Pfizer
New York, 10001, United States
NCT Number: NCT07200128
This study is a secondary analysis of the Adelphi Real World Alopecia Areata II United States Disease Specific Programmes database. This database contains data from a cross-sectional study capturing linked physician and patient survey data for dermatologists who treat alopecia areata and patients diagnosed with alopecia areata in the United States. The retrospective analysis of these data will evaluate experiences of patients and dermatologists receiving/prescribing ritlecitinib for severe alopecia areata in the United States. Specifically, the study will describe characteristics of patients who received ritlecitinib for severe alopecia areata, including demographics, clinical characteristics at the time of starting ritlecitinib, and their alopecia areata-related treatment history. The study will also report dermatologist satisfaction with treatment and change in the patient's alopecia areata severity and disease activity from the start of ritlecitinib to different time points on treatment.
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Notify Me18 year and older
All sexes
Observational
New York, 10001, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Aged 18 years or older with severe alopecia areata
As provided in real world practice
Time frame: 11/15/2023 to 06/10/2024
Time frame: 11/15/2023 to 06/10/2024
Time frame: 11/15/2023 to 06/10/2024
Pfizer
Industry
Satisfaction and Treatment Experiences With RitlEcitiNib And Traditional Treatments for Severe Alopecia Areata Among Adults in the United States (SERENATA)
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