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Clinical Trial in Females for Female Pattern Hair Loss


A Phase 3 Multi-Center Parallel Design Clinical Trial to Compare the Efficacy and Safety of 5% Minoxidil Foam vs. Vehicle in Females for the Treatment of Female Pattern Hair Loss (Androgenetic Alopecia)




This is a six month clinical trial to evaluate the effectiveness and safety in women with Female Pattern Hair Loss (FPHL), comparing a 5% minoxidil topical foam (MTF) formulation applied once a day versus a topical foam vehicle (placebo) formulation applied once a day.

Study Status: Completed


Condition Intervention Phase
Androgenetic Alopecia Drug: 5% Minoxidil Topical Foam
Drug: Vehicle Topical Foam
Phase 3

Verified by Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc. August, 2012

Sponsored by: Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc.
Information provided by: Johnson & Johnson Consumer and Personal Products Worldwide identifier: NCT01226459

Study Type: Interventional

Study Design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Cleveland Clinic
Cleveland, Ohio 44195
United States

Rita A Wanser., Study Director

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