drugset / Trial / NCT06497985

A Study of Tucidinostat in Combination With Sintilimab and Bevacizumab in MSS/pMMR Colorectal Cancer Patients

NCT06497985

Phase 3 Recruiting 430 enrolled Chipscreen Biosciences, Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

A randomised, open-label, multicenter phase III study to evaluate the efficacy and safety of tucidinostat in combination with sintilimab and bevacizumab versus fruquintinib monotherapy in MSS/pMMR colorectal cancer patients.

Timeline

Start
2024-12-06
Primary completion
2028-05-31
Completion
2028-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 7.5 mg/kg Intravenous
Comparator Fruquintinib Small molecule 5 mg Oral
Subject Sintilimab Monoclonal antibody 200 mg Intravenous
Subject Tucidinostat Small molecule 30 mg Oral

Indications