Last reviewed · How we verify

S-1 and cisplatin

Asan Medical Center · Phase 3 active Small molecule

S-1 is a combination of three components that inhibit thymidylate synthase and other enzymes in the pyrimidine synthesis pathway, while cisplatin is a platinum-based alkylating agent that cross-links DNA, together producing synergistic cytotoxic effects against cancer cells.

S-1 is a combination of three components that inhibit thymidylate synthase and other enzymes in the pyrimidine synthesis pathway, while cisplatin is a platinum-based alkylating agent that cross-links DNA, together producing synergistic cytotoxic effects against cancer cells. Used for Gastric cancer (advanced or metastatic), Gastroesophageal junction cancer.

At a glance

Generic nameS-1 and cisplatin
Also known asTS-1 and cisplatin
SponsorAsan Medical Center
Drug classFluoropyrimidine antimetabolite + platinum-based alkylating agent
TargetThymidylate synthase (S-1); DNA (cisplatin)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

S-1 (tegafur, gimeracil, oteracil potassium) is an oral fluoropyrimidine prodrug that inhibits thymidylate synthase and other nucleotide synthesis enzymes, disrupting DNA replication. Cisplatin covalently binds to DNA, forming interstrand and intrastrand cross-links that prevent DNA replication and transcription. The combination exploits complementary mechanisms of action to enhance cytotoxic activity against rapidly dividing tumor cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: