Chronic Rhinosinusitis With Nasal Polyps
Conditions
Keywords
biofilm, antibiotic-resistant infections
Brief summary
TRL1068 is expected to eliminate the pathogen-protecting biofilm in Chronic Rhinosinusitis, thus making these bacteria substantially more susceptible to established antibiotic treatment regimens. This initial study is to assess overall safety and pharmacokinetics (PK) of TRL1068. The goal of the development program is to demonstrate effectiveness of TRL1068 in difficult to treat bacterial infections such as in CRS.
Detailed description
Chronic rhinosinusitis with nasal polyps (CRSwNP) is associated with significant morbidity and decreased quality of life. Defects in the epithelial cell barrier, increased exposure to pathogenic and colonized bacteria, and dysregulation of the host immune system are all thought to play prominent roles in disease pathogenesis. Colonization with S. aureus or P. aureus are associated with recalcitrant disease and biofilm formation, making eradication difficult. Distribution of topical solutions in the unoperated sinuses has been observed to be less than 2% of the total irrigation volume, with almost no penetration in the frontal and sphenoid sinuses. For those patients with mucosal edema from infection and chronic inflammation, distribution is probably significantly less when applied topically. Intravenously administered TRL1068 is expected to achieve effective anti-biofilm levels throughout the sinonasal space for several weeks. TRL1068 is a monoclonal human antibody that rapidly eliminates biofilm at very low concentrations, thus making the targeted bacterial pathogens substantially more sensitive to standard of care antibiotic treatment regimen and greatly accelerating clinical improvement and potential for bacterial eradication.
Interventions
DRUGTRL1068
A human IgG1κ (G1m1,17 (z,a); Km3 allotype) monoclonal antibody
Sponsors
Trellis Bioscience LLC
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
single group, all subjects will receive 15 mg/kg of TRL1068 on Day 1
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
1. Age 18 to 85 years, inclusive 2. Diagnosis of chronic rhinosinusitis with: 1. Acute exacerbation of CRSwNP with increased sinonasal discharge OR 2. Acute exacerbation post-functional endoscopic sinus surgery (FESS) with increased sinonasal discharge AND 3. Sinonasal culture positive for SA or PA without concomitant fungal infection in culture or PCR 3. Symptoms and culture results justify initiation of topical and/or systemic antibiotic treatment 4. Willing and able to provide written informed consent 5. Willing to perform and comply with all study procedures including attending clinic visits as scheduled 6. Men and women of child bearing potential (WOCBP) must be willing to practice a highly effective method of contraception that may include, but is not limited to, abstinence, sex only with persons of the same sex, monogamous relationship with vasectomized partner, vasectomy, hysterectomy, bilateral tubal ligation, licensed hormonal methods, intrauterine device (IUD), or use of spermicide combined with a barrier method (e.g., condom, diaphragm) for 28 days before receiving the investigational product (IP) and through Day 50.
Exclusion criteria
1. Active malignancy, or history of malignancy or chemotherapy within the past 2 years other than history of localized or surgical removal of focal skin cancer, or cervical cancer in situ treated successfully in the past by local treatment (including but not limited to cryotherapy or laser therapy) or by hysterectomy 2. Any chronic or acute bacterial infection other than acute exacerbation of CRS 3. Concomitant intrasinal culture or 16S PCR indicative of concomitant fungal infection 4. Allergic fungal rhinosinusitis, characterized by elevated antifungal IgE and eosinophilic mucus 5. Receiving or recently received another investigational drug (within 30 days of Day 1, or 5 half-lives of the investigational drug, whichever is longer) 6. Received a COVID-19 vaccine or booster within 14 days of planned Day 1 or planned COVID-19 vaccination within 14 days after Day 1 7. Positive serum test for pregnancy, pregnant, or nursing women 8. History of drug or alcohol abuse that, in the opinion of the Investigator, would interfere with the subject's ability to comply with the study requirements 9. Any other comorbidity or condition that, in the opinion of the Investigator would make the subject unsuitable for the study or unable to comply with the study requirements
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Assess the immunogenicity of TRL1068 as measured by anti-drug antibodies (ADAs) | 6 weeks | Anti-drug antibodies (ADA), i.e. anti-TRL1068 antibodies in serum will determined by electrochemiluminescence assay |
| Characterize the pharmacokinetics (PK) of TRL1068 in intrasinal concentrations (AUCINF) | 6 weeks | Individual subject TRL1068 AUCINF intrasinal will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacodynamics (PD) of TRL1068 (time to resolution of bacterial pathogen infection) | 6 weeks | Cultures will be tested for bacterial pathogen presence by bacterial culture and/or PCR assessment. Time to resolution of bacterial pathogen infection is defined as the number of days from start of current acute exacerbation to the day when testing by bacterial culture and/or PCR assessment are reported as negative. Descriptive statistics will be performed including mean, median and confidence interval. |
| Characterize the pharmacodynamics (PD) of TRL1068 (time to resolution of signs and symptoms of acute exacerbation) | 6 weeks | Patients will be evaluated for signs and symptoms of acute exacerbation using SNOT-22 scoring. Time to resolution of signs and symptoms of acute exacerbation is defined as the day when the SNOT-22 score is back to pre-acute exacerbation score. |
| Characterize the pharmacokinetics (PK) of TRL1068 in serum (AUCLAST) | 6 weeks | Individual subject TRL1068 AUCLAST in serum will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Incidence of abnormal physical exam findings | 6 weeks | Clinically-significant abnormal physical exam findings will be reviewed |
| Incidence of abnormal serum chemistries and hematology | 6 weeks | Clinically-significant abnormal laboratory results will be reviewed |
| Incidence of abnormal vital signs (temperature) | 6 weeks | Clinically-significant abnormal temperatures will be reviewed |
| Incidence of abnormal vital signs (blood pressure) | 6 weeks | Clinically-significant abnormal blood pressures will be reviewed |
| Incidence of abnormal vital signs (heart rate) | 6 weeks | Clinically-significant abnormal heart rates will be reviewed |
| Incidence of Adverse Events (AEs) and Serious Adverse Events (SAEs) | 7 weeks | reported AEs and SAEs will be reviewed |
| Characterize the pharmacokinetics (PK) of TRL1068 in serum (Cmax) | 6 weeks | Individual subject TRL1068 Cmax in serum will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in serum (Cmin) | 6 weeks | Individual subject TRL1068 Cmin in serum will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in serum (Tmax) | 6 weeks | Individual subject TRL1068 Tmax in serum will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in serum (AUCINF) | 6 weeks | Individual subject TRL1068 AUCINF in serum will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in intrasinal concentrations (Cmax) | 6 weeks | Individual subject TRL1068 Cmax intrasinal will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in intrasinal concentrations (Cmin) | 6 weeks | Individual subject TRL1068 Cmin intrasinal will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in intrasinal concentrations (Tmax) | 6 weeks | Individual subject TRL1068 Tmax intrasinal will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
| Characterize the pharmacokinetics (PK) of TRL1068 in intrasinal concentrations (AUCLAST) | 6 weeks | Individual subject TRL1068 AUCLAST intrasinal will be determined by ELISA and derived PK parameters will be summarized using descriptive statistics. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Assess the incidence of improvement of baseline symptoms of chronic rhinosinusitis (CRS) after intravenous TRL1068 | 7 weeks | signs and symptoms will be measured using the SNOT-22 |
| Assess time to improvement of baseline symptoms of CRS as compared with previous duration of acute exacerbations | 7 weeks | signs and symptoms will be measured using the SNOT-22 and compared with historical data |
Other
| Measure | Time frame | Description |
|---|---|---|
| Assess the effects of treatment on the intrasinal microbiome | 6 weeks | intrasinal culture and PCR results will be reviewed |
Contacts
Primary ContactAnton (Tony) Leighton, MD
Backup ContactAdriane Kisch-Hancock
Outcome results
None listed