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

Phase 3

Completed

Conditions: Chronic Plaque Psoriasis

Interventions: Drug: ARQ-151 0.3% cream
Drug: ARQ-151 vehicle cream

Registration Number: NCT04211389

Lead Sponsor: Arcutis Biotherapeutics, Inc.

Brief Summary: 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

Detailed Description: 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

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 442

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

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
ARQ-151 cream 0.3%	ARQ-151 0.3% cream	Active comparator
ARQ-151 cream vehicle	ARQ-151 vehicle cream	Placebo comparator

Primary Outcome Measures

Name	Time	Method
Number of Participants Achieving Success on the Investigator Global Assessment (IGA) Scale	Week 8	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.

Secondary Outcome Measures

Name	Time	Method
Number of Participants Achieving Success in Intertriginous Investigator Global Assessment (I-IGA) Scale Assessment of Disease Severity at Week 8	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.
Number of Participants Achieving Psoriasis Area Severity Index-90 (PASI-90)	Baseline (Day 1) and Week 8	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 to Achieve Psoriasis Area Severity Index-50 (PASI-50)	From start of treatment to achievement of PASI-50 or study completion/early termination (maximum duration = 124 days)	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.
Number of Participants Achieving Psoriasis Area Severity Index-75 (PASI-75)	Baseline (Day 1) and Week 8	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.
Change From Baseline in Psoriasis Symptoms Diary (PSD) Score	Baseline (Day 1) and Weeks 4 and 8	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.
Number of Participants Achieving I-IGA Score of 'Clear' at Week 8	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.
Number of Participants Achieving Success in Worst Itch Numerical Rating Scale (WI-NRS) Pruritus Score	Baseline (Day 1) and Week 2, Week 4, Week 8	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.

Trial Locations

Locations (39): Arcutis Biotherapeutics Clinical Site 203
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Scottsdale, Arizona, United States
Arcutis Biotherapeutics Clinical Site 215
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Santa Monica, California, United States
Arcutis Biotherapeutics Clinical Site 239
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Beverly Hills, California, United States
Arcutis Biotherapeutics Clinical Site 223
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Boynton Beach, Florida, United States
Arcutis Biotherapeutics Clinical Site 208
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Santa Monica, California, United States
Arcutis Biotherapeutics Clinical Site 227
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Saint Joseph, Missouri, United States
Arcutis Biotherapeutics Clinical Site 233
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Knoxville, Tennessee, United States
Arcutis Biotherapeutics Clinical Site 210
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West Jordan, Utah, United States
Arcutis Biotherapeutics Clinical Site 224
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New Orleans, Louisiana, United States
Arcutis Biotherapeutics Clinical Site 237
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DeLand, Florida, United States
Arcutis Biotherapeutics Clinical Site 236
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Portsmouth, New Hampshire, United States
Arcutis Biotherapeutics Clinical Site 206
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Arlington, Texas, United States
Arcutis Biotherapeutics Clinical Site 225
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Encino, California, United States
Arcutis Biotherapeutics Clinical Site 232
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Winnepeg, Manitoba, Canada
Arcutis Biotherapeutics Clinical Site 230
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Richmond, Virginia, United States
Arcutis Biotherapeutics Clinical Site 216
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Fridley, Minnesota, United States
Arcutis Biotherapeutics Clinical Site 205
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Ajax, Ontario, Canada
Arcutis Biotherapeutics Clinical Site 240
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Reno, Nevada, United States
Arcutis Biotherapeutics Clinical Site 221
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Murfreesboro, Tennessee, United States
Arcutis Biotherapeutics Clinical Site 207
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Surrey, British Columbia, Canada
Arcutis Biotherapeutics Clinical Site 220
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San Diego, California, United States
Arcutis Biotherapeutics Clinical Site 231
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Las Vegas, Nevada, United States
Arcutis Biotherapeutics Clinical Site 238
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Houston, Texas, United States
Arcutis Biotherapeutics Clinical Site 212
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Detroit, Michigan, United States
Arcutis Biotherapeutics Clinical Site 222
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Oklahoma City, Oklahoma, United States
Arcutis Biotherapeutics Clinical Site 217
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Louisville, Kentucky, United States
Arcutis Biotherapeutics Clinical Site 228
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Largo, Florida, United States
Arcutis Biotherapeutics Clinical Site 211
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Lake Charles, Louisiana, United States
Arcutis Biotherapeutics Clinical Site 229
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Broomall, Pennsylvania, United States
Arcutis Biotherapeutics Clinical Site 226
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Surrey, British Columbia, Canada
Arcutis Biotherapeutics Clinical Site 234
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Fredericton, New Brunswick, Canada
Arcutis Biotherapeutics Clinical Site 218
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Barrie, Ontario, Canada
Arcutis Biotherapeutics Clinical Site 214
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Indianapolis, Indiana, United States
Arcutis Biotherapeutics Clinical Site 209
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Sweetwater, Florida, United States
Arcutis Biotherapeutics Clinical Site 201
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North Miami Beach, Florida, United States
Arcutis Biotherapeutics Clinical Site 235
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Toronto, Ontario, Canada
Arcutis Biotherapeutics Clinical Site 213
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Metairie, Louisiana, United States
Arcutis Biotherapeutics Clinical Site 204
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Windsor, Ontario, Canada
Arcutis Biotherapeutics Clinical Site 219
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Las Vegas, Nevada, United States