Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: Latisse Versus Placebo
Completed
Allergan
Phase 4
2011-03-01
The primary purpose of this study is to assess efficacy and safety of Latisse (bimatoprost
.03% ophthalmic solution) applied to the lateral and medial eyebrows. The primary outcome is
a increase in overall eyebrow prominence as measured by at least a 1-grade increase on the
Global Eyebrow Assessment (GEyA) scale, from baseline to the end of the treatment which will
be day 270 period.
Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosis of the Eyebrows: Latisse Versus Placebo
Completed
Kenneth Beer
Phase 4
2011-03-01
The primary purpose of this study is to assess efficacy and safety of Latisse (bimatoprost
.03% ophthalmic solution) applied to the lateral and medial eyebrows. The primary outcome is
a increase in overall eyebrow prominence as measured by at least a 1-grade increase on the
Global Eyebrow Assessment (GEyA) scale, from baseline to the end of the treatment which will
be day 270 period.
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