Status:
UNKNOWN
Study to Evaluate Safety and Activity of TRL1068 in Chronic Rhinosinusitis
Lead Sponsor:
Trellis Bioscience LLC
Conditions:
Chronic Rhinosinusitis With Nasal Polyps
Eligibility:
All Genders
18-85 years
Phase:
PHASE1
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...
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 c...
Eligibility Criteria
Inclusion
- Age 18 to 85 years, inclusive
- Diagnosis of chronic rhinosinusitis with:
- Acute exacerbation of CRSwNP with increased sinonasal discharge OR
- Acute exacerbation post-functional endoscopic sinus surgery (FESS) with increased sinonasal discharge AND
- Sinonasal culture positive for SA or PA without concomitant fungal infection in culture or PCR
- Symptoms and culture results justify initiation of topical and/or systemic antibiotic treatment
- Willing and able to provide written informed consent
- Willing to perform and comply with all study procedures including attending clinic visits as scheduled
- 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
- 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
- Any chronic or acute bacterial infection other than acute exacerbation of CRS
- Concomitant intrasinal culture or 16S PCR indicative of concomitant fungal infection
- Allergic fungal rhinosinusitis, characterized by elevated antifungal IgE and eosinophilic mucus
- Receiving or recently received another investigational drug (within 30 days of Day 1, or 5 half-lives of the investigational drug, whichever is longer)
- 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
- Positive serum test for pregnancy, pregnant, or nursing women
- 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
- 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
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 1 2025
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT05355207
Start Date
January 1 2024
End Date
January 1 2025
Last Update
April 12 2023
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.