None listed
Conditions
Brief summary
This study is being conducted to look at the safety and immune response (how the immune system of the human body reacts) to a vaccine for SARS-CoV-2 (the virus responsible for COVID-19 infection) when administered as an intramuscular injection (an injection directly into the muscle) to the upper arm of healthy participants, on two occasions at least 28 days apart.
Interventions
This study will be conducted in two parts: Part 1 and Part 2.
Part 1 of the study will evaluate single ascending doses (SAD) and multiple ascending doses (MAD) of SARS-CoV-2 Sclamp vaccine in healthy adult participants of age more than or equal to 18 years to less than or equal to 55 years. Part 2 of the study will evaluate multiple ascending doses (MAD) of SARS-CoV-2 Sclamp vaccine administered as an intramuscular injection in older healthy adult participants of age 56 years and above.
Parti
This study will be conducted in two parts: Part 1 and Part 2. Part 1 of the study will evaluate single ascending doses (SAD) and multiple ascending doses (MAD) of SARS-CoV-2 Sclamp vaccine in healthy adult participants of age more than or equal to 18 years to less than or equal to 55 years. Part 2 of the study will evaluate multiple ascending doses (MAD) of SARS-CoV-2 Sclamp vaccine administered as an intramuscular injection in older healthy adult participants of age 56 years and above. Participants in both Parts 1 and 2 will be randomized to receive Treatment A, B, C and D or placebo in the respective Cohorts. • Treatment A: SARS-CoV-2 Sclamp vaccine 5 micrograms (mcg) in 0.5 milliliter (mL) suspension, as an intramuscular injection, administered as two separate doses at least 28 days apart on Day 1 and 29 • Treatment B: SARS-CoV-2 Sclamp vaccine 15 mcg in 0.5 mL suspension, as an intramuscular injection, administered as two separate doses at least 28 days apart on Day 1 and 29 • Treatment C: SARS-CoV-2 Sclamp vaccine 45 mcg in 0.5 mL suspension, as an intramuscular injection, administered as two separate doses at least 28 days apart on Day 1 and 29 • Treatment D: SARS-CoV-2 Sclamp vaccine 45 mcg in 0.5 mL suspension, as an intramuscular injection, administered as the first dose on Day 1, followed by placebo as the second dose at least 28 days apart on Day 29 Part 1 and Part 2 will include 3 Cohorts each. • Part 1, Cohort 1- Treatment A (24 participants) or placebo (8 participants) • Part 1, Cohort 2- Treatment B (24 participants) or placebo (8 participants) • Part 1, Cohort 3- Treatment C (24 participants) and Treatment D (24 participants) or placebo (8 participants) • Part 2, Cohort 1- Treatment A (24 participants) or placebo (8 participants) • Part 2, Cohort 2- Treatment B (24 participants) or placebo (8 participants) • Part 2, Cohort 3- Treatment C (24 participants) or placebo (8 participants) A total of 216 subjects are planned to be included in the study. The anticipated study duration for any individual participant is up to approximately 14 months.
Sponsors
University of Queensland
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Subject, Caregiver, Outcomes Assessor)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Part 1 1. Healthy male or non-pregnant female, greater than or equal to 18 and less than or equal to 55 years of age, with BMI greater than 18 and less than 34.0 kg/metres sqaured and body weight greater than or equal to 50.0 kg for males and greater than or equal to 45.0 kg for females. 2. Healthy as defined by: a.The absence of clinically significant illness and surgery within 28 days prior to dosing. Subjects displaying signs or symptoms of an acute and/or febrile illness within 24 hours pre-dose (with at least 3 symptom-free pre-dose days required) will be carefully evaluated for upcoming illness/disease. Inclusion is at the discretion of the Investigator, and the subject may have their scheduled dosing postponed until the condition resolves. b.The absence of clinically significant history of neurological, endocrine, cardiovascular, respiratory, haematological, immunological, psychiatric, gastrointestinal, renal, hepatic, and metabolic disease. 3.Non-smokers or social smokers (defined as the equivalent of fewer than 10 cigarettes per week). Ex-heavy smokers (heavy smoking defined as the equivalent of 25 or more cigarettes per day) may be admitted if they have quit, or reduced their cigarette intake to the defined level of social smoking, for a period of at least 1 year. 4.Women of childbearing potential (WOCBP) or men whose sexual partners are WOCBP must be able and willing to use at least 2 highly effective methods of contraception commencing at least 28 days prior to enrolment, during the study and for 3 months after last treatment administration. A female subject is considered to be a WOCBP following menarche and until she is in a post-menopausal state for 12 consecutive months (without an alternative medical cause) or otherwise permanently sterile (for which acceptable methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy). A follicle-stimulating hormone (FSH) test may be used to confirm postmenopausal state. Examples of acceptable methods of contraceptive methods (for female subjects) to be used throughout the study include: a. Simultaneous use of hormonal contraceptives, started at least 28 days prior to first study treatment (active or placebo) administration and must agree to use the same hormonal contraceptive throughout the study, and condom for the male partner; b. Simultaneous use of intra-uterine contraceptive device, placed at least 28 days prior to first study treatment administration, and condom for the male partner; c. Simultaneous use of diaphragm or cervical cap and male condom for the male partner, started at least 28 days prior to first study treatment administration; d. Sterile male partner (vasectomized since at least 6 months prior to first study treatment administration); e. True abstinence, defined as no sexual intercourse (heterosexual couples), for at least 28 days prior to first study treatment administration and for at least the duration of the study. Periodic abstinence and withdrawal are not acceptable methods. 