Last reviewed · How we verify
An Open-label Study Assessing Long-term Safety of Glycopyrronium in Subjects With Primary Axillary Hyperhidrosis
This is an open-label, long-term safety study of glycopyrronium topical wipes, enrolling up to 660 subjects with primary axillary hyperhidrosis who participated in either the DRM04-HH04 or DRM04-HH05 studies.
Details
| Lead sponsor | Journey Medical Corporation |
|---|---|
| Phase | Phase 3 |
| Status | COMPLETED |
| Enrolment | 564 |
| Start date | 2015-08 |
| Completion | 2016-12 |
Conditions
- Hyperhidrosis
Interventions
- Glycopyrronium Topical Wipes
Primary outcomes
- Long-term Safety Assessed Through Adverse Events and Local Skin Reactions — Day 1 - Week 44
The Total Participants at risk are based on the Safety population, defined as, Participants who were randomized and received at least one confirmed dose of study drug.
Countries
United States, Germany