跳至主要内容
临床试验/EUCTR2012-004867-38-IT
EUCTR2012-004867-38-IT进行中(未招募)1 期

Safety and efficacy of nonacog beta pegol (N9-GP) in Previously Untreated Patients with Haemophila B.An open-label single-arm multicentre non-controlled phase 3a trial investigating safety and efficacyof nonacog beta pegol (N9-GP) in prophylaxis and treatment of bleeding episodes in previouslyuntreated patients with haemophilia B (FIX activity =2%) - An open-label single-arm multicentre non-controlled phase 3a trial investigating safety and efficacy

OVO NORDISK. S.P.A.0 个研究点目标入组 50 人开始时间: 2018年2月15日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

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
Male

入选标准

  • - Informed consent obtained before any trial-related activities. Trialrelated
  • activities are any procedures that are carried out as part of the
  • trial, including activities to determine suitability for the trial
  • - Male, < 6 years of age at the time of signing informed consent
  • - Patients with the diagnosis of haemophilia B (FIX activity level = 2%)
  • based on medical records or central laboratory results
  • - Previously untreated or exposed to FIX containing products less than
  • or equal to 3 exposure days (5 previous exposure days to blood
  • components are acceptable)
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 1
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Any history of FIX inhibitors (defined by medical records)
  • - Known or suspected hypersensitivity to trial product or related
  • - Previous participation in this trial. Participation is defined as first dose
  • administered of trial product
  • - Receipt of any investigational medicinal product within 30 days before
  • - Congenital or acquired coagulation disorder other than haemophilia B
  • - Any chronic disorder or severe disease which, in the opinion of the
  • Investigator, might jeopardise patient's safety or compliance with the
  • - Patient's parent(s)/LAR(s) mental incapacity, unwillingness to
  • cooperate, or a language barrier precluding adequate understanding and
  • cooperation

研究者

发起方
OVO NORDISK. S.P.A.

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