Pertussis, Pertussis Immunisation
Conditions
Keywords
B. pertussis Vaccine, BPZE1, Immunogenicity, Safety
Brief summary
This is a randomized, partially blind, placebo controlled, clinical trial evaluating a single intranasal dose of BPZE1 in healthy adults. The study will evaluate a lyophilized formulation of the product, with the goal of testing for the optimal dose for subsequent clinical trials. Fifty healthy adults, 18-49 years of age will be randomized to one of the four following treatment groups in a 3:3:3:1 ratio: 10\^7 colony forming units (CFU) of BPZE1 administered by VaxINator device, 10\^9 CFU of BPZE1 administered by VaxINator device, placebo administered by VaxINator device, 10\^9 CFU of BPZE1 administered by needleless tuberculin syringe. Study duration will be approximately 12 months with a subject participation duration of approximately 6 months. The primary objective of this study is to assess the safety and tolerability of a single intranasal dose of either 10\^7 or 10\^9 CFU of lyophilized BPZE1 vaccine.
Detailed description
This is a phase 2a, single center, randomized, partially blind, placebo controlled, clinical trial evaluating a single intranasal dose of either 10\^7 colony forming units (CFU) or 10\^9 CFU of BPZE1 in healthy adults. The study will evaluate a lyophilized formulation of the product, with the goal of testing for the optimal dose for subsequent clinical trials. Fifty healthy adults, 18-49 years of age will be randomized to one of the four following treatment groups in a 3:3:3:1 ratio: 10\^7 CFU of BPZE1 administered by VaxINator device, 10\^9 CFU of BPZE1 administered by VaxINator device, placebo administered by VaxINator device, 10\^9 CFU of BPZE1 administered by needleless tuberculin syringe. Study duration will be approximately 12 months with a subject participation duration of approximately 6 months. The primary objective of this study is to assess the safety and tolerability of a single intranasal dose of either 10\^7 or 10\^9 CFU of lyophilized BPZE1 vaccine. The secondary objectives of this study are: 1) to assess the humoral immunogenicity of lyophilized BPZE1 vaccine at Day 15, Day 29 and Day 181 following receipt of one intranasal dose of 10\^7 or 10\^9 CFU of BPZE1; 2) to assess mucosal immunogenicity of lyophilized BPZE1 vaccine at Day 29 and Day 181 following receipt of one intranasal dose of 10\^7 or 10\^9 CFU of BPZE1; 3) to evaluate nasal clearance of BPZE1 by culture at Day 29 (and if still positive, at Day 46) following receipt of one intranasal dose of lyophilized BPZE1 vaccine of 10\^7 or 10\^9 CFU of BPZE1.
Interventions
BIOLOGICALBPZE1
Lyophilized, live-attenuated Bordetella pertussis vaccine reconstituted with sterile water for injection (SWFI) and administered as a single intranasal dose of either 10\^7 colony forming units (CFU) or 10\^9 CFU.
OTHERPlacebo
The placebo consists of the same constituents in the same quantities as the BPZE1 investigational vaccines, absent the attenuated B. pertussis cells, reconstituted with sterile water for injection (SWFI).
Sponsors
National Institute of Allergy and Infectious Diseases (NIAID)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
Yes
Inclusion criteria
Subjects eligible to participate in this study must meet all inclusion criteria: 1. Provide written informed consent prior to initiation of any study procedures. 2. Able to understand and comply with planned study procedures and be available for all study visits. 3. Males or non-pregnant females, 18-49 years of age, inclusive. 4. In good health\*. \*As determined by medical history and physical examination to evaluate acute or currently ongoing chronic medical diagnoses or conditions, defined as those that have been present for at least 90 days that would affect the assessment of the safety of subjects or the immunogenicity of study vaccinations. Chronic medical diagnoses or conditions should be stable for the last 60 days. This includes no change in chronic prescription medication, dose, or frequency because of deterioration of the chronic medical diagnosis or condition in the 60 days prior to enrollment. Any prescription change that is due to change of health care provider, insurance company, etc., or that is done for financial reasons, if it is in the same class of medication, will not be considered a deviation of this inclusion criterion. Any change in prescription medication due to improvement of a disease outcome, as determined by the site principal investigator or appropriate sub-investigator, will not be considered a deviation of this inclusion criterion. Subjects may be on chronic or as needed (prn) medications if, in the opinion of the site principal investigator or appropriate sub-investigator, they pose no additional risk to subject safety or assessment of reactogenicity and immunogenicity and do not indicate a worsening of medical diagnosis or condition. Similarly, medication changes after enrollment and study vaccination are acceptable provided there was no deterioration in the subject's chronic medical condition that necessitated a medication change, and there is no additional risk to the subject or interference with the evaluation of responses to study vaccination. Note: Topical and inhaled medications (with the exception of inhaled or nasal corticosteroids within 30 days prior to enrollment), herbals, vitamins, and supplements are permitted. 5. Oral temperature is \< / = 100 degrees Fahrenheit. 6. Pulse is 45 to 100 bpm, inclusive\*. \*Pulse can be 45 to 50 bpm, inclusive, if no other symptoms are present. Otherwise, pulse should be 50-100 bpm. 7. Systolic blood pressure is 85 to 150 mm Hg, inclusive. 8. Diastolic blood pressure is 55 to 95 mm Hg, inclusive. 9. White blood cell count is 3,900 cells/microliter or greater\*. \*Abnormalities in white blood count, hemoglobin, platelet count, alanine aminotransferase, and serum creatinine that are suspected to be due to laboratory anomalies may be repeated once to ensure accuracy; additionally, otherwise eligible subjects with grade 1 abnormalities in these values may be considered for enrollment if, in the opinion of the investigator (or clinician on the 1572), the abnormalities are not clinically significant and do not pose additional risk to the study or the volunteer. 10. Hemoglobin is 13.0 g/dL or greater (men) or 11.8 g/dL or greater (women)\*. \*Abnormalities in white blood count, hemoglobin, platelet count, alanine aminotransferase, and serum creatinine that are suspected to be due to laboratory anomalies may be repeated once to ensure accuracy; additionally, otherwise eligible subjects with grade 1 abnormalities in these values may be considered for enrollment if, in the opinion of the investigator (or clinician on the 1572), the abnormalities are not clinically significant and do not pose additional risk to the study or the volunteer. 11. Platelet count is 135,000 cells/microliter or greater\*. \*Abnormalities in white blood count, hemoglobin, platelet count, alanine aminotransferase, and serum creatinine that are suspected to be due to laboratory anomalies may be repeated once to ensure accuracy; additionally, otherwise eligible subjects with grade 1 abnormalities in these values may be considered for enrollment if, in the opinion of the investigator (or clinician on the 1572), the abnormalities are not clinically significant and do not pose additional risk to the study or the volunteer. 