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A Study to Evaluate the Safety and Efficacy of ATx201 in Subjects With Moderate Atopic Dermatitis
This is a Phase 2, 3-week, single-center, double-blind, randomized, two-arm, vehicle controlled study, with each individual receiving both active and vehicle treatment. Approximately 30 subjects with moderate atopic dermatitis will receive topically applied ATx201 CREAM 2% and matching vehicle once daily for 3 weeks (5 mg/cm2/day), without occlusion. ATx201 and vehicle will be applied on two separate target lesions of moderate atopic dermatitis (lesions of at least 3 × 3 cm, excluding the face, scalp, genitals, hands, and feet, ideally from the same anatomical location).
Details
| Lead sponsor | UNION therapeutics |
|---|---|
| Phase | PHASE2 |
| Status | COMPLETED |
| Enrolment | 31 |
| Start date | Mon Sep 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Mon Mar 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Atopic Dermatitis
Interventions
- ATx201 2% Cream
- ATx201 Cream Vehicle
Countries
Canada