Drug intelligence / Profile preview

INBRX-109 + 5-fluorouracil + irinotecan

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

Overview

INBRX-109 + 5-fluorouracil + irinotecan is a **combination therapy** involving a recombinant, humanized tetravalent monoclonal antibody (INBRX-109) that targets death receptor 5 (DR5), together with two chemotherapeutic agents, **5-fluorouracil** and **irinotecan**. INBRX-109 acts as a DR5 agonist, inducing apoptosis in cancer cells via clustering of DR5, leading to activation of caspase-8 and downstream executioner caspases-3 and -7. 5-fluorouracil is a pyrimidine analog that inhibits thymidylate synthase and RNA/DNA synthesis; irinotecan is a topoisomerase I inhibitor that promotes DNA damage and cell death. The combination is under investigation in **solid tumors including sarcomas and colorectal adenocarcinoma**. INBRX-109 is developed by Inhibrx and marketed as ozekibart for clinical trials[1][2][3][4][5][6].

Brand names
ozekibart
Other names
INBRX-109 + 5-fluorouracil + irinotecan
02

Targets

TOP1 (DNA Topoisomerase I)TS (Thymidylate synthase)TNFRSF10B (DR5)

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