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临床试验/NL-OMON32383
NL-OMON32383已完成3 期

Plerixafor and G-CSF for the Mobilisation of Peripheral Blood Stem Cells for Autologous Stem Cell Transplantation in Patients with Non-Hodgkin*s Lymphoma (NHL), Hodgkin*s Disease (HD) or Multiple Myeloma (MM) * Safety Study in a General Autologous Transplant Population - MOZ00808

Genzyme0 个研究点目标入组 4 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
Genzyme
入组人数
4

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1.Diagnosis of MM, NHL, or HD in partial response (PR) or complete response (CR)
  • 2.Eligible and planned for an autologous haematopoietic stem cell transplantation
  • 4.At least 18 years of age (inclusive)

排除标准

  • 1. History of any acute or chronic leukaemia (including myelodysplastic syndrome)
  • 2. Prior allogeneic transplantation or more than one prior autologous transplantation
  • 3. Failed previous CD34+ cell collection attempts (either due to insufficient yield in apheresis product, or ineligible for apheresis because of inadequate mobilisation of CD34+ cells into peripheral blood)
  • 4. Less than 4 weeks since last anti-cancer therapy (including chemotherapy, biologic/immunologic, radiation) or less than 6 weeks if prior therapy with nitrosourea or mitomycin (for therapies with long-acting agents, a treatment-free interval of at least 2 half-lives should be considered) with the exception of
  • - Treatment with thalidomide, dexamethasone, lenalidomide (Revlimid*), and/or bortezomib (Velcade*) which is allowed up to 7 days prior to the first dose of G-CSF.

研究者

发起方
Genzyme

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