跳至主要内容
临床试验/EUCTR2006-001164-24-IT
EUCTR2006-001164-24-IT进行中(未招募)不适用

MAINTENANCE TREATMENT WITH ALEMTUZUMAB Campath AS AN ALTERNATIVE TO ALLOGENIC TRANSPLANTATION IN PATIENTS WITHOUT COMPATIBLE DONOR IN PATIENTS WITH PERIPHERAL T CELL LYMPHOMA - ND

G.I.S.L. - GRUPPO ITALIANO STUDIO LINFOMI0 个研究点目标入组 25 人开始时间: 2006年8月3日最近更新:
适应症
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
25

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

  • - Histologically confirmed diagnosis of Peripheral T cell Lymphoma Entheropathy-type T-cell Lymphoma; Hepatosplenic T-cell Lymphoma; Subcutaneous Panniculitis-like T-cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Peripheral T-cell Lymphoma, unspecified - Stage I IV - Performance Status ECOG 0 3 - Age 18 65 years - CD52 positivity - Previous induction therapy with CHOP or DHAP, followed by autologous bone marrow transplantion - Complete or partial 75 response at the time of inclusion into the study - HIV, HbsAg, HCV negativity - CMV Ag and/or Ab anti CMV IgM negativity - ANC 1.500 x 109/L and PLT 75 x 109/L - Normal renal and hepatic functions - LVEF 50 - Documented absence of infections - No previous or concomitant neoplasms - No CNS involvement - Use of effective contraception - Negative pregnancy test - 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Cardiopathy- LVEF 40 - No previous treatment - Myelodysplasic syndromes - HbsAg, HIV and HCV-RNA positivity

研究者

发起方
G.I.S.L. - GRUPPO ITALIANO STUDIO LINFOMI

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