Study of Glycopyrronium in Axillary Hyperhydrosis

Status Completed

Clinical Trial Summary

The study is a randomized, double-blind, vehicle controlled, parallel group study, designed to assess the efficacy and safety of glycopyrronium topical wipes, once daily, compared to vehicle in subjects with axillary hyperhidrosis.

Clinical Trial Description

This is a randomized, double-blind vehicle controlled study to assess the efficacy and safety of glycopyrronium topical wipes compared to vehicle in subjects with axillary hyperhidrosis. Safety will be assessed through lab tests, ECG, physical exams and vital signs. ;

Study Design

Related Conditions & MeSH terms

Hyperhidrosis

Clinical Trial Details

NCT number	NCT02530281
Study type	Interventional
Source	Journey Medical Corporation
Contact
Status	Completed
Phase	Phase 3
Start date	July 2015
Completion date	March 2016

View Details

See also
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