Overview
Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female Pattern Hair Loss
Status:
Completed
Completed
Trial end date:
2012-09-01
2012-09-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
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.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AllerganTreatments:
Bimatoprost
Minoxidil
Pharmaceutical Solutions
Criteria
Inclusion Criteria:- 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
Exclusion Criteria:
- 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