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Irinotecan/Cetuximab

Gruppo Italiano per lo studio dei Carcinomi dell'Apparato Digerente · Phase 3 active Small molecule

Irinotecan inhibits topoisomerase I to damage cancer cell DNA, while cetuximab blocks EGFR signaling to prevent tumor growth and enhance chemotherapy sensitivity.

Irinotecan inhibits topoisomerase I to damage cancer cell DNA, while cetuximab blocks EGFR signaling to prevent tumor growth and enhance chemotherapy sensitivity. Used for Metastatic colorectal cancer, EGFR-positive or wild-type KRAS, Advanced colorectal cancer as first-line or later-line therapy.

At a glance

Generic nameIrinotecan/Cetuximab
Also known asCPT11/Cetuximab
SponsorGruppo Italiano per lo studio dei Carcinomi dell'Apparato Digerente
Drug classCombination chemotherapy and monoclonal antibody
TargetTopoisomerase I (irinotecan); EGFR (cetuximab)
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

Irinotecan is a topoisomerase I inhibitor that causes DNA damage in rapidly dividing cancer cells. Cetuximab is a monoclonal antibody targeting the epidermal growth factor receptor (EGFR), which blocks growth signaling and enhances the efficacy of chemotherapy. The combination leverages synergistic effects in EGFR-expressing colorectal cancers.

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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