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临床试验/CTIS2022-502386-13-00
CTIS2022-502386-13-00招募中1 期

A Phase 3 Open-label Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of CSL312 (Garadacimab) in the Prophylactic Treatment of Hereditary Angioedema in Pediatric Subjects 2 to 11 Years of Age - CSL312_3003

CSL Behring LLC0 个研究点目标入组 20 人开始时间: 2023年6月22日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 17(—)
性别
All

入选标准

  • Male or female, Aged 2 to 11 years, inclusive, with body weight = 10th percentile based on age, Diagnosed with clinically confirmed C1-INH HAE, Experienced = 2 HAE attacks during the 6 months before Screening

排除标准

  • Concomitant diagnosis of another form of angioedema, such as idiopathic or acquired angioedema, recurrent angioedema associated with urticaria, or HAE type III, Use of C1-INH products, androgens, antifibrinolytics, approved or future approved medications, or other small molecule medications for routine prophylaxis against HAE attacks, Participation in another interventional clinical study, Having laboratory clinical abnormalities assessed as clinically significant by the investigator in results of hematology or chemistry assessments performed during Screening, Currently receiving a therapy not permitted during the study, Being pregnant or breastfeeding

研究者

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