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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02087943
Other study ID # CC-10004-AD-001
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date June 2014
Est. completion date February 2016

Study information

Verified date April 2017
Source Amgen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A study to evaluate the efficacy and safety of apremilast (CC-10004) in subjects with moderate to severe atopic dermatitis


Recruitment information / eligibility

Status Completed
Enrollment 191
Est. completion date February 2016
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Males or females, aged = 18 years (= 20 for Japanese subjects) at the time of consent.

2. Have a diagnosis of atopic dermatitis for = 12 months.

3. Have moderate to severe atopic dermatitis which is considered inappropriate for topical therapy or which cannot be adequately controlled by topical therapy.

4. Meet the laboratory criteria as defined per protocol

5. Females of Childbearing Potential (FCBP) must have a negative pregnancy test at Screening and Baseline. Sexually active FCBP must use one of the approved contraceptive options required per protocol while on and for at least 28 days after the last dose of study medication

6. Male subjects (including those who have had a vasectomy) who engage in activity in which conception is possible must use barrier contraception while on and for at least 28 days after the last dose of study medication.

Exclusion Criteria:

1. Active tuberculosis (TB) or a history of inadequately treated tuberculosis.

2. Positive for hepatitis B surface antigen or hepatitis C antibody

3. Pregnant or breast feeding

4. History of allergy to any component of the study medication.

5. Active skin infection requiring systemic antimicrobials at Baseline.

Study Design


Intervention

Drug:
Apremilast
Orally twice a day (BID)
Apremilast
Orally twice a day (BID)
Placebo
Orally twice a day (BID)
Placebo
Orally twice a day (BID)

Locations

Country Name City State
Canada Ultranova Skincare Barrie Ontario
Canada Eastern Canada Cutaneous Research Associates Ltd Halifax Nova Scotia
Canada Innovaderm Research Montreal Quebec
Canada Centre Dermatologique du Quebec Metropolitain Ste-Foy Quebec
Canada Chih-Ho Hong Medical, Inc. Surrey British Columbia
Canada K. Papp Clinical Research Waterloo Ontario
Japan Kokubu Abashiri Dermatology Clinic Abashiri-shi, Hokkaido
Japan Asanuma Dermatology Clinic Chitose-shi, Hokkaido
Japan Fukuoka University Hospital Dermatology Fukuoka-shi, Fukuoka
Japan Hatamoto Dermatology Clinic Fukuoka-shi, Fukuoka
Japan Tashiro Clinic Iizuka-shi, Fukuoka
Japan Kokubu Dermatology Kitami-shi, Hokkaido
Japan Kyoto University Hospital Kyoto
Japan University Hospital, Kyoto Prefectural University of Medicine Kyoto-City
Japan Sapporo Skin Clinic Sapporo-shi, Hokkaido
Japan NTT Medical Center Tokyo Shinagawa-ku, Tokyo
United States Advanced Medical Research Atlanta Georgia
United States Emory Clinic Atlanta Georgia
United States Bakersfield Dermatology and Skin Cancer Medical Group Bakersfield California
United States Northwestern University Northwestern Medical Faculty Foundation Chicago Illinois
United States Northwestern Medicine Lake Forest Hospital Lake Forest Illinois
United States Dartmouth Hitchcock Medical Center Lebanon New Hampshire
United States Dermatology Research Associates Los Angeles California
United States Dermatology Specialists, PSC Louisville Kentucky
United States Mount Sinai Medical Center New York New York
United States NYU Department of Dermatology New York New York
United States Virginia Clinical Research Inc Norfolk Virginia
United States Renstar Medical Research Ocala Florida
United States Arizona Research Center Phoenix Arizona
United States Oregon Health and Science University Portland Oregon
United States PMG Research of Winston-Salem LLC Winston-Salem North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Amgen

Countries where clinical trial is conducted

United States,  Canada,  Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage Change From Baseline in the Eczema Area and Severity Index (EASI) Score at Week 12. EASI is a validated composite scoring system integrating the proportion of the body region (area) involved and the intensity of key signs of atopic dermatitis (AD). A representative lesion is selected for each of the four body regions for assessing the intensity of each of the four signs (erythema, induration /papulation, excoriation, and lichenification). Symptoms (eg, pruritus) and secondary signs (eg, xerosis, scaling) are excluded from the assessment. The total EASI score ranges from 0 to 72. A higher score indicated worse disease status, and a negative change from baseline indicated improvement. Baseline to Week 12
Secondary Percentage of Participants Who Achieved a Score of 0 (Cleared) or 1 (Almost Cleared) and at Least a 2-point Reduction From Baseline in a Static Physician's Global Assessment of Acute Signs (sPGA-A) at Week 12. The sPGA-A is intended to assess the global severities (ie, a "visual average" integrating all areas of AD) of key acute clinical signs of AD, including erythema, induration/papulation, oozing/crusting (lichenification excluded) based on a 5-point scale of cleared (0), almost cleared (1), mild (2), moderate (3) and severe (4). Baseline to Week 12
Secondary Percentage of Participants Who Achieved at Least a 50% Reduction From Baseline in the EASI Score (EASI 50) at Week 12 The EASI 50 reduction (defined as = 50% reduction from baseline in EASI score) was selected to serve as the key responder endpoint. A = 50% improvement is clinically meaningful for this population. Baseline to Week 12
Secondary The Percentage Change From Baseline in the Average Weekly Pruritus Numerical Rating Scale (NRS) Score at Week 4 The participant completed a daily diary recording the average intensity of pruritus they experienced during the preceding 24 hrs. The intensity of pruritus was assessed using a validated 11-point NRS, ranging from 0 ("no pruritus") to 10 ("the worst pruritus imaginable"). It should be noted that this NRS is distinct from the pruritus, Visual Analogue Scale (VAS) in the Modified SCORAD Index with respect to recall period (three days for the VAS). The weekly NRS score was calculated as the average of the NRS scores over 7 days within the specified week. A higher score indicated worse disease status, and a negative change from baseline indicated improvement. Baseline to Week 4
Secondary Number of Participants With Treatment Emergent Adverse Events (TEAEs) During the Placebo Controlled Period A TEAE is an adverse event with a start date on or after the date of the first dose of IP and no later than 28 days after the last dose of IP for participants who discontinued early. An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (ie, any clinically significant adverse change in the frequency or intensity of a pre existing condition) should be considered an AE. A serious AE is any which results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect; constitutes an important medical event. Baseline to Week 12
Secondary Number of Participants With TEAEs During the Apremilast Exposure Period A TEAE is an adverse event with a start date on or after the date of the first dose of investigational product (IP) and no later than 28 days after the last dose of IP. An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (ie, any clinically significant adverse change in the frequency or intensity of a pre existing condition) should be considered an AE. A serious AE is any which results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect; constitutes an important medical event. Baseline to Week 24; median duration of apremilast 30 mg was 23.3 weeks and 22.4 weeks for apremilast 40 mg