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USEL/Leucovorin

Hokkaido Gastrointestinal Cancer Study Group · Phase 3 active Small molecule

Leucovorin is a folate analog that inhibits the enzyme dihydrofolate reductase, which is involved in DNA synthesis and repair.

Leucovorin is a folate analog that inhibits the enzyme dihydrofolate reductase, which is involved in DNA synthesis and repair. Used for Rescue after high-dose methotrexate therapy, Dihydropyrimidine dehydrogenase deficiency.

At a glance

Generic nameUSEL/Leucovorin
Also known asLeucovorin
SponsorHokkaido Gastrointestinal Cancer Study Group
Drug classAntifolate
TargetDihydrofolate reductase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

By inhibiting dihydrofolate reductase, leucovorin reduces the levels of tetrahydrofolate, a necessary cofactor for thymidylate synthase. This action is particularly important in cancer treatment, as it allows for the increased efficacy of 5-fluorouracil, a chemotherapeutic agent that also targets thymidylate synthase.

Approved indications

Common side effects

Key clinical trials

Primary sources

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