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Clinical Trials/2024-517024-20-00
2024-517024-20-00
Recruiting
Phase 1/2

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 sites in 1 country190 target enrollmentNovember 22, 2024

Overview

Phase
Phase 1/2
Intervention
trifluridine/tipiracil + XB2001
Conditions
Not specified
Sponsor
Centr Georges Francois Leclerc
Enrollment
190
Locations
14
Primary Endpoint
Overall survival
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

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.

Detailed Description

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

Registry
euclinicaltrials.eu
Start Date
November 22, 2024
End Date
TBD
Last Updated
11 months ago
Study Type
Interventional
Study Design
Single Group

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pr François GHIRINGHELLI

Scientific

Centr Georges Francois Leclerc

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Experimental arm

trifluridine/tipiracil + XB2001

Intervention: trifluridine/tipiracil + XB2001

Control arm

trifluridine/tipiracil + placebo

Intervention: trifluridine/tipiracil + placebo

Outcomes

Primary Outcomes

Overall survival

Time Frame: 6-month

Maximum Tolerated Dose (MTD) of XB2001

Time Frame: At the end of Cycle 1 (each cycle is 28 days)

Study Sites (14)

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