BOSTON--(BUSINESS WIRE)--Akili Interactive Labs, Inc. and Pfizer Inc. (NYSE: PFE) today presented positive topline data showing that Akili’s proprietary technology platform detected a statistically significant difference between subjects with and without brain amyloidosis, the primary biomarker for Alzheimer’s risk. The study was part of a collaborative trial designed by Pfizer and Akili, and topline results were presented at the International Conference on Clinical Trials for Alzheimer’s Disease in San Diego, CA.
The technology, derived from the company’s patent-pending cognitive measurement platform, differentiated between older healthy subjects positive for amyloid deposits in their brains versus an age-matched comparison group of amyloid-negative subjects, both in change over time (p=0.04) and at the completion visit after 28-day remote self-administration protocol (p<0.008). All metrics were obtained from study participant interaction with the cognitive assessment tool, which is designed to operate as a fast-paced action video game on a tablet. Importantly, compliance with the tool was high, and no safety concerns were reported during the study.
“These initial results suggest that our digital biomarkers may have the potential to serve as non-invasive options to screening procedures such as PET imaging scans requiring the administration of radioactive ligands or lumbar punctures,” said Eddie Martucci, President and CEO of Akili. “We’re also excited by the potential for early detection of neurological dysfunction, and we’re looking forward to further exploring that potential on our own and with strategic partners.”
“We are encouraged by the results of this trial, and we look forward to exploring ways that we might be able to implement innovative new technologies like the Akili platform into the clinical trial process,” said Ole Isacson, Senior Vice President and Chief Scientific Officer, Neuroscience, Pfizer. “Alzheimer’s disease is a particularly complex disease about which we still have much to learn. These results are a step in the right direction in our mission of making a difference in the lives of Alzheimer’s patients and their families.”
The non-exclusive collaboration between Akili and Pfizer was established in 2014 to assess the potential correlation between Akili’s proprietary digital biomarkers and one or more of the accepted neurological markers for asymptomatic Alzheimer’s Disease.
The double-blind study was conducted as a parallel protocol where individuals were accepted into the study only if they were judged healthy by screening criteria. All accepted individuals were then given a quantitative PET scan to determine brain amyloid presence, as amyloid accumulation is generally considered to be a biomarker and risk factor for eventual development of Alzheimer’s disease. All participants also received a full neurological work-up including magnetic resonance imaging (MRI) and non-Akili cognitive endpoints including measures of memory and attention. Further analyses of a variety of digital metrics from this study that correlate with the PET, MRI and other patient data are underway.
About Alzheimer’s Disease
Alzheimer’s Disease is a chronic,
progressive, neurodegenerative disorder characterized by loss of memory
and other important mental functions. The type, severity, sequence, and
progression of mental changes vary widely, and It represents an enormous
burden on victims of the disease and their family. Alzheimer’s is the
most common form of dementia in people over the age of 65, and it is
estimated to affect more than 5 million Americans. It is the sixth
leading cause of death in the United States, and there is currently no
cure.
About Akili’s Technology
Akili's technologies are based on a
proprietary neuroscience approach developed to target specific
neurological systems through sensory and digital mechanics. The
company's lead, patent-pending technology platform (used in this trial)
is based on cognitive science exclusively licensed from the lab of Dr.
Adam Gazzaley at the University of California, San Francisco, and
proprietary adaptive algorithms developed at Akili, all built into
action video game interfaces. The platform powers both assessment and
treatment products, which deploy real-time, adaptive cognitive
challenges and interventions, respectively. Both products target the
brain's interference processing system (an individual's core ability to
process multiple streams of information), a key function underlying
cognitive control.
Akili is currently conducting multiple clinical trials of its leading digital medicine platform across a variety of patient populations, including pediatric ADHD, autism spectrum disorder (in collaboration with Autism Speaks), depression, Alzheimer’s disease and traumatic brain injury.
About Akili Interactive Labs, Inc.
Akili is
building clinically validated cognitive treatments and assessments that
are delivered in an action video game interface. Leveraging
medical-grade science and consumer-grade software technology, the
company is seeking to produce a new type of medical product that can
offer safe and effective scalable treatment and better monitoring for
patients across a range of mental health and neurological conditions.
The company was founded by PureTech
Health (PRTC.L), together with leading neuroscientists and game
designers. Akili has garnered investment from Shire PLC, Amgen Ventures
and Merck Ventures BV, Amsterdam, The Netherlands, a subsidiary of Merck
KGaA, Darmstadt, Germany (known as M Ventures in the United States and
Canada), and it has strategic partnerships with Pfizer Inc. and Autism
Speaks.
