跳至主要内容
临床试验/NCT07483268
NCT07483268进行中(未招募)不适用

A Prospective Study of Stapokibart Injection in Patients With CRSwNP

Chengdu Kangnuoxing Biopharma,Inc.1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2026年5月29日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
600
试验地点
1

研究概览

简要总结

This study is a open label, prospective study to evaluate the safety of Stapokibart Injection in subjects with CRSwNP.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Participants aged 18 years or older at the time of informed consent and provide voluntary informed consent to participate in the study before inclusion in the study.
  • Physician decision to treat the participant with Stapokibart Injection for CRSwNP (according to the China-specific prescribing information) made prior to and independently of the participant's participation in the study.

排除标准

  • Known history of allergic reaction to Stapokibart Injection.
  • Participants currently or plan participating in any interventional clinical trial.
  • Participants with hematologic malignancies.
  • Women with pregnant.
  • Any condition that, in the opinion of the Investigator, may interfere with the participant's ability to participate in the study.

研究者

发起方
Chengdu Kangnuoxing Biopharma,Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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