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临床试验/EUCTR2016-002383-13-NL
EUCTR2016-002383-13-NL进行中(未招募)1 期

mbilical cord blood transplantation in high-risk hematological patients using stemregenin-1 expanded hematopoietic stem cells.A feasibility study focussing on engraftment and hematopoietic recovery. - Cord Blood Expansion (SR-1)

Erasmus MC0 个研究点开始时间: 2016年9月12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
Erasmus MC

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

  • - Age 18-70 years inclusive
  • - Diagnosis of poor-risk hematological malignancy or (V)SAA relapsing after or failing immunosuppressive therapy and meeting the criteria for a MUD allo SCT
  • - Lacking a sufficiently matched volunteer unrelated donor or lacking such a donor within the required time period of = 2 months in case of urgently needed alloSCT
  • - Availability of 1 (=5/6) matched UCB graft with a nuclear cell count > 2,7 x 107/kg (see paragraph 8.2).
  • - Availability of an back-up autograft, harvested and frozen earlier in the course of treatment, (harvest according to local aphersis policies)
  • - WHO performance status 0-2
  • - Written informed consent
  • 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 9
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1

排除标准

  • Bilirubin and/or transaminases > 2.5 x normal value
  • Creatinine clearance < 40 ml/min
  • Cardiac dysfunction as defined by:
  • -Reduced left ventricular function with an ejection fraction < 45% as measured by MUGA scan or echocardiogram (another method for measuring cardiac function is acceptable)
  • - Unstable angina
  • - Unstable cardiac arrhythmias
  • Pulmonary function test with VC, FEV1 and/ or DCO < 50%
  • Active, uncontrolled infection
  • History of high dose (= 8 Gy) total body irradiation
  • Pregnant or lactating females
  • HIV positivity

研究者

发起方
Erasmus MC

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