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Completed Phase 2 Interventional Results available

Safety and Efficacy of IDP-123 Lotion to Tazorac® Cream, in the Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT02938494

Public ClinicalTrials.gov record NCT02938494. 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 2, 2026, 11:46 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 Phase 2, Multi-Center, Double-Blind, Randomized, Vehicle-Controlled, Study to Compare the Safety and Efficacy of IDP-123 Lotion to Tazorac® (Tazarotene) Cream, in the Treatment of Acne Vulgaris

Brief summary

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

Safety and Efficacy of IDP-123 Lotion (0.045% tazarotene) to Tazorac® (tazarotene) Cream, 0.1%, in the Treatment of Acne Vulgaris

Study identification

NCT ID
NCT02938494
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
210 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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
Oct 31, 2015
Primary completion
Jun 30, 2016
Completion
Aug 31, 2016
Last update posted
Sep 22, 2020

2015 – 2016

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
Valeant Site 03 Encinitas California 92024
Valeant Site 04 Fremont California 94538
Valeant Site 06 Los Angeles California 90036
Valeant Site 14 Sacramento California 95819
Valeant Site 01 Santa Monica California 90404
Valeant Site 05 Colorado Springs Colorado 80915
Valeant Site 08 Coral Gables Florida 33146
Valeant Site 10 Miami Florida 33175
Valeant Site 09 Miramar Florida 33027
Valeant Site 12 Louisville Kentucky 40202
Valeant Site 13 Louisville Kentucky 40217
Valeant Site 02 Rockville Maryland 20850
Valeant Site 07 Fridley Minnesota 55432
Valeant Site 16 Chapel Hill North Carolina 27517
Valeant Site 15 High Point North Carolina 27262
Valeant Site 11 Philadelphia Pennsylvania 19103

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 NCT02938494, 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 22, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02938494 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →