跳至主要内容
临床试验/NCT07200128
NCT07200128已完成不适用

Satisfaction and Treatment Experiences With RitlEcitiNib And Traditional Treatments for Severe Alopecia Areata Among Adults in the United States (SERENATA)

Pfizer1 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2025年2月3日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
123
试验地点
1
主要终点
% of patients for whom their clinician was "satisfied" with current control of alopecia areata

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged 18 years or older with severe alopecia areata

排除标准

  • 未提供

研究组 & 干预措施

Patients with severe Alopecia Areata

干预措施: Ritlecitinib (Drug)

结局指标

主要结局

% of patients for whom their clinician was "satisfied" with current control of alopecia areata

时间窗: 11/15/2023 to 06/10/2024

% of patients with clinician-assessed mild, moderate, or severe disease

时间窗: 11/15/2023 to 06/10/2024

% of patients with clinician assessed progressive, stable, or improving disease

时间窗: 11/15/2023 to 06/10/2024

次要结局

未报告次要终点

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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