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Completed Phase 3 Interventional Results available

Safety and Efficacy of IDP-118 in the Treatment of Plaque Psoriasis

ClinicalTrials.gov ID: NCT02462070

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT02462070. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 10:50 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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-118 in the Treatment of Plaque Psoriasis

Brief summary

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

The objective of the study is to evaluate the safety and efficacy of a topical lotion.

Study identification

NCT ID
NCT02462070
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
203 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
Aug 11, 2015 (Actual)
Primary completion
Nov 8, 2016 (Actual)
Completion
Dec 1, 2016 (Actual)
Last update posted
Aug 20, 2020

2015 – 2016

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Valeant Site 3 Mobile Alabama 36601 —
Valeant Site 9 Beverly Hills California 90210 —
Valeant Site 12 Encino California 91316 —
Valeant Site 10 San Diego California 92093 —
Valeant Site 1 Santa Rosa California 95403 —
Valeant Site 16 Denver Colorado 80123 —
Valeant Site 2 Tampa Florida 33601 —
Valeant Site 7 South Bend Indiana 46601 —
Valeant Site 8 Louisville Kentucky 40202 —
Valeant Site 13 Clinton Township Michigan 48036 —
Valeant Site 14 Rochester New York 14603 —
Valeant Site 6 Nashville Tennessee 37115 —
Valeant Site 5 Austin Texas 73344 —
Valeant Site 4 Houston Texas 77001 —
Valeant Site 11 Norfolk Virginia 23501 —
Valeant Site 15 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 NCT02462070, 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 20, 2020 · Synced Nov 12, 2026

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