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Completed Phase 2 Interventional Results available

Dose Range Study of CD5789 in Acne Vulgaris

ClinicalTrials.gov ID: NCT01616654

Public ClinicalTrials.gov record NCT01616654. 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 Jul 22, 2026, 5:05 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 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

Study identification

NCT ID
NCT01616654
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Galderma R&D
Industry
Enrollment
304 participants

Conditions and interventions

Conditions

Interventions

  • CD5789 25 µg/g cream Drug
  • CD5789 50 µg/g cream Drug
  • CD5789 100 µg/g cream Drug
  • Tazarotene 0.1% gel Drug
  • Vehicle cream Drug

Drug

Eligibility (public fields only)

Age range
12 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
Jun 19, 2012
Primary completion
Jul 23, 2013
Completion
Jun 11, 2014
Last update posted
Sep 19, 2021

2012 – 2014

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Total Skin and Beauty Dermatology Center, PC Birmingham Alabama 35205
Parexel Early Phase Glendale California 91206
Odyssey Medispa Marina del Rey California 90292
Rady Children's Hospital San Diego California 92123
FXM Research Corp Miami Miami Florida 33175
FMX Research Miramar Miramar Florida 33027
Meda Phase, Inc Newnan Georgia 30263
Deaconess Clinic, Inc. Evansville Indiana 47713
Dermatology Specialists PC Louisville Kentucky 40202
Hamzavi Dermatology Fort Gratiot Michigan 48059
Somerset Skin Centre Troy Michigan 48084
Skin Specialists, PC Omaha Nebraska 68144
Academic Dermatology Associates Albuquerque New Mexico 87106
Zoe Drealos, MD High Point North Carolina 27262
PMG Research of Wilmington Wilmington North Carolina 28401
Central Sooner Research Norman Oklahoma 73069
Oregon Dermatology and Research Center Portland Oregon 97210
Palmetto Clinical Trial Services, LLC Greenville South Carolina 29607
Arlington Center for Dermatology Arlington Texas 76011
Suzanne Bruce and Associates P.A. The Center for Skin Research Houston Texas 77056
Stephen Miller MD San Antonio Texas 78229
Center for Clinical Studies Webster Texas 77598
Dermatology Research Center Salt Lake City Utah 84124
The Education & Research Foundation, Inc. Lynchburg Virginia 24501

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01616654, 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 Sep 19, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01616654 live on ClinicalTrials.gov.

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