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Topical Medication

IDP-118 Lotion for Psoriasis

Phase 4
Recruiting
Research Sponsored by Bausch Health Americas, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Is 4 to 16 years 11 months of age at time of informed consent/assent obtained.
Verbal and written informed consent/assent obtained from the participant and/or parent or legal guardian.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0 (predose), 1, 2, 4, 8, 12, and 24 hours postdose
Awards & highlights

Summary

This trial tests a special lotion called IDP-118 for children with moderate to severe plaque psoriasis. It aims to ensure the lotion is safe, see how much gets into the body, and check if it affects stress-related hormones. The goal is to find a safe and effective treatment for these children. IDP-118 is a combination of halobetasol propionate and tazarotene, which has shown effectiveness in treating moderate-to-severe plaque psoriasis in adults.

Who is the study for?
This trial is for children aged 4 to nearly 17 with moderate to severe plaque psoriasis, covering at least 10% of their body excluding face, scalp, and certain areas. They must have normal adrenal function and agree to avoid sun/UV exposure. Girls able to have children must use birth control during the study.
What is being tested?
The trial tests IDP-118 Lotion's safety and effects on the body when applied topically in kids with plaque psoriasis. It also checks if it affects adrenal gland hormones by measuring cortisol levels after a stimulation test.
What are the potential side effects?
Potential side effects are not detailed here but may include skin reactions at the application site or systemic effects due to absorption through the skin which could influence hormone levels.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 4 and 16 years old.
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I have moderate to severe psoriasis, not including my face, scalp, underarms, or skin folds.
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I have psoriasis covering 10% of my body, excluding my face, scalp, and certain areas.
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I can stay out of the sun and away from UV lights during the study.
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I am willing to use birth control during the study.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0 (predose), 1, 2, 4, 8, 12, and 24 hours postdose
This trial's timeline: 3 weeks for screening, Varies for treatment, and 0 (predose), 1, 2, 4, 8, 12, and 24 hours postdose for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Pharmacokinetics: : Maximum Observed Drug (Halobetasol Propionate, Tazarotene, or Tazarotenic Acid) Concentration in Plasma (Cmax) of IDP-118 Lotion Analytes
Secondary study objectives
Proportion of Participants With Hypothalamic-Pituitary-Adrenal (HPA) Axis Suppression at Week 8

Trial Design

1Treatment groups
Experimental Treatment
Group I: IDP-118 LotionExperimental Treatment1 Intervention
Two cohorts of pediatric participants (1 cohort of participants age 12 to 16 years 11 months and 1 cohort of participants age 4 to 11 years 11 months) will apply IDP-118 Lotion to Investigator identified lesions affecting a minimum of 10% body surface area (BSA) once daily for 8 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
IDP-118 Lotion
2016
Completed Phase 3
~1590

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Topical corticosteroids and retinoids are common treatments for psoriasis, working through anti-inflammatory and keratolytic mechanisms, respectively. Corticosteroids reduce inflammation and immune response, alleviating redness, swelling, and itching. Retinoids normalize skin cell growth and differentiation, reducing scales and plaques. Combining these treatments, as in the IDP-118 lotion, targets multiple disease pathways, offering a more effective and comprehensive symptom management for psoriasis patients.
Investigation of anti-inflammatory and anti-proliferative activities promoted by photoactivated cationic porphyrin.

Find a Location

Who is running the clinical trial?

Bausch Health Americas, Inc.Lead Sponsor
262 Previous Clinical Trials
81,991 Total Patients Enrolled
24 Trials studying Psoriasis
11,512 Patients Enrolled for Psoriasis
Anya LoncaricStudy DirectorBausch Health Americas, Inc.
39 Previous Clinical Trials
20,618 Total Patients Enrolled
4 Trials studying Psoriasis
3,813 Patients Enrolled for Psoriasis
Varsha BhattStudy DirectorBausch Health Americas, Inc.
8 Previous Clinical Trials
994 Total Patients Enrolled
2 Trials studying Psoriasis
61 Patients Enrolled for Psoriasis

Media Library

IDP-118 Lotion (Topical Medication) Clinical Trial Eligibility Overview. Trial Name: NCT03988439 — Phase 4
Psoriasis Research Study Groups: IDP-118 Lotion
Psoriasis Clinical Trial 2023: IDP-118 Lotion Highlights & Side Effects. Trial Name: NCT03988439 — Phase 4
IDP-118 Lotion (Topical Medication) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03988439 — Phase 4
Psoriasis Patient Testimony for trial: Trial Name: NCT03988439 — Phase 4
~10 spots leftby Sep 2025