Core Insights - ProMIS Neurosciences Inc. is advancing its Phase 1b clinical trial, PRECISE-AD, for PMN310, a therapeutic candidate targeting toxic oligomers in Alzheimer's Disease (AD) [2][6] - The company has received Fast Track designation from the FDA for PMN310, indicating its potential to address unmet medical needs in AD [2][10] - The ongoing trial has enrolled over 50% of the planned 128 patients, reflecting a swift enrollment process [2][7] Company Overview - ProMIS Neurosciences is a clinical-stage biotechnology company focused on developing therapeutic antibodies for neurodegenerative diseases, including AD, ALS, and PD [8] - The company's proprietary platform, EpiSelect, identifies toxic misfolded proteins, enabling the design of selective therapeutic antibodies [3][8] Clinical Trial Details - The PRECISE-AD trial is a randomized, double-blind, placebo-controlled study assessing the safety, tolerability, and pharmacokinetics of PMN310 at multiple ascending doses [7] - The trial aims to evaluate the effects of PMN310 on biomarkers associated with AD pathology and clinical outcomes, with a primary focus on safety [6][7] - Interim data from the trial is expected to be reported in Q2 2026, with topline results anticipated by Q4 2026 [2][10] Presentation and Conference Participation - ProMIS Neurosciences will present its findings at the Alzheimer's Association International Conference 2025, highlighting the PRECISE-AD trial and the EpiSelect platform [1][4] - Key presentations will include discussions on the design and validation of the EpiSelect platform and the ongoing clinical trial [4][5]