drugset / Trial / NCT06563986

FTD-TPI, Bevacizumab, and Radioembolization With 166Ho-microspheres in Refractory Metastatic Colorectal Cancer

NCT06563986

Phase 2 Recruiting 40 enrolled UMC Utrecht
NaSingle-groupOpen-labelTreatment

Summary

Extrahepatic disease progression limits clinical efficacy of individualized radioembolization for patients with refractory metastatic colorectal cancer (mCRC). In the same patient population, trifluridine/tipiracil (FTD-TPI) and bevacizumab lead to disease control and overall survival benefit and may be a radiosensitizer. The purpose of this study is to determine safety, tolerability, and activity of individualized radioembolization with 166Holmium (166Ho)-microspheres combined with FTD-TPI and bevacizumab.

Timeline

Start
2024-06-18
Primary completion
2028-01
Completion
2028-06

Drugs

EvaluationDrugModalityDoseRoute
Subject 166-Ho microspheres Unknown Other
Background Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Background TAS-102 Small molecule 35 mg/m2 Oral

Indications