Psoriasis Clinical Trial

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

Summary

Suppression Potential of Topically Applied IDP-118 Lotion and HP Monad Lotion in Subjects with Moderate to Severe Plaque Psoriasis.

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Full Description

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.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Male or Female of any race, at least 18 years old of age (inclusive)
Freely provides both written and oral informed consent.
Has a clinical diagnosis of psoriasis at the Baseline visit with an Investigator's Global Assessment Score of 3 or 4. The face, scalp ,axillae, and intertriginous areas are to be excluded in this calculation.
Has an area of plaque psoriasis for topical treatment that involves a BSA of at least 20%.
The willing and able to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural and artificial) for the duration of the study.

Key Exclusion Criteria:

Has spontaneously improving or rapidly deteriorating plaque psoriasis or postural psoriasis, as determined by the investigator.
Presents with psoriasis that was treated with prescription medication and failed to respond to presents).
Has a history of adrenal disease.
Presents with any other concurrent skin conditions that could interfere with the evaluation of the treatment areas, as determined by the investigator.
Is pregnant, nursing, or planning pregnancy during the study period.

Study is for people with:

Psoriasis

Phase:

Phase 1

Estimated Enrollment:

94

Study ID:

NCT03058744

Recruitment Status:

Completed

Sponsor:

Bausch Health Americas, Inc.

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There are 12 Locations for this study

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Valeant Site 12
Anaheim California, 92801, United States
Valeant Site 05
Encino California, 91436, United States
Valeant Site 01
San Diego California, 92093, United States
Valeant Site 07
Santa Rosa California, 95401, United States
Valeant Site 10
Orange Park Florida, 32065, United States
Valeant Site 09
Sanford Florida, 32771, United States
Valeant Site 08
Atlanta Georgia, 30301, United States
Valeant Site 04
Plainfield Indiana, 46168, United States
Valeant Site 06
New York New York, 10001, United States
Valeant Site 11
Philadelphia Pennsylvania, 19019, United States
Valeant Site 03
Austin Texas, 73301, United States
Valeant Site 02
Katy Texas, 77449, United States

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 1

Estimated Enrollment:

94

Study ID:

NCT03058744

Recruitment Status:

Completed

Sponsor:


Bausch Health Americas, Inc.

How clear is this clinincal trial information?

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