drugset / Trial / NCT07012954

ctDNA-Guided Cetuximab or Bevacizumab Plus Trifluridine/Tipiracil in RAS/BRAF Wild-Type mCRC

NCT07012954

Phase 1/2 Recruiting 64 enrolled Sun Yat-sen University
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this randomized controlled clinical trial is to evaluate the efficacy of ctDNA-guided rechallenge with cetuximab plus trifluridine/tipiracil compared with bevacizumab plus trifluridine/tipiracil in patients with treatment-refractory, RAS/BRAF wild-type metastatic colorectal cancer.

Timeline

Start
2025-06-01
Primary completion
2027-12-31
Completion
2030-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Subject Cetuximab Monoclonal antibody 500 mg/m2 Intravenous
Background trifluridine/tipiracil Unknown 35 mg/m2 Oral

Indications