Study of Trifarotene Cream to Assess Risk of a Trophic Acne Scar Formation
Completed · Phase 4
Conditions studied: Acne Vulgaris
In brief
The purpose of this study is to evaluate the safety and efficacy of trifarotene 50 microgram per gram (mcg/g) cream compared to its vehicle on the risk of formation of atrophic acne scars after 24 weeks of treatment in facial acne participants assessed by atrophic acne scars count.
Key facts
- Study ID
- NCT04856904
- Run by
- Galderma R&D
- People needed
- 121
- Starts
- 2021-05-28
- Expected to finish
- 2023-06-30
- Last updated by the study team
- 2024-06-11
Who can join
Age: 17 and older, up to 35. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Galderma Investigational Site #8873 — Scottsdale, Arizona, United States
- Galderma Investigational Site #8447 — Fort Smith, Arkansas, United States
- Galderma Investigational Site #8608 — Santa Monica, California, United States
- Galderma Investigational Site #9928 — Boynton Beach, Florida, United States
- Galderma Investigational Site #8295 — Miami, Florida, United States
- Galderma Investigational Site #8883 — Miramar, Florida, United States
- Galderma Investigational Site #8189 — Snellville, Georgia, United States
- Galderma Investigational Site #8367 — Arlington Heights, Illinois, United States
- Galderma Investigational Site #8838 — Darien, Illinois, United States
- Galderma Investigational Site #8601 — Metairie, Louisiana, United States
- Galderma Investigational Site #9936 — New Orleans, Louisiana, United States
- Galderma Investigational Site #8108 — Las Vegas, Nevada, United States
- Galderma Investigational Site #8881 — Stony Brook, New York, United States
- Galderma Investigational Site #8886 — Sugarloaf, Pennsylvania, United States
- Galderma Investigational Site #9920 — Arlington, Texas, United States
- Galderma Investigational Site #9918 — Peterborough, Ontario, Canada
- Galderma Investigational Site #9927 — Saint-Jérôme, Quebec, Canada
- Galderma Investigational Site #6167 — Nantes, France
Full record on ClinicalTrials.gov
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