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UFT (uracil, tegafur)

Taiho Pharmaceutical Co., Ltd. · Phase 3 active Small molecule

UFT is a combination of uracil and tegafur that inhibits thymidylate synthase to block DNA synthesis and induce cancer cell death.

UFT is a combination of uracil and tegafur that inhibits thymidylate synthase to block DNA synthesis and induce cancer cell death. Used for Colorectal cancer, Gastric cancer, Breast cancer.

At a glance

Generic nameUFT (uracil, tegafur)
SponsorTaiho Pharmaceutical Co., Ltd.
Drug classFluoropyrimidine antimetabolite
TargetThymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Tegafur is a prodrug of 5-fluorouracil (5-FU) that is converted in the body to the active form. Uracil is included to inhibit dihydropyrimidine dehydrogenase, the enzyme responsible for 5-FU catabolism, thereby increasing and prolonging 5-FU exposure. Together, they act as a fluoropyrimidine antimetabolite that disrupts nucleotide synthesis and DNA replication in rapidly dividing cancer cells.

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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