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NCT02651220 · ClinicalTrials.gov registry record · Phase 3

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

A Phase 3 study of Acne, sponsored by Actavis.

Completed
Registry status
Phase 3
Development phase
1,001
Enrollment target
20
Study locations

NCT02651220: Completed Phase 3 study of Acne, sponsored by Actavis.

NCT02651220 is a Phase 3 study of Acne that has completed, run by Actavis. The registered enrollment target is 1,001 participants, above the 104-participant average among 26 other Acne trials with a reported enrollment target (863% higher). The trial reports 20 study locations across 9 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02651220, a Phase 3 study of Acne, has completed, sponsored by Actavis.

COMPLETED
Registry status
Phase 3
Development phase
1,001 participants
Enrollment target
20
Study locations

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
Actavis

79 total trials

What the finished NCT02651220 record still lists

NCT02651220 is an interventional study that assigns participants to a tested intervention. Its 1,001 participants enrollment target places it among the larger protocols in the corpus, above the 104-participant average among 26 other Acne trials with a reported enrollment target (863% higher).

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.

NCT02651220 names 20 study sites across 9 states, led by California, Florida, Arizona.

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.

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).

Who is sponsoring clinical trial NCT02651220?

This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Acne

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02651220's enrollment target sits among peer trials

1,001 1st of 26 higher than 26 of 26 other Acne trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Acne trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02651220, the US trial registry maintained by the National Library of Medicine. NCT02651220 (large enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.