drugset / Trial / NCT05521438
Safety, Tolerability and Efficacy of QRX003 Lotion in Subjects With Netherton Syndrome
RandomizedParallel-groupTriple-blindTreatment
Summary
This study has been designed to determine the safety, tolerability and efficacy of QRX003 lotion 2%, 4% QAM or 4% BID in subjects with Netherton Syndrome (NS) in comparison to vehicle
Timeline
- Start
- 2022-06-23
- Primary completion
- 2025-12-30
- Completion
- 2026-12-31
Outcome
Met primary endpoint
release “Summary of CL-QRX003-004 Interim Results in Netherton Syndrome The primary endpoint of 1-grade improvement or greater for IGA on all of the treatment area met” quoinpharma.com ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | QRX003 | Unknown | 2 % | Topical |
| Subject | QRX003 | Unknown | 4 % | Topical |