Clinical Trials Directory

Trials / Completed

CompletedNCT00891982

A Clinical Study to Evaluate the Tolerability of a Topical Antibiotic and Retinoid Used in a Combined Regimen With a BPO Wash

A Phase 3B, Multicenter, Assessor-Blinded Study of the Tolerability of Clindamycin 1%-Tretinoin 0.025% Gel Used in Conjunction With Benzoyl Peroxide 4% Wash in Subjects With Mild to Moderate Facial Acne Vulgaris

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Stiefel, a GSK Company · Industry
Sex
All
Age
12 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the tolerability of a combined regimen of a topical antibiotic and retinoid and a benzoyl peroxide wash.

Conditions

Interventions

TypeNameDescription
DRUGCTGel/ BPO WashBenzoyl Peroxide (BPO) wash will be used once daily in the morning for 28 days Clindamycin and Tretinoin (CT) gel will be used once daily in the evening for 28 days.
DRUGSoap Free Cleanser and CTGelSoap Free Cleanser will be used once daily in the morning for 28 days Clindamycin and Tretinoin gel will be used once daily in the evening for 28 days.

Timeline

Start date
2009-04-01
Primary completion
2009-06-01
Completion
2009-06-05
First posted
2009-05-01
Last updated
2017-05-24
Results posted
2011-07-25

Locations

5 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00891982. Inclusion in this directory is not an endorsement.

A Clinical Study to Evaluate the Tolerability of a Topical Antibiotic and Retinoid Used in a Combined Regimen With a BPO (NCT00891982) · Clinical Trials Directory