跳至主要内容
临床试验/NCT06665217
NCT06665217尚未招募2 期

Glofitamab, Polatuzumab Vedotin, Zanubrutinib, Lenalidomide and Prednisone in Previously Untreated Diffuse Large B-Cell Lymphoma

Navy General Hospital, Beijing0 个研究点目标入组 80 人开始时间: 2025年9月24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
尚未招募
发起方
入组人数
80
主要终点
Overall Response Rate (ORR)

研究概览

简要总结

The goal of this phase 2 trial is to test the safety and efficacy of G-Pola-ZLP as induction therapy in patients with DLBCL.

详细描述

The investigators will evaluate safety and efficacy of G-Pola-ZLP as induction therapy in Previously Untreated Diffuse Large B-Cell Lymphoma. ORR(Overall response rate, progression-free survival (PFS), Overall survival (OS), Adverse events (AEs) will be assessed.

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
14 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pathologically confirmed Diffuse Large B Cell Lymphoma according World Health Organization (WHO) classification;
  • Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF).
  • Patient must understand and voluntarily sign an ICF prior to any study-specific assessments/procedures being conducted;
  • Patient is willing and able to adhere to the study visit schedule and other protocol requirements;
  • Patient has not received chemotherapy previously.
  • Anticipated life expectancy at least 3 months

排除标准

  • Active or uncontrolled infections requiring systemic treatment within 14 days before enrollment.
  • Any instability of systemic disease, including but not limited to severe cardiac, liver, kidney, or metabolic disease need therapy.
  • Pregnant or lactating women

研究组 & 干预措施

Induction Therapy

Experimental

Patients were treated by G-Pola-ZLP as Induction Therapy

干预措施: Glofitamab, Polatuzumab Vedotin, Zanubrutinib, Lenalidomide and Prednisone as Induction Therapy (Drug)

结局指标

主要结局

Overall Response Rate (ORR)

时间窗: 1 year

ORR was defined as the proportion of patients who achieved CR or PR as their best response

次要结局

  • Overall Survival (OS)(through study completion, an average of 2 years)
  • Progression Free Survival (PFS)(2 years)

研究者

发起方
Navy General Hospital, Beijing
申办方类型
Other
责任方
Principal Investigator
主要研究者

Liren Qian

Associate Chief Physician, Associate Professor

Navy General Hospital, Beijing

相似试验