Diadem Announces Publication of Clinical Data Showing Its AlzoSure® Biomarker Test Accurately Predicts Progression to Alzheimer’s Disease Six Years Before Diagnosis
—AlzoSure® Predict Identifies Individuals Who Will Progress to Alzheimer’s Disease (AD) Up to Six Years Before Diagnosis with High Accuracy (AUC=.99) Using Simple Blood Draw—
—Prognostic Performance for Progression to Alzheimer’s Significantly Better than Conventional PET Amyloid Imaging (P<0.001)—
—As a Simple, Accessible Accurate Prognostic Blood Test for AD, AlzoSure Predict Epitomizes World Alzheimer’s Month September Campaign Focus on Early Diagnosis—
Consistent with earlier studies of AlzoSure® Predict, its prognostic performance in the new study was high, predicting the onset of AD dementia up to six years before symptoms appeared in individuals who were classified as either cognitively normal (CN) or as having minor cognitive impairment (MCI) at baseline, achieving AUC values of around 99% over the years of study follow-up. The data also confirm the test’s capability to discriminate between patients at different stages of cognitive decline, from asymptomatic to mild impairment to full AD dementia. In this 482-patient cohort from the Australian Imaging, Biomarkers and Lifestyle (AIBL) study, AlzoSure® Predict also demonstrated superior predictive performance to standard PET imaging measures of amyloid load (P<0.001), as well as AD-related genetic biomarkers .
The Diadem AlzoSure® Predict assay uses a proprietary antibody, U-p53AZ, to measure blood levels of an unfolded conformational variant of the p53 protein that has been implicated in the pathogenesis of AD. The analysis is based on longitudinal data from the AIBL study cohort spanning the AD continuum from cognitive normal to fully symptomatic AD. Patients were followed for up to 144 months. The data include comparative results from PET imaging and other commonly used AD diagnostic tools.
Colin Louis Masters MD FAA AO is laureate professor of pathology at the University of Melbourne and Head of the Neuropathology and Neurodegeneration Laboratory at Australia’s Florey Institute of Neuroscience and Mental Health, one of the largest and most respected brain research centers in the world. Dr. Masters, who was not involved with the new study, commented, “Despite growing interest in biomarkers allowing early identification of individuals at risk for Alzheimer’s, more than half of AD patients still lack a formal diagnosis, and opportunities for early intervention to slow or stop disease progression are missed. Most seriously, progress in developing disease modifying treatments has been hampered by the lack of accessible prognostic biomarkers to identify those who could benefit from early treatment. These encouraging data suggest that AlzoSure® Predict could play a valuable role in identifying at-risk patients many years in advance, enabling earlier interventions now and better clinical studies of investigational AD therapies going forward.”
Tamas Bartfai, PhD, Chair of Diadem’s Medical Advisory Board and formerly Professor and Chairman of Molecular and Integrative Neurosciences and Director of the Dorris Neuroscience Center at the Scripps Research Institute, noted, “These new data using samples from multiple well-known biobanks confirm that AlzoSure® Predict, a blood-based, easily accessible test, can identify individuals who will progress to symptomatic Alzheimer’s disease six or more years in advance. They are being published as we prepare to highlight September as Alzheimer’s Disease International’s World Alzheimer’s Month, focusing this year on
the importance of early diagnosis. An accessible, accurate blood-based biomarker test like AlzoSure® Predict has the potential to make possible early interventions to slow or stop disease progression and to enable more effective enrollment for the multiple clinical studies of new therapeutics. In view of the growing evidence supporting the test’s utility, I am optimistic that the further validation studies that are now underway will confirm these results, paving the way for AlzoSure Predict® to become available to patients and their physicians.”
Paul Kinnon, CEO of Diadem, added, “These study results reflect years of innovative research by Diadem scientific co-founder Professor Daniela Uberti, a leader in investigating the role of this conformational p53 variant in the development of Alzheimer’s disease. The new data reinforce and validate our prior studies showing that AlzoSure® Predict can identify individuals who will progress to Alzheimer’s dementia years before symptoms are evident, and it does so more accurately than established diagnostic tools such as PET imaging of amyloid load. Best of all, our biomarker test is blood-based, simple, and affordable, making it accessible for a variety of applications, including broad-based patient screening. We aim to complete additional validation studies in the coming months and are targeting a global launch in collaboration with strategic partners next year.” Diadem is developing the AlzoSure® Predict assay as a simple, non-invasive plasma-based biomarker test to accurately predict the probability that a patient with asymptomatic mild cognitive impairment will progress to Alzheimer’s dementia. The company’s patented technology uses an analytical method that includes a proprietary antibody developed by Diadem designed to bind to the conformational variant U-p53AZ protein and its target sequences. Diadem is currently conducting a follow-up study using additional longitudinal data from different cohorts and centers in Europe and the United States to validate these newly published findings and compare and correlate the potential of U-p53AZ as a blood-based biomarker with traditionally studied markers of AD pathology. Results are expected later this year.
About Alzheimer’s Disease
There are about 50 million people suffering from dementia worldwide. Alzheimer’s disease is the most common form and accounts for 60-70% of cases. At present there are no disease modifying treatments for Alzheimer's, and therapies to treat symptoms are limited. There are about 10 million new cases per year, and the incidence is rising rapidly as the population ages. The current total cost of care is enormous--estimated at $1 trillion in the U.S. annually and expected to double by 2030. Currently, diagnosis of Alzheimer’s disease is slow, inconclusive, invasive and expensive. Development of effective therapies for Alzheimer’s has been hindered by the lack of accurate and cost-effective prognostic and diagnostic methods.
Diadem was founded as a spin-off of the University of Brescia (Italy). The company is developing the first blood-based prognostic test for the early detection of dementia, with a focus on Alzheimer’s disease. The lack of accurate, accessible and affordable diagnostic tools is a major contributor to the absence of effective treatments for this devastating condition. As a result, patients are not diagnosed until late in the illness, when effective treatment is no longer possible. Diadem’s rapid, accurate and cost effective blood-based prognostic test makes it possible for the first time to identify patients early in the disease process, when effective interventions and better outcomes are far more feasible. The utility of the approach has been demonstrated in early clinical studies. Additional retrospective and prospective clinical trials are ongoing and planned to further validate clinical claims and support widespread adoption and use. Diadem’s founding lead investor is Milan-based Panakes Partners, a venture capital firm that finances promising high potential biomedical companies in Europe and Israel. Diadem is preparing for rapid commercialization of its initial Alzheimer’s prognostic via a global launch in collaboration with strategic partners.