Drug intelligence / Profile preview

aflibercept + S-1

Development stage
Unknown
Lead developer
Regeneron Pharmaceuticals
Modality
Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Aflibercept + S-1 is an investigational **combination regimen** evaluated in clinical trials for the treatment of advanced solid tumors. **Aflibercept** is a recombinant fusion protein that binds to and inhibits vascular endothelial growth factors (VEGF-A, VEGF-B) and placental growth factor, thereby blocking angiogenesis and tumor progression. **S-1** is an oral fluoropyrimidine formulation containing tegafur (a prodrug of 5-fluorouracil), gimeracil (an inhibitor of 5-FU catabolism), and oteracil (which reduces gastrointestinal toxicity by decreasing 5-FU activation in the gut). The combination aims to provide additive or synergistic anti-cancer effects by combining anti-angiogenic therapy with cytotoxic chemotherapy. It has been studied in Japanese patients with metastatic or unresectable solid malignancies, primarily in phase I trials to assess safety, tolerability, and recommended dosing. The combination is administered as intravenous aflibercept every two weeks plus oral S-1 in cycles[1].

Brand names
aflibercept + S-1
Other names
aflibercept + S-1
02

Targets

TS (Thymidylate synthase)DPYD (Dihydropyrimidine dehydrogenase)VEGFA (Vascular endothelial growth factor A)PGF (Placental Growth Factor)VEGFB (Vascular endothelial growth factor B)

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