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临床试验/NCT06764017
NCT06764017招募中2 期

A Single-arm, Multicenter, Prospective Clinical Study of CHiR (chidamide, Zanubrutinib, and Lenalidomide) for Newly Diagnosed MYC- and BCL2-positive Diffuse Large B-cell Lymphoma (DLBCL) in Elderly Patients Intolerant to Chemotherapy.

First Affiliated Hospital of Ningbo University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年2月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
30
试验地点
1
主要终点
the complete remission rate (CRR)

研究概览

简要总结

The objective of exploring the application of CHiR is to evaluate its therapeutic efficacy and safety in newly diagnosed elderly patients with diffuse large B-cell lymphoma (DLBCL) aged 70 and above, and to investigate the genetic subtypes that may benefit from CHiR. The primary endpoint is the complete remission rate (CRR) at the end of 8 cycles.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
70 Years 至 100 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

CHiR

Experimental

The combined regimen of chidamide, zanubrutinib, and lenalidomide (CHiR) is employed to treat elderly patients with double-expressor lymphoma. This study aims to explore the efficacy and safety of this regimen in newly diagnosed elderly patients with diffuse large B-cell lymphoma (DLBCL) who are intolerant to chemotherapy.

干预措施: CHiR-DEL (Drug)

结局指标

主要结局

the complete remission rate (CRR)

时间窗: Each cycle consists of 21 days, with a total of 8 cycles.

The primary endpoint is the complete remission rate (CRR) at the end of 8 cycles.

次要结局

未报告次要终点

研究者

发起方
First Affiliated Hospital of Ningbo University
申办方类型
Network
责任方
Principal Investigator
主要研究者

Lixia Sheng

Chief Physician

First Affiliated Hospital of Ningbo University

研究点 (1)

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