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
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