Trials / Completed
CompletedNCT01616654
Dose Range Study of CD5789 in Acne Vulgaris
A Randomized, Multi-center, Investigator-blind, Vehicle- and Active-controlled, Phase 2 Study to Assess the Efficacy and Safety of Different Concentrations of CD5789 Cream Applied Once Daily in Subjects With Moderate to Severe Acne Vulgaris
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 304 (actual)
- Sponsor
- Galderma R&D · Industry
- Sex
- All
- Age
- 12 Years – 35 Years
- Healthy volunteers
- Not accepted
Summary
To assess the efficacy and safety of different concentrations of CD5789 cream in participants with acne vulgaris for the purpose of dose identification.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | CD5789 25 µg/g cream | CD5789 25 µg/g cream applied once daily |
| DRUG | CD5789 50 µg/g cream | CD5789 50 µg/g cream applied once daily |
| DRUG | CD5789 100 µg/g cream | CD5789 100 µg/g cream applied once daily |
| DRUG | Tazarotene 0.1% gel | Tazarotene 0.1% gel applied once daily |
| DRUG | Vehicle cream | Vehicle cream applied once daily |
Timeline
- Start date
- 2012-06-20
- Primary completion
- 2013-07-24
- Completion
- 2014-06-12
- First posted
- 2012-06-12
- Last updated
- 2021-09-20
- Results posted
- 2021-09-20
Locations
24 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01616654. Inclusion in this directory is not an endorsement.