The purpose of the proposed project is to conduct a Phase 2a mechanistic clinical proof of concept study of an investigational drug, T3D-959 which is being developed for the treatment of cognitive and functional decline in Alzheimer's disease patients. T3D-959 has successfully completed Phase I studies, and with data demonstrating robust entry into the brain in a rat pharmacokinetic study. T3D-959 is a novel, orally delivered, small molecule, dual nuclear receptor agonist, formerly targeted as a type 2 diabetes therapy and now being re-positioned as a potential disease-modifying therapy for Alzheimer's disease (AD) and mild cognitive impairment (MCI). The project goal is to test the hypothesis that T3D- 959 can mechanistically act in the brain of AD patients to produce desired changes in glucose metabolism (as measured by FDG-PET) and brain function (as measured by BOLD fMRI). These imaging modalities are currently being utilized as surrogate measures of potential efficacy in treating AD. If T3D- 959 treatment produces desired changes in glucose metabolism and brain function, the drug could have disease remedial potential and this study could provide supportive clinical data that justifies the pursuit of longer term clinical studies of the potentia of T3D-959 to slow, stop or reverse cognitive and functional decline in AD patients. The clinical trial is an adaptive, sequential enrollment design involving 24-36 mild-to-moderate AD patients dosed orally once-a-day for 2 weeks. The project has 3 key objectives: i. To determine the potential of T3D-959 to improve cerebral glucose metabolism (CMRgl). Low CMRgl is a hallmark of AD and a better predictor of future cognitive impairment than amyloid plaqe or tau bundle load. ii. To determine the potential of T3D-959 to improve memory-related hippocampal functional connectivity (resting state default mode network activity). iii. Determine appropriate doses for future clinical studies (dose range finding). The therapeutic approach to be tested is based on two suppositions; (A) ameliorating multiple pathologies in the disease with a single therapy may provide a superior clinical benefit than therapeutic approaches which target a single pathology (e.g. beta amyloid plaques) and (B) correcting insulin resistance in the brain, (a key driver of AD pathophysiology) may be disease remedial.

Public Health Relevance

Alzheimer's disease today is the costliest disease to the American healthcare system with no marketed drug therapies that can slow, stop or reverse the course of this malady. The purpose of the proposed project is to conduct a mechanistic proof of concept Phase 2a study of an investigational drug, T3D-959, which has successfully completed Phase I. The project aims to demonstrate that T3D-959 has the potential to be an effective disease remedial drug therapy for treating cognitive impairment in Alzheimer's disease. The therapeutic approach to be tested is based on two suppositions; (A) ameliorating multiple defects in the disease with a single therapy may provide a superior clinical benefit than therapeutic approaches which target a single defect (e.g. beta amyloid plaques) and (B) correcting insulin resistance in the brain, (a key driver of Alzheimer's disease pathophysiology) may alter the course of disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
5R44AG049510-02
Application #
9034522
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Ryan, Laurie M
Project Start
2015-03-15
Project End
2017-02-28
Budget Start
2016-03-01
Budget End
2017-02-28
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
T3 Therapeutics, Inc.
Department
Type
DUNS #
079219893
City
Research Triangle Park
State
NC
Country
United States
Zip Code
27709
de la Monte, Suzanne M; Tong, Ming; Wands, Jack R (2018) The 20-Year Voyage Aboard the Journal of Alzheimer's Disease: Docking at 'Type 3 Diabetes', Environmental/Exposure Factors, Pathogenic Mechanisms, and Potential Treatments. J Alzheimers Dis 62:1381-1390
Tong, Ming; Leão, Raiane; Vimbela, Gina V et al. (2017) Altered temporal lobe white matter lipid ion profiles in an experimental model of sporadic Alzheimer's disease. Mol Cell Neurosci 82:23-34
Lee, Han-Kyu; Kwon, Bumsup; Lemere, Cynthia A et al. (2017) mTORC2 (Rictor) in Alzheimer's Disease and Reversal of Amyloid-? Expression-Induced Insulin Resistance and Toxicity in Rat Primary Cortical Neurons. J Alzheimers Dis 56:1015-1036
de la Monte, Suzanne M; Tong, Ming; Schiano, Irio et al. (2017) Improved Brain Insulin/IGF Signaling and Reduced Neuroinflammation with T3D-959 in an Experimental Model of Sporadic Alzheimer's Disease. J Alzheimers Dis 55:849-864
de la Monte, Suzanne M (2017) Insulin Resistance and Neurodegeneration: Progress Towards the Development of New Therapeutics for Alzheimer's Disease. Drugs 77:47-65
Andreani, Tomas; Tong, Ming; Gundogan, Fusun et al. (2016) Differential Effects of 3rd Trimester-Equivalent Binge Ethanol and Tobacco-Specific Nitrosamine Ketone Exposures on Brain Insulin Signaling in Adolescence. J Diabetes Relat Disord 1:
Yu, Rosa; Deochand, Chetram; Krotow, Alexander et al. (2016) Tobacco Smoke-Induced Brain White Matter Myelin Dysfunction: Potential Co-Factor Role of Smoking in Neurodegeneration. J Alzheimers Dis 50:133-48
Tong, Ming; Deochand, Chetram; Didsbury, John et al. (2016) T3D-959: A Multi-Faceted Disease Remedial Drug Candidate for the Treatment of Alzheimer's Disease. J Alzheimers Dis 51:123-38
Tong, Ming; Dominguez, Cesar; Didsbury, John et al. (2016) Targeting Alzheimer's Disease Neuro-Metabolic Dysfunction with a Small Molecule Nuclear Receptor Agonist (T3D-959) Reverses Disease Pathologies. J Alzheimers Dis Parkinsonism 6:
de la Monte, Suzanne M (2014) Type 3 diabetes is sporadic Alzheimer?s disease: mini-review. Eur Neuropsychopharmacol 24:1954-60