Maximal Usage Pharmacokinetics and Safety of ARQ-151 in Children With Plaque Psoriasis (ARQ-151-216)

NCT ID: NCT04746911

Last Updated: 2023-03-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-03-01
• Study Completion Date: 2022-05-11

Brief Summary

This is a Phase 2, open label, maximal usage PK and safety study of ARQ-151 cream 0.3% in pediatric subjects (ages 2 to 5 years old) with plaque psoriasis:

Conditions

Psoriasis; Plaque Psoriasis

Study Design

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

Study Groups

ARQ-151 cream 0.3%

Open label study of ARQ-151 cream 0.3% applied once daily for 4 weeks

Group Type: EXPERIMENTAL

ARQ-151 cream 0.3%

Intervention Type: DRUG

ARQ-151 cream 0.3% applied to chronic plaque psoriasis lesions once a day for 4 weeks

Interventions

ARQ-151 cream 0.3%

ARQ-151 cream 0.3% applied to chronic plaque psoriasis lesions once a day for 4 weeks

Intervention Type: DRUG

Other Intervention Names

Topical roflumilast

Eligibility Criteria

Inclusion Criteria

• Informed consent of parent(s) or legal guardian.
• Males or females, 2 to 5 years old (inclusive).
• Clinical diagnosis of psoriasis vulgaris of at least 2 months duration as determined by the Investigator or through subject interview. Stable disease for the past 3 weeks.
• Psoriasis vulgaris on the face, extremities, trunk, and/or intertriginous areas involving at least 2% of BSA (excluding the scalp, palms, and soles).
• An Investigator Global Assessment of disease severity (IGA) of at least Mild ('2') at Baseline.
• Subject has adequate venous access for PK sampling in areas not involved by plaque psoriasis and not being treated with ARQ-151 (e.g., back of the hands).
• In good health as judged by the Investigator, based on medical history, physical examination, 12-lead electrocardiogram (ECG), serum chemistry labs and hematology values.
• 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

• Subjects with any serious medical or psychiatric condition or clinically significant laboratory, ECG, vital signs, or physical examination abnormality that would prevent study participation or place the subject at significant risk, as judged by the Investigator.
• Planned initiation or changes to concomitant medication that could, in the opinion of the Investigator, affect psoriasis vulgaris
• Current diagnosis of non-plaque form of psoriasis (e.g., guttate, erythrodermic/exfoliative, palmoplantar only involvement, or pustular psoriasis). Current diagnosis of drug-induced psoriasis.
• Subjects with any condition on the treatment area which, in the opinion of the Investigator, could confound efficacy measurements.
• Subjects who cannot discontinue the use of strong cytochrome P-450 CYP3A4 inducers for 2 weeks prior to Baseline/Day 1and during the study period.
• Subjects who cannot discontinue the use of strong cytochrome P-450 CYP3A4 inhibitors for 2 weeks prior to Baseline/Day 1 and during the study period.
• Subjects who are unwilling to refrain from prolonged sun exposure and from using a tanning bed or other artificial light emitting devices (LEDs) for 4 weeks prior to Baseline/Day 1 and during the study.
• Subjects who cannot discontinue specific systemic therapies and/or topical therapies prior to the Baseline/Day 1 and during the study period according to the protocol.
• Subjects with any infection requiring oral or intravenous administration of antibiotics, antifungal or antiviral agents within 2 weeks prior to Baseline/Day 1.

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 5 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Arcutis Biotherapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David Berk, MD

Role: STUDY_DIRECTOR

Arcutis Biotherapeutics, Inc.

Locations

Arcutis Clinical Site 603

Mountain Brook, Alabama, United States

Arcutis Clinical Site 604

Scottsdale, Arizona, United States

Arcutis Clinical Site 609

Fountain Valley, California, United States

Arcutis Clinical Site 618

Los Angeles, California, United States

Arcutis Clinical Site 608

Los Angeles, California, United States

Arcutis Clinical Site 611

Rancho Santa Margarita, California, United States

Arcutis Clinical Site 610

Boca Raton, Florida, United States

Arcutis Clinical Site 602

Coral Gables, Florida, United States

Arcutis Clinical Site 613

Delray Beach, Florida, United States

Arcutis Clinical Study Site 628

Miami, Florida, United States

Arcutis Clinical Site 607

Miami, Florida, United States

Arcutis Clinical Site 627

West Lafayette, Indiana, United States

Arcutis Clinical Site 606

Arlington, Texas, United States

Arcutis Clinical Site 619

Frisco, Texas, United States

Arcutis Clinical Study Site 619

Frisco, Texas, United States

Arcutis Clinical Site 605

Houston, Texas, United States

Arcutis Clinical Site 621

Toronto, Ontario, Canada

Arcutis Clinical Site 630

Santo Domingo, , Dominican Republic

Countries

United States; Canada; Dominican Republic

References

Hebert AA, Guide SV, Groysman V, Gonzalez ME, Blanco D, Laquer V, Seal MS, Thurston A, Krupa D, Snyder S, Burnett P, Chu DH, Berk DR, Higham RC. Early Evidence of Safety, Clinical Benefit, and Pharmacokinetics of Roflumilast Cream 0.3% Once Daily for Treatment of Mild or Moderate Plaque Psoriasis in Children Aged 2-11 Years. Pediatr Dermatol. 2025 Aug 27. doi: 10.1111/pde.70013. Online ahead of print.

Reference Type: DERIVED

PMID: 40862624 (View on PubMed)

Other Identifiers

ARQ-151-216

Identifier Type: -

Identifier Source: org_study_id