A Clinical Trial Evaluating the Safety and Efficacy of IDP-110 in Patients With Acne Vulgaris
NCT00663286 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1399
Last updated 2008-04-22
Summary
The purpose of this study is to assess the effectiveness of IDP-110 in treating patients with acne vulgaris.
Conditions
- Acne Vulgaris
Interventions
- DRUG
-
IDP-110
Topical application for 12 weeks
- DRUG
-
Clindamycin
Topical application for 12 weeks
- DRUG
-
Benzoyl peroxide
Topical application for 12 weeks
- DRUG
-
Vehicle
Topical application for 12 weeks
Sponsors & Collaborators
-
Dow Pharmaceutical Sciences
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-10-31
- Primary Completion
- 2007-08-31
Countries
- United States
Study Locations
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