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Study details
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A Safety and Pharmacokinetics Trial of IDP-122 Lotion in Children With Psoriasis

Bausch Health Americas, Inc.
NCT IDNCT03987763ClinicalTrials.gov data as of Apr 2026
Phase

Phase 4

Target enrollment

45

Study length

about 6.7 years

Ages

6–17

Locations

7 sites in CA, FL, SC +1

What this study is about

This trial is testing the safety, how much of halobetasol propionate (HP) is absorbed into the body, and if it affects the HPA axis for topically applied IDP-122 lotion in children with moderate to severe plaque psoriasis. The treatment will be applied topically.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take IDP-122 Lotion

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
topical

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug routes

topical

Endpoints

Primary: Pharmacokinetics: Maximum Observed Drug (Halobetasol Propionate) Concentration in Plasma (Cmax) of IDP-122 Lotion Analytes

Body systems

Dermatology