CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 46 enrolled
Drug / intervention
RVL-1201 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01848041
NCT01848041Phase 2Completed

A Randomized, Double-Masked, Placebo-Controlled Phase 1/2a Study of the Efficacy and Safety of Two Dosing Regimens of RVL-1201 in the Treatment of Acquired Blepharoptosis

RVL Pharmaceuticals, Inc.·interventional·Posted May 7, 2013·Updated Nov 26, 2021

In Brief

A Phase 2 clinical trial evaluating RVL-1201 and RVL-1201 Vehicle Placebo for Blepharoptosis. Completed, enrolled 46 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBlepharoptosis
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMay 7, 2013
Enrollment StartMay 1, 2013
Primary CompletionJan 1, 2014
Study CompletionFeb 1, 2014
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 13.2 years ago

Interventions

RVL-1201drug

RVL-1201 0.1% Ophthalmic Solution

RVL-1201 Vehicle Placebodrug

RVL-1201 Vehicle Placebo