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Cognition Therapeutics has reached full enrollment in its expanded access program for Zervimesine (CT1812) in dementia with Lewy Bodies (DLB). The program was made possible by a generous donation from a participant's family in the Phase 2 SHIMMER study. The Company is pursuing input from the FDA on a registrational program for DLB, with a Type C meeting scheduled for January. Zervimesine has not been approved by regulatory authorities, and its safety and efficacy have not been fully characterized.

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