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UFT adjuvant chemotherapy

Translational Research Center for Medical Innovation, Kobe, Hyogo, Japan · Phase 3 active Small molecule

UFT is a combination of uracil and tegafur (a prodrug of fluorouracil) that inhibits thymidylate synthase to disrupt DNA synthesis in cancer cells.

UFT is a combination of uracil and tegafur (a prodrug of fluorouracil) that inhibits thymidylate synthase to disrupt DNA synthesis in cancer cells. Used for Adjuvant chemotherapy for colorectal cancer, Gastric cancer adjuvant treatment.

At a glance

Generic nameUFT adjuvant chemotherapy
Also known asAdjuvant chemotherapy with tegafur-uracil
SponsorTranslational Research Center for Medical Innovation, Kobe, Hyogo, Japan
Drug classAntimetabolite chemotherapy
TargetThymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

UFT combines uracil with tegafur, a prodrug that is metabolized to fluorouracil (5-FU), a classic antimetabolite chemotherapy agent. The fluorouracil component inhibits thymidylate synthase, blocking dTMP synthesis and disrupting DNA replication in rapidly dividing cancer cells. Uracil acts as a modulator to enhance and prolong the cytotoxic effects of fluorouracil.

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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