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Drug: gemcitabine, S-1

Osaka Medical Center for Cancer and Cardiovascular Diseases · Phase 2 active Small molecule

Inhibits DNA synthesis by inhibiting ribonucleotide reductase and DNA polymerase alpha

Inhibits DNA synthesis by inhibiting ribonucleotide reductase and DNA polymerase alpha Used for Pancreatic cancer, Breast cancer, Non-small cell lung cancer.

At a glance

Generic nameDrug: gemcitabine, S-1
Also known asgemzer, TS-1
SponsorOsaka Medical Center for Cancer and Cardiovascular Diseases
Drug classNucleoside analog
TargetRibonucleotide reductase, DNA polymerase alpha
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Gemcitabine is a nucleoside analog that is metabolized into its active forms, which are then incorporated into DNA, causing chain termination during DNA replication. S-1 is a combination of tegafur (a prodrug of 5-fluorouracil), gimeracil (a dihydropyrimidine dehydrogenase inhibitor), and oteracil (a cytosine deaminase inhibitor), which enhances the antitumor activity of 5-fluorouracil while reducing its gastrointestinal toxicity.

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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