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COMPLETED Phase 3

Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus Epiduo® Forte Gel in Treatment of Acne Vulgaris

NCT02651220 · View on ClinicalTrials.gov ↗

Study Summary

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Multiple-Site Clinical Study to Evaluate the Therapeutic Equivalence and Safety of adapalene and benzoyl peroxide gel, 0.3%/2.5% (Actavis Laboratories UT, Inc.) to Epiduo® Forte (adapalene and benzoyl peroxide) gel 0.3%/2.5% (Galderma) in the treatment of Acne Vulgaris

Conditions Studied

Interventions

  • DRUG placebo gel
  • DRUG Epiduo® Forte Gel
  • DRUG Adapalene and Benzoyl Peroxide Gel

Study Locations (20)

California

  • Site 112 — Anaheim
  • Site 110 — Long Beach
  • Site 111 — Los Angeles
  • Site 104 — San Diego
  • Site 113 — West Covina

Florida

  • Site 101 — Brandon
  • Site 119 — Jacksonville
  • Site 114 — Miami
  • Site 115 — Miami
  • Site 116 — Miramar

Arizona

  • Site 103 — Mesa
  • Site 109 — Tucson

Indiana

  • Site 105 — Carmel
  • Site 120 — New Albany

Other

  • Site 117 — Belize City
  • Site 118 — Belize City

Illinois

  • Site 102 — Arlington Heights

Nevada

  • Site 107 — Henderson

North Carolina

  • Site 106 — High Point

Trial Details

FieldValue
Enrollment Target 1,001 participants
Start Date 2015-11
Est. Completion 2016-10
Phase Phase 3

Sponsor

Actavis

16 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02651220

The ClinicalTrials.gov registry entry for NCT02651220 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 1,001 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Actavis, which has 16 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 Acne appearing as the primary indexed condition, and to 3 interventions — of which placebo gel 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: NCT02651220 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT02651220 about?

NCT02651220 is a clinical study titled "Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus Epiduo® Forte Gel in Treatment of Acne Vulgaris". A Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Multiple-Site Clinical Study to Evaluate the Therapeutic Equivalence and Safety of adapalene and benzoyl peroxide gel, 0.3%/2.5% (Actavis Laboratories UT, Inc.) to Epiduo® Forte (adapalene and benzoyl peroxide) gel 0.3%/2.5% (Galderma)...

What is the current status of trial NCT02651220?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,001 participants. The study started on 2015-11. Estimated completion is 2016-10.

What conditions does trial NCT02651220 study?

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

What interventions are being tested in trial NCT02651220?

The interventions under investigation include: placebo gel (DRUG), Epiduo® Forte Gel (DRUG), Adapalene and Benzoyl Peroxide Gel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02651220?

This trial is sponsored by Actavis, which has 16 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02651220 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Illinois, Indiana. 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