5. WOCBP must have a negative urine pregnancy test (and negative serum pregnancy test in the event of a positive urine test) prior to receiving each dose. 6. Male subjects (including men who have had a vasectomy) with a pregnant partner, a female partner not of childbearing potential, or a same sex partner, must agree to use a condom from the first study treatment administration until at least 90 days after the last study treatment administration. 7. Male subjects must be willing not to donate sperm until 90 days following the last study treatment administration. 8. Must be able to attend all visits for the duration of the study and to comply with all study procedures according to the study schedule. 9. Capable of, and have given, written consent. Part 2 Subjects must meet all of the following criteria to be included in the study: 1. Healthy male or non-pregnant female equal to 56 years of age, with BMI >18 and <34.0 kg/m2 and body weight equal to 50.0 kg for males and equal to 45.0 kg for females. 2. Healthy as defined by: a. The absence of clinically significant illness and surgery within 28 days prior to dosing. Subjects displaying signs or symptoms of an acute and/or febrile illness within 24 hours pre-dose (with at least 3 symptom-free pre-dose days required) will be carefully evaluated for upcoming illness/disease. Inclusion pre-dosing is at the discretion of the Investigator, and the subject may have their scheduled dosing postponed until the condition resolves. b. The absence of clinically significant history of a pre-existing medical condition that is not stable (neurological, endocrine, cardiovascular, respiratory, haematological, immunological, psychiatric, gastrointestinal, renal, hepatic, and metabolic disease). A stable medical condition is defined as disease not requiring significant change in therapy or hospitalization for worsening disease during the 3 months before enrolment. 3. Non-smokers or social smokers (defined as the equivalent of fewer than 10 cigarettes per week). Ex-heavy smokers (heavy smoking defined as the equivalent of 25 or more cigarettes per day) may be admitted if they have quit,or reduced their cigarette intake to the defined level of social smoking, for a period of at least 12 months. 4. Women of childbearing potential (WOCBP) or men whose sexual partners are WOCBP must be able and willing to use at least 2 highly effective methods of contraception commencing at enrolment, during the study and for 3 months after last treatment administration. A female subject is considered to be a WOCBP following menarche and until she is in a post-menopausal state for 12 consecutive months (without an alternative medical cause) or otherwise permanently sterile (for which acceptable methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy). A follicle-stimulating hormone (FSH) test may be used to confirm post-menopausal state. Examples of acceptable methods of contraceptive methods (for female subjects) to be used throughout the study include: a. Simultaneous use of hormonal contraceptives, started at least 28 days prior to first study treatment administration and must agree to use the same hormonal contraceptive throughout the study, and condom for the male partner; b. Simultaneous use of intra-uterine contraceptive device, placed at least 28 days prior to first study treatment administration, and condom for the male partner; c. Simultaneous use of diaphragm or cervical cap and male condom for the male partner, started at least 28 days prior to first study treatment administration; d. Sterile male partner (vasectomized since at least 6 months prior to first study treatment administration); e. True abstinence, defined as no sexual intercourse with a male partner, (for heterosexual couples) for at least 28 days prior to first study treatment administration and for at least the duration of the study. Periodic abstinence and withdrawal are not acceptable methods. 5. WOCBP must have a negative urine pregnancy test prior to receiving each dose. 6. Male subjects (including men who have had a vasectomy) with a pregnant partner, a female partner not of childbearing potential, or a same sex partner, must agree to use a condom from the first study treatment administration until at least 90 days after the last study treatment administration. 7. Male subjects must be willing not to donate sperm until 90 days following the last study treatment administration. 8. Must be able to attend all visits for the duration of the study and to comply with all study procedures according to the study schedule. 9. Capable of, and have given, written informed consent.
