Skip to main content
PMN

ProMIS Neurosciences Inc.

Biopharma developer (SEC filing verified)·Phase 1·Toronto, ON, Canada·CEO: Mr. Neil K. Warma M.B.A.
Neurology

PMN evidence brief

What we can confirm

BioSniper Score:
6.3 / 10
Market Cap:
$121.6M
Lead Asset:
pmn310 (Phase 1)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $121.6M · Lead Asset: pmn310 (Phase 1)
BioSniper AIPage evidence connected

Prepared research question

What matters most for PMN—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · PMN

ProMIS Neurosciences Inc. (PMN) is a clinical-stage biotechnology company developing monoclonal antibodies targeting toxic misfolded proteins in neurodegenerative diseases, with lead candidate PMN310 for Alzheimer's disease currently in a Phase 1b trial.

Key risk: No product revenue

6.3/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$121.6M

Cash Runway

—

Lead Asset

pmn310 (Phase 1)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 2 clinical trials for ProMIS Neurosciences Inc..

AI OverviewAI overview is shown in English only.

ProMIS Neurosciences Inc. (PMN) is a clinical-stage biotechnology company developing monoclonal antibodies targeting toxic misfolded proteins in neurodegenerative diseases, with lead candidate PMN310 for Alzheimer's disease currently in a Phase 1b trial.

  • Lead candidate PMN310 is a monoclonal antibody designed to selectively target toxic amyloid-beta oligomers in Alzheimer's disease [sec_mda · as of 2026-05-12].
  • PRECISE-AD Phase 1b trial fully enrolled; six-month interim data expected Q2 2026 and final top-line results Q4 2026 [sec · filed 2025-09-03].
  • Cash and equivalents of $53.4M as of 2026-06-30 [sec].
  • Net loss of $11.7M for the period ended 2026-06-30 [sec].
  • FDA granted Fast Track Designation for PMN310 in Alzheimer's disease [news · published 2025-08-13].

What works

  • PMN310 has shown a favorable safety profile with no treatment-related serious adverse events and no cases of amyloid-related imaging abnormalities (ARIA) reported to date [news · published 2026-03-25].
  • The company's technology platform uses protein biology, physics, and supercomputing to selectively target toxic misfolded proteins, potentially reducing interference with normal protein function [sec_mda · as of 2026-05-12].
  • FDA Fast Track Designation for PMN310 may enable priority review and more frequent interactions with the agency [news · published 2025-08-13].
  • Cash runway extended through 2027 following $53.4M in cash as of mid-2026 [news · published 2026-08-14].

What to weigh

  • The company has not yet generated product revenue and may not become profitable even if product sales begin [sec_mda · as of 2026-08-13].
  • Operating loss of $40.2M for the year ended December 31, 2025, and an accumulated deficit [sec_mda · as of 2026-03-25].
  • If additional capital is not raised, the company may need to significantly delay, reduce, or eliminate development of product candidates [sec_mda · as of 2026-08-13].
  • The company's ability to continue as a going concern has been previously questioned due to limited cash runway [sec_mda · as of 2025-08-13].

From the filings

Quoted directly from source documents.

  • PMN310 selectively targets toxic amyloid-beta oligomers

    “PMN310, a monoclonal antibody designed to treat AD by selectively targeting toxic, misfolded oligomers of amyloid-beta.”

    SEC MD&A · May 12, 2026

  • No ARIA cases observed in PRECISE-AD trial

    “no cases of amyloid-related imaging abnormalities observed to date”

    SEC filings · September 3, 2025

  • FDA Fast Track Designation for PMN310

    “U.S. FDA Grants Fast Track Designation for PMN310 in Alzheimer’s Disease”

    News · August 13, 2025

Catalyst timeline

  • 2023-11-18 · Phase 1a start (PMN310 single ascending dose in healthy volunteers) — Initiation of first-in-human study for PMN310.
  • 2024-12-13 · Phase 1b start (PMN310 multiple ascending dose in early Alzheimer's patients) — Start of PRECISE-AD trial in patients with early Alzheimer's disease.
Risks & what to watch (4)›

Key risks

  • No product revenue — Company has no approved products and may never achieve profitability even if sales begin [sec_mda · as of 2026-08-13].
  • Capital dependency — Failure to raise capital could force significant delays or termination of development programs [sec_mda · as of 2026-08-13].
  • Accumulated deficit — Operating loss of $40.2M in 2025 and ongoing accumulated deficit [sec_mda · as of 2026-03-25].
  • Clinical trial uncertainty — Phase 1b data not yet released; efficacy and safety beyond current cohorts unknown [sec · filed 2025-09-03].

What to watch

  • Six-month interim data from PRECISE-AD Phase 1b trial expected Q2 2026 [sec · filed 2025-09-03].
  • Final top-line results from PRECISE-AD anticipated Q4 2026 [sec · filed 2025-09-03].
  • Cash runway and any additional financing rounds, given prior going-concern warnings [news · published 2026-08-14].
  • Progress of second lead candidate PMN267 for ALS [sec_mda · as of 2026-05-12].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated September 24, 2026 · How we verify sources →

Run ProMIS Neurosciences Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available ProMIS Neurosciences Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.8

D/E 0.15 · 0% dilution

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal8.0

2 buys · 0 sells (180d)

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

25

Total value held

$78.0M

Showing top 10 of 25 institutional holders of ProMIS Neurosciences Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
1.6%
Days to cover
3.5
Shares short
138,078
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

PMN short interest

Governance

Frequently asked questions

What is the AI investment thesis for ProMIS Neurosciences Inc.?

ProMIS Neurosciences Inc. (PMN) is a clinical-stage biotechnology company developing monoclonal antibodies targeting toxic misfolded proteins in neurodegenerative diseases, with lead candidate PMN310 for Alzheimer's disease currently in a Phase 1b trial.

What is ProMIS Neurosciences Inc.'s lead drug candidate?

ProMIS Neurosciences Inc.'s most advanced tracked candidate is pmn310 (Phase 1) for Alzheimer Disease, Early Onset; Healthy Participants.

Who is the CEO of ProMIS Neurosciences Inc.?

Mr. Neil K. Warma M.B.A. is the chief executive officer of ProMIS Neurosciences Inc. (PMN).

Where is ProMIS Neurosciences Inc. headquartered?

ProMIS Neurosciences Inc. (PMN) is headquartered in Toronto, ON, Canada.

What therapeutic areas does ProMIS Neurosciences Inc. focus on?

ProMIS Neurosciences Inc. develops therapies across Neurology.

923 companies304,840 SEC filings22,636 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.