Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female Pattern Hair Loss

Completed · Phase 2

Conditions studied: Alopecia, Baldness

In brief

This study will evaluate the safety and efficacy of 3 doses of bimatoprost solution compared with vehicle and over-the-counter (OTC) minoxidil 2% solution in women with female pattern hair loss. All treatments will be provided in a double-blinded fashion except for minoxidil 2% solution which will be provided open-label.

Key facts

Study ID

NCT01325350

Run by

Allergan

People needed

306

Starts

2011-06-01

Expected to finish

2012-09-01

Last updated by the study team

2014-04-09

Who can join

Age: 18 and older, up to 59. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Mild to moderate female pattern hair loss with ongoing hair loss for at least 1 year
• Willingness to have micro-dot-tattoo applied to scalp
• Willingness to maintain same hair style, length and hair color during study

You may not qualify if…

• Drug or alcohol abuse within 12 months
• HIV positive
• Received hair transplants or had scalp reductions
• Use of hair weaves, hair extensions or wigs within 3 months
• Oral or topical minoxidil treatment within 6 months
• Application of topical steroids or nonsteroidal anti-inflammatory drugs (NSAIDs) to scalp within 4 weeks

Where it is running

• Study site — Portland, Oregon, United States
• Study site — Berlin, Germany

Full record on ClinicalTrials.gov

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