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rilvegostomig + gemcitabine + cisplatin

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

**Rilvegostomig + gemcitabine + cisplatin** is a combination regimen currently under clinical investigation, particularly in the ARTEMIDE-Biliary01 Phase III clinical trial for the adjuvant treatment of patients with biliary tract cancer (BTC) who have undergone surgical resection[1][3]. Rilvegostomig is a bispecific monoclonal antibody that targets both the PD-1 (programmed death-1) and TIGIT (T cell immunoreceptor with Ig and ITIM domains) immune checkpoints, enhancing anti-tumor immune response by blocking two major suppressive pathways used by cancer to evade immune detection[1][2][3]. By combining rilvegostomig with standard cytotoxic chemotherapeutics gemcitabine and cisplatin, the regimen aims to synergistically improve cancer cell eradication: rilvegostomig reinvigorates immune-mediated destruction, while gemcitabine and cisplatin directly kill rapidly dividing tumor cells[1][3]. The regimen is administered intravenously. Rilvegostomig is developed by AstraZeneca, derived from Compugen’s antibody technology[2].

Other names
cisplatin + gemcitabine + AZD2936CISGEM + Rilvegostomig
02

Targets

TIGIT (T cell immunoreceptor with Ig and ITIM domains)PDCD1 (Programmed cell death protein 1 receptor)

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