The Aim of This Study is to Assess the Efficacy and Safety of Chidamide, Regorafenib in Combination With Iparomlimab and Tuvonralimab for the Treatment of Advanced Colorectal Cancer in Third-line Therapy and Subsequent Lines.

PHASE2RecruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

April 10, 2025

Primary Completion Date

April 30, 2027

Study Completion Date

September 30, 2027

Conditions
Advanced Colorectal Cancer in the Third-line Treatment and BeyondpMMR/MSS Advanced Colorectal Cancer
Interventions
DRUG

chidamide, regorafenib, and iparomlimab/tuvonralimab

All patients were treated with the following regimen: Chidamide: 30mg per dose, twice a week; Regorafenib: 80mg per dose, once a day, orally for 3 weeks, followed by a 1-week rest, and repeated every 4 weeks; Iparomlimab/Tuvonralimab: 5mg/kg, once every 3 weeks, intravenous infusion.

Trial Locations (1)

200003

RECRUITING

Department of Medical Oncology, Second Affiliated Hospital of Naval Medical University, Shanghai

All Listed Sponsors
lead

Shanghai Changzheng Hospital

OTHER