The aim of this proposal is to develop a novel class of Alzheimer's Disease (AD) therapeutics acting via a hitherto unexplored mechanism of action. AD is the sixth-leading cause of death in the United States with no known cure. The burden on families and caregivers of patients is immense, with the annual cost of care approaching $1 trillion. The exorbitant strain of AD arises, in large part, to the lack of effective, innovative ad disease-modifying treatment options. A prominent pathological feature of AD is a robust activation of the neuronal lysosomal pathway, endocytosis and autophagy - disturbances of which are associated with lysosomal cytotoxicity and represent one of the earliest manifestations in sporadic AD. Furthermore, dysfunction in lysosomal storage and indigestibility of glycosaminoglycans (GAGs) such as heparan sulfate GAGs (HS-GAGs) is also the primary cause of several neurodegenerative diseases known as mucopolysaccharidoses. HS-GAGs interact with key molecules implicated in AD pathogenesis, i.e., ¿-amyloid (Abeta), Tau and Apolipoprotein E. Our biotechnology company has discovered a new series of proprietary compounds called Glycosaminoglycan-Interacting Small Molecule (GISMO). These molecules work via a unique mechanism of action to inhibit protein interactions with HS-GAGs, and as such, represent a novel therapeutic approach for the treatment of AD. The goal of this proposal is to develop a novel AD therapeutic that inhibits uptake of HS-GAG/Abeta protein aggregates via endo-lysosomal route. Consequently, GISMO compounds are expected to prevent lysosomal storage of HS-GAGs (complexed with Abeta) and protect nerve cells against lysosomal dysfunction and cytotoxicity. Furthermore, GISMO compounds may also dissipate already aggregated Abeta bound to GAGs and reduce further accumulation of extracellular Abeta, by dissociating the Abeta-GAG complexes. During this project, Specific Aim 1 is to evaluate 24 already identified lead compounds for in vitro potency and safety; Specific Aim 2 is to perform lead optimization to improve safety and selectivity; and Specific Aim 3 is to assess pharmacokinetic properties of lead compounds to identify brain-penetrant compounds. The successful completion of these studies will result in identification of three optimized lead compounds that will be subjected to in vivo testing in animal models of AD, with the subsequent aim of identifying a Preclinical Candidate for IND-enabling studies.
Public Health Relevance Statement: Public Health Relevance: Alzheimer's disease is a progressive neurologic disease of the brain leading to the irreversible loss memory and cognitive performance which become severe enough to impede social or occupational functioning. This chronic, debilitating disorder results in a devastating burden on the families and caregivers of patients, with the rising costs o care in the United States exceeding $170 billion a year. The goal of this Phase I SBIR proposal is to develop a novel and orally effective small molecule for the treatment of Alzheimer's disease. The drugs described in this proposal act via a novel and highly differentiated mechanism of action and are postulated to exhibit an improved efficacy / safety risk compared to the current standard of care.
NIH Spending Category: Aging; Alzheimer's Disease; Biotechnology; Brain Disorders; Dementia; Neurodegenerative; Neurosciences
Project Terms: Acute; Alzheimer's Disease; Alzheimer's disease model; Amyloid; Amyloid beta-Protein; analog; Animal Model; Apolipoprotein E; Area Under Curve; Autophagocytosis; base; Binding (Molecular Function); Bioavailable; Biological Assay; Biotechnology; Brain; Brain Diseases; Caring; Cause of Death; Cell Culture Techniques; Cell Line; Cell surface; Cells; Characteristics; Chemicals; Chronic; Cognitive; Complex; cost; cytotoxicity; Disease; drug development; drug discovery; Drug Kinetics; Endocytosis Pathway; Evaluation; Exhibits; extracellular; Family Caregiver; Functional disorder; Glycosaminoglycans; Goals; Half-Life; Hand; Heparin Binding; Heparitin Sulfate; high throughput screening; Human; improved; In Vitro; in vitro Assay; in vivo; Incubated; inhibitor/antagonist; innovation; Lead; lead series; Measures; Memory Loss; Mucopolysaccharidoses; Mus; neuroblastoma cell; Neurodegenerative Disorders; Neurologic; Neurons; neuroprotection; novel; novel therapeutic intervention; Occupational; Pathogenesis; Patients; Performance; Pharmaceutical Preparations; Pharmacy (field); Phase; Plasma; polysulfated glycosaminoglycan; pre-clinical; prevent; Property; protein aggregate; Proteins; public health relevance; research study; Risk; Rodent; Route; Safety; Series; Small Business Innovation Research Grant; small molecule; social; standard of care; Structure; tau Proteins; Testing; Therapeutic; Toxic effect; United States; uptake; Work
