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drug_type
RELEVANT_DRUG
intervention_type
Antibody-drug conjugate (ADC)
drug_description
TROP-2–directed antibody–drug conjugate with a topoisomerase I payload.
nci_thesaurus_concept_id
C166409
nci_thesaurus_preferred_term
Sacituzumab Tirumotecan
nci_thesaurus_definition
An antibody-drug conjugate (ADC) composed of a humanized immunoglobulin G1 kappa (IgG1k) monoclonal antibody directed against the tumor-associated antigen (TAA) trophoblast cell surface protein 2 (trophoblast antigen 2; calcium signal transducer 2; TROP2; TROP-2; TACSTD2; GA733-1; M1S1) conjugated, via a methyl sulfonyl pyrimidine linker, to the belotecan derivative and topoisomerase I inhibitor tirumotecan, with potential antineoplastic activity. Upon administration of sacituzumab tirumotecan, sacituzumab targets and binds to TROP2 expressed on tumor cells. Upon both extracellular pH-sensitive cleavage and intracellular enzymatic cleavage of the linker, tirumotecan is released and inhibits DNA topoisomerase I activity, thereby inhibiting DNA replication and resulting in cell cycle arrest and apoptosis in tumor cells expressing TROP2. In addition, the bystander effect induced by sacituzumab tirumotecan further inhibits tumor cell proliferation. TROP2 is a transmembrane protein overexpressed in various tumors while its expression is low and/or restricted in normal, healthy tissues; its expression is associated with enhanced tumor aggressiveness, metastasis, drug resistance and increased tumor cell survival.
drug_category
ANTIBODY DRUG CONJUGATE
drug_class
Conjugate
drug_delivery_route
Intravenous
drug_mechanism_of_action
TROP-2–targeting humanized IgG1 ADC; after binding and internalization, pH/enzymatic cleavage of the linker releases the topoisomerase I inhibitor tirumotecan, inhibiting DNA replication and causing cell-cycle arrest and apoptosis, with a bystander killing effect.
drug_name
Sacituzumab tirumotecan
nct_id_drug_ref
NCT06145308