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L-leucovorin

Gruppo Oncologico del Nord-Ovest · Phase 3 active Small molecule

L-leucovorin is a reduced folate that enhances the cytotoxic activity of fluorouracil by stabilizing the ternary complex between fluorodeoxymonophosphate, thymidylate synthase, and the reduced folate cofactor.

L-leucovorin is a reduced folate that enhances the cytotoxic activity of fluorouracil by stabilizing the ternary complex between fluorodeoxymonophosphate, thymidylate synthase, and the reduced folate cofactor. Used for Colorectal cancer (in combination with fluorouracil), Metastatic colorectal cancer, Adjuvant treatment of colorectal cancer.

At a glance

Generic nameL-leucovorin
Also known asI-LV, Lederfolin
SponsorGruppo Oncologico del Nord-Ovest
Drug classReduced folate cofactor / chemotherapy adjuvant
TargetThymidylate synthase (indirect; acts as cofactor)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

L-leucovorin (the active L-isomer of folinic acid) acts as a cofactor that potentiates fluorouracil (5-FU) efficacy in cancer chemotherapy. By providing reduced folate, it increases the formation and stability of the inhibitory complex that blocks thymidylate synthase, thereby enhancing 5-FU's ability to disrupt DNA synthesis in rapidly dividing cancer cells. This combination is a standard component of many colorectal and other solid tumor chemotherapy regimens.

Approved indications

Common side effects

Key clinical trials

Primary sources

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