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A Study to Learn About the Medicine Called Ritlecitinib in Adults With Severe Alopecia Areata in Real-world Settings

Pfizer logo

Pfizer

Status

Completed

Conditions

Severe Alopecia Areata

Treatments

Drug: Ritlecitinib

Study type

Observational

Funder types

Industry

Identifiers

NCT07200128
B7981115

Details and patient eligibility

About

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.

Enrollment

123 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Aged 18 years or older with severe alopecia areata

Trial design

123 participants in 1 patient group

Patients with severe Alopecia Areata
Treatment:
Drug: Ritlecitinib

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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