Lindsay Burns
A neuroscientist, biotechnology leader, drug developer, and Olympic medalist. Her career spans basic research in neurodegenerative disease, drug discovery and clinical testing.
Dr. Burns is an independent consultant in all areas of neuroscience drug development.
About
Lindsay Burns, PhD
Lindsay has built a life at the intersection of scientific rigor, persistence and high performance.
Raised in Montana on a fourth-generation ranch, she went on to study psychobiology at Harvard and earn a PhD in neuroscience at the University of Cambridge, UK. She is an author on 40 peer-reviewed publications and a named inventor on 21 U.S. patents. For over ten years, Lindsay reviewed grant applications for the National Institute on Aging, a part of the National Institutes of Health.
Lindsay has taken novel scientific ideas from discovery through clinical development, including advancing a novel small molecule (simufilam) from target discovery to Phase 3 clinical testing.
For nearly 20 years, she trained under legendary drug developer Nadav Friedmann, PhD, MD. Her biotechnology experience spans neuropharmacology, analgesia, oncology and Alzheimer’s disease.
Earlier, Lindsay spent eight years on the U.S. National Rowing Team, earning four World Championship medals and an Olympic silver medal. She continues to bring a highly competitive drive to science, consulting, and the challenges she chooses to pursue.
From Discovery to Development
From Discovery to Development
Question the Expected
Question the Expected
Beyond Neuroscience
Beyond Neuroscience
Journal
Publications
Explore Lindsay Burns' published research and scholarly contributions through her ORCID public record, which provides a comprehensive and up-to-date list of her peer-reviewed publications.
Articles
Latest Reads
Filamin A Phosphorylation at S2152: a molecular switch fueling cancer and neurodegeneration
Lindsay H. Burns & Alex Romero (2026)
Filamin A (FLNA) plays a key role in cell structure and signaling, with abnormal phosphorylation linked to cancer progression, inflammation, and Alzheimer’s disease. Targeting these changes may offer new therapeutic opportunities.
Phase 3 Randomized Clinical Trials of Simufilam in Mild-to-moderate Alzheimer’s Disease
James W. Kupiec, Anton P. Porsteinsson, Raymond S. Turner, et. al. (2026)
Reports findings from two Phase 3 trials evaluating simufilam in mild-to-moderate Alzheimer’s disease. While the treatment was safe and well tolerated, the trials did not meet their primary or secondary endpoints.
Simufilam Reverses Aberrant Receptor Interactions of Filamin A in Alzheimer’s Disease
Hoau-Yan Wang. Erika Cecon, Julie Dam, Zhe Pei, Ralf Jockers, Lindsay H. Burns (2023)
Examines simufilam’s proposed mechanism in Alzheimer’s disease, focusing on its effects on abnormal filamin A–receptor interactions. Findings suggest it may reduce amyloid-related signaling and inflammatory activity linked to AD.
Simufilam Suppresses Overactive mTOR and Restores its Sensitivity to Insulin in Alzheimer’s Disease Patient Lymphocytes
Hoau-Yan Wang, Zhe Pei, Kuo-Chieh Lee, Boris Nikolov, Tamara Doehner, et. al. (2023)
Targeting α7 Nicotinic Acetylcholine Receptors and Their Protein Interactions in Alzheimer's Disease Drug Development
Lindsay H. Burns, Zhe Pei, Hoau-Yan Wang (2023)
Altered filamin A enables amyloid beta-induced tau hyperphosphorylation and neuroinflammation in Alzheimer’s disease
Lindsay H. Burns & Hoau-Yan Wang (2017)
Explores altered filamin A (FLNA) as a potential therapeutic target in Alzheimer’s disease. Highlights its role in amyloid-driven tau pathology and neuroinflammation, as well as the potential of PTI-125 to disrupt these processes.
Get In Touch
For consulting inquiries around grant writing, help with manuscripts, or early development advice, please send a message describing your project.