Exclusion criteria
Part 1: Subjects to whom any of the following applies will be excluded from the study: 1. Any clinically significant abnormality or vital sign abnormality at physical examination (including baseline high blood pressure [140/90] after 3 repeated measurements or high random blood sugar [non-fasting]), clinically significant abnormal laboratory test results or positive test for HIV, hepatitis B, or hepatitis C found during medical screening. 2. Any acute or chronic ongoing illness which, in the judgement of the investigator, may preclude the subject’s participation. 3. Any subject that has an active COVID-19 infection (positive COVID-19 test: nasal/oropharyngeal swab and/or positive serum antibody response) at screening, or Day 1, or has been in close contact with someone who has an active COVID-19 infection, or has recovered from a previous COVID-19, SARS-CoV--1, or MERS infection. 4. Positive pregnancy, urine drug screen, or alcohol breath test at screening. 5. Known history of allergic reactions or hypersensitivity to vaccines, or to any excipient in the formulation (including the adjuvant, MF59C.1). 6. Presence of a known, or suspected, impairment of the immune system including, but not limited to, HIV, autoimmune disorders, immunosuppressant therapy, and diabetes mellitus. 7. History of a known, or suspected, respiratory system disorder including, but not limited to, cystic fibrosis, reactive airway disease, emphysema, chronic bronchitis, chronic obstructive pulmonary disease (COPD), or asthma, excluding childhood asthma. 8. History of significant alcohol abuse within 12 months year prior to screening. 9. Positive test for drugs of abuse (such as marijuana/tetrahydrocannabinol [THC] products, amphetamine, methamphetamine, methadone, barbiturates, benzodiazepines, cocaine, opiates, methylenedioxymethamphetamine [MDMA], or phencyclidine [PCP]) at screening, prior to dosing, or a history of drug abuse within 12 months prior to screening. 10. Participation in a clinical research study involving the administration of an investigational, or marketed, drug or device within 30 days prior to receiving the first treatment administration, or administration of a biological product in the context of a clinical research study within 90 days prior to the first dosing, or concomitant participation in an investigational study involving no drug, vaccine, or device administration, or intent to participate in another clinical study at any time during the conduct of the study. 11. Use of medications for the timeframes specified below, with the exception of hormonal contraceptives and medications exempted by the Investigator on a case-by-case basis because they are judged to interfere with subject safety e.g., topical drug products without significant systemic absorption are permissible: a. Prescription medication within 14 days prior to the first dosing; b. Any medication, or treatments, that may affect the immune system such as allergy injections, immunoglobulin, interferon, immunomodulators, cytotoxic drugs, or other drugs known to be frequently associated with significant major organ toxicity within 90 days prior to enrolment; c. Any registered vaccine administered within 30 days prior to enrolment in the study, or who plan to receive any non-study vaccines within 28 days of the second dose of the study vaccine d. Any other investigational coronavirus vaccine i.e. SARS--CoV-1, SARS--CoV-2, MERS etc. at any time prior to, or during, the study. e. Over-the-counter products within 7 days prior to the first dosing, with the exception of the occasional use of paracetamol (up to 2 g daily) and standard dose vitamins. 12. Donation of plasma within 7 days prior to dosing. Donation or loss of blood (excluding volume drawn at screening) of 50 mL to 499 mL of blood within 30 days, or more than 499 mL within 56 days prior to the first dosing. 13. Receipt of blood products within 2 months prior to the first study treatment administration (Day 1), or planned receipt of blood products during the study period. 14. Breast-feeding subject, or subject who plans to breastfeed from the time of first dose through 60 days after last study treatment administration. 15. Presence of tattoos, scarring, skin discoloration, or any other skin disturbances at the injection site which, in the opinion of the Investigator, may inhibit the ability to effectively perform an injection site assessment. 16. Employee or immediate relative of an employee of the clinical site, any of its affiliates or partners, or Syneos Health. 17. Any reason which, in the opinion of the Investigator, would interfere with the primary study objectives or prevent the subject from participating in the study. Part 2 Subjects to whom any of the following applies will be excluded from the study: 1. Any clinically significant abnormality or vital sign abnormality at physical examination, or uncontrolled hypertension in adults aged < 56 years and older ,or high random blood sugar [non-fasting]), clinically significant abnormal laboratory test results or positive test for HIV, hepatitis B, or hepatitis C found during medical screening. 