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临床试验/EUCTR2020-004725-23-GR
EUCTR2020-004725-23-GR进行中(未招募)1 期

Administration of rapidly generated multipathogen-specific T-Lymphocytes for the Treatment of AdV, CMV, EBV, BKV and Aspergillus fumigatus infections post Allogeneic Stem Cell Transplant - Penta-STs-001

Ge???? ??s???µe?? Tessa??????? Ge?????? ?apa????????0 个研究点目标入组 10 人开始时间: 2022年9月15日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
10

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

性别
All

入选标准

  • 1)Received prior myeoloablative or nonmyeloablative allogeneic hematopoietic stem cell transplant.
  • 2)Cells administered as treatment for single or multiple infections/reactivations of one or more of the following pathogens: AdV, CMV, EBV, ??V and AF (see 2.2.1 definitions).
  • 3)Karnofsky/Lansky score of = 50.
  • 4)ANC > 500/µl.
  • 5)Bilirubin = 2x*, AST < 3x*, Serum creatinine = 2x*, Hemoglobin > 8.0 g/dl.
  • 6)Pulse oximetry of > 90% on room air.
  • 7)Available pentavalent-specific T cells.
  • 8)Negative pregnancy test (if female of childbearing potential)
  • 9)Patient capable of providing 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 10
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • 1)Received ATG, or Campath or other T cell immunosuppressive monoclonal antibodies in the last 28 days.
  • 2)Steroids > 0.5 mg/kg/day prednisone.
  • 3)Received donor lymphocyte infusion in last 28 days.
  • 4)GVHD = grade 2.
  • 5)Active and uncontrolled relapse of malignancy.
  • 6)Patients with other uncontrolled infections

研究者

发起方
Ge???? ??s???µe?? Tessa??????? Ge?????? ?apa????????

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