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Completed Phase 3 Interventional Results available

A Study Comparing Tazarotene Cream 0.1% to TAZORAC® (Tazarotene) Cream 0.1% and Both to a Placebo Control in the Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT02886715

Public ClinicalTrials.gov record NCT02886715. 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, 6:08 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 Multi-Center, Double-Blind, Randomized, Vehicle-Controlled, Parallel-Group Study Comparing Tazarotene Cream 0.1% to TAZORAC® (Tazarotene) Cream 0.1% and Both Active Treatments to a Vehicle Control in the Treatment of Acne Vulgaris

Study identification

NCT ID
NCT02886715
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Fougera Pharmaceuticals Inc.
Industry
Enrollment
1,110 participants

Conditions and interventions

Conditions

Interventions

  • Tazarotene Cream 0.1% Drug
  • Tazorac® Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 40 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 20, 2016
Primary completion
May 30, 2017
Completion
May 30, 2017
Last update posted
Aug 16, 2018

2016 – 2017

United States locations

U.S. sites
25
U.S. states
9
U.S. cities
23
Facility City State ZIP Site status
Fougera Investigational Site Tucson Arizona 85712
Fougera Investigational Site Conway Arkansas 72034
Fougera Investigational Site Hot Springs Arkansas 71913
Fougera Investigational Site Anaheim California 92801
Fougera Investigational Site La Mesa California 91942
Fougera Investigational Site Long Beach California 90806
Fougera Investigational Site Long Beach California 90813
Fougera Investigational Site Los Angeles California 90010
Fougera Investigational Site North Hollywood California 91606
Fougera Investigational Site San Diego California 92108
Fougera Investigational Site San Ramon California 94582
Fougera Investigational Site Upland California 91786
Fougera Investigational Site West Covina California 91790
Fougera Investigational Site Coral Gables Florida 33134
Fougera Investigational Site Miami Florida 33015
Fougera Investigational Site Miami Florida 33175
Fougera Investigational Site Miami Gardens Florida 33169
Fougera Investigational Site Miramar Florida 33027
Fougera Investigational Site Sweetwater Florida 33172
Fougera Investigational Site Plainfield Indiana 46168
Fougera Investigational Site High Point North Carolina 27262
Fougera Investigational Site Hazleton Pennsylvania 18201
Fougera Investigational Site Upper Saint Clair Pennsylvania 15241
Fougera Investigational Site Chattanooga Tennessee 37421
Fougera Investigational Site Austin Texas 78759

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 NCT02886715, 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 Aug 16, 2018 · Synced Jul 22, 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 NCT02886715 live on ClinicalTrials.gov.

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