2. Any acute or chronic ongoing illness which, in the judgement of the investigator, may preclude the subject’s participation. 3. Any subject that has an active COVID-19 infection (positive COVID-19 test: nasal/oropharyngeal swab and/or positive serum antibody response) at screening, or Day 1, or has been in close contact with someone who has an active COVID-19 infection, or has recovered from a previous COVID-19, SARS-CoV-1, or MERS infection. 4. Positive pregnancy, urine drug screen, or alcohol breath test at screening. 5. Known history of allergic reactions or hypersensitivity to vaccines, or to any excipient in the formulation (including the adjuvant, MF59C.1). 6. Presence of a known, or suspected, impairment of the immune system including, but not limited to, HIV, autoimmune disorders, immunosuppressant therapy, and diabetes mellitus. 7. History of a known, or suspected, or currently unstable medical condition that may expose the participant to an increased risk for severe SARS-CoV-2 disease, such as a respiratory system disorder including, but not limited to, cystic fibrosis, reactive airway disease, emphysema, chronic bronchitis, chronic obstructive pulmonary disease (COPD), or asthma, excluding childhood asthma, uncontrolled hypertension, ischemic or structural heart disease, chronic kidney disease, chronic liver disease, endocrine disorder and neurological illness. 8. History of significant alcohol abuse within 12 months prior to screening. 9. Positive test for drugs of abuse (such as marijuana/tetrahydrocannabinol [THC] products, amphetamine, methamphetamine, methadone, barbiturates, benzodiazepines, cocaine, opiates, methylenedioxymethamphetamine [MDMA], or phencyclidine [PCP]) at screening, prior to dosing, or a history of drug abuse within 12 months prior to screening. 10. Participation in a clinical research study involving the administration of an investigational, or marketed, drug or device within 30 days prior to receiving the first treatment administration, or administration of a biological product in the context of a clinical research study within 90 days prior to the first dosing, or concomitant participation in an investigational study involving no drug, vaccine, or device administration, or intent to participate in another clinical study at any time during the conduct of the study. 11. Use of medications for the timeframes specified below, with the exception of hormonal contraceptives and medications exempted by the Investigator on a case-by-case basis because they are judged to interfere with subject safety e.g., topical drug products without significant systemic absorption are permissible: a. Prescription medication within 14 days prior to the first dosing that in the opinion of the Investigator could impact the subjects safe participation in the study; b. Any medication, or treatments, that may affect the immune system such as allergy injections, immunoglobulin, interferon, immunomodulators, cytotoxic drugs, or other drugs known to be frequently associated with significant major organ toxicity within 90 days prior to enrolment; c. Any registered vaccine administered within 30 days prior to enrolment in the study, or who plan to receive any non-study vaccines within 28 days of the second dose of the study vaccine d. Any other investigational coronavirus vaccine i.e. SARS-CoV-1, SARS-CoV-2, MERS etc. at any time prior to, or during, the study. e. Over-the-counter products within 7 days prior to the first dosing, that in the opinion of the investigator could impact the subjects safe participation in the study. Paracetamol (up to 2 g daily) and standard dose vitamins will be permitted. 12. Donation of plasma within 7 days prior to dosing. Donation or loss of blood (excluding volume drawn at screening) of 50 mL to 499 mL of blood within 30 days, or more than 499 mL within 56 days prior to the first dosing. 13. Receipt of blood products within 2 months prior to the first study treatment administration (Day 1), or planned receipt of blood products during the study period. 14. Breast-feeding subject, or subject who plans to breastfeed from the time of first dose through 60 days after last study treatment administration. 15. Presence of tattoos, scarring, skin discoloration, or any other skin disturbances at the injection site which, in the opinion of the Investigator, may inhibit the ability to effectively perform an injection site assessment. 16. Employee or immediate relative of an employee of the clinical site, any of its affiliates or partners, or Syneos Health. 17. Any reason which, in the opinion of the Investigator, would interfere with the primary study objectives or prevent the subject from participating in the study. 18. Permanent resident in an aged care facility (nursing or aged care home.
Outcome results
None listed