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Completed Phase 3 Interventional Results available

Safety and Efficacy of IDP-122 in the Treatment of Participants With Plaque Psoriasis

ClinicalTrials.gov ID: NCT02514577

Public ClinicalTrials.gov record NCT02514577. 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 Oct 18, 2026, 1:29 PM 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 3, Multicenter, Double-Blind, Randomized, Vehicle Controlled Clinical Study to Assess the Safety and Efficacy of IDP-122 in the Treatment of Plaque Psoriasis

Brief summary

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

This study is to evaluate the safety and efficacy of a topical lotion when applied once daily to adult participants with moderate to severe plaque psoriasis (defined as an Investigator's Global Assessment \[IGA\] score of 3 or 4).

Study identification

NCT ID
NCT02514577
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
217 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Nov 7, 2015 (Actual)
Primary completion
May 1, 2017 (Actual)
Completion
May 1, 2017 (Actual)
Last update posted
Jan 27, 2020

2015 – 2017

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Valeant Site 11 Hot Springs Arkansas 71901 —
Valeant Site 1 Encinitas California 92023 —
Valeant Site 10 Encino California 91436 —
Valeant Site 12 Santa Rosa California 95401 —
Valeant Site 13 Atlanta Georgia 30301 —
Valeant Site 7 Boise Idaho 83701 —
Valeant Site 6 Rockville Maryland 20847 —
Valeant Site 4 Ann Arbor Michigan 48103 —
Valeant Site 8 Clarkston Michigan 48346 —
Valeant Site 15 Las Vegas Nevada 89101 —
Valeant Site 9 Raleigh North Carolina 27601 —
Valeant Site 5 Knoxville Tennessee 37901 —
Valeant Site 3 Austin Texas 73301 —
Valeant Site 2 San Antonio Texas 78201 —
Valeant Site 14 Spokane Washington 99201 —

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 NCT02514577, 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 Jan 27, 2020 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02514577 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →