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
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
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Experimental arm
trifluridine/tipiracil + XB2001
干预措施: trifluridine/tipiracil + XB2001 (Drug)
Control arm
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
Pr François GHIRINGHELLI
Scientific
Centr Georges Francois Leclerc
