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Completed Phase 3 Interventional Results available

A Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects With Common Facial Acne - W0260-301

ClinicalTrials.gov ID: NCT01017146

Public ClinicalTrials.gov record NCT01017146. 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 24, 2026, 8:30 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 Multicenter, Randomized, Double-Blind, Vehicle-Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of Tazarotene Foam, 0.1%, in Subjects With Acne Vulgaris

Study identification

NCT ID
NCT01017146
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Stiefel, a GSK Company
Industry
Enrollment
744 participants

Conditions and interventions

Conditions

Interventions

  • Tazarotene foam Drug
  • Vehicle Foam Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 45 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
Sep 30, 2009
Primary completion
Oct 31, 2010
Completion
Oct 31, 2010
Last update posted
Jan 17, 2017

2009 – 2010

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Cherry Creek Research, Inc. Denver Colorado 80209
Cosmetic Medicine & Treatment Research Insttitute, Inc. Miami Beach Florida 33140
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46260
Minnesota Clinical Study Center Fridley Minnesota 55432
Academic Dermatology Associates Albuquerque New Mexico 87106
DermResearch Center of New York, Inc. Stony Brook New York 11790
Dermatology Consulting Services High Point North Carolina 27262
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
The Dermatology Research of Cincinnati Cincinnati Ohio 45220
Group Health Associates Cincinnatti Ohio 45220
Haber Dermatology & Cosmetic Surgery, Inc. South Euclid Ohio 44118
Oregon Dermatology and Research Center Portland Oregon 97210
Yardley Dermatology Associates Yardley Pennsylvania 19067
The Skin Wellness Center, PC Knoxville Tennessee 37922
Dermatology Research Associates, Inc. Nashville Tennessee 37203
DermResearch, Inc. Austin Texas 78759
J & S Studies, Inc. College Station Texas 77845
Dermatology Treatment & Research Center Dallas Texas 75230
Aurora Advanced Healthcare, Inc. Clinical Research Center Milwaukee Wisconsin 53209

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 NCT01017146, 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 Jan 17, 2017 · Synced Jul 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01017146 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →