Drug intelligence / Profile preview

abituzumab + cetuximab + irinotecan

Development stage
Unknown
Lead developer
Merck
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

Abituzumab + cetuximab + irinotecan is an investigational combination therapy evaluated primarily for the treatment of metastatic colorectal cancer (mCRC), particularly in patients with KRAS wild-type tumors. Abituzumab (EMD 525797) is a humanized monoclonal IgG2 antibody that targets integrin αv heterodimers, notably αvβ5 and αvβ6 integrins, which are implicated in tumor progression and metastasis. Cetuximab is a chimeric monoclonal antibody targeting the epidermal growth factor receptor (EGFR), inhibiting downstream signaling involved in cell proliferation and survival. Irinotecan is a small molecule chemotherapeutic agent that inhibits topoisomerase I, leading to DNA damage and apoptosis in rapidly dividing cells. The combination has been studied in phase I/II clinical trials as second-line therapy for patients with KRAS wild-type mCRC who have progressed after oxaliplatin-containing regimens. The rationale for combining these agents lies in their complementary mechanisms—targeting both integrin-mediated tumor microenvironment interactions and EGFR-driven signaling pathways while providing cytotoxic chemotherapy[1][3][4].

02

Targets

αVβ6 (Integrin αVβ6)EGFR T790M (Epidermal growth factor receptor T790M mutant)TOP1 (DNA Topoisomerase I)αVβ5 (Integrin αVβ5)

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