Trials / Completed
CompletedNCT01391273
Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypotrichosis
A Multicenter, Double-masked, Randomized, Parallel-group Study Assessing the Safety and Efficacy of Once-Daily Application of Bimatoprost Solution 0.03% Compared to Vehicle in Increasing Overall Eyelash Prominence in Japanese Subjects With Hypotrichosis of the Eyelashes
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 173 (actual)
- Sponsor
- Allergan · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the safety and efficacy of bimatoprost solution 0.03% compared with vehicle in Japanese adults with hypotrichosis of the eyelashes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | bimatoprost solution 0.03% | One drop of bimatoprost solution 0.03% applied along each upper eyelid margin once daily in the evening for 4 months. |
| DRUG | bimatoprost vehicle solution | One drop of bimatoprost vehicle solution applied along each upper eyelid margin once daily in the evening for 4 months. |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2012-05-19
- Completion
- 2012-05-19
- First posted
- 2011-07-12
- Last updated
- 2019-07-08
- Results posted
- 2013-07-09
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT01391273. Inclusion in this directory is not an endorsement.