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Completed Phase 1 Interventional

Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis

ClinicalTrials.gov ID: NCT03058744

Public ClinicalTrials.gov record NCT03058744. 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 Jun 26, 2026, 2:51 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 1b Open Label, Randomized Study Evaluating the Absorption and Systemic Pharmacokinetics and HPA Axis Suppression Potential of Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects With Moderate to Severe Plaque Psoriasis

Study identification

NCT ID
NCT03058744
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
94 participants

Conditions and interventions

Conditions

Interventions

  • IDP-118 Lotion Drug
  • HP Monad Lotion Drug
  • Ultravate Cream Drug
  • Tazorac Cream Drug

Drug

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
Mar 31, 2015
Primary completion
Nov 30, 2016
Completion
Dec 31, 2016
Last update posted
Jun 8, 2017

2015 – 2017

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
Valeant Site 12 Anaheim California 92801
Valeant Site 05 Encino California 91436
Valeant Site 01 San Diego California 92093
Valeant Site 07 Santa Rosa California 95401
Valeant Site 10 Orange Park Florida 32065
Valeant Site 09 Sanford Florida 32771
Valeant Site 08 Atlanta Georgia 30301
Valeant Site 04 Plainfield Indiana 46168
Valeant Site 06 New York New York 10001
Valeant Site 11 Philadelphia Pennsylvania 19019
Valeant Site 03 Austin Texas 73301
Valeant Site 02 Katy Texas 77449

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 NCT03058744, 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 Jun 8, 2017 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03058744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →