Drug intelligence / Profile preview

iparomlimab + tuvonralimab + gemcitabine + cisplatin

Development stage
Unknown
Lead developer
Qilu Pharmaceutical
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

This combination therapy consists of iparomlimab and tuvonralimab (collectively known as QL1706) administered in conjunction with the chemotherapy agents gemcitabine and cisplatin (GC). QL1706 is a bifunctional MabPair product developed by Qilu Pharmaceutical that simultaneously targets the PD-1 and CTLA-4 immune checkpoint pathways to enhance anti-tumor immune responses. Gemcitabine is a nucleoside metabolic inhibitor that interferes with DNA synthesis, while cisplatin is a platinum-based agent that causes DNA cross-linking and apoptosis. This specific four-drug regimen is being evaluated as a first-line treatment for advanced intrahepatic cholangiocarcinoma (ICC) in clinical trials sponsored by Fudan University, aiming to provide superior efficacy over standard chemotherapy or single-checkpoint inhibitor combinations.

Other names
Iparomlimab and Tuvonralimab Combined With Gemcitabine and CisplatinQL1706 plus GCQL-1706 plus GCQL 1706 plus GC
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)DNARNR (Ribonucleotide reductase)

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