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LV5FU2

Centre Hospitalier Universitaire de Besancon · Phase 3 active Small molecule

LV5FU2 is a combination chemotherapy regimen that inhibits thymidylate synthase and DNA synthesis to kill rapidly dividing cancer cells.

LV5FU2 is a combination chemotherapy regimen that inhibits thymidylate synthase and DNA synthesis to kill rapidly dividing cancer cells. Used for Metastatic colorectal cancer, Advanced gastric cancer.

At a glance

Generic nameLV5FU2
SponsorCentre Hospitalier Universitaire de Besancon
Drug classAntimetabolite chemotherapy combination
TargetThymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

LV5FU2 combines leucovorin (folinic acid), 5-fluorouracil (5-FU), and additional agents to enhance antimetabolite activity. Leucovorin potentiates 5-FU by stabilizing its binding to thymidylate synthase, thereby increasing the inhibition of DNA and RNA synthesis in cancer cells. This combination is designed to improve efficacy in colorectal and other solid tumors.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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