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Capecitabine, Cyclophosphamide

Vastra Gotaland Region · Phase 2 active Small molecule

Capecitabine is a prodrug that is converted into 5-fluorouracil, which interferes with DNA synthesis, thereby inhibiting cancer cell growth. Cyclophosphamide is an alkylating agent that attaches an alkyl group to the DNA of cancer cells, thereby interfering with their replication.

Capecitabine is a prodrug that is converted into 5-fluorouracil, which interferes with DNA synthesis, thereby inhibiting cancer cell growth. Cyclophosphamide is an alkylating agent that attaches an alkyl group to the DNA of cancer cells, thereby interfering with their replication. Used for Metastatic breast cancer, Advanced colorectal cancer.

At a glance

Generic nameCapecitabine, Cyclophosphamide
SponsorVastra Gotaland Region
Drug classAntineoplastic
TargetThymidylate synthase, DNA
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Capecitabine's mechanism of action is similar to that of 5-fluorouracil, a thymidylate synthase inhibitor. Cyclophosphamide's mechanism of action involves the formation of DNA cross-links, which prevent DNA replication and transcription. This leads to cell death, particularly in rapidly dividing cancer 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

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