Condition: Atopic Dermatitis · Atopic Dermatitis, Unspecified · Dermatitis, Atopic · Sponsor: Pfizer
This is a prospective, multi-center observational study characterizing clinical and patient reported outcomes of patients receiving abrocitinib for moderate-to-severe atopic dermatitis (M2S AD) who had inadequate response (or intolerance) to ≤2 previous biologic therapies approved for M2S AD in the United States. The aim of this study is to measure the effectiveness of abrocitinib in a real-world setting in patients with moderate-to-severe atopic dermatitis, with inadequate response or intolerance to ≤2 biologic therapies.
This description comes directly from the study's public registry record.
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| Allergy and Asthma Medical Group and Research Center | San Diego, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06899204