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喘息の成人患者におけるルンセキミグ(SAR443765)の長期安全性および有効性評価。
基本情報
- NCT ID
- NCT06609239
- ステータス
- 募集中
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 900
- 治験依頼者名
- Sanofi
概要
This is a phase 2, open-label extension study to evaluate the long-term safety and efficacy of lunsekimig in adult participants with asthma who have previously completed the parent studies. After completion of the parent study, eligible participants will be offered the opportunity to participate in the long-term extension (LTE) study with lunsekimig. The study duration will be up to 100 weeks with a treatment duration being up to 96 weeks.
対象疾患
Asthma
介入
Lunsekimig(DRUG)
依頼者(Sponsor)
サノフィ株式会社(INDUSTRY)