drug_type
RELEVANT_DRUG
intervention_type
Drug
drug_description
An anti-EGFR antibody–drug conjugate (ADC) with a drug–antibody ratio of 8 that couples an EGFR-specific monoclonal antibody to a high-potency DNA topoisomerase I inhibitor. After binding EGFR and internalization, it releases the topo I inhibitor to cause DNA damage and apoptosis; the antibody component may also inhibit EGFR signaling.
nci_thesaurus_concept_id
C206272
nci_thesaurus_definition
An antibody-drug conjugate (ADC) composed of an immunoglobulin G1 (IgG1) monoclonal antibody directed against the tumor-associated antigen (TAA) epidermal growth factor receptor (EGFR) conjugated, via a cleavable linker, to a topoisomerase I inhibitor (TOP1i), with potential antineoplastic activity. Upon administration of anti-EGFR/TOP1i ADC HLX42, the anti-EGFR monoclonal antibody moiety targets and binds to EGFR expressed on tumor cells. Upon binding and cleavage in the tumor microenvironment (TME), the TOP1i moiety inhibits DNA topoisomerase I activity, thereby inhibiting DNA replication which results in cell cycle arrest and tumor cell apoptosis. This inhibits the proliferation of EGFR-expressing tumor cells. HLX42 also induces bystander killing activity. EGFR, a receptor tyrosine kinase mutated in many tumor cell types, plays a key role in tumor cell proliferation and tumor vascularization.
drug_mesh_term
Antibody-Drug Conjugates
drug_category
ANTIBODY DRUG CONJUGATE
drug_class
Conjugate
drug_delivery_route
Intravenous
drug_mechanism_of_action
EGFR-targeting IgG1 monoclonal antibody conjugated via a cleavable linker to a high-potency topoisomerase I inhibitor. After binding EGFR on tumor cells and internalization/cleavage, it releases the TOP1 inhibitor to block DNA topoisomerase I, causing DNA damage, replication arrest, and apoptosis; the antibody may also inhibit EGFR signaling and can mediate bystander killing.
drug_name
HLX42
nct_id_drug_ref
NCT06210815