This market will resolve to "Yes" if the U.S. Food and Drug Administration (FDA) grants approval of intismeran autogene for any indication by December 31, 2027, 11:59 PM ET.
Otherwise, this market will resolve to "No".
Intismeran autogene refers to the individualized neoantigen therapy developed by Moderna and Merck and evaluated in the Phase 3 INTerpath-001 trial (NCT05933577), also known as mRNA-4157 and V940, together with any brand, trade, or nonproprietary name later assigned to that product, as well as any renamed or modified version that the relevant company or the FDA identify as the same product or a direct continuation of the V940/mRNA-4157 program.
Differences in neoantigen composition between patients will not affect resolution.
Changes to the product's formulation will not affect resolution, provided the FDA approves the product described above.
Approval as part of a combination regimen will qualify.
Wat zijn de huidige kansen voor FDA approves skin cancer vaccine by which date??
Polymarket prijst December 31, op 68% per 21 augustus 2026.
Wanneer wordt FDA approves skin cancer vaccine by which date? afgewikkeld?
FDA approves skin cancer vaccine by which date? wordt naar verwachting op 31 december 2027 afgewikkeld.
Hoe wordt FDA approves skin cancer vaccine by which date? afgewikkeld?
Polymarket wikkelt deze markt als volgt af: This market will resolve to "Yes" if the U.S. Food and Drug Administration (FDA) grants approval of intismeran autogene for any indication by December 31, 2027, 11:59 PM ET.