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COMPLETED Phase 3

Study of the Safety and Efficacy of RVL-1201 in the Treatment of Acquired Blepharoptosis

NCT02436759 · View on ClinicalTrials.gov ↗

Study Summary

This is a Phase 3 study is to evaluate the safety and efficacy of RVL-1201 Ophthalmic Solution in the treatment of acquired blepharoptosis (ptosis) and to assess the safety and comfort of RVL-1201 Ophthalmic Solution for an extended dosing period of 6 weeks.

Conditions Studied

Interventions

  • DRUG RVL-1201
  • DRUG RVL-1201 Vehicle Placebo

Study Locations (14)

California

  • — Artesia
  • — Newport Beach
  • — Rancho Cordova
  • — Santa Maria

Florida

  • — Fort Myers
  • — Largo
  • — Plantation
  • — Sarasota

Kansas

  • — Pittsburg
  • — Shawnee Mission

Georgia

  • — Roswell

Ohio

  • — Mason

Pennsylvania

  • — Kingston

Tennessee

  • — Nashville

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2015-05
Est. Completion 2016-11
Phase Phase 3

Sponsor

RVL Pharmaceuticals

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02436759

The ClinicalTrials.gov registry entry for NCT02436759 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is RVL Pharmaceuticals, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acquired Blepharoptosis appearing as the primary indexed condition, and to 2 interventions — of which RVL-1201 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02436759 reports 14 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02436759 about?

NCT02436759 is a clinical study titled "Study of the Safety and Efficacy of RVL-1201 in the Treatment of Acquired Blepharoptosis". This is a Phase 3 study is to evaluate the safety and efficacy of RVL-1201 Ophthalmic Solution in the treatment of acquired blepharoptosis (ptosis) and to assess the safety and comfort of RVL-1201 Ophthalmic Solution for an extended dosing period of 6 weeks.

What is the current status of trial NCT02436759?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 140 participants. The study started on 2015-05. Estimated completion is 2016-11.

What conditions does trial NCT02436759 study?

This clinical trial studies the following conditions: Acquired Blepharoptosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02436759?

The interventions under investigation include: RVL-1201 (DRUG), RVL-1201 Vehicle Placebo (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02436759?

This trial is sponsored by RVL Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02436759 being conducted?

This trial has 14 study locations across California, Florida, Georgia, Kansas, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial