Twin Trial of PDE4 Inhibition With Roflumilast for the Management of Plaque Psoriasis

Arcutis Biotherapeutics, Inc.442 enrolled

Overview

This study will assess the safety and efficacy of ARQ-151 cream vs placebo applied once a day for 56 days by subjects with chronic plaque psoriasis

This is a parallel group, double blind, vehicle-controlled study in which ARQ-151 cream or vehicle is applied once daily x 8 weeks to subjects with psoriasis

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

442

Conditions

Chronic Plaque Psoriasis

Interventions

ARQ-151 0.3% creamDRUG

ARQ-151 0.3% cream

ARQ-151 vehicle creamDRUG

ARQ-151 vehicle cream

Eligibility

Sex: ALLMin age: 2 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Participants legally competent to sign and give informed consented and if appropriate assent as required by local laws * Males and females ages 2 years and older (inclusive) * Clinical diagnosis of psoriasis vulgaris of at least 6 months duration (3 months for children) as determined by the Investigator * Females of childbearing potential (FOCBP) must have a negative pregnancy test at Screening (Visit 1) and Baseline (Visit 2). In addition, sexually active FOCBP must agree to use at least one form of highly effective contraception throughout the trial. * In good health as judged by the Investigator, based on medical history, physical examination, serum chemistry labs, hematology values, and urinalysis. * Subjects considered reliable and capable of adhering to the Protocol and visit schedule, according to the judgment of the Investigator. Exclusion Criteria: * Planned excessive exposure of treated area(s) to either natural or artificial sunlight, tanning bed or other LED. * Females who are pregnant, wishing to become pregnant during the study, or are breast-feeding. * Previous treatment with ARQ-151 or its active ingredient * Subjects with any serious medical condition or laboratory abnormality that would prevent study participation or place the subject at significant risk, as determined by the Investigator. * Subjects with a history of chronic alcohol or drug abuse within 6 months of initiation of investigational product * 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

Locations (39)

Outcomes

Primary Outcomes

Number of Participants Achieving Success on the Investigator Global Assessment (IGA) Scale

The number of participants achieving "success" in IGA assessment of disease severity at Week 8 is presented for each arm. Success was defined as achievement of an IGA score of 0 ('clear') or 1 ('almost clear') at Week 8, accompanied by a ≥2-grade improvement from baseline IGA score. The IGA is 5-point scale assessing the severity of plaque psoriasis, with scores ranging from 0 ('clear') to 4 ('severe'), and higher scores indicate greater symptom severity. The IGA scores are based on observed data, whereas odds ratio and p-values were calculated using multiple imputation of missing values.

Time frame: Week 8

Secondary Outcomes

Time to Achieve Psoriasis Area Severity Index-50 (PASI-50)

The Psoriasis Area and Severity Index (PASI) is widely used for the measurement of severity of psoriasis. PASI combines the assessment of the severity of lesions and the area affected into a single score in the range from 0 (no disease) to 72 (maximal disease), with higher scores indicating greater symptom severity. The time to achieve PASI-50 (defined as a 50% reduction from baseline in PASI score) is presented, and is based on observed data only. Participants are included whether they achieved PASI-50 or not.

Time frame: From start of treatment to achievement of PASI-50 or study completion/early termination (maximum duration = 124 days)

Number of Participants Achieving Psoriasis Area Severity Index-75 (PASI-75)

The Psoriasis Area and Severity Index (PASI) is widely used for the measurement of severity of psoriasis. PASI combines the assessment of the severity of lesions and the area affected into a single score in the range from 0 (no disease) to 72 (maximal disease), with higher scores indicating greater symptom severity. The number of participants achieving PASI-75 (defined as a 75% reduction from baseline in PASI score) at Week 8 is presented. Participant counts are based on observed data only.

Time frame: Baseline (Day 1) and Week 8

Number of Participants Achieving Psoriasis Area Severity Index-90 (PASI-90)

Data from ClinicalTrials.gov

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Arcutis Biotherapeutics Clinical Site 203

Scottsdale, Arizona, United States

Arcutis Biotherapeutics Clinical Site 239

Beverly Hills, California, United States

Arcutis Biotherapeutics Clinical Site 225

Encino, California, United States

Arcutis Biotherapeutics Clinical Site 220

San Diego, California, United States

Arcutis Biotherapeutics Clinical Site 208

Santa Monica, California, United States

Arcutis Biotherapeutics Clinical Site 215

Santa Monica, California, United States

Arcutis Biotherapeutics Clinical Site 223

Boynton Beach, Florida, United States

Arcutis Biotherapeutics Clinical Site 237

DeLand, Florida, United States

Arcutis Biotherapeutics Clinical Site 228

Largo, Florida, United States

Arcutis Biotherapeutics Clinical Site 201

North Miami Beach, Florida, United States

...and 29 more locations

The Psoriasis Area and Severity Index (PASI) is widely used for the measurement of severity of psoriasis. PASI combines the assessment of the severity of lesions and the area affected into a single score in the range from 0 (no disease) to 72 (maximal disease), with higher scores indicating greater symptom severity. The number of participants achieving PASI-90 (defined as a 90% reduction from baseline in PASI score) at Week 8 is presented. Participant counts are based on observed data only.

Time frame: Baseline (Day 1) and Week 8

Number of Participants Achieving Success in Intertriginous Investigator Global Assessment (I-IGA) Scale Assessment of Disease Severity at Week 8

The number of participants with I-IGA score ≥2 at baseline achieving "success" in IGA assessment of disease severity at Week 8 is presented (observed data only) for each arm. Success was defined as achievement of an I-IGA score of 0 ('clear') or 1 ('almost clear') at Week 8, accompanied by a ≥2-grade improvement from baseline I-IGA score. The IGA is a 5-point scale assessing the severity of plaque psoriasis, with scores ranging from 0 ('clear') to 4 ('severe'), and higher scores indicate greater symptom severity.

Time frame: Week 8

Number of Participants Achieving I-IGA Score of 'Clear' at Week 8

The number of participants achieving an IGA score of 0 ('clear') at Week 8 is presented (observed data only) for each arm. The I-IGA is a 5-point scale assessing the severity of intertriginous area plaque psoriasis, with scores ranging from 0 ('clear') to 4 ('severe'), and higher scores indicate greater symptom severity.

Time frame: Week 8

Number of Participants Achieving Success in Worst Itch Numerical Rating Scale (WI-NRS) Pruritus Score

The number of participants achieving success in WI-NRS is presented. Success is defined as achievement of a ≥ 4-point reduction in WI-NRS pruritus score in participants with WI-NRS pruritus score ≥ 4 at baseline. The WI-NRS is a 10 point scale ranging from 0 ('no itch') to 10 ('worst itch imaginable') the participant experienced in the past 24 hours, with higher scores indicating greater symptoms severity. Results are based on observed data only.

Time frame: Baseline (Day 1) and Week 2, Week 4, Week 8

Change From Baseline in Psoriasis Symptoms Diary (PSD) Score

The PSD is a 16-item questionnaire asking subjects to rate the severity of psoriasis-related symptoms in the past 24 hours. Each question is scored from 0 ("no symptoms") to 10 ("worst imaginable symptoms"). Scores range from 0 to 160, with higher scores indicating greater symptom severity. The least squares (LS) mean (95% CI) change in PSD total score relative to baseline is presented for each treatment arm, with decreases from baseline indicating symptom improvement.

Time frame: Baseline (Day 1) and Weeks 4 and 8