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Completed Phase 2 Interventional Accepts healthy volunteers

Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris

ClinicalTrials.gov ID: NCT03003247

Public ClinicalTrials.gov record NCT03003247. 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 6, 2026, 11:02 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, Randomized, Double-Blind, Vehicle- Controlled, Parallel-Group, Clinical Study Comparing the Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris

Brief summary

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

Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris

Study identification

NCT ID
NCT03003247
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
364 participants

Conditions and interventions

Eligibility (public fields only)

Age range
9 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

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
Aug 30, 2016
Completion
Sep 29, 2016
Last update posted
Dec 17, 2017

2015 – 2016

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Valeant Site 15 Encino California 91316
Valeant Site 13 Lake Mary Florida 32746
Valeant Site 16 Miami Florida 33101
Valeant Site 14 Tampa Florida 33601
Valeant Site 02 West Palm Beach Florida 33401
Valeant Site 21 Atlanta Georgia 30302
Valeant Site 23 South Bend Indiana 46601
Valeant Site 09 Detroit Michigan 48204
Valeant Site 24 Minneapolis Minnesota 55401
Valeant Site 11 Saint Joseph Missouri 64502
Valreant Site 05 New York New York 10001
Valeant Site 06 New York New York 10002
Valeant Site 01 Chapel Hill North Carolina 27517
Valeant Site 17 High Point North Carolina 27268
Valeant Site 22 Columbus Ohio 43085
Valeant Site 04 Knoxville Tennessee 37901
Valeant Site 07 Austin Texas 73301
Valeant Site 12 Austin Texas 78701
Valeant Site 18 San Antonio Texas 78204
Valeant Site 25 Spokane Washington 99202

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03003247, 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 Dec 17, 2017 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03003247 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →