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临床试验/2024-517024-20-00
2024-517024-20-00招募中1/2 期

Multicentric Randomized Phase I/II Study to Evaluate Efficacy of Trifluridine/Tipiracil Plus XB2001 (Anti-IL-1α True Human Antibody) Versus Trifluridine/Tipiracil Plus Placebo in Metastatic Colorectal Cancer Patients After Failure of Oxaliplatin, Irinotecan, Fluoropyrimidine

Centr Georges Francois Leclerc14 个研究点 分布在 1 个国家目标入组 190 人开始时间: 2024年11月22日最近更新:
干预措施
相关药物

试验速览

阶段
1/2 期
状态
招募中
入组人数
190
试验地点
14
主要终点
Overall survival

研究概览

简要总结

Unresectable metastatic colorectal cancer (mCRC) remains an incurable disease. After failure of conventional treatments involving fluoropyrimidines, oxaliplatin and irinotecan in combination or not with biotherapies targeting EGFR and VEGF; regorafenib shows a modest improvement in overall survival. Recently, trifluridine/tipiracil has also shown efficacy in phase 3 with an overall survival of around 7 months. Trifluridine/tipiracil has become the standard of care for advanced mCRC in most western countries. However, the objective response rate remains very low and the survival gain remains moderate (+2 months). Therefore, new strategies are needed to ensure that mCRC patients who have received multiple lines of therapy can receive more effective treatments.

Based on previous clinical trials on IL-1 inhibition and our preclinical data, IL-1 inhibition may increase the efficacy of trifluridine/tipiracil. The goal is to test whether the addition of XB2001 to trifluridine/tipiracil could be synergistic.

详细描述

This project proposes to evaluate trifluridine/tipiracil plus XB2001 in patients with metastatic colorectal cancer previously treated with oxaliplatin, fluoropyrimidine and irinotecan in combination or not with an anti-angiogenic and an anti-EGFR for RAS Wild type tumor.

The project will consist of a randomized (1:1 ratio), double-blind, non-comparative, multi-center Phase II study with two treatment arms:

  • Experimental arm: trifluridine/tipiracil + XB2001
  • Control arm: trifluridine/tipiracil + placebo

研究设计

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

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
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

Experimental arm

Experimental

trifluridine/tipiracil + XB2001

干预措施: trifluridine/tipiracil + XB2001 (Drug)

Control arm

Placebo Comparator

trifluridine/tipiracil + placebo

干预措施: trifluridine/tipiracil + placebo (Drug)

结局指标

主要结局

Overall survival

时间窗: 6-month

Maximum Tolerated Dose (MTD) of XB2001

时间窗: At the end of Cycle 1 (each cycle is 28 days)

次要结局

未报告次要终点

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Pr François GHIRINGHELLI

Scientific

Centr Georges Francois Leclerc

研究点 (14)

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