At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 564 enrolled
Drug / intervention
Glycopyrronium Topical Wipesdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
An Open-label Study Assessing Long-term Safety of Glycopyrronium in Subjects With Primary Axillary Hyperhidrosis
In Brief
A Phase 3 clinical trial evaluating Glycopyrronium Topical Wipes for Hyperhidrosis. Completed, enrolled 564 participants across 48 sites in 2 countries.
Detailed Summary
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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHyperhidrosis
CountriesGermany, United States
Collaborators--
Timeline
Phase 3CompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartAug 2015
First PostedSep 2015
Primary CompletionDec 2016
TodayJul 2026
First PostedSep 18, 2015
Enrollment StartAug 1, 2015
Primary CompletionDec 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 10.8 years ago
Interventions
Glycopyrronium Topical Wipesdrug
Glycopyrronium Topical Wipes