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Completed Phase 3 Interventional Results available

To Study Generic Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Glenmark Generics, Ltd) in the Treatment of Acne Vulgaris.

ClinicalTrials.gov ID: NCT02465632

Public ClinicalTrials.gov record NCT02465632. 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 Oct 17, 2026, 5:58 PM EDT

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

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multiple-Site Study to Evaluate the Therapeutic Equivalence of a Generic Clindamycin 1%/Benzoyl Peroxide 5% Topical Gel (Glenmark Generics, Ltd) to the Marketed Product BenzaClin® Topical Gel, Clindamycin 1%/Benzoyl Peroxide 5% (Valeant Pharmaceuticals, US) in the Treatment of Acne Vulgaris.

Brief summary

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

This is a randomized, double-blind, multiple-site, placebo-controlled, parallel-group study, designed to compare the efficacy and safety of generic Clindamycin 1%/ Benzoyl peroxide 5% topical gel (Glenmark Generics, Ltd), and the marketed product BenzaClin® Topical Gel, Clindamycin 1%/ Benzoyl peroxide 5% (Valeant Pharmaceuticals, US) in the treatment of acne vulgaris.

Study identification

NCT ID
NCT02465632
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
1,100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 40 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Apr 2015 (Type not available)
Primary completion
Nov 2015 (Actual)
Completion
Dec 2015 (Actual)
Last update posted
Jun 28, 2017

2015

United States locations

U.S. sites
13
U.S. states
6
U.S. cities
12
Facility City State ZIP Site status
Glenmark Investigational Site 13 Anaheim California — —
Glenmark Investigational Site 6 Long Beach California — —
Glenmark Investigational Site 15 Los Angeles California — —
Glenmark Investigational Site12 West Covina California — —
Glenmark Investigational Site 4 Brandon Florida — —
Glenmark Investigational Site 1 Miami Florida — —
Glenmark Investigational Site 8 Miami Florida — —
Glenmark Investigational Site 9 Miramar Florida — —
Glenmark Investigational Site 2 St. Petersburg Florida — —
Glenmark Investigational Site 5 Louisville Kentucky — —
Glenmark Investigational Site7 Upper Saint Clair Pennsylvania — —
Glenmark Investigational Site 14 Greenville South Carolina — —
Glenmark Investigational Site 3 Nashville Tennessee — —

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 NCT02465632, 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 28, 2017 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02465632 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →