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Trial of PDE4 Inhibition With Roflumilast for the Management of Atopic Dermatitis (INTEGUMENT-II)

Phase 3
Completed
Conditions
Atopic Dermatitis Eczema
Interventions
Drug: Vehicle cream
Registration Number
NCT04773600
Lead Sponsor
Arcutis Biotherapeutics, Inc.
Brief Summary

This study will assess the safety and efficacy of ARQ-151 cream vs vehicle applied once a day for 4 weeks by subjects with atopic dermatitis (eczema). This is a parallel group, double blind, vehicle-controlled study in which ARQ-151 0.15% cream or vehicle is applied once daily (qd) for 4 weeks by participants with atopic dermatitis.

Detailed Description

This is a parallel group, double blind, vehicle-controlled study in which ARQ-151 cream or vehicle is applied once daily for 4 weeks to subjects with atopic dermatitis.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
683
Inclusion Criteria
  1. Participants legally competent to sign and give informed consent and, if appropriate, assent as required by local laws.
  2. Males and females, ages 6 years and older at time of signing Informed Consent (Screening). Only subjects 18 years and older will be enrolled at sites located in the province of Québec in Canada.
  3. Diagnosed with atopic dermatitis 6 months duration (3 months for children), as determined by the Investigator. Stable disease for the past 4 weeks with no significant flares in atopic dermatitis before screening.
  4. Females of childbearing potential (FOCBP) must have a negative serum pregnancy test at Screening and a negative urine pregnancy test at Baseline/Day 1. In addition, sexually active FOCBP must agree to use at least one form of a highly effective or barrier method of contraception throughout the trial.
  5. In good health as judged by the Investigator.
  6. Subjects 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 clinically significant abnormality that would prevent study participation or place the subject at significant risk, as judged by the Investigator
  2. Has unstable AD or any consistent requirement for high potency topical steroids.
  3. 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.
  4. Females who are pregnant, wishing to become pregnant during the study, or are breast-feeding.
  5. Previous treatment with ARQ-151.
  6. Subjects with a history of chronic alcohol or drug abuse within 6 months prior to Screening.
  7. Parent(s)/legal guardian(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.
  8. 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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Roflumilast Cream 0.15%Roflumilast CreamParticipants apply roflumilast cream 0.15% once daily (qd) for 4 weeks.
Vehicle CreamVehicle creamParticipants apply vehicle cream qd for 4 weeks.
Primary Outcome Measures
NameTimeMethod
Achievement of Validated Investigator Global Assessment for Atopic Dermatitis (vIGA-AD) Success at Week 4Week 4

The percentage of participants achieving viGA-AD "success" is presented with multiple imputation of missing observations. viGA-AD "success" is defined as a viGA-AD score of 'clear' or 'almost clear' PLUS a 2-grade improvement from Baseline. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (reported only in integers of 0 to 4 where 0 is clear), with higher scores indicative of greater symptom severity.

Secondary Outcome Measures
NameTimeMethod
Achievement of vIGA-AD Success at Week 4 in Participants With "Moderate" Baseline ScoresWeek 4

The percentage of participants with moderate baseline scores achieving viGA-AD "success" is presented with multiple imputation of missing observations. viGA-AD "success" is defined as a viGA-AD score of 'clear' or 'almost clear' PLUS a 2-grade improvement from baseline in participants with a 'moderate' baseline viGA-AD score. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (0 'clear' to 4 'severe'), with higher scores indicative of greater symptom severity.

vIGA-AD Success at Week 2Week 2

The percentage of participants achieving viGA-AD "success" is presented with multiple imputation of missing observations. viGA-AD "success" is defined as a viGA-AD score of 'clear' or 'almost clear' PLUS a 2-grade improvement from Baseline. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (reported only in integers of 0 to 4 where 0 is clear), with higher scores indicative of greater symptom severity.

vIGA-AD Success at Week 1Week 1

The percentage of participants achieving viGA-AD "success" is presented with multiple imputation of missing observations. viGA-AD "success" is defined as a viGA-AD score of 'clear' or 'almost clear' PLUS a 2-grade improvement from Baseline. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (reported only in integers of 0 to 4 where 0 is clear), with higher scores indicative of greater symptom severity.

Achievement of a 4-point Reduction at Week 4 in the Average, Weekly Worst Itch Numeric Rating Scale (WI-NRS) in Participants With Baseline WI-NRS Score ≥4Week 4

The percentage of participants with a baseline WI-NRS ≥ 4 achieving WI-NRS success is presented with multiple imputation of missing observations. The WI-NRS is a simple, single item scale to assess the subject-reported severity of this symptom, on a scale ranging from 0 ("no itch") to 10 ("worst imaginable itch") the participant experienced in the previous 24 hours (higher scores indicate higher itch severity).

Achievement of a 4-point Reduction at Week 2 in the WI-NRS in Participants With Baseline WI-NRS Score ≥4Week 2

The percentage of participants with a baseline WI-NRS ≥ 4 achieving WI-NRS success is presented with multiple imputation of missing observations. The WI-NRS is a simple, single item scale to assess the subject-reported severity of this symptom, on a scale ranging from 0 ("no itch") to 10 ("worst imaginable itch") the participant experienced in the previous 24 hours (higher scores indicate higher itch severity).

Achievement of a 4-point Reduction at Week 1 in the WI-NRS in Participants With Baseline WI-NRS Score ≥4Week 1

The percentage of participants with a baseline WI-NRS ≥ 4 achieving WI-NRS success is presented with multiple imputation of missing observations. The WI-NRS is a simple, single item scale to assess the subject-reported severity of this symptom, on a scale ranging from 0 ("no itch") to 10 ("worst imaginable itch") the participant experienced in the previous 24 hours (higher scores indicate higher itch severity).

Achievement of ≥75% Decrease From Baseline at Week 4 in the Eczema Area and Severity Index (EASI-75)Week 4

The percentage of participants achieving EASI-75 is presented with multiple imputation of missing observations. EASI-75 is a \~75% reduction from the baseline EASI score. EASI combines the assessment of the severity of lesions and the area affected into a single total score in the range 0 (no disease) to 72 (maximal disease). To calculate the EASI, the sum = of the severity rating (0 to 3 with 3 being the most severe) for four clinical signs are multiplied with the numerical value of the area affected and with the percentage of the four body areas.

Achievement of vIGA-AD Score of 'Clear' or 'Almost Clear' at Week 4Week 4

The percentage of participants scoring 'clear' or 'almost clear' on viGA-AD is presented with multiple imputation of missing observations. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (0 'clear' to 4 'severe'), with higher scores indicative of greater symptom severity.

Achievement of vIGA-AD Score of 'Clear' or 'Almost Clear' at Week 2Week 2

The percentage of participants scoring 'clear' or 'almost clear' on viGA-AD is presented with multiple imputation of missing observations. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (0 'clear' to 4 'severe'), with higher scores indicative of greater symptom severity.

Achievement of vIGA-AD Score of 'Clear' or 'Almost Clear' at Week 1Week 1

The percentage of participants scoring 'clear' or 'almost clear' on viGA-AD is presented with multiple imputation of missing observations. The viGA-AD is a static evaluation of qualitative overall AD severity. This global assessment scale is an ordinal scale with five severity grades (0 'clear' to 4 'severe'), with higher scores indicative of greater symptom severity.

Trial Locations

Locations (53)

Arcutis Clinical Site 34

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Rockville, Maryland, United States

Arcutis Clinical Site 36

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San Diego, California, United States

Arcutis Clinical Site 41

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Miami, Florida, United States

Arcutis Clinical Site 02

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San Antonio, Texas, United States

Arcutis Clinical Site 54

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Centennial, Colorado, United States

Arcutis Clinical Site 31

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Birmingham, Alabama, United States

Arcutis Clinical Site 55

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Boca Raton, Florida, United States

Arcutis Clinical Site 30

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Coral Gables, Florida, United States

Arcutis Clinical Site 13

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Santa Monica, California, United States

Arcutis Clinical Site 51

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Fort Smith, Arkansas, United States

Arcutis Clinical Site 19

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San Diego, California, United States

Arcutis Clinical Site 46

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Inglewood, California, United States

Arcutis Clinical Site 37

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Delray Beach, Florida, United States

Arcutis Clinical Site 58

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Miami, Florida, United States

Arcutis Clinical Site 42

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Lake Charles, Louisiana, United States

Arcutis Clinical Site 62

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Boise, Idaho, United States

Arcutis Clinical Site 01

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High Point, North Carolina, United States

Arcutis Clinical Site 18

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Charleston, South Carolina, United States

Arcutis Clinical Site 24

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Hershey, Pennsylvania, United States

Arcutis Clinical Site 33

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Stony Brook, New York, United States

Arcutis Clinical Site 07

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Pittsburgh, Pennsylvania, United States

Arcutis Clinical Site 38

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Mandeville, Louisiana, United States

Arcutis Clinical Site 03

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College Station, Texas, United States

Arcutis Clinical Site 06

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Metairie, Louisiana, United States

Arcutis Clinical Site 245

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Saint Joseph, Missouri, United States

Arcutis Clinical Site 21

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Fort Gratiot, Michigan, United States

Clinical Site 05

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Austin, Texas, United States

Arcutis Clinical Site 32

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Orem, Utah, United States

Arcutis Clinical Site 17

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Norfolk, Virginia, United States

Arcutis Clinical Site 12

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Calgary, Alberta, Canada

Arcutis Clinical Site 20

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Ajax, Ontario, Canada

Arcutis Clinical Site 26

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Winnipeg, Manitoba, Canada

Arcutis Clinical Site 23

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London, Ontario, Canada

Arcutis Clinical Site 16

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Waterloo, Ontario, Canada

Arcutis Clinical Site 11

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Sanford, Florida, United States

Arcutis Clinical Site 61

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Troy, Michigan, United States

Clinical Site 04

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Plainfield, Indiana, United States

Arcutis Clinical Site 57

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West Palm Beach, Florida, United States

Arcutis Clinical Site 43

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Louisville, Kentucky, United States

Arcutis Clinical Site 63

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Baton Rouge, Louisiana, United States

Arcutis Clinical Site 29

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Clinton Township, Michigan, United States

Arcutis Clinical Site 39

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Rochester, New York, United States

Arcutis Clinical Site 53

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New York, New York, United States

Arcutis Clinical Site 15

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North Charleston, South Carolina, United States

Arcutis Clinical Site 35

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Charleston, South Carolina, United States

Arcutis Clinical Site 52

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Pflugerville, Texas, United States

Arcutis Clinical Site 09

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Surrey, British Columbia, Canada

Arcutis Clinical Site 25

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Toronto, Ontario, Canada

Arcutis Clinical Site 27

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Québec, Quebec, Canada

Arcutis Clinical Site 22

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Burke, Virginia, United States

Arcutis Clinical Site 59

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Frisco, Texas, United States

Arcutis Clinical Site 250

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Grapevine, Texas, United States

Arcutis Clinical Site 08

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Drummondville, Quebec, Canada

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