12. Alanine aminotransferase is \< 45 U/L (women) or 62 U/L (men)\*. \*Abnormalities in white blood count, hemoglobin, platelet count, alanine aminotransferase, and serum creatinine that are suspected to be due to laboratory anomalies may be repeated once to ensure accuracy; additionally, otherwise eligible subjects with grade 1 abnormalities in these values may be considered for enrollment if, in the opinion of the investigator (or clinician on the 1572), the abnormalities are not clinically significant and do not pose additional risk to the study or the volunteer. 13. Serum creatinine is \< / = 1.25 mg/dL (men) or 1.11 mg/dL (women)\*. \*Abnormalities in white blood count, hemoglobin, platelet count, alanine aminotransferase, and serum creatinine that are suspected to be due to laboratory anomalies may be repeated once to ensure accuracy; additionally, otherwise eligible subjects with grade 1 abnormalities in these values may be considered for enrollment if, in the opinion of the investigator (or clinician on the 1572), the abnormalities are not clinically significant and do not pose additional risk to the study or the volunteer. 14. Negative serum HIV antibody assay. 15. Women of childbearing potential\* must use an acceptable contraception method\*\* from 30 days before study vaccination until 60 days after vaccination. \*Not sterilized via tubal ligation, bilateral oophorectomy, salpingectomy, hysterectomy, or successful Essure(R) placement (permanent, non-surgical, non-hormonal sterilization) with documented radiological confirmation test at least 90 days after the procedure, and still menstruating or \< 1 year has passed since the last menses if menopausal. * Includes non-male sexual relationships, abstinence from sexual intercourse with a male partner, monogamous relationship with vasectomized partner who has been vasectomized for 180 days or more prior to the subject receiving study vaccination, barrier methods such as condoms or diaphragms/cervical caps with spermicide, effective intrauterine devices, NuvaRing(R), and licensed hormonal methods such as implants, injectables or oral contraceptives (the pill). 16. Women of childbearing potential must have a negative urine or serum pregnancy test within 24 hours prior to study vaccination.
Exclusion criteria
1. Have immunosuppression as a result of an underlying illness or treatment, or use of anticancer chemotherapy or radiation therapy (cytotoxic) within 3 years prior to study vaccination. 2. Have known or suspected active chronic autoinflammatory condition. 3. Have known active neoplastic disease (excluding non-melanoma skin cancer) or a history of any hematologic malignancy. 4. Have a history of persistent asthma, major anatomic nasopharyngeal abnormality, or sinus polyp disease due to chronic sinusitis\*. \*If a patient has a history of nasopharyngeal surgery such as, but not limited to rhinoplasty, tonsillectomy or sinus surgery, adequate healing time per the judgement of the investigator must occur prior to enrollment. 5. Have known hepatitis B or hepatitis C infection. 6. Have a history of alcohol or drug abuse within 5 years prior to study vaccination. 7. Currently untreated or clinically unstable (in the opinion of the investigator) schizophrenia, bipolar disease, or other psychiatric diagnosis that may interfere with subject compliance or safety evaluations. 8. Have been hospitalized for psychiatric illness, history of suicide attempt, or confinement for danger to self or others within 5 years prior to study vaccination. 9. Have received corticosteroids (including oral, parenteral, inhaled, nasal, or intra-articular) of any dose within 30 days prior to study vaccination. 10. Individual with PT serum IgG antibodies \> / = 20 IU/mL and / or PRN serum IgG antibodies \> / = 125 IU/ml. 11. Unwilling to refrain from smoking tobacco for 28 days post vaccination. 12. Receipt of immunoglobulin or blood derived products within 90 days of enrollment. 13. Receipt of a vaccine against pertussis in the past 2 years. 14. Receipt of a live vaccine within 30 days of study vaccination or an inactivated vaccine within 14 days of study vaccination. 15. Planned vaccination with a licensed vaccine within 28 days of study vaccination. 16. History of severe allergic reaction (e.g., anaphylaxis) or Bell's palsy, or Guillain-Barre syndrome, after a previous dose of any diphtheria toxoid-tetanus toxoid-, or pertussis-containing vaccine, or encephalopathy within 7 days of administration of a previous pertussis containing vaccine. 17. History of a progressive neurologic disorder. 18. In close contact\* with children less than 1 year of age or contact with persons with known immunocompromising conditions. \*Close contact includes sharing a household, serving as a healthcare worker, or working professionally in settings with repeated exposures. 19. Receipt of B. pertussis-active antibiotics\* within 7 days prior to vaccination. \*B. pertussis active antibiotics include macrolides, fluoroquinolones, trimethoprim-sulfamethoxazole, tetracyclines. 20. Known hypersensitivity to any component of the study vaccine. 21. Hypersensitivity to azithromycin, which may be used in the event of ongoing BPZE1 colonization. 22. Any condition that, in the opinion of the investigator, might interfere with objectives of the study or safety to the individual. 23. Acute illness, including temperature \> 100 degrees Fahrenheit within one week prior to vaccination\*. * Enrollment may be postponed if acute illness occurs; subjects must remain within the screening window, however, and must be rescreened if \> 30 days elapses prior to enrollment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Day 1 through Day 15 | The solicited systemic reactogenicity events included fever, feverishness, fatigue, malaise, myalgia, arthralgia, headache, and rash/hypersensitivity. |
| Number of Participants Experiencing Adverse Events of Special Interest (AESIs) | Day 1 through Day 29 | AESIs included medically attended wheezing events given the route of study product administration and the nature of the study product. |
| Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs) | Day 1 through Day 181 | NOCMCs are defined as new medical conditions, not present at the time of screening or enrollment, that require ongoing medical care and intervention. |
| Number of Participants Experiencing Serious Adverse Events (SAEs) | Day 1 through Day 181 | An adverse event was considered serious if, in the view of either the site principal investigator or sponsor, it resulted in any of the following outcomes: death, a life-threatening adverse event, inpatient hospitalization or prolongation of existing hospitalization, a persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, or a congenital anomaly/birth defect, or, when, based upon appropriate medical judgment they may jeopardize the participant and may require medical or surgical intervention to prevent one of the outcomes listed in this definition. |
| Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Day 1 through Day 15 | The solicited local reactogenicity events included runny nose, stuffy nose/congestion, nasal pain/irritation, epistaxis, sneezing, sinus pressure/pain, sore/irritated throat, cough, and shortness of breath/wheezing. |
| Number of Participants Experiencing Unsolicited Non-Serious AEs | Day 1 through Day 29 | Adverse events were defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product regardless of its causal relationship to the study treatment. Unsolicited non-serious AEs were documented and reported from the time of vaccination through Day 29. |
| Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Day 1 through Day 15 | Solicited local reactogenicity events include runny nose, stuffy nose/congestion, nasal pain/irritation, epistaxis, sneezing, sinus pressure/pain, sore/irritated throat, cough, and shortness of breath/wheezing. They were graded as grade 1 (mild), grade 2 (moderate), or grade 3 (severe). Severe local events were those that required medical care or caused significant discomfort that prevented daily activity, including sore/irritated throat preventing eating or drinking and cough preventing sleep. Severe epistaxis events were bleeding events that required a medical encounter. Severe stuffy nose/congestion events caused the participant to be unable to breathe through the nose or to seek medical care. |
| Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Day 1 through Day 15 | Solicited systemic reactogenicity events include fever, feverishness, fatigue, malaise, myalgia, arthralgia, headache, and rash/hypersensitivity. They were graded as grade 1 (mild), grade 2 (moderate), and grade 3 (severe). For all symptoms except rash and fever, an event was considered severe if it caused significant interference and prevented daily activity. Severe rash/hypersensitivity events were those that caused generalized urticaria, anaphylaxis, or angioedema or localized urticaria that required medical encounter. Severe fever was a temperature exceeding 38.9°C. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. The geometric mean FIM-IgA titer and FIM-IgG titer were calculated for each study arm. |
| Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen via a bead-based assay. The geometric mean PRN-IgA titer and PRN-IgG titer were calculated for each study arm. |
| Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) pertussis antigen via a bead-based assay. The geometric mean PT-IgA titer and PT-IgG titer were calculated for each study arm. |
| Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin, filamentous hemagglutinin, pertactin, and fimbriae 2/3 pertussis antigens. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA or antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to at least one pertussis antigen at each and across immunogenicity timepoints (Day 15, Day 29, and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin, filamentous hemagglutinin, pertactin, and fimbriae 2/3 pertussis antigens. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA levels or antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to at least two pertussis antigens at each and across all immunogenicity timepoints (Day 15, Day 29, and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 29 and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis vaccine antigens via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted to at least one pertussis antigen at each and any immunogenicity timepoint was calculated. |
| Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures | Day 29 and Day 46 | Colonization of live B. pertussis organism was assessed from a nasopharyngeal swab performed 28 days after vaccine administration (Day 29) to ensure all participants were cleared of colonization. Standard microbiologic techniques were used to assess the presence of B. pertussis by culture. If any participants were positive for B. pertussis culture at Day 29, they were asked to return at Day 46 for a repeat culture. If the participant was not positive for B. pertussis at Day 29, no subsequent nasopharyngeal samples for culture were collected. |
| Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA levels and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA and IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to FHA-IgA and FHA-IgG at any and each immunogenicity timepoint (Day 15, Day 29, and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA levels and IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to FIM-IgA or FIM-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or and Day 181) was calculated. |
| Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Screening, Day 29, Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FHA-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm. |
| Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Screening, Day 29, Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FHA-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm. |
| Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Screening, Day 29, Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PRN-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm. |
| Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Screening, Day 29, and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PT-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm. |
| Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. The geometric mean FHA-IgA titer and FHA-IgG titer were calculated for each study arm. |
| Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA and antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to PRN-IgA and PRN-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or Day 181) were calculated. |
| Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA/IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to PT-IgA and PT-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 29 and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted FHA-IgA at each and any immunogenicity timepoint (Day 29 or Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 29 and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted FIM-IgA at each and any immunogenicity timepoint (Day 29 and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 29 and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted PRN-IgA at each and any immunogenicity timepoint (Day 29 and Day 181) was calculated. |
| Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 29 and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was calculated for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted PT-IgA at each immunogenicity timepoint (Day 29 and Day 181) was calculated. |
| Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Screening, Day 29, Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FIM-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm. |
| Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Screening, Day 29, and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FIM-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm. |
| Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Screening, Day 29, and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PRN-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm. |
| Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Screening, Day 29, and Day 181 | Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PT-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm. |
| Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen. The fold rise in FHA-IgA from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm. |
| Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen. The fold rise in FIM-IgA and FIM-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm. |
| Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen. The fold rise in PRN-IgA and PRN-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm. |
| Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | Day 1, Day 15, Day 29, and Day 181 | Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) pertussis antigen. The fold rise in PT-IgA and PT-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm. |
Countries
United States
Participant flow
Recruitment details
The study population includes 50 healthy adults,18-49 years of age, inclusive, who meet all eligibility criteria. Participants were enrolled between 01NOV2018 and 06DEC2019.
