INTerpath-001 de-risks the neoantigen platform; a disclosed-data gate routes the re-rating The phase 3 win converts Moderna oncology optionality into a concrete FDA 2027 track on an equal Merck profit share. A magnitude and timing gate at the center sends the de-risking credit either to a justified re-rating (pipeline optionality holds) or to multiple compression (weak magnitude or a slip). patient neoantigen mRNA LNP + T-cell · PD-1 block INTerpath-001 intismeran + Keytruda beats Keytruda alone RFS · DMFS beat lung bladder kidney same intismeran platform · phase 2/3 FDA path 2027 · Merck 50/50