Question · Q4 2025
Pujada from JPMorgan Chase & Co. asked for clarification on the potential registrational pathway for REC-4881 in FAP, including regulatory updates and plans for patient population expansion.
Answer
CEO Najat Khan stated that Recursion Pharmaceuticals is preparing for initial FDA engagement in the first half of 2026 to discuss the registrational study design, patient population, and endpoints, supported by strong durability and polyp burden reduction data, as well as natural history data. She also mentioned ongoing recruitment for the 18-and-over cohort and dose optimization efforts, with further clinical data anticipated in the first half of 2027.
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