2026 Bloom Burton & Co. Healthcare Investor Conference
Logotype for ProMIS Neurosciences Inc

ProMIS Neurosciences (PMN) 2026 Bloom Burton & Co. Healthcare Investor Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for ProMIS Neurosciences Inc

2026 Bloom Burton & Co. Healthcare Investor Conference summary

16 Jun, 2026

Operational and financial update

  • Recently secured $175 million in financing, ensuring funding through the end of next year, led by major investors including Ally Bridge, Janus, and Wellington.

  • Company is publicly listed on Nasdaq and maintains operations in Boston, Cambridge, and Vancouver.

  • Fast track designation from the FDA was obtained last year for the lead Alzheimer's program.

  • Actively planning for both internal funding and potential pharma partnerships for future phase III trials.

  • Management team includes leaders with extensive CNS and neurodegenerative disease experience.

Platform and scientific differentiation

  • Proprietary platform enables design of highly selective antibodies targeting misfolded proteins, using computational and AI-driven approaches.

  • Lead asset, PMN310, targets toxic amyloid beta oligomers in Alzheimer's, avoiding plaque and monomer binding.

  • Differentiation from competitors centers on selective targeting, aiming to reduce ARIA side effects seen with current drugs.

  • In-house studies confirm PMN310 does not bind plaque, unlike other marketed antibodies.

  • Pipeline includes candidates for ALS (TDP-43) and Parkinson’s/Lewy body dementia (alpha-synuclein).

Clinical development and trial progress

  • Phase I-B trial in Alzheimer's is fully enrolled with 144 patients, exceeding initial targets due to strong site and patient interest.

  • Study is placebo-controlled, double-blind, with three ascending dose cohorts and robust clinical and biomarker endpoints.

  • Interim blinded analysis focused on safety and biomarker trends is expected early Q3, with top-line results in early Q1 next year.

  • Phase I-A in healthy volunteers showed safety, tolerability, and sufficient blood-brain barrier penetration.

  • Planning to accelerate SubQ formulation development and design phase III registration study based on phase I-B outcomes.

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