A successful trial of a drug for memory loss in people with Alzheimer’s disease and schizophrenia brings treatment one step closer.
VU319 is the first Vanderbilt end-to-end drug discovery effort, starting from the earliest basic science research through human clinical trials. The effort spanned a high-throughput screening hit-to-candidate selection to completion of a clinical trial.
“This milestone highlights Vanderbilt’s ability to drive discovery from research to clinical impact,” said vice chancellor for academic affairs, Cybele Raver.
“The success of VU319 exemplifies how collaboration and innovation can bring real hope to patients and families facing Alzheimer’s and other neurodegenerative diseases.”
John Kuriyan, dean of basic sciences and University Distinguished Professor of Biochemistry and Chemistry, said: “The successful phase I trial of VU319 marks a potentially transformative step in drug development for Alzheimer’s, showcasing Vanderbilt’s capacity to translate fundamental research into therapeutic discovery that brings the hope of real clinical impact.”
“After more than a decade of basic and translational research, the WCNDD was finally able to disclose how VU319, a unique M1 PAM, was discovered and profiled,” said Craig Lindsley, executive director of the WCNDD.
In addition to treating Alzheimer’s disease, which affects roughly 6.9 million people over age 65 and has no known cure, VU319 has shown potential to treat memory loss in schizophrenia, prion diseases, Rett syndrome, vascular dementia, and Lewey body dementia.
“Funding from the National Institute of Mental Health allowed the WCNDD to discover and develop VU319. An important philanthropic gift from the William K. Warren Foundation then enabled us to partner with DavosPharma to conduct critical early-stage studies and earn approval from the FDA as an investigational new drug, paving the way for the Alzheimer’s Association award to Dr. Paul Newhouse for the Phase I trial,” Lindsley said.
“Overall, it has been incredibly rewarding to drive a programme from the most basic discovery stage and translate it into human clinical testing, all at Vanderbilt.”
The neurotransmitter acetylcholine is responsible for learning and memory, but in Alzheimer’s and other neurodegenerative diseases, such as schizophrenia, it is one of the first that stops working and disables neurons from functioning properly. VU319, an M1 positive allosteric modulator, increases the efficacy of the endogenous neurotransmitter acetylcholine at the M1 receptor, acting as a dimmer switch to “turn-up” the gain on the receptor selectively, providing the best possible therapeutic index.
In the human trial, the researchers saw signs of target engagement at the highest dose of the treatment that was tested and saw no side effects typical of other drugs working on the same area of the brain.
Following this successful phase I SAD clinical trial, the WCNDD is continuing to develop additional back-up M1 PAMs to enter into human clinical testing.
