Effectiveness and Safety Study of Tezepelumab in Adults & Adolescent Participants With Severe Asthma in the United States
| 适应症 | Asthma |
|---|---|
| 分期 | 4期 |
| 申办方 | AstraZeneca |
| 状态 | 已完成 |
| 受试者人数 | 286 人 |
| 干预(药物) | Tezepelumab |
| 开始日期 | 2022年4月29日 |
| 完成日期 | 2025年10月1日 |
| 结果公布日 | 2026年7月16日 |
摘要
To asses effectiveness and safety of tezepelumab in adult and adolescent participants with severe asthma including several under-studied populations in the United States.
Annualized Asthma Exacerbation Rate (AAER)
| Tezepelumab | 2.8783 ± 2.69 Adjusted rate (exacerbations per year) |
|---|---|
| Tezepelumab | 0.8665 ± 0.71 Adjusted rate (exacerbations per year) |
在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文
同一适应症的其他试验
- A Study of Remote Asthma Management Using an Integrated Artificial Intelligence-assisted E — Mayo Clinic
- Developing a Childhood Asthma Risk Passive Digital Marker — Indiana University
- A Study Testing the Superiority of CHF 1535 pMDI 800/24µg Total Daily Dose Compared With C — Chiesi Farmaceutici S.p.A.
- A Study Evaluating the Efficacy and Safety of Lebrikizumab in Adult Patients With Mild to — Hoffmann-La Roche
- A Study of Lebrikizumab in Participants With Uncontrolled Asthma Who Are on Inhaled Cortic — Hoffmann-La Roche
- Administration of ARS-1 or Albuterol in Subjects With Persistent Asthma — ARS Pharmaceuticals, Inc.