Participants by arm
| Arm | Count |
|---|---|
| BPZE1 10^7 CFU by VaxINator 800 microliters (10\^7 CFU) of BPZE1 administered intranasally with the VaxINator device on Day 1. | 15 |
| BPZE1 10^9 CFU by VaxINator 800 microliters (10\^9 CFU) of BPZE1 administered intranasally with the VaxINator device on Day 1. | 15 |
| BPZE1 10^9 CFU by Syringe 800 microliters (10\^9 CFU) of BPZE1 administered intranasally with a needleless tuberculin syringe on Day 1. | 5 |
| Placebo by VaxINator 800 microliters of Placebo administered intranasally with the VaxINator device on Day 1. | 15 |
| Total | 50 |
Baseline characteristics
| Characteristic | BPZE1 10^7 CFU by VaxINator | BPZE1 10^9 CFU by VaxINator | BPZE1 10^9 CFU by Syringe | Placebo by VaxINator | Total |
|---|---|---|---|---|---|
| Age, Continuous | 30.3 years STANDARD_DEVIATION 10.7 | 29.1 years STANDARD_DEVIATION 8.8 | 30.2 years STANDARD_DEVIATION 8.9 | 30.9 years STANDARD_DEVIATION 9.5 | 30.1 years STANDARD_DEVIATION 9.3 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 1 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 15 Participants | 15 Participants | 5 Participants | 14 Participants | 49 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 5 Participants | 1 Participants | 0 Participants | 2 Participants | 8 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 10 Participants | 14 Participants | 5 Participants | 13 Participants | 42 Participants |
| Sex: Female, Male Female | 9 Participants | 9 Participants | 2 Participants | 11 Participants | 31 Participants |
| Sex: Female, Male Male | 6 Participants | 6 Participants | 3 Participants | 4 Participants | 19 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 15 | 0 / 15 | 0 / 5 | 0 / 15 |
| other Total, other adverse events | 11 / 15 | 14 / 15 | 3 / 5 | 13 / 15 |
| serious Total, serious adverse events | 0 / 15 | 0 / 15 | 0 / 5 | 0 / 15 |
Outcome results
Primary
Number of Participants Experiencing Adverse Events of Special Interest (AESIs)
AESIs included medically attended wheezing events given the route of study product administration and the nature of the study product.
Time frame: Day 1 through Day 29
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Adverse Events of Special Interest (AESIs) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Adverse Events of Special Interest (AESIs) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Adverse Events of Special Interest (AESIs) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Adverse Events of Special Interest (AESIs) | 0 Participants |
Primary
Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs)
NOCMCs are defined as new medical conditions, not present at the time of screening or enrollment, that require ongoing medical care and intervention.
Time frame: Day 1 through Day 181
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs) | 1 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing New Onset Chronic Medical Conditions (NOCMCs) | 0 Participants |
Primary
Number of Participants Experiencing Serious Adverse Events (SAEs)
An adverse event was considered serious if, in the view of either the site principal investigator or sponsor, it resulted in any of the following outcomes: death, a life-threatening adverse event, inpatient hospitalization or prolongation of existing hospitalization, a persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions, or a congenital anomaly/birth defect, or, when, based upon appropriate medical judgment they may jeopardize the participant and may require medical or surgical intervention to prevent one of the outcomes listed in this definition.
Time frame: Day 1 through Day 181
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Serious Adverse Events (SAEs) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Serious Adverse Events (SAEs) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Serious Adverse Events (SAEs) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Serious Adverse Events (SAEs) | 0 Participants |
Primary
Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events
Solicited local reactogenicity events include runny nose, stuffy nose/congestion, nasal pain/irritation, epistaxis, sneezing, sinus pressure/pain, sore/irritated throat, cough, and shortness of breath/wheezing. They were graded as grade 1 (mild), grade 2 (moderate), or grade 3 (severe). Severe local events were those that required medical care or caused significant discomfort that prevented daily activity, including sore/irritated throat preventing eating or drinking and cough preventing sleep. Severe epistaxis events were bleeding events that required a medical encounter. Severe stuffy nose/congestion events caused the participant to be unable to breathe through the nose or to seek medical care.
Time frame: Day 1 through Day 15
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Runny nose | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Nasal pain/irritation | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sore/irritated throat | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sneezing | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Cough | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Epistaxis | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Shortness of breath/wheezing | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Stuffy nose/congestion | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sinus pressure/pain | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sore/irritated throat | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Cough | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Stuffy nose/congestion | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Shortness of breath/wheezing | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Nasal pain/irritation | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Runny nose | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Epistaxis | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sneezing | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sinus pressure/pain | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Nasal pain/irritation | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Cough | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sneezing | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Shortness of breath/wheezing | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Stuffy nose/congestion | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sore/irritated throat | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sinus pressure/pain | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Epistaxis | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Runny nose | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Shortness of breath/wheezing | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Runny nose | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Stuffy nose/congestion | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Nasal pain/irritation | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Epistaxis | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sneezing | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sore/irritated throat | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Cough | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Local Reactogenicity Adverse Events | Sinus pressure/pain | 0 Participants |
Primary
Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs
Solicited systemic reactogenicity events include fever, feverishness, fatigue, malaise, myalgia, arthralgia, headache, and rash/hypersensitivity. They were graded as grade 1 (mild), grade 2 (moderate), and grade 3 (severe). For all symptoms except rash and fever, an event was considered severe if it caused significant interference and prevented daily activity. Severe rash/hypersensitivity events were those that caused generalized urticaria, anaphylaxis, or angioedema or localized urticaria that required medical encounter. Severe fever was a temperature exceeding 38.9°C.
