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临床试验/EUCTR2007-000902-55-DE
EUCTR2007-000902-55-DE进行中(未招募)不适用

Prospective Phase II Pilot study of Rabbit Antithymocyte globulin(ATG, Thymoglobuline®, Genzyme) with Ciclosporin for Patients withAcquired Aplastic Anaemia and comparison with matched historicalpatients treated with horse ATG and Ciclosporin: a Study from theEuropean Blood and Marrow Transplant (EBMT) Severe AplasticAnaemia Working Party

EBMT (European Group for Blood and Marrow Transplantation)0 个研究点目标入组 35 人开始时间: 2009年9月29日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
35

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

  • 1) To define aplastic anaemia there must be at least two of the following:
  • (1) haemoglobin < 10g/dl;
  • (2) platelet count < 50 x 109/l;
  • (3) neutrophil count < 1.5 x 109/l,
  • and a hypocellular bone marrow on bone marrow biopsy
  • 1.1) SAA as defined by a hypocellular bone marrow of <25% cellularity and 2 of the following 3 peripheral blood criteria: neutrophil count < 0.5 x 109/l, platelets < 20 x 109/l and/or reticulocytes < 20 x 109/l
  • 1.2) NSAA as defined by a hypocellular bone marrow and cytopenia in at least two cell lines AND neutrophil count > 0.5 x 109/l, and red cell and/or platelet transfusion dependence
  • 1.3) Acquired AA
  • 2) Time from diagnosis to study registration = 6mths
  • 3) No prior treatment except for haemopoietic growth factors given for no more than 4 weeks, or prior treatment with androgens.
  • 4) Age = 16yrs (= 18yrs in Germany and Switzerland), with no upper age limit.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1) Eligibility for an HLA-matched sibling donor transplant for SAA patients
  • 2) Prior therapy with ATG or CSA
  • 3) Haematopoeitic growth factors more than 4 weeks before study enrollment
  • 4) Diagnosis of Fanconi anaemia, dyskeratosis congenita or congenital bone mar¬row failure syndrome
  • 5) Evidence of myelodysplastic disease
  • 6) Paroxysmal nocturnal haemoglobinuria with evidence of significant haemolysis, history of PNH associated thrombosis or a PNH clone > 50% by flow cytometry
  • 7) Diagnosis or previous history of carcinoma (except local cervical, basal cell, squamous cells, or melanoma)
  • 8) Subject is pregnant (e.g. positive HCG test) or is breast feeding
  • 9) Severe uncontrolled infection or unexplained fever > 38oC
  • 10) Subjects who have hepatic, renal cardiac, metabolic or other concur¬rent diseases of such severity that life expectancy is less than 3 months

研究者

发起方
EBMT (European Group for Blood and Marrow Transplantation)

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Prospective Phase II Pilot study of Rabbit... | 临床试验