跳至主要内容
临床试验/EUCTR2007-000902-55-GB
EUCTR2007-000902-55-GB进行中(未招募)1 期

Prospective Phase II study of Rabbit Antithymocyte globulin (ATG, Thymoglobuline®, Genzyme) with Ciclosporin for Patients with Acquired Aplastic Anaemia and comparison with matched historical patients treated with horse ATG and Ciclosporin

EBMT (European group for Blood and Marrow Transplantation)0 个研究点目标入组 35 人开始时间: 2007年6月26日最近更新:
适应症
相关药物

试验速览

阶段
1 期
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

入选标准

  • 1.To define aplastic anaemia there must be at least two of the following:
  • · haemoglobin < 10g/dl
  • · platelet count < 50 x 109/l
  • · 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 two of the following:
  • · neutrophil count < 0.5 x 109/l,
  • · platelets < 20 x 109/l
  • · reticulocytes < 20 x 109/l 16
  • 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 haematopoietic growth factors given for no more than 4 weeks, or prior treatment with androgens.
  • 4. Age = 16yrs (= 18yrs in Germany in accordance with German law), with no upper age limit
  • Are the trial subjects under 18? yes
  • 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 marrow 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 concurrent 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)

相似试验

进行中(未招募)
1 期
Prospective Phase II Pilot study of Rabbit Antithymocyte globulin (ATG, Thymoglobuline®, Genzyme) with Ciclosporin for Patients with Acquired Aplastic Anaemia and comparison with matched historical patients treated with horse ATG and CiclosporiAquired aplastic anaemia and transfusion dependent non-severe aplastic anaemiaMedDRA version: 9.1Level: LLTClassification code 10002274Term: Anemia aplastic
EUCTR2007-000902-55-FREBMT (European group for Blood and Marrow Transplantation)35
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
EUCTR2007-000902-55-DEEBMT (European Group for Blood and Marrow Transplantation)35
进行中(未招募)
不适用
A Phase II Study of Efficacy of Rabbit Antithymocyte Globulin (rATG) in patients with Low and Itermediate-1 Risk Mylodysplastic Syndrome - Genzyme ThymoHEMO1206: Phase II study of Thymoglobulin in MDS patients
EUCTR2007-002532-28-DEGenzyme Europe BV43
进行中(未招募)
1 期
A Phase II Study of Efficacy of Rabbit Anti-thymocyte Globulin (rATG) in patients with Low and Itermediate-1 Risk Mylodysplastic Syndrome - Genzyme ThymoHEMO1206: Phase II study of Thymoglobulin in MDS patients
EUCTR2007-002532-28-GBGenzyme Europe BV43
进行中(未招募)
不适用
A Phase II Study of Efficacy of Rabbit Anti-thymocyte Globulin (rATG) in patients with Low and Itermediate-1 Risk Mylodysplastic Syndrome - Genzyme ThymoHEMO1206: Phase II study of Thymoglobulin in MDS patientsow And Intermediate-1 Risk Myelodysplastic Syndrome in adult patients 60 years or youngerMedDRA version: 9.1Level: LLTClassification code 10028533Term: Myelodysplastic syndrome
EUCTR2007-002532-28-NLGenzyme Europe BV43