Drug intelligence / Profile preview

ABBV-621 + FOLFIRI + bevacizumab

Development stage
Unknown
Lead developer
AbbVie
Modality
Small Molecules, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

ABBV-621 + FOLFIRI + bevacizumab is an investigational multi-drug combination regimen being evaluated primarily for metastatic or previously-treated colorectal cancer, particularly in RAS-mutant subpopulations. The regimen consists of: - **ABBV-621 (eftozanermin alfa)**, a second-generation TRAIL receptor agonist (recombinant fusion protein) that binds to the death receptors DR4 and DR5 on tumor cells, inducing apoptosis via caspase-dependent pathways. - **FOLFIRI**, a standard chemotherapy regimen composed of three drugs: irinotecan (topoisomerase I inhibitor), fluorouracil (5-FU, a pyrimidine antimetabolite), and folinic acid (leucovorin, enhances 5-FU activity). - **Bevacizumab**, a monoclonal antibody targeting vascular endothelial growth factor A (VEGF-A) to inhibit angiogenesis. The combination is delivered intravenously and is under investigation for its safety, tolerability, and preliminary antitumor activity in colorectal cancer, with additional interest in solid tumors. ABBV-621 is developed by AbbVie, and the broader regimen may involve manufacturers of the constituent drugs[3][5][2].

Other names
eftozanermin alfa + FOLFIRI + bevacizumab
02

Targets

TNFRSF10A (Death receptor 4)TS (Thymidylate synthase)TOP1 (DNA Topoisomerase I)VEGFA (Vascular endothelial growth factor A)TNFRSF10B (DR5)

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