Time frame: Day 1 through Day 15
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Headache | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Feverishness | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Feverishness | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Headache | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Feverishness | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Headache | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Headache | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Feverishness | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Severe Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 0 Participants |
Primary
Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs)
The solicited local reactogenicity events included runny nose, stuffy nose/congestion, nasal pain/irritation, epistaxis, sneezing, sinus pressure/pain, sore/irritated throat, cough, and shortness of breath/wheezing.
Time frame: Day 1 through Day 15
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sore/irritated throat | 4 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sinus pressure/pain | 1 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Shortness of breath/wheezing | 2 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Epistaxis | 1 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Nasal pain/irritation | 1 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Stuffy nose/congestion | 8 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Cough | 6 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sneezing | 4 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Runny nose | 6 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sneezing | 5 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sore/irritated throat | 4 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sinus pressure/pain | 4 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Stuffy nose/congestion | 8 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Runny nose | 7 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Nasal pain/irritation | 1 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Shortness of breath/wheezing | 1 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Cough | 2 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Epistaxis | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sneezing | 1 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Runny nose | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Stuffy nose/congestion | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Nasal pain/irritation | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Epistaxis | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sinus pressure/pain | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sore/irritated throat | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Cough | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Shortness of breath/wheezing | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sore/irritated throat | 3 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Epistaxis | 1 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Nasal pain/irritation | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Shortness of breath/wheezing | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Cough | 2 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Stuffy nose/congestion | 6 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sinus pressure/pain | 2 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Sneezing | 3 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Local Reactogenicity Adverse Events (AEs) | Runny nose | 5 Participants |
Primary
Number of Participants Experiencing Solicited Systemic Reactogenicity AEs
The solicited systemic reactogenicity events included fever, feverishness, fatigue, malaise, myalgia, arthralgia, headache, and rash/hypersensitivity.
Time frame: Day 1 through Day 15
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fever | 1 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Feverishness | 1 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 4 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 3 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 0 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Headache | 5 Participants |
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 1 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 3 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 2 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Feverishness | 2 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Headache | 9 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 3 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 4 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Headache | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 2 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 1 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 1 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 1 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Feverishness | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fatigue (tiredness) | 5 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Malaise (general unwell feeling) | 2 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Feverishness | 1 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Fever | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Myalgia (body aches/muscular pain) | 1 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Rash/hypersensitivity | 0 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Headache | 8 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Solicited Systemic Reactogenicity AEs | Arthralgia (joint pain) | 1 Participants |
Primary
Number of Participants Experiencing Unsolicited Non-Serious AEs
Adverse events were defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product regardless of its causal relationship to the study treatment. Unsolicited non-serious AEs were documented and reported from the time of vaccination through Day 29.
Time frame: Day 1 through Day 29
Population: The safety population consists of all participants who received the study vaccine and for whom any data on safety were available
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Number of Participants Experiencing Unsolicited Non-Serious AEs | 3 Participants |
| BPZE1 10^9 CFU by VaxINator | Number of Participants Experiencing Unsolicited Non-Serious AEs | 3 Participants |
| BPZE1 10^9 CFU by Syringe | Number of Participants Experiencing Unsolicited Non-Serious AEs | 1 Participants |
| Placebo by VaxINator | Number of Participants Experiencing Unsolicited Non-Serious AEs | 5 Participants |
Secondary
Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM)
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen. The fold rise in FIM-IgA and FIM-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 15 | 1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 29 | 2.1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 181 | 1.4 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 15 | 1.1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 29 | 1.6 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 181 | 1.2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 181 | 2.8 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 15 | 1.5 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 15 | 1.1 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 181 | 2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 29 | 2.2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 29 | 2.6 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 29 | 3.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 181 | 2.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 15 | 1 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 181 | 1.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 29 | 1.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 15 | 1.1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 29 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 181 | 0.9 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 29 | 0.7 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgG - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Fimbriae 2/3 (FIM) | IgA - Day 181 | 1.1 fold rise |
Secondary
Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN)
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen. The fold rise in PRN-IgA and PRN-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who have received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 29 | 0.9 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 15 | 0.7 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 29 | 1.7 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 181 | 0.9 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 181 | 1.5 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 15 | 1 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 29 | 2.3 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 181 | 2.5 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 15 | 1.5 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 29 | 3.2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 15 | 1.6 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 181 | 3.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 15 | 1.1 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 181 | 1.5 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 15 | 0.9 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 29 | 2.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 181 | 0.9 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 29 | 1.2 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 181 | 0.9 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 15 | 1.1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 29 | 1.1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgA - Day 181 | 1.3 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 15 | 1.1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertactin (PRN) | IgG - Day 29 | 0.9 fold rise |
Secondary
Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT)
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) pertussis antigen. The fold rise in PT-IgA and PT-IgG from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who have received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 15 | 1.3 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 29 | 1.4 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 181 | 1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 15 | 1.1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 29 | 1.5 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 181 | 1.9 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 181 | 1.4 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 15 | 1.2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 15 | 1.9 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 181 | 1.8 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 29 | 1.9 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 29 | 1.4 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 29 | 1.4 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 181 | 1 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 15 | 0.7 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 181 | 1.1 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 29 | 1.5 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 29 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 181 | 0.9 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 29 | 1.2 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgG - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline of Serum IgA and Serum IgG ELISA Titers to Pertussis Toxin (PT) | IgA - Day 181 | 1.4 fold rise |
