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Completed Phase 3 Interventional Results available

CD5789 (Trifarotene) Long Term Safety Study on Acne Vulgaris

ClinicalTrials.gov ID: NCT02189629

Public ClinicalTrials.gov record NCT02189629. 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 Jun 26, 2026, 11:34 AM EDT

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

Official title

A LONG-TERM SAFETY AND EFFICACY STUDY OF CD5789 (Trifarotene) 50 µg/g CREAM IN SUBJECTS WITH ACNE VULGARIS

Study identification

NCT ID
NCT02189629
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Galderma R&D
Industry
Enrollment
453 participants

Conditions and interventions

Conditions

Interventions

  • CD5789 (trifarotene) Drug

Drug

Eligibility (public fields only)

Age range
9 Years and older
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
Feb 22, 2015
Primary completion
Feb 22, 2017
Completion
Feb 22, 2017
Last update posted
Nov 13, 2019

2015 – 2017

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Galderma Investigational Site Mobile Alabama 36608
Galderma Investigational Site Rogers Arkansas 72758
Galderma Investigational Site Sacramento California 95819
Galderma Investigational Site San Diego California 92123
Galderma Investigational Site Miami Florida 33175
Galderma Investigational Site Miramar Florida 33027
Galderma Investigational Site Newnan Georgia 30277
Galderma Investigational Site Louisville Kentucky 40241
Galderma Investigational Site Albuquerque New Mexico 87107
Galderma Investigational Site New York New York 10155
Galderma Investigational Site High Point North Carolina 27262
Galderma Investigational Site Beachwood Ohio 44122
Galderma Investigational Site Portland Oregon 97210
Galderma Investigational Site Knoxville Tennessee 37922

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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02189629, 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 Nov 13, 2019 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02189629 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →