Overview

Safety and Efficacy Study of RVL-1201 in Acquired Blepharoptosis

Status:
Completed
Trial end date:
2014-02-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
RevitaLid Inc.
RVL Pharmaceuticals, Inc.
Treatments:
Ophthalmic Solutions
Oxymetazoline
Pharmaceutical Solutions
Phenylephrine