Difference between revisions of "Belzutifan (Welireg)"
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
*8/13/2021: Approved for adult patients with von Hippel-Lindau (VHL) disease who require therapy for associated [[Renal cell carcinoma|renal cell carcinoma (RCC)]], [[CNS hemangioblastoma|central nervous system (CNS) hemangioblastomas]], or [[Pancreatic NET|pancreatic neuroendocrine tumors (pNET)]], not requiring immediate surgery. ''(Based on MK-6482-004)'' | *8/13/2021: Approved for adult patients with von Hippel-Lindau (VHL) disease who require therapy for associated [[Renal cell carcinoma|renal cell carcinoma (RCC)]], [[CNS hemangioblastoma|central nervous system (CNS) hemangioblastomas]], or [[Pancreatic NET|pancreatic neuroendocrine tumors (pNET)]], not requiring immediate surgery. ''(Based on MK-6482-004)'' | ||
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+ | ==Also known as== | ||
+ | *'''Code names:''' MK6482, PT2977 | ||
+ | *'''Brand name:''' Welireg | ||
[[Category:Drugs]] | [[Category:Drugs]] |
Revision as of 12:31, 4 December 2022
Mechanism of action
From the NCI Drug Dictionary: An orally active, small molecule inhibitor of hypoxia inducible factor (HIF)-2alpha (HIF-2a), with potential antineoplastic activity. Upon oral administration, belzutifan binds to and blocks the function of HIF-2alpha, thereby preventing HIF-2alpha heterodimerization and its subsequent binding to DNA. This results in decreased transcription and expression of HIF-2alpha downstream target genes, many of which regulate hypoxic signaling. This inhibits cell growth and survival of HIF-2alpha-expressing tumor cells.
Diseases for which it is used
History of changes in FDA indication
- 8/13/2021: Approved for adult patients with von Hippel-Lindau (VHL) disease who require therapy for associated renal cell carcinoma (RCC), central nervous system (CNS) hemangioblastomas, or pancreatic neuroendocrine tumors (pNET), not requiring immediate surgery. (Based on MK-6482-004)
Also known as
- Code names: MK6482, PT2977
- Brand name: Welireg