Clinical Trials Directory

Trials / Completed

CompletedNCT00441415

Efficacy and Safety of Fixed Combination Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel in the Treatment of Acne Vulgaris

Efficacy and Safety of Fixed Combination Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel Compared to Clindamycin 0.1% / Benzoyl Peroxide 5% Gel in the Treatment of Acne Vulgaris

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
272 (actual)
Sponsor
Galderma R&D · Industry
Sex
All
Age
12 Years – 35 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to demonstrate the non-inferior efficacy of Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel when compared to Clindamycin 1% / Benzoyl Peroxide 5% Gel in Subjects with acne vulgaris after a 12-week treatment period.

Conditions

Interventions

TypeNameDescription
DRUGAdapalene BPO

Timeline

Start date
2007-02-01
Primary completion
2007-10-01
Completion
2007-10-01
First posted
2007-02-28
Last updated
2021-02-17

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00441415. Inclusion in this directory is not an endorsement.

Efficacy and Safety of Fixed Combination Adapalene 0.1% / Benzoyl Peroxide 2.5% Gel in the Treatment of Acne Vulgaris (NCT00441415) · Clinical Trials Directory