The Efficacy and Safety of Neoadjuvant Therapy With Iparomlimab and Tuvonralimab in Locally Advanced MSI-H/dMMR Colorectal Cancer: An Prospective, Single-Arm Study (Neo-IT)

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

August 20, 2025

Primary Completion Date

August 30, 2027

Study Completion Date

August 30, 2030

Conditions
dMMR/MSI-H-type Rectal Adenocarcinoma
Interventions
DRUG

Ipalolimab and Tovorilimab

1.Active Ingredients: Ipalolimab and Tovorilimab (a dual-functional combination antibody consisting of Ipalolimab, a recombinant humanized monoclonal antibody targeting programmed death receptor-1 \[PD-1\], and Tovorilimab, a recombinant humanized monoclonal antibody targeting cytotoxic T-lymphocyte-associated protein-4 \[CTLA-4\]). 2.Specification: 50 mg (2 mL) per vial. 3.Dosage and Administration: Administer via intravenous infusion at a recommended dose of 5 mg/kg every 3 weeks.

Trial Locations (1)

310016

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine,, Hangzhou

All Listed Sponsors
lead

Sir Run Run Shaw Hospital

OTHER