跳至主要内容
临床试验/CTIS2023-503830-27-00
CTIS2023-503830-27-00招募中1 期

A Randomized, Open-Label, Phase 2 Study Evaluating Lymphodepletion With Fludarabine, Cyclophosphamide, And ALLO-647, Vs. Fludarabine And Cyclophosphamide Alone, In Subjects With Relapsed/Refractory Large B-Cell Lymphoma (LBCL) Receiving ALLO-501A Allogeneic CAR T Cell Therapy - ALLO-647-201

Allogene Therapeutics Inc.0 个研究点目标入组 70 人开始时间: 2023年3月30日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
70

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 65+(—)
性别
All

入选标准

  • Histologically confirmed diagnosis of relapsed/refractory large B-cell lymphoma at last relapse per WHO 2017, Relapsed or refractory disease after at least 2 lines of chemotherapy, Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1., Absence of significant donor (product)-specific anti-HLA antibodies (DSA) at screening., Adequate hematological function, Adequate Renal Function, Adequate Liver Function

排除标准

  • Active central nervous system (CNS) involvement by malignancy, Hypocellular bone marrow for age, Autologous or allogeneic HSCT within last 6 months (24 weeks) prior to lymphodepletion.

研究者

发起方
Allogene Therapeutics Inc.

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