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临床试验/EUCTR2022-000763-45-IT
EUCTR2022-000763-45-IT进行中(未招募)1 期

Global Registry for Long-Term Follow-up of Patients Participating in Clinical Trials with Posoleucel (ALVR105) - ALVR105

AlloVir, Inc.0 个研究点目标入组 500 人开始时间: 2022年6月21日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
AlloVir, Inc.
入组人数
500

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. Participation in an Allovir-sponsored PSL clinical trial, regardless of treatment assignment (PSL or placebo) and completion status (completion, early discontinuation).
  • 2. Patient received at least one infusion of PSL or placebo.
  • 3. Patient is willing and able to provide written informed consent to participate in the registry, or a parent or legal guardian is willing and able to provide written informed consent and the potential paediatric participant is able to provide assent in a manner approved by the Institutional Review Board/Independent Ethics Committee and local
  • regulations.
  • 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 250
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 105

排除标准

  • 未提供

研究者

发起方
AlloVir, Inc.

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