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Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris
NCT03003247 · View on ClinicalTrials.gov ↗
Study Summary
Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris
Conditions Studied
Interventions
- DRUG IDP-120 Gel
- DRUG IDP 120 Component A Gel
- DRUG IDP 120 Component B Gel
- DRUG IDP 120 Vehicle Gel
Study Locations (20)
Florida
- Valeant Site 13 — Lake Mary
- Valeant Site 16 — Miami
- Valeant Site 14 — Tampa
- Valeant Site 02 — West Palm Beach
Texas
- Valeant Site 07 — Austin
- Valeant Site 12 — Austin
- Valeant Site 18 — San Antonio
New York
- Valreant Site 05 — New York
- Valeant Site 06 — New York
North Carolina
- Valeant Site 01 — Chapel Hill
- Valeant Site 17 — High Point
California
- Valeant Site 15 — Encino
Georgia
- Valeant Site 21 — Atlanta
Indiana
- Valeant Site 23 — South Bend
Michigan
- Valeant Site 09 — Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 364 participants |
| Start Date | 2015-11 |
| Est. Completion | 2016-09-30 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03003247
The ClinicalTrials.gov registry entry for NCT03003247 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 364 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bausch Health Americas, which has 55 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Acne Vulgaris appearing as the primary indexed condition, and to 4 interventions — of which IDP-120 Gel is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03003247 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Florida, Texas, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03003247 about?
NCT03003247 is a clinical study titled "Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris". Efficacy and Safety of IDP-120 Gel in the Treatment of Acne Vulgaris
What is the current status of trial NCT03003247?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 364 participants. The study started on 2015-11. Estimated completion is 2016-09-30.
What conditions does trial NCT03003247 study?
This clinical trial studies the following conditions: Acne Vulgaris. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03003247?
The interventions under investigation include: IDP-120 Gel (DRUG), IDP 120 Component A Gel (DRUG), IDP 120 Component B Gel (DRUG), IDP 120 Vehicle Gel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03003247?
This trial is sponsored by Bausch Health Americas, which has 55 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03003247 being conducted?
This trial has 20 study locations across California, Florida, Georgia, Indiana, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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