drugset / Trial / NCT02676310

Safety, Tolerability, and Pharmacokinetics of Bimatoprost in Men With Androgenetic Alopecia (AGA)

NCT02676310

Phase 1 Terminated 53 enrolled Allergan
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a safety, tolerability, and pharmacokinetics study of bimatoprost in male patients with androgenetic alopecia (AGA).

Timeline

Start
2016-03
Primary completion
2017-01
Completion
2017-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 0.25 ml Topical
Subject Bimatoprost Other / unclassified 0.3 % Topical
Subject Bimatoprost Other / unclassified 1 % Topical
Subject Bimatoprost Other / unclassified 1 ml Topical
Subject Bimatoprost Other / unclassified 3 % Topical

Indications