Study Evaluating Efficacy and Safety of PF-04965842 and Dupilumab in Adult Subjects With Moderate to Severe Atopic Dermatitis on Background Topical Therapy

Completed · Phase 3 · Has a placebo group

Conditions studied: Dermatitis, Dermatitis, Atopic, Eczema, Skin Diseases, Skin Diseases, Genetic, Genetic Diseases, Inborn, Skin Diseases, Eczematous, Hypersensitivity, Hypersensitivity, Immediate, Immune System Diseases

In brief

B7451029 is a Phase 3 study to investigate PF-04965842 in adult patients who have moderate to severe atopic dermatitis and use background topical therapy. The efficacy of two dosage strengths of PF-04965842, 100 mg and 200 mg taken orally once daily will be evaluated relative to placebo over 12 weeks. The efficacy of the two dosage strengths of PF-04965842 will be compared with dupilumab in terms of pruritus relief at 2 weeks. The two dosage strengths of PF-04965842 and dupilumab 300 mg injected subcutaneously once every two weeks (with a loading dose of 600 mg injected on the first day) will also be evaluated relative to placebo over 16 weeks. The safety of the investigational products will be evaluated over the duration of the study. Subjects will use non-medicated emollient at least twice a day and medicated topical therapy such as corticosteroids, calcineurin inhibitors or PDE4 inhibitors, as per protocol guidance, to treat active lesions during the study. Subjects who are randomized to receive one of the two dosage strengths of PF-04965842 will also receive placebo injectable study drug every two weeks until Week 16 and then will continue on receiving only the oral study drug for 4 weeks. Subjects who are randomized to receive dupilumab injections every two weeks will also receive oral placebo to be taken once daily until Week 16 and will then continue to receive only the oral placebo for 4 weeks. Subjects who are randomized to the placebo arms, will receive both daily oral placebo and injectable placebo every two weeks until Week 16, after which they will receive either 100 mg or 200 mg of PF-04965842 taken orally once daily for 4 weeks, dependent upon which arm they have been allocated to. Eligible subjects will have an option to enter a long-term extension study after completing 20 weeks of treatment.

Key facts

Study ID

NCT03720470

Run by

Pfizer

People needed

838

Starts

2018-10-29

Expected to finish

2020-03-06

Last updated by the study team

2021-01-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female subjects aged 18 years or older at the time of informed consent
• Diagnosis of atopic dermatitis (AD) for at least 1 year and current status of moderate to severe disease (>= the following scores: BSA 10%, IGA 3, EASI 16, Pruritus NRS severity 4)
• Documented recent history (within 6 months before the screening visit) of inadequate response to treatment with medicated topical therapy for AD for at least 4 weeks, or who have required systemic therapies for control of their disease.
• Must be willing and able to comply with standardized background topical therapy, as per protocol guidelines throughout the study
• Female subjects who are of childbearing potential must not be intending to become pregnant, currently pregnant, or lactating. The following conditions apply:
• Female subjects of childbearing potential must have a confirmed negative pregnancy test prior to randomization;
• Female subjects of childbearing potential must agree to use a highly effective method of contraception for the duration of the active treatment period and for at least 28 days after the last dose of investigational product.
• Female subjects of non-childbearing potential must meet at least 1 of the following criteria:
• Have undergone a documented hysterectomy and/or bilateral oophorectomy;
• Have medically confirmed ovarian failure; or
• Achieved postmenopausal status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause and have a serum follicle stimulating hormone (FSH) level confirming the postmenopausal state.
• All other female subjects (including female subjects with tubal ligations) are considered to be of childbearing potential.
• If receiving concomitant medications for any reason other than AD, must be on a stable regimen prior to Day 1 and through the duration of the study

You may not qualify if…

• Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study
• Medical history including thrombocytopenia, coagulopathy or platelet dysfunction, Q wave interval abnormalities, current or history of certain infections, cancer, lymphoproliferative disorders and other medical conditions at the discretion of the investigator
• Unwilling to discontinue current AD medications prior to the study or require treatment with prohibited medications during the study
• Other active nonAD inflammatory skin diseases or conditions affecting skin
• Prior treatment with JAK inhibitors
• Previous treatment with dupilumab
• Unwilling to discontinue current AD medications prior to the study or require treatment with prohibited medications during the study

Where it is running

• The University Of Alabama At Birmingham — Birmingham, Alabama, United States
• Marvel Research, LLC — Huntington Beach, California, United States
• Alliance Research Centers — Laguna Hills, California, United States
• Allergy & Asthma Care Center of Southern California — Long Beach, California, United States
• Allergy & Asthma Associates of Southern California dba Southern California Research — Mission Viejo, California, United States
• Dermatology Specialists, Inc. — Murrieta, California, United States
• MedDerm Associates — San Diego, California, United States
• Clinical Science Institute — Santa Monica, California, United States
• Synexus Clinical Research US, Inc. — Santa Rosa, California, United States
• IMMUNOe Research Centers — Centennial, Colorado, United States
• Renaissance Research and Medical Group, Inc — Cape Coral, Florida, United States
• C & R Research Services USA, Inc — Coral Gables, Florida, United States
• Florida Academic Centers Research and Education, LLC — Coral Gables, Florida, United States
• Moonshine Research Center, Inc. — Doral, Florida, United States
• Solutions Through Advanced Research, Inc. — Jacksonville, Florida, United States
• Olympian Clinical Research — Largo, Florida, United States
• Savin Medical Group LLC — Miami, Florida, United States
• Wellness Clinical Research, LLC — Miami Lakes, Florida, United States
• ForCare Clinical Research — Tampa, Florida, United States
• Research Institute of Southeast, LLC — West Palm Beach, Florida, United States
• Research Institute of the Southeast, LLC — West Palm Beach, Florida, United States
• Columbus Regional Research Institute — Columbus, Georgia, United States
• Idaho Allergy and Research — Eagle, Idaho, United States
• ASR, LLC — Nampa, Idaho, United States
• Clinical Research Center of Alabama, LLC — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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