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NCT04214639 · ClinicalTrials.gov registry record · Phase 3

Clinical Study Comparing the Efficacy and Safety of IDP-126 Gel in the Treatment of Acne Vulgaris

A Phase 3 study of Acne Vulgaris, sponsored by Bausch Health Americas.

Completed
Registry status
Phase 3
Development phase
183
Enrollment target
13
Study locations

NCT04214639 is a Phase 3 study of Acne Vulgaris that has completed, run by Bausch Health Americas. The registered enrollment target is 183 participants, below the 273-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (33% lower). The trial reports 13 study locations across 10 states.

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The verdict

NCT04214639, a Phase 3 study of Acne Vulgaris, has completed, sponsored by Bausch Health Americas.

COMPLETED
Registry status
Phase 3
Development phase
183 participants
Enrollment target
13
Study locations

Study Summary

This is a multicenter, randomized, double-blind, vehicle-controlled, 12-week study designed to assess the safety, tolerability, and efficacy of IDP-126 Gel in comparison IDP-126 Vehicle Gel at Weeks 2, 4, 8, and 12.

Conditions Studied

Interventions

  • DRUG IDP-126 Gel
  • DRUG IDP-126 Vehicle Gel

Study Locations (13)

Florida

  • Bausch Site 102 - Boynton Beach
  • Bausch Site 111 - North Miami Beach
  • Bausch Site 106 - Sanford

Ontario

  • Bausch Site 101 - Barrie
  • Bausch Site 113 - Waterloo

Arkansas

  • Bausch Site 110 - Bryant

California

  • Bausch Site 104 - Fremont

Colorado

  • Bausch Site 109 - Denver

Nevada

  • Bausch Site 103 - Las Vegas

New York

  • Bausch Site 114 - New York

North Carolina

  • Bausch Site 105 - High Point

Trial Details

FieldValue
Enrollment Target 183 participants
Start Date 2020-01-17
Est. Completion 2021-01-18
Phase Phase 3

Sponsor

Bausch Health Americas

168 total trials

What the Registry Record Tells You About NCT04214639

The ClinicalTrials.gov registry entry for NCT04214639 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 183 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 273-participant average among 67 other Acne Vulgaris trials with a reported enrollment target (33% lower). The listed sponsor is Bausch Health Americas, which has 168 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Acne Vulgaris appearing as the primary indexed condition, and to 2 interventions - of which IDP-126 Gel is the first listed.

NCT04214639 reports 13 study locations spanning 10 distinct geographic areas - top geographies include Florida, Ontario, Arkansas.

Frequently Asked Questions

What is clinical trial NCT04214639 about?

NCT04214639 is a clinical study titled "Clinical Study Comparing the Efficacy and Safety of IDP-126 Gel in the Treatment of Acne Vulgaris". This is a multicenter, randomized, double-blind, vehicle-controlled, 12-week study designed to assess the safety, tolerability, and efficacy of IDP-126 Gel in comparison IDP-126 Vehicle Gel at Weeks 2, 4, 8, and 12.

What is the current status of trial NCT04214639?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 183 participants. The study started on 2020-01-17. Estimated completion is 2021-01-18.

What conditions does trial NCT04214639 study?

This clinical trial studies the following conditions: Acne Vulgaris.

What interventions are being tested in trial NCT04214639?

The interventions under investigation include: IDP-126 Gel (DRUG), IDP-126 Vehicle Gel (DRUG).

Who is sponsoring clinical trial NCT04214639?

This trial is sponsored by Bausch Health Americas, which has 168 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04214639 being conducted?

This trial has 13 study locations across Arkansas, California, Colorado, Florida, Nevada. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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