ProMIS Neurosciences
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ProMIS Neurosciences (PMN) investor relations material

ProMIS Neurosciences H.C. Wainwright 28th Annual Global Investment Conference summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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H.C. Wainwright 28th Annual Global Investment Conference summary15 Sep, 2026

Company overview and technology

  • Focuses on neurodegenerative diseases using monoclonal antibodies to target misfolded proteins, with a platform originating from University of British Columbia and now based in Cambridge, MA.

  • Lead candidate, PMN310, is in clinical trials for Alzheimer's, with additional pipeline assets for ALS and Parkinson's.

  • Technology enables selective targeting of toxic oligomers, avoiding monomers and plaque, differentiating from current market therapies.

  • Strong patent position and leadership team, with robust financial backing through 2027 following a $175 million financing.

Clinical trial design and interim results

  • Phase I-B study in early Alzheimer's (MCI) enrolled 144 patients across 22 U.S. sites, fully enrolled and dosed by December, with top-line results expected Q1 2027.

  • Study is placebo-controlled, double-blind, with three dosing arms and a 3:1 randomization, conducted over 12 months.

  • Interim six-month analysis showed a superb safety profile, with zero cases of ARIA-E and no treatment-related serious adverse events or dropouts.

  • Biomarker analysis indicated a 15% decline in p-tau217 and similar trends in MTBR-tau243, suggesting target engagement.

  • Safety and biomarker signals were consistent even in high-risk APOE4 carriers, a population underserved by current therapies.

Market opportunity and future plans

  • Current Alzheimer's drugs have modest efficacy and significant ARIA-related side effects, leaving a large unmet need for safer, more effective therapies.

  • PMN310's differentiated mechanism and safety profile position it to capture significant market share, especially in preclinical and high-risk populations.

  • Fast Track designation from FDA enables efficient regulatory engagement.

  • Planning for a phase III registration study and development of a subcutaneous formulation is underway.

  • Financial resources are sufficient to support ongoing development and pipeline expansion beyond upcoming data milestones.

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Q3 202613 Nov, 2026
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