ALZpath and Siemens Healthineers Sign Licensing Agreement  Read the full announcement →

Global Momentum and Validation Grows at AAIC for ALZpath Proprietary pTau217 Antibody Use in Alzheimer’s Disease Research, Diagnosis, and Treatment

ALZpath pTau217 antibody data included in 37 submissions at AAIC, building on 90 Publications Across 18 Countries demonstrating ALZpath’s superior sensitivity and accuracy in blood-based tests for Alzheimer’s disease

CARLSBAD, Calif., July 28, 2025 – ALZpath, Inc., a leading developer of innovative diagnostic tools for Alzheimer’s disease, announced today that data highlighting the ALZpath pTau217 antibody will be showcased in seven presentations and 30 posters at the Alzheimer’s Association International Conference (AAIC) taking place July 27-31 in Toronto. These studies demonstrate increasing scientific evidence of the reliability of ALZpath’s proprietary pTau217 antibody in blood-based assays for early detection of Alzheimer’s disease. See the full list of presentations and posters here.

“This growing body of evidence and the incorporation of our pTau217 antibody across leading research and clinical diagnostic platforms affirms the confidence the global Alzheimer’s community has in our product,” said Mike Banville, CEO and President of ALZpath. “As the field advances toward earlier and more accessible detection of Alzheimer’s disease, we are proud that our antibody is positioned to support a wide array of research and clinical applications across diverse studies and populations.”

Since its inception in 2023, the ALZpath pTau217 antibody has been featured in 90 publications, including 60 original research papers that have generated 34,510 individual data points using assays incorporating ALZpath’s antibody in original research. To date, the antibody has also been featured in 157 posters and presentations at other international scientific conferences.

The 90 publications highlight the widespread use of the ALZpath pTau217 antibody across 18 countries, including the United States, Canada, China, Italy, Korea, South Korea, Spain, and Sweden. Nearly 90 percent of the original studies involved cohorts larger than 100 participants, while 42 percent included ethnically and demographically diverse populations. Additionally, eight direct comparison studies have evaluated the ALZpath antibody against other pTau217 antibodies and biomarkers, reinforcing its reliability and clinical relevance.

Notably, ALZpath’s antibody was showcased in one of the largest population-based investigations of Alzheimer’s disease pathology, the HUNT study, led by Anita Sunde of Stavanger University Hospital, and presented at AD/PD™ 2025. Researchers used ALZpath’s pTau217 assay to analyze 11,486 samples, including nearly 9,000 individuals over 70, to measure the prevalence of Alzheimer’s-related brain changes.

“We congratulate our collaborators on their many achievements, and we look forward to our continued work together to build the future of Alzheimer’s disease diagnostics,” said Banville.

About ALZpath

ALZpath, Inc. is a leader in blood test-based diagnostic solutions for Alzheimer’s disease. Its proprietary pTau217 antibody, used in many of the most advanced and widely available blood-based tests, is helping transform how Alzheimer’s disease is detected, treated, and monitored. Through licensing agreements with global industry leaders and collaborations with world-class laboratories, ALZpath enables partners to deliver accurate, scalable testing to clinicians and patients worldwide. The company’s innovations have earned numerous industry honors, including Time Magazine Best Inventions (2024), Fast Company Most Innovative Companies (2025) and BioTech Breakthrough “Diagnostic Innovation of the Year” (2025).

To learn more, visit https://alzpath.bio/ and follow ALZpath on LinkedIn, X, BlueSky, and Facebook .

ALZpath Media Contact

Jessica Hoffman
FINN Partners
Jessica.hoffman@finnpartners.com 

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “may,” “will,” “expect,” “plan,” “anticipate,” “estimate,” “intend” and similar expressions (as well as other words or expressions referencing future events, conditions, or circumstances) are intended to identify forward-looking statements. Forward-looking statements in this news release are based on ALZpath’s expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties. Factors that may cause ALZpath’s actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in ALZpath’s filings with the U.S. Securities and Exchange Commission, including the “Risk Factors” sections contained therein. Except as required by law, ALZpath assumes no obligation to update any forward-looking statements contained herein to reflect any change in expectations, even as new information becomes available.