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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Safety and Efficacy of IDP-122 Lotion When Applied Topically to Subjects With Moderate to Severe Plaque Psoriasis

ClinicalTrials.gov ID: NCT02785185

Public ClinicalTrials.gov record NCT02785185. 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, 10:26 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, Double-Blind, Randomized, Vehicle-Controlled Study to Compare the Safety and Efficacy of IDP-122 Lotion (0.01% Halobetasol Propionate) to Ultravate® (Halobetasol Propionate) Cream, in the Treatment of Plaque Psoriasis

Brief summary

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

A Phase 2, Multi-Center, Double-Blind, Randomized, Vehicle-Controlled Study.

Study identification

NCT ID
NCT02785185
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
150 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Jun 2016 (Actual)
Primary completion
Dec 2, 2016 (Actual)
Completion
Jan 2017 (Actual)
Last update posted
Aug 27, 2020

2016 – 2017

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
13
Facility City State ZIP Site status
Valeant Site 05 Rogers Arkansas 75758 —
Valeant Site 10 Beverly Hills California 90210 —
Valeant Site 09 Carlsbad California 92008 —
Valeant Site 13 Los Angeles California 90045 —
Valeant Site 12 Santa Monica California 90404 —
Valeant Site 07 Coral Gables Florida 33134 —
Valeant Site 11 North Miami Beach Florida 33162 —
Valeant Site 03 Sanford Florida 32771 —
Valeant Site 08 Albany Indiana 47150 —
Valeant Site 04 Louisville Kentucky 40202 —
Valeant Site 06 Fridley Minnesota 55432 —
Valeant Site 02 High Point North Carolina 27262 —
Valeant Site 01 Houston Texas 77065 —

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 NCT02785185, 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 Aug 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 NCT02785185 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →