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Completed Phase 3 Interventional Accepts healthy volunteers Results available

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

ClinicalTrials.gov ID: NCT02651220

Public ClinicalTrials.gov record NCT02651220. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 3:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT02651220
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Actavis Inc.
Industry
Enrollment
1,001 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 40 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2015
Primary completion
Mar 31, 2016
Completion
Sep 30, 2016
Last update posted
Jun 22, 2020

2015 – 2016

United States locations

U.S. sites
18
U.S. states
8
U.S. cities
17
Facility City State ZIP Site status
Site 103 Mesa Arizona 85202
Site 109 Tucson Arizona 85712
Site 112 Anaheim California 92804
Site 110 Long Beach California 90813
Site 111 Los Angeles California 92210
Site 104 San Diego California 92108
Site 113 West Covina California 91790
Site 101 Brandon Florida 33511
Site 119 Jacksonville Florida 32256
Site 114 Miami Florida 33015
Site 115 Miami Florida 33175
Site 116 Miramar Florida 33027
Site 102 Arlington Heights Illinois 60005
Site 105 Carmel Indiana 46032
Site 120 New Albany Indiana 47150
Site 107 Henderson Nevada 89052
Site 106 High Point North Carolina 27262
Site 108 Rhinelander Wisconsin 54501

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02651220, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 22, 2020 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02651220 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →