drugset / Trial / NCT01848041

Safety and Efficacy Study of RVL-1201 in Acquired Blepharoptosis

NCT01848041 ↗

Phase 1/2 Completed 46 enrolled RVL Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is an exploratory, proof of concept study to evaluate the safety and efficacy of RVL-1201 dosed once or twice daily for 14 days compared to a placebo (vehicle) control in patients with ptosis.

Timeline

Start
2013-05
Primary completion
2014-01
Completion
2014-02

Drugs

EvaluationDrugModalityDoseRoute
Subject RVL-1201 Unknown 0.1 % Other

Indications