Secondary
Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA)
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to perform a bead-based assay to measure serum IgA and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen. The fold rise in FHA-IgA from baseline was calculated for each participant and the geometric mean of the fold rise was calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 15 | 0.8 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 29 | 1.4 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 181 | 1.2 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 15 | 1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 29 | 1.7 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 181 | 1.8 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 181 | 1.7 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 15 | 1.2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 15 | 1.3 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 181 | 2.1 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 29 | 2.5 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 29 | 1.5 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 29 | 3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 181 | 2.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 15 | 0.8 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 181 | 1.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 29 | 1.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 15 | 1.4 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 29 | 0.9 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 181 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 29 | 0.8 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgG - Day 15 | 1.1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 15 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Baseline Serum IgA and Serum IgG ELISA Titers to Filamentous Hemagglutinin (FHA) | IgA - Day 181 | 1.1 fold rise |
Secondary
Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FHA-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.2 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 181 | 0.8 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 181 | 2 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.7 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 181 | 0.4 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Filamentous Hemagglutinin-specific IgA (FHA-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.2 fold rise |
Secondary
Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FIM-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.7 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.1 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 181 | 6.7 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 29 | 6.2 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.7 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.6 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Fimbriae-Specific IgA (FIM-IgA) to Total IgA by Nasal Aspirate | Day 181 | 0.8 fold rise |
Secondary
Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PRN-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.1 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.1 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 181 | 3.5 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 29 | 3.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.3 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 181 | 3.3 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.8 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertactin-Specific IgA (PRN-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1 fold rise |
Secondary
Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PT-IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. The geometric mean fold rise of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.9 fold rise |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.3 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.6 fold rise |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 29 | 1.4 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 29 | 0.9 fold rise |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.6 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 29 | 2.2 fold rise |
| Placebo by VaxINator | Geometric Mean Fold Rise From Screening of the Ratio of Pertussis Toxin-Specific IgA (PT-IgA) to Total IgA by Nasal Aspirate | Day 181 | 1.2 fold rise |
Secondary
Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. The geometric mean FHA-IgA titer and FHA-IgG titer were calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 15 | 19.99 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 181 | 5.13 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 15 | 3.06 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 29 | 33.49 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 181 | 32.73 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 1 | 19.59 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 1 | 3.83 Titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 29 | 5.27 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 181 | 32.92 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 1 | 19.65 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 29 | 29.4 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 29 | 8.67 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 15 | 23.19 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 15 | 4.66 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 181 | 7.52 Titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 1 | 3.54 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 15 | 12.78 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 29 | 20.9 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 181 | 19.62 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 181 | 2.81 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 15 | 1.75 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 1 | 1.21 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 1 | 16.59 Titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 29 | 3.68 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 181 | 13.84 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 15 | 2.62 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 29 | 2.21 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 181 | 3.3 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 29 | 11.96 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgA - Day 1 | 2.71 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 1 | 12.81 Titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Filamentous Hemagglutinin | IgG - Day 15 | 14.14 Titer |
Secondary
Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. The geometric mean FIM-IgA titer and FIM-IgG titer were calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 181 | 80.27 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 29 | 7.07 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 29 | 84.12 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 1 | 51.71 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 1 | 3.40 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 181 | 5.30 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 15 | 3.27 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 15 | 56.73 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 15 | 4.26 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 29 | 41.30 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 181 | 45.32 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 15 | 24.17 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 1 | 3.94 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 29 | 8.84 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 181 | 8.01 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 1 | 15.98 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 1 | 1.85 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 29 | 5.92 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 29 | 160.50 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 1 | 129.14 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 181 | 159.90 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 15 | 2.04 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 15 | 129.80 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 181 | 4.29 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 181 | 21.84 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 1 | 2.68 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 15 | 2.68 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 29 | 1.79 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgA - Day 181 | 2.69 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 1 | 24.48 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 15 | 25.30 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Fimbriae 2/3 | IgG - Day 29 | 24.35 titer |
Secondary
Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen via a bead-based assay. The geometric mean PRN-IgA titer and PRN-IgG titer were calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 1 | 10.53 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 15 | 7.69 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 29 | 9.32 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 181 | 7.90 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 1 | 38.69 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 15 | 38.59 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 29 | 65.11 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 181 | 53.49 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 15 | 26.42 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 1 | 17.68 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 15 | 6.21 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 181 | 44.92 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 29 | 41.07 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 181 | 12.19 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 29 | 12.38 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 1 | 3.82 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 29 | 58.20 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 29 | 8.02 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 181 | 5.43 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 1 | 48.47 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 15 | 41.42 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 181 | 42.76 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 1 | 3.57 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 15 | 4.07 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 29 | 3.19 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 181 | 4.10 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 15 | 3.22 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgA - Day 1 | 2.88 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 1 | 8.81 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 181 | 11.36 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 29 | 7.63 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertactin | IgG - Day 15 | 9.58 titer |
Secondary
Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure serum IgA levels and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) pertussis antigen via a bead-based assay. The geometric mean PT-IgA titer and PT-IgG titer were calculated for each study arm.
