drugset / Trial / NCT02530281

Study of Glycopyrronium in Axillary Hyperhydrosis

NCT02530281 ↗

Phase 3 Completed 344 enrolled Journey Medical Corporation
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2015-07
Primary completion
2016-03
Completion
2016-03

Outcome

Mixed primary results

registry NUMBER Glycopyrronium: 52.8 percent of subjects NCT02530281 ↗

registry NUMBER Vehicle: 28.3 percent of subjects NCT02530281 ↗

registry Glycopyrronium vs Vehicle; p <0.001; Cochran-Mantel-Haenszel NCT02530281 ↗

registry Glycopyrronium vs Vehicle; p =0.065; ANCOVA NCT02530281 ↗

registry LEAST_SQUARES_MEAN Glycopyrronium: -100.56 (Standard Deviation 98.151) mg/5 min NCT02530281 ↗

registry LEAST_SQUARES_MEAN Vehicle: -88.08 (Standard Deviation 95.695) mg/5 min NCT02530281 ↗

registry Glycopyrronium vs Vehicle; p =0.001; ANCOVA NCT02530281 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycopyrronium Unknown 3.75 % Topical