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capecitabine-irinotecan

Dutch Colorectal Cancer Group · Phase 3 active Small molecule

Capecitabine-irinotecan combines a prodrug of fluorouracil with a topoisomerase I inhibitor to target rapidly dividing cancer cells.

Capecitabine-irinotecan combines a prodrug of fluorouracil with a topoisomerase I inhibitor to target rapidly dividing cancer cells. Used for Metastatic colorectal cancer.

At a glance

Generic namecapecitabine-irinotecan
SponsorDutch Colorectal Cancer Group
Drug classTopoisomerase I inhibitor and thymidylate synthase inhibitor
TargetTopoisomerase I and thymidylate synthase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Capecitabine is converted into 5-fluorouracil, which is then phosphorylated into its active form, 5-fluorodeoxyuridylate. This inhibits thymidylate synthase, leading to DNA damage and cell death. Irinotecan, on the other hand, inhibits topoisomerase I, preventing DNA replication and transcription.

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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