ProMIS Neurosciences Inc. has announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to their lead therapeutic candidate, PMN310, for the treatment of Alzheimer's disease. This designation underscores the potential of PMN310 to address a critical unmet need by providing a more targeted and safer treatment option for Alzheimer's patients. The Fast Track status allows for enhanced engagement with the FDA, potentially expediting the approval process. ProMIS is currently conducting the PRECISE-AD Phase 1b trial, focusing on the safety, tolerability, and efficacy of PMN310, with interim results expected in Q2 2026. This development marks a significant milestone for ProMIS and the Alzheimer's community in the pursuit of more effective treatments.
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