Time frame: Day 1, Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 1 | 0.66 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 15 | 0.86 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 29 | 0.91 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 181 | 0.82 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 1 | 3.36 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 15 | 3.65 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 29 | 5.20 titer |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 181 | 6.39 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 15 | 4.77 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 1 | 4.00 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 15 | 0.92 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 181 | 5.67 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 29 | 5.41 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 181 | 0.86 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 29 | 0.95 titer |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 1 | 0.48 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 29 | 15.01 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 29 | 1.29 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 181 | 0.91 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 1 | 10.10 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 15 | 7.36 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 181 | 10.86 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 1 | 0.91 titer |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 15 | 0.88 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 29 | 0.99 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 181 | 1.28 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 15 | 0.80 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgA - Day 1 | 0.82 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 1 | 3.41 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 181 | 3.09 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 29 | 3.42 titer |
| Placebo by VaxINator | Geometric Mean Titer by Serum IgA and Serum IgG to Pertussis Toxin | IgG - Day 15 | 3.38 titer |
Secondary
Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FHA-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Screening | 0.0154 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0178 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.011 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0263 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0229 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Screening | 0.0133 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0109 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0069 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Screening | 0.0251 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Screening | 0.0147 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0154 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FHA-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0185 Titer Ratio |
Secondary
Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of FIM-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Screening | 0.0023 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0039 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0021 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Screening | 0.0012 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0073 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0078 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0074 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Screening | 0.0073 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0052 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0015 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0017 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal FIM-IgA to Total IgA by Nasal Aspirate | Screening | 0.0023 Titer Ratio |
Secondary
Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PRN-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Screening | 0.0167 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0157 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0186 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Screening | 0.007 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0244 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0231 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0083 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Screening | 0.0063 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0207 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Screening | 0.0106 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0102 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PRN-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0087 Titer Ratio |
Secondary
Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The ratio of PT-IgA to total mucosal IgA was computed for each participant and the geometric mean of the ratio was calculated for each study arm.
Time frame: Screening, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who have received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (GEOMETRIC_MEAN) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Screening | 0.0014 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0016 Titer Ratio |
| BPZE1 10^7 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0013 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Screening | 0.0011 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0017 Titer Ratio |
| BPZE1 10^9 CFU by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0015 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0018 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Screening | 0.0021 Titer Ratio |
| BPZE1 10^9 CFU by Syringe | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0033 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Screening | 0.0011 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 181 | 0.0013 Titer Ratio |
| Placebo by VaxINator | Geometric Mean Titer Ratio of Mucosal PT-IgA to Total IgA by Nasal Aspirate | Day 29 | 0.0024 Titer Ratio |
Secondary
Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to filamentous hemagglutinin (FHA) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted FHA-IgA at each and any immunogenicity timepoint (Day 29 or Day 181) was calculated.
Time frame: Day 29 and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 181 | 8 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 29 | 20 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Any Time Point | 20 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Any Time Point | 67 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 29 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 181 | 53 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 181 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Any Time Point | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 29 | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Any Time Point | 40 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 29 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Mucosal IgA Levels | Day 181 | 43 percentage of participants |
Comparison: Any time pointp-value: 0.271Barnard's exact test
Comparison: Any time pointp-value: 0.226Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA levels and serum IgG levels (in ELISA units/mL) to filamentous hemagglutinin (FHA) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA and IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to FHA-IgA and FHA-IgG at any and each immunogenicity timepoint (Day 15, Day 29, and Day 181) was calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 20 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 17 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 47 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 7 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 33 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 33 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 7 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 20 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 67 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 67 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 40 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 21 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 33 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Filamentous Hemagglutinin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 7 percentage of participants |
Comparison: IgA, any time pointp-value: 0.526Barnard's exact test
Comparison: IgA, any time pointp-value: 0.1Barnard's exact test
Comparison: IgG, any time pointp-value: 0.055Barnard's exact test
Comparison: IgG, any time pointp-value: 0.023Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to fimbriae 2/3 (FIM) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted FIM-IgA at each and any immunogenicity timepoint (Day 29 and Day 181) was calculated.
Time frame: Day 29 and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 181 | 8 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Any Time Point | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 29 | 27 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 29 | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Any Time Point | 80 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 181 | 80 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Any Time Point | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 181 | 60 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Any Time Point | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 181 | 14 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Mucosal IgA Levels | Day 29 | 7 percentage of participants |
Comparison: Any time pointp-value: 0.783Barnard's exact test
Comparison: Any time pointp-value: 0.001Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to fimbriae 2/3 (FIM) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA levels and IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to FIM-IgA or FIM-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or and Day 181) was calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 0 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 0 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 20 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 20 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 8 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 17 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 13 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 20 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 53 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Fimbriae 2/3 as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 0 percentage of participants |
Comparison: IgA, any time pointp-value: 0.174Barnard's exact test
Comparison: IgA, any time pointp-value: 0.006Barnard's exact test
Comparison: IgG, any time pointp-value: 0.745Barnard's exact test
Comparison: IgG, any time pointp-value: 0.023Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin, filamentous hemagglutinin, pertactin, and fimbriae 2/3 pertussis antigens. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA or antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to at least one pertussis antigen at each and across immunogenicity timepoints (Day 15, Day 29, and Day 181) was calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 67 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 33 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 53 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 42 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 67 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 93 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 93 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 100 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 60 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 57 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 40 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 73 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 47 percentage of participants |
Comparison: At any time pointp-value: 0.807Barnard's exact test
Comparison: At any time pointp-value: 0.043Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis vaccine antigens via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted to at least one pertussis antigen at each and any immunogenicity timepoint was calculated.
Time frame: Day 29 and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Any Time Point | 60 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 181 | 50 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 29 | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Any Time Point | 93 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 181 | 93 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 29 | 73 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Any Time Point | 80 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 181 | 80 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Any Time Point | 80 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 181 | 50 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to One or More Pertussis Antigens as Measured by the Ratio of Antigen-Specific Mucosal IgA Levels to Total Mucosal IgA Levels | Day 29 | 73 percentage of participants |
Comparison: Any time pointp-value: 1Barnard's exact test
Comparison: Any time pointp-value: 0.009Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertactin (PRN) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was computed for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted PRN-IgA at each and any immunogenicity timepoint (Day 29 and Day 181) was calculated.
