A Dose-Ranging Study Evaluating the Safety and Efficacy of IDP-107 in Patients With Acne Vulgaris
NCT01194375 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 180
Last updated 2012-07-02
Summary
The purpose of this study is to evaluate the safety and efficacy of IDP-107 versus placebo in treating patients with acne vulgaris.
Conditions
- Acne Vulgaris
Interventions
- DRUG
-
Low Strength IDP-107
Once a day for 16 weeks
- DRUG
-
High Strength IDP-107
Once a day for 16 weeks
- DRUG
-
Once a day for 16 weeks
Sponsors & Collaborators
-
Dow Pharmaceutical Sciences
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-09-30
- Primary Completion
- 2011-12-31
- Completion
- 2011-12-31
Countries
- United States
- Canada
Study Locations
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