An Open-label Single Center, Proof of Concept Study Evaluating the Efficacy of Roflumilast Foam 0.3% in Pediatric Patients With Non-Segmental Vitiligo (NSV)

NCT ID: NCT07105254

Last Updated: 2025-08-08

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-08-01
• Study Completion Date: 2026-06-15

Brief Summary

An open-label single center, proof of concept study evaluating the efficacy of Roflumilast foam 0.3% in pediatric subjects with Non-Segmental Vitiligo (NSV)

Conditions

Non-segmental Vitiligo

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Open-label single center, proof of concept study evaluating the efficacy of Roflumilast foam 0.3%

Group Type: EXPERIMENTAL

Roflumilast topical 0.3% foam

Intervention Type: DRUG

Roflumilast 0.3% topical foam

Interventions

Roflumilast topical 0.3% foam

Roflumilast 0.3% topical foam

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female subjects aged 2 years but less than 18 years

2. Pediatric and adolescent subjects: Informed consent of parent(s) or legal guardian, and, if age appropriate, assent by the subjects, as required by local laws.

3. Diagnosis of non-segmental vitiligo based on clinical history and dermatology examination for at least 3 months.

4. Diagnosis of non-segmental vitiligo with the following:

1. BSA affected < 10% AND

2. At least 0.5% BSA affected on the face. AND

3. Pigmented hair within some of the areas of vitiligo on the face

5. In good health as judged by the Investigator, based on the medical history, and dermatology examination.

6. Subjects and parent(s)/legal guardian (s) are considered reliable and capable of adhering to the Protocol and visit schedule, according to the judgment of the Investigator.

Exclusion Criteria

1. Subjects with any serious medical condition or physical examination abnormality that would prevent study participation or place the subject at significant risk, as judged by the Investigator.

2. Subjects with known or suspected:

1. Severe renal insufficiency

2. Moderate to severe hepatic disorders (Child-Pugh B or C)

3. Subjects who cannot discontinue prohibited medications and treatments prior to the Baseline visit and during the study, including (any biologic or experimental therapy within 12 weeks (or 5 half-lives), phototherapy within 4 weeks, immunomodulating treatments within 4 weeks, or topical treatments within 1 week.

3. Subjects who are unwilling to refrain from using a tanning bed or other artificial light emitting devices (LEDs) for 4 weeks prior to Baseline/Day 1 and during the study.

4. Subjects with diagnosis of other forms of vitiligo (e.g. Segmental), other differential diagnosis of vitiligo or other skin depigmentation disorders (e.g. Piedbaldism, pityriasis alba, leprosy, post-inflammatory hypopigmentation, progressive macule hypomelanosis, nevus anemicus, chemical leukoderma and tinea versicolor) that would interfere with the evaluations of the effect of the study medication, as determined by the Investigator.

5. Subjects with known genetic dermatological conditions that overlap with non-segmental vitiligo.

6. Known allergies to excipients in Roflumilast foam (petrolatum, isopopyl palmitate, methylparaben, propylparaben, diethylene glycol monomethyl ether, hexylene glycol, cetylseteary alcohol, dicetyl phosphase and ceteth-10 phosphate)

7. Subjects who cannot discontinue systemic CYP3A4 inhibitors or dual inhibitors that inhibit both CYP3A4 and CYP1A2 simultaneously (e.g. Erythromycin, ketoconazole, fluvoxamine, enoxacin, cimetidine)

8. Subjects who have received oral roflumilast (Daxas®, Daliresp®) within 4 weeks prior to Baseline/Day 1.

9. Females who are pregnant, wishing to become pregnant during the study, or are breast feeding.

10. Previous treatment with Roflumilast cream or foam for vitiligo in the past 3 months.

11. Parent (s)/legal guardians (s) who are unable to communicate, read, or understand the local language (s). Subjects who are unable to communicate, read or understand the local language, or who display another condition, which in the Investigator's opinion, makes them unsuitable for clinical study participation.

12. Subjects who are family members of the clinical study site, clinical study staff, or sponsor, or family members of enrolled subjects living in the same house.

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Arcutis Biotherapeutics, Inc.

INDUSTRY

Sponsor Role: collaborator

Derm Texas, PLLC

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kelly Warren, MD

Role: PRINCIPAL_INVESTIGATOR

Derm Texas, PLLC

Locations

Derm Texas

Dallas, Texas, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Amanda Harvey, Study Coordinator

Role: CONTACT

aharvey@derm-texas.com

2148456426

Facility Contacts

Amanda Study Coordinator

Role: primary

aharvey@derm-texas.com

214-845-6426

Other Identifiers

20251829

Identifier Type: -

Identifier Source: org_study_id