Time frame: Day 29 and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 29 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 181 | 8 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Any Time Point | 13 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 181 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Any Time Point | 53 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Any Time Point | 80 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 181 | 80 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 29 | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Any Time Point | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Mucosal IgA Levels | Day 181 | 21 percentage of participants |
Comparison: Any time pointp-value: 0.745Barnard's exact test
Comparison: Any time pointp-value: 0.068Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertactin (PRN) pertussis antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA and antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to PRN-IgA and PRN-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or Day 181) were calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 17 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 33 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 25 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 7 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 0 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 13 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 67 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 33 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 80 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 67 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 53 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 36 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertactin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 20 percentage of participants |
Comparison: IgA, any time pointp-value: 0.023Barnard's exact test
Comparison: IgA, any time pointp-value: 0.142Barnard's exact test
Comparison: IgG, any time pointp-value: 0.526Barnard's exact test
Comparison: IgG, any time pointp-value: 0.142Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels
Nasal aspirate samples were collected from all participants at screening (baseline), Day 29, and Day 181 to measure total mucosal IgA levels via ELISA assay and mucosal IgA levels to pertussis toxin (PT) pertussis antigen via a bead-based assay. Total mucosal IgA levels were reported in µg/mL; antigen-specific IgA results were reported in ELISA units/mL. The titer ratio of antigen-specific IgA to total mucosal IgA was calculated for each participant at each time point, and the fold rise from baseline of this ratio was subsequently calculated for each participant. Seroconversion was defined as at least a 2-fold rise in antigen-specific titer ratios post-baseline compared to baseline titer ratios. The percentage of participants who seroconverted PT-IgA at each immunogenicity timepoint (Day 29 and Day 181) was calculated.
Time frame: Day 29 and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Any Time Point | 40 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 29 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 181 | 42 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Any Time Point | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 29 | 33 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 181 | 40 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 29 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Any Time Point | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 181 | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 181 | 14 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Day 29 | 53 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Mucosal IgA Levels | Any Time Point | 53 percentage of participants |
Comparison: Any time pointp-value: 0.585Barnard's exact test
Comparison: Any time pointp-value: 1Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin (PT) antigen. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA/IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to PT-IgA and PT-IgG at any and each immunogenicity timepoint (Day 15, Day 29, or and Day 181) was calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 13 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 25 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 53 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 33 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 17 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 60 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 13 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 47 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 40 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 20 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 33 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 20 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 15 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 29 | 33 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Any Time Point | 13 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 181 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgG - Day 29 | 7 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 15 | 33 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Day 181 | 50 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Pertussis Toxin as Measured by Serum IgA and Serum IgG Levels | IgA - Any Time Point | 60 percentage of participants |
Comparison: IgA, any time pointp-value: 0.836Barnard's exact test
Comparison: IgA, any time pointp-value: 1Barnard's exact test
Comparison: IgG, any time pointp-value: 0.526Barnard's exact test
Comparison: IgG, any time pointp-value: 0.119Barnard's exact test
Secondary
Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels
Approximately 10 mL of venous blood was collected from participants immediately prior to the first study vaccination on Day 1 (baseline), Day 15, Day 29, and Day 181 to measure via a bead-based assay serum IgA and serum IgG levels (in ELISA units/mL) to pertussis toxin, filamentous hemagglutinin, pertactin, and fimbriae 2/3 pertussis antigens. Seroconversion was defined as at least a 2-fold rise in antigen-specific IgA levels or antigen-specific IgG levels post-baseline compared to baseline levels. The percentage of participants who seroconverted to at least two pertussis antigens at each and across all immunogenicity timepoints (Day 15, Day 29, and Day 181) was calculated.
Time frame: Day 15, Day 29, and Day 181
Population: The Immunogenicity Population includes all participants who received the study vaccination and contributed both pre-vaccination samples and either at least one post vaccination sample for humoral immunogenicity testing for which results were reported, or at least one post vaccination nasal sample for which results were reported.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 53 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 7 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 27 percentage of participants |
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 25 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 53 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 73 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 67 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 73 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 20 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 60 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 60 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 181 | 36 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 15 | 27 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Any Time Point | 53 percentage of participants |
| Placebo by VaxINator | Percentage of Participants Achieving Seroconversion to Two or More Pertussis Antigens as Measured by Serum IgA or Serum IgG Levels | Day 29 | 20 percentage of participants |
Comparison: Any time pointp-value: 1Barnard's exact test
Comparison: Any time pointp-value: 0.301Barnard's exact test
Secondary
Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures
Colonization of live B. pertussis organism was assessed from a nasopharyngeal swab performed 28 days after vaccine administration (Day 29) to ensure all participants were cleared of colonization. Standard microbiologic techniques were used to assess the presence of B. pertussis by culture. If any participants were positive for B. pertussis culture at Day 29, they were asked to return at Day 46 for a repeat culture. If the participant was not positive for B. pertussis at Day 29, no subsequent nasopharyngeal samples for culture were collected.
Time frame: Day 29 and Day 46
Population: The Per Protocol (PP) Population includes all participants in the immunogenicity population, excluding participants ineligible at baseline. Data is excluded from PP analyses from visits after major protocol deviations and study visits that occurred greater than 3 days out of window. Data from 1 participant was excluded from the BPZE1 10\^7 CFU by VaxINator group due to receipt of immunosuppressive therapy within 30 days of study vaccination.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| BPZE1 10^7 CFU by VaxINator | Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures | Day 29 | 0 percentage of participants |
| BPZE1 10^9 CFU by VaxINator | Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures | Day 29 | 0 percentage of participants |
| BPZE1 10^9 CFU by Syringe | Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures | Day 29 | 0 percentage of participants |
| Placebo by VaxINator | Percentage of Participants With Detectable B. Pertussis From Nasopharyngeal Cultures | Day 29 | 0 percentage of participants |