The best correlate of memory deficits in Alzheimer?s disease (AD) patients is not A? plaque burden or neurofibrillary tangles, but synapse loss, which is thought to occur early in the disease process before the onset of clinical symptoms. We have developed a novel compound called M3 that can effectively enhance structural and functional plasticity of synapses. This compound has been proved to provide significant benefits in two mouse models of AD (APPSw/Ind mice and rTg4510 mice), including improved cognitive functions, restored synaptic integrity, reduced neurodegeneration, reduced tau phosphorylation and neurofibrillary tangles, and reduced amyloid plaques. M3 has excellent potency, solubility, stability, specificity, and thus far no overt safety concerns. M3 meets all Late Stage Entry Criteria. In Year 1, we will focus on IND-enabling studies and IND preparation and filing. Our milestones are (i) completion of IND-enabling studies, (ii) production of a GMP batch for clinical studies, and (iii) active IND. In Year 2, we will focus on a single ascending dose (SAD) study. Our milestones are (i) IRB approval, (ii) completion of SAD study, and (iii) MTD and single dose PK established. In Year 3, we will focus on a multiple ascending dose (MAD) study. Our milestones are (i) completion of MAD study and (ii) MTD and repeat dose PK established.

Public Health Relevance

A large number of studies have indicated that the best correlate of memory deficits in Alzheimer?s disease (AD) patients is synapse loss, which is thought to occur early in the disease process before the onset of clinical symptoms. Our research team has developed a novel compound that can effectively enhance structural and functional plasticity of synapses. We have demonstrated that our compound provides profound efficacy in two mouse models of AD. This compound is a potential new therapeutic drug for AD. The focuses of this study are (i) conducting Investigational New Drug (IND)-enabling studies to meet the requirements for filing an IND (FDA approval for human clinical trials) and (ii) conducting First-in-Human (Phase I) clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01AG068822-01
Application #
10045319
Study Section
Special Emphasis Panel (ZAG1)
Program Officer
Yuan, Jean
Project Start
2020-09-15
Project End
2023-08-31
Budget Start
2020-09-15
Budget End
2021-08-31
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Ohio State University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210