drugset / Trial / NCT06202001

Irinotecan, TAS-102 Plus Bevacizumab as a Second-Line Therapy in mCRC Patients

NCT06202001

NaSingle-groupOpen-labelTreatment

Summary

In mCRC, response to second-line chemotherapy is limited, and few treatment options are available. It is urgent to design an optimal second-line treatment regimen to improve the response rate and prolong the survival of patients with mCRC. Several studies preliminarily demonstrated that irinotecan, TAS-102 plus bevacizumab regimen could bring promising efficacy with a tolerable safety profile for patients with mCRC as a second-line treatment. This phase I/II study was aimed to determine the recommended phase II dose (RP2D) of the combination of TAS-102, irinotecan, and bevacizumab for future clinical trials in patients with mCRC refractory to both fluoropyrimidine and oxaliplatin and to evaluate its safety and preliminary efficacy.

Timeline

Start
2022-10-01
Primary completion
2025-09-30
Completion
2026-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 5 mg/kg
Subject Irinotecan Small molecule 135 mg/m2
Subject Irinotecan Small molecule 150 mg/m2
Subject Irinotecan Small molecule 165 mg/m2
Subject Irinotecan Small molecule 180 mg/m2
Subject Trifluridine/tipiracil Unknown 20 mg/m2
Subject Trifluridine/tipiracil Unknown 25 mg/m2
Subject Trifluridine/tipiracil Unknown 30 mg/m2
Subject Trifluridine/tipiracil Unknown 35 mg/m2

Indications