drugset / Trial / NCT07116577

Radiotherapy Combined QL1706, TAS-102 and Bevacizumab in mCRC

NCT07116577

Phase 2 Not yet recruiting 37 enrolled Jinan Central Hospital
NaSingle-groupOpen-labelTreatment

Summary

This single-center, single-arm, prospective study plans to enroll patients with advanced colorectal cancer who have failed first-line or higher systemic therapies. Participants will receive a combination of iparomlimab and tuvonralimab (QL1706), trifluridine/tipiracil (TAS-102), bevacizumab, and palliative radiotherapy. The efficacy and safety of this combination therapy will be evaluated by assessing objective response rate (ORR), progression-free survival (PFS), overall survival (OS), disease control rate (DCR), and safety profile.

Timeline

Start
2025-08-31
Primary completion
2027-08-31
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Subject Iparomlimab Monoclonal antibody Intravenous
Subject TAS-102 Small molecule 35 mg/m2 Oral
Subject Tuvonralimab Monoclonal antibody Intravenous

Indications