EUCTR2016-001503-23-NL进行中（未招募）1 期
Prospective Follow-up Study for Patients who Completed Study ALX0681-C301 (HERCULES) to Evaluate Long-term Safety and Efficacy of Caplacizumab (Post-HERCULES)
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- Ablynx NV
- 入组人数
- 92
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Each potential subject must satisfy all of the following criteria to be enrolled in the study:
- •1.Completed the Final (28 day) FU visit in Study ALX0681-C301.
- •2.Is =18 years of age at the time of signing the informed consent form (ICF).
- •3.Provided informed consent prior to initiation of any study specific activity/procedure.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 89
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 3
排除标准
- •The criteria for exclusion are the following:
- •1.Not being able/willing to comply with the study protocol procedures.
- •2.Currently enrolled in a clinical study with another investigational drug or device.
研究者
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