A Clinical Study of T3011 in Combination With Toripalimab and Regorafenib in Patients With Colorectal Cancer

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

April 2, 2024

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions
Colorectal Cancer Metastatic
Interventions
BIOLOGICAL

T3011 hepatic artery infusion

The study was divided into two dose groups, T3011 3×10\^8 PFU/time (HAI) and T3011 1×10\^9 PFU/time (HAI), with a 3+3 dose escalation design. After the completion of the lead-in period, the patient entered the combination therapy period(combination therapy with T3011 hepatic artery infusion , Regorafenib and Toripalimab),and the dosage of T3011 was determined according to the safety observation results of the lead-in period, the dose of toripalimab was 80mg intravenously, and regorafenib was 80mg orally once a day.

DRUG

toripalimab

The combination therapy period: toripalimab, 80mg intravenous ,D2 and D16, 4 weeks per cycle

DRUG

regorafenib

The combination therapy period: regorafenib ,80mg orally once a day, D1-D21,4 weeks per cycle

All Listed Sponsors
collaborator

Immvira Co., Limited

UNKNOWN

lead

China Medical University, China

OTHER

NCT06283303 - A Clinical Study of T3011 in Combination With Toripalimab and Regorafenib in Patients With Colorectal Cancer | Biotech Hunter | Biotech Hunter