drugset / Trial / NCT05521438

Safety, Tolerability and Efficacy of QRX003 Lotion in Subjects With Netherton Syndrome

NCT05521438 ↗

Phase 2/3 Active not recruiting 30 enrolled Quoin Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
Subject QRX003 Unknown 2 % Topical
Subject QRX003 Unknown 4 % Topical

Indications