Drug intelligence / Profile preview

sonesitatug vedotin + rilvegostomig + 5-fluorouracil + capecitabine

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

This is an investigational combination therapy comprising four drugs: - **sonesitatug vedotin** (AZD0901/CMG901): a Claudin 18.2-targeted antibody-drug conjugate (ADC) delivering monomethyl auristatin E, a microtubule inhibitor, for selective killing of tumor cells expressing CLDN18.2. - **rilvegostomig** (AZD2936): a PD-1/CTLA-4 bispecific monoclonal antibody, functioning as an immune checkpoint inhibitor, currently in early phase clinical trials. - **5-fluorouracil**: a pyrimidine analog antimetabolite that inhibits thymidylate synthase, impairing DNA synthesis. - **capecitabine**: an oral prodrug of 5-fluorouracil, also inhibiting thymidylate synthase after conversion in vivo. The combination is under clinical study for treatment of advanced or metastatic gastric or gastroesophageal junction adenocarcinoma expressing Claudin 18.2[2][3].

02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TS (Thymidylate synthase)MicrotubuleCTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)Claudin 18.2

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