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Biological and Environmental Research Ontology
| Id | http://purl.obolibrary.org/obo/NCIT_C171577
http://purl.obolibrary.org/obo/NCIT_C171577
|
|---|---|
| Preferred Name | Ifinatamab Deruxtecan |
| Definitions |
An antibody-drug conjugate (ADC) composed of a humanized monoclonal antibody against the immunoregulatory protein B7-homologue 3 (B7-H3, CD276) conjugated, via an enzymatically cleavable tetrapeptide-based linker, to the cytotoxic DNA topoisomerase I inhibitor and exatecan (DX-8951) derivative DXd (MAAA-1181a; MAAA-1181), with potential antineoplastic activity. Upon administration of the anti-B7-H3/DXd ADC DS-7300a, the anti-B7-H3 antibody targets and binds to B7-H3-expressing tumor cells. Upon cellular uptake and lysosomal degradation of the linker, DXd targets and binds to DNA topoisomerase I, thereby stabilizing the cleavable complex between topoisomerase I and DNA, resulting in DNA breaks, inhibition of DNA replication and apoptosis. This inhibits the proliferation of B7-H3-expressing tumor cells. B7-H3, a type I transmembrane protein and a member of the B7 co-stimulatory protein superfamily, is overexpressed on certain tumor cell types and on various immune cells. It plays a key role in tumor growth and immune responses. The ADC allows for reduced systemic exposure and enhanced delivery of the cytotoxic agent DXd.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | An antibody-drug conjugate (ADC) composed of a humanized monoclonal antibody against the immunoregulatory protein B7-homologue 3 (B7-H3, CD276) conjugated, via an enzymatically cleavable tetrapeptide-based linker, to the cytotoxic DNA topoisomerase I inhibitor and exatecan (DX-8951) derivative DXd (MAAA-1181a; MAAA-1181), with potential antineoplastic activity. Upon administration of the anti-B7-H3/DXd ADC DS-7300a, the anti-B7-H3 antibody targets and binds to B7-H3-expressing tumor cells. Upon cellular uptake and lysosomal degradation of the linker, DXd targets and binds to DNA topoisomerase I, thereby stabilizing the cleavable complex between topoisomerase I and DNA, resulting in DNA breaks, inhibition of DNA replication and apoptosis. This inhibits the proliferation of B7-H3-expressing tumor cells. B7-H3, a type I transmembrane protein and a member of the B7 co-stimulatory protein superfamily, is overexpressed on certain tumor cell types and on various immune cells. It plays a key role in tumor growth and immune responses. The ADC allows for reduced systemic exposure and enhanced delivery of the cytotoxic agent DXd. |
|---|---|
| prefLabel | Ifinatamab Deruxtecan
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| label | Ifinatamab Deruxtecan
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| NCI_META_CUI | CL1405790
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| PDQ_Closed_Trial_Search_ID | 801901
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| code | C171577
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| Has_Target | |
| prefixIRI | NCIT:C171577
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| in_subset |
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| Display_Name | Ifinatamab Deruxtecan
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| Preferred_Name | Ifinatamab Deruxtecan
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| FDA_UNII_Code | C6I0GC0GX5
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| Contributing_Source |
CTRP
FDA
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| Maps_To | Anti-B7-H3/DXd Antibody-drug Conjugate DS-7300a
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| CAS_Registry | 2484870-92-8
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| NCI_Drug_Dictionary_ID | 801901
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| type | |
| Is_Value_For_GDC_Property | |
| subClassOf | |
| PDQ_Open_Trial_Search_ID | 801901
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| Semantic_Type | Pharmacologic Substance
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