Drug intelligence / Profile preview

IBI363 + capecitabine

Development stage
Unknown
Lead developer
Innovent Biologics
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Oral
01

Overview

IBI363 + capecitabine is an investigational combination regimen that pairs the novel bispecific fusion protein IBI363 (also known as TAK-928) with the oral chemotherapy agent capecitabine. Developed by Innovent Biologics and partnered with Takeda, IBI363 is a first-in-class PD-1/alpha-biased IL-2 bispecific fusion protein designed to simultaneously block the PD-1/PD-L1 immune checkpoint pathway and selectively activate the IL-2 pathway on tumor-specific T cells, thereby enhancing anti-tumor immunity while minimizing systemic toxicity. Capecitabine is a fluoropyrimidine carbamate prodrug that is converted to 5-fluorouracil (5-FU) in vivo, acting as an antimetabolite to inhibit DNA synthesis and cell division. This combination is primarily being evaluated in clinical trials, often alongside oxaliplatin (as part of the XELOX regimen), for the treatment of advanced or metastatic gastric or gastroesophageal junction adenocarcinoma.

Other names
capecitabine + IBI363capecitabine + TAK-928IBI363 + capecitabineIBI363 + XelodaTAK-928 + capecitabineTAK-928 + Xeloda
02

Targets

IL2RA (Interleukin-2 receptor alpha subunit)PDCD1 (Programmed cell death protein 1 receptor)TS (Thymidylate synthase)

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