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