drugset / Trial / NCT05799443

Efficacy and Safety of SBRT Followed by Tislelizumab Plus Cetuximab and Irinotecan in Patients With Previously Treated RAS Wild-type Advanced Refractory Colorectal Cancer

NCT05799443 ↗

Phase 2 Unknown 23 enrolled Fujian Cancer Hospital
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the efficacy and safety of SBRT followed by tislelizumab plus cetuximab and irinotecan in patients with previously treated RAS wild-type advanced refractory colorectal cancer

Timeline

Start
2023-04-05
Primary completion
2024-04-05
Completion
2025-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 500 mg/m2 —
Subject Irinotecan Small molecule 180 mg/m2 —
Subject Tislelizumab Monoclonal antibody 200 mg —

Indications