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Jul 28, 2026 12:30 PM

Small-Cap ProMIS Neurosciences Says Lead Drug Shows Encouraging Action in Early Alzheimer's Study

ProMIS Neurosciences announced positive interim Phase 1b trial data for its Alzheimer's drug candidate PMN310, showing zero ARIA-E.

ProMIS Neurosciences Inc. (NASDAQ:PMN) reported positive blinded six-month interim safety and biomarker results from its ongoing Phase 1b PRECISE-AD trial evaluating lead drug candidate PMN310 in patients with mild cognitive impairment due to Alzheimer's disease.

The clinical-stage biopharmaceutical company develops therapies targeting toxic misfolded proteins linked to neurodegenerative diseases.

Favorable Safety Profile Across Genotypes

The blinded interim analysis included 136 Alzheimer's disease patients and showed a favorable safety profile across all genotypes.

No cases of amyloid-related imaging abnormalities with edema (ARIA-E) were reported as of the data cutoff date. Total ARIA incidence was 4.4%, with all cases limited to mild, asymptomatic amyloid-related imaging abnormalities-microhemorrhages (ARIA-H).

The company also reported no treatment-related serious adverse events and no drug-related patient discontinuations.

Safety Maintained In High-Risk APOE4 Patients

The favorable safety profile was also observed among high-risk APOE4 carriers, who represented 61% of the trial population, including 11% who were homozygotes.

ProMIS noted that this patient group remains underserved by many currently approved amyloid-targeting therapies.

Early Biomarker Movement And Differentiated Mechanism

On a blinded basis, 68.5% of patients exhibited a decline from baseline in plasma pTau217, and 62.5% showed a decline in CSF MTBR-tau243, contrasting with expected natural-history increases.

These trends potentially reflect the trial's 3:1 active-to-placebo randomization.

However, because treatment allocations remain blinded, these observations do not constitute a determination of clinical efficacy.

PMN310 utilizes a differentiated, oligomer-selective mechanism engineered to selectively bind toxic amyloid-beta oligomers while avoiding plaque, aiming to decouple potential efficacy from ARIA risk.

The trial remains ongoing, with unblinded 12-month topline results, including efficacy data, expected in the first quarter of 2027.

By selectively targeting toxic oligomers, PMN310 “has the potential to deliver the benefits of amyloid-directed therapy without the ARIA burden that has constrained this class of drugs,” said Neil Warma, CEO of ProMIS Neurosciences.

“The absence of ARIA-E, an overall favorable safety profile, and early biomarker movement together align with our expectations based on our prior studies,” Warma added.

PMN Stock Price Activity: ProMIS Neurosciences shares were up 18.67% at $13.90 at the time of publication on Tuesday, according to Benzinga Pro data.

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