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Completed Phase 4 Interventional Results available

Study of Trifarotene Cream to Assess Risk of a Trophic Acne Scar Formation

ClinicalTrials.gov ID: NCT04856904

Public ClinicalTrials.gov record NCT04856904. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 10:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Evaluation of the Risk of Atrophic Acne Scar Formation During Treatment of Acne Vulgaris Subjects With Trifarotene 50 μg/g Cream Versus Vehicle Cream Over 24 Weeks

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT04856904
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Galderma R&D
Industry
Enrollment
121 participants

Conditions and interventions

Eligibility (public fields only)

Age range
17 Years to 35 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 27, 2021
Primary completion
Feb 7, 2023
Completion
Jun 29, 2023
Last update posted
Jun 10, 2024

2021 – 2023

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Galderma Investigational Site #8873 Scottsdale Arizona 85260
Galderma Investigational Site #8447 Fort Smith Arkansas 72916
Galderma Investigational Site #8608 Santa Monica California 90404
Galderma Investigational Site #9928 Boynton Beach Florida 33437
Galderma Investigational Site #8295 Miami Florida 33136
Galderma Investigational Site #8883 Miramar Florida 33027
Galderma Investigational Site #8189 Snellville Georgia 30078
Galderma Investigational Site #8367 Arlington Heights Illinois 60005
Galderma Investigational Site #8838 Darien Illinois 60561
Galderma Investigational Site #8601 Metairie Louisiana 70001
Galderma Investigational Site #9936 New Orleans Louisiana 70130
Galderma Investigational Site #8108 Las Vegas Nevada 89148
Galderma Investigational Site #8881 Stony Brook New York 11790
Galderma Investigational Site #8886 Sugarloaf Pennsylvania 18249
Galderma Investigational Site #9920 Arlington Texas 76011

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04856904, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 10, 2024 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04856904 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →