Clinical Trials Directory

Trials / Completed

CompletedNCT02566369

Efficacy and Safety of CD5789 (Trifarotene) 50μg/g Cream Versus Vehicle Cream in Acne Vulgaris

A Multi-Center, Randomized, Double-Blind, Parallel-Group Vehicle Controlled Study To Compare The Efficacy And Safety Of CD5789 (Trifarotene) 50μg/g Cream Versus Vehicle Cream In Subjects With Acne Vulgaris

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
1,208 (actual)
Sponsor
Galderma R&D · Industry
Sex
All
Age
9 Years
Healthy volunteers
Not accepted

Summary

Assessment of the efficacy and safety of CD5789 (trifarotene) 50μg/g cream applied once daily for 12 weeks in subjects with acne vulgaris.

Detailed description

Clinical Trial for each subject is approximately 14 weeks and are randomized to one of the two treatments for 12 weeks. Subjects must be 9 years of age and older with acne vulgaris.

Conditions

Interventions

TypeNameDescription
DRUGCD5789 (trifarotene) 50μg/g creamCD5789 (trifarotene) 50µg/g cream applied once daily for 12 weeks.
DRUGPlacebo creamPlacebo cream applied once daily for 12 weeks

Timeline

Start date
2015-11-30
Primary completion
2017-11-14
Completion
2017-11-14
First posted
2015-10-02
Last updated
2019-11-12
Results posted
2019-08-22

Locations

124 sites across 5 countries: United States, Canada, Germany, Hungary, Puerto Rico

Source: ClinicalTrials.gov record NCT02566369. Inclusion in this directory is not an endorsement.