NL-OMON44118已完成3 期
Efficacy and Safety of NNC 0129-0000-1003 during Surgical Procedures in Patients with Haemophilia A - Pathfinder3
ovo Nordisk0 个研究点目标入组 1 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1
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
- 18 至 99(—)
入选标准
- •- Ongoing participation in the pathfinder2 (NN7088-3859) trial and having received *5 doses of N8-GP
- •- Undergoing major surgery
排除标准
- •- Known or suspected hypersensitivity to trial product including allergy to hamster protein or related products
- •- Previous withdrawal from the pathfinder2 (NN7088-3859) trial after administration of trial product, except interruption due to inclusion in this pathfinder3 trial (NN7088-3860)
- •- The receipt of any investigational medicinal product (except N8-GP) within 30 days prior to enrolment into the trial.
- •- FVIII inhibitors * 0.6 BU/mL at screening
- •- Previous arterial thrombotic events (e.g. myocardial infarction and intracranial thrombosis) or previous deep venous thrombosis or pulmonary embolism (as defined by available medical records)
- •- Immune modulating or chemotherapeutic medication
研究者
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