Mirvetuximab Soravtansine
This antibody-drug conjugate targets folate receptor alpha, a protein found on the surface of many ovarian cancer cells, delivering a potent cell-killing agent called a maytansinoid directly to tumor cells while sparing most normal tissues. It provides a targeted treatment option for platinum-resistant ovarian cancer patients whose tumors express high levels of the folate receptor.
Lĩnh vực điều trị
Cơ chế tác dụng
As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.
HBD / HBA
- / -
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Câu hỏi thường gặp
This antibody-drug conjugate targets folate receptor alpha, a protein found on the surface of many ovarian cancer cells, delivering a potent cell-killing agent called a maytansinoid directly to tumor cells while sparing most normal tissues. It provides a targeted treatment option for platinum-resistant ovarian cancer patients whose tumors express high levels of the folate receptor.
As a monoclonal antibody, it binds with high specificity to its target antigen, modulating the immune response through mechanisms including receptor blockade, immune cell engagement, or targeted cytotoxicity.
Yes, Mirvetuximab Soravtansine is an approved drug. It has reached clinical phase 4. It is classified as a Antibody drug conjugate.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3545132. Open-access bioactivity database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-02-27.
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