Difference between revisions of "Mirvetuximab soravtansine (Elahere)"
(Created page with "==Mechanism of action== From the [https://www.cancer.gov/publications/dictionaries/cancer-drug/def/mirvetuximab-soravtansine NCI Drug Dictionary]: An immunoconjugate consistin...") |
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
− | *11 | + | *2022-11-14: Granted accelerated approval for adult patients with folate receptor alpha positive, platinum-resistant [[Ovarian cancer|epithelial ovarian, fallopian tube, or primary peritoneal cancer]], who have received one to three prior systemic treatment regimens. ''(Based on SORAYA)'' |
+ | *2024-03-22: Approved for adult patients with folate receptor alpha positive, platinum-resistant [[Ovarian cancer|epithelial ovarian, fallopian tube, or primary peritoneal cancer]], who have received one to three prior systemic treatment regimens. Patients are selected based on an FDA-approved test. ''(Based on MIRASOL)'' | ||
==Also known as== | ==Also known as== | ||
− | *'''Code name:''' | + | *'''Code name:''' IMGN-853 |
*'''Generic name:''' mirvetuximab soravtansine-gynx | *'''Generic name:''' mirvetuximab soravtansine-gynx | ||
*'''Brand name:''' Elahere | *'''Brand name:''' Elahere | ||
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[[Category:Protein expression-specific medications]] | [[Category:Protein expression-specific medications]] | ||
− | [[Category: | + | [[Category:Anti-FOLR1 antibody-drug conjugates]] |
− | |||
[[Category:Microtubule inhibitors]] | [[Category:Microtubule inhibitors]] | ||
[[Category:Ovarian cancer medications]] | [[Category:Ovarian cancer medications]] | ||
− | [[Category:FDA approved in | + | [[Category:FDA approved in 2022]] |
Latest revision as of 23:15, 3 June 2024
Mechanism of action
From the NCI Drug Dictionary: An immunoconjugate consisting of the humanized monoclonal antibody M9346A against folate receptor 1 (FOLR1) conjugated, via the disulfide-containing cleavable linker sulfo-SPDB, to the cytotoxic maytansinoid DM4, with potential antineoplastic activity. The anti-FOLR1 monoclonal antibody moiety of mirvetuximab soravtansine targets and binds to the cell surface antigen FOLR1. After antibody-antigen interaction and internalization, the immunoconjugate releases DM4, which binds to tubulin and disrupts microtubule assembly/disassembly dynamics, thereby inhibiting cell division and cell growth of FOLR1-expressing tumor cells. FOLR1, a member of the folate receptor family is overexpressed on a variety of epithelial-derived cancer cells. The sulfo-SPDB linker prevents cleavage in the bloodstream and may improve this agent’s efficacy in multidrug resistant tumor cells.
Diseases for which it is used
History of changes in FDA indication
- 2022-11-14: Granted accelerated approval for adult patients with folate receptor alpha positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens. (Based on SORAYA)
- 2024-03-22: Approved for adult patients with folate receptor alpha positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens. Patients are selected based on an FDA-approved test. (Based on MIRASOL)
Also known as
- Code name: IMGN-853
- Generic name: mirvetuximab soravtansine-gynx
- Brand name: Elahere