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NCT02932306 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of IDP-121 and IDP-121 Vehicle Lotion in the Treatment of Acne Vulgaris

A Phase 3 study, sponsored by Bausch Health Americas.

Completed
Registry status
Phase 3
Development phase
820
Enrollment target

NCT02932306: Completed Phase 3 study, sponsored by Bausch Health Americas.

NCT02932306 is a Phase 3 study that has completed, run by Bausch Health Americas. The registered enrollment target is 820 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02932306, a Phase 3 study, has completed, sponsored by Bausch Health Americas.

COMPLETED
Registry status
Phase 3
Development phase
820 participants
Enrollment target

Study Summary

The objective of this study was to evaluate the efficacy, safety, and tolerability of a once daily topical application of IDP-121 Lotion compared with its vehicle (IDP-121 Vehicle Lotion) in participants with moderate to severe acne vulgaris (acne) (that is, acne having an Evaluator's Global Severity Score \[EGSS\] of 3 \[moderate\] or 4 \[severe\]).

Primary Outcome

Noninflammatory lesions were defined as follows: Open comedones (blackhead) - plugged hair follicle with dilated/open orifice, black in color; and Closed comedones (whitehead) - plugged hair follicle: small opening at skin surface. For noninflammatory facial lesions, open and closed comedones were recorded as a single count.

Interventions

  • DRUG IDP-121 Vehicle Lotion
  • DRUG IDP-121 Lotion

Trial Details

FieldValue
Enrollment Target 820 participants
Start Date 2015-11-03
Est. Completion 2017-02-22
Phase Phase 3
Bausch Health Americas

168 total trials

What the finished NCT02932306 record still lists

NCT02932306 is an interventional study that assigns participants to a tested intervention. The registered 820 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which IDP-121 Vehicle Lotion is the first listed.

NCT02932306 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02932306 about?

NCT02932306 is a clinical study titled "Efficacy and Safety of IDP-121 and IDP-121 Vehicle Lotion in the Treatment of Acne Vulgaris". The objective of this study was to evaluate the efficacy, safety, and tolerability of a once daily topical application of IDP-121 Lotion compared with its vehicle (IDP-121 Vehicle Lotion) in participants with moderate to severe acne vulgaris (acne) (that is, acne having an Evaluator's Global Severit...

What is the current status of trial NCT02932306?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 820 participants. The study started on 2015-11-03. Estimated completion is 2017-02-22.

What interventions are being tested in trial NCT02932306?

The interventions under investigation include: IDP-121 Vehicle Lotion (DRUG), IDP-121 Lotion (DRUG).

Who is sponsoring clinical trial NCT02932306?

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

How this trial's enrollment target compares

Where NCT02932306's enrollment target sits among peer trials

820 404th of 2000 higher than 1,596 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02932306, the US trial registry maintained by the National Library of Medicine. NCT02932306 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.