Alzheimer's disease (AD) occurs in one out of eight Americans of age 65 and affects 43% of the elderly over 85. Current FDA-approved drugs provide short-term symptomatic relief of AD. There is a pressing need to discover new disease-modifying medications. AD is multifactorial in origin and progression. A drug attenuating several underlying factors is a preferred therapy for AD. Nomethiazoles are a class of small molecules that address synaptic dysfunction through NO/cGMP signaling and harness the neuroprotective and GABA-mimetic activities of a methylthiazole (MZ) pharmacophore. Activation of the NO/cGMP/CREB signaling pathway, essential for learning and memory, is known to be attenuated in AD brains; whereas, the MZ pharmacophore provides neuroprotection against neuronal loss and has anti-inflammatory actions in the brain. Preliminary data show that nomethiazoles reverse cognitive deficits, slow A accumulation, and provide a positive biomarker profile in AD transgenic mouse models. We have: positive data on the prototype nomethiazole in four different AD mouse models; a U01-funded drug discovery project that yielded 4 candidate 2nd generation nomethiazoles; and STTR Phase 1 data indicating improved pharmacokinetic properties of 2 of these candidates. The objective of this Phase 2 proposal is to de-risk and select one drug candidate for future full IND-enabling studies.
In Aims 1 and 2, two advanced mouse models of AD will be used to select the preferred nomethiazole and to provide a unique spectrum of preclinical animal efficacy data: 1) E4FAD a transgenic mouse model of familial AD, incorporating human apoE4, the major genetic risk factor for AD, which increases risk 20-fold and is biased against women; and 2) an accelerated oxidative stress model of age- related AD that manifests age-dependent hallmark AD biomarkers, neuronal loss, and cognitive decline.
In Aim 1, rescue and reversal of cognitive decline will be studied in these models.
In Aim 2, quantitative biomarkers will be measured of target engagement, attenuation of AD hallmark pathology and inflammation, and rescue of synaptic and neuronal function.
In Aim 3, drug scale-up, selected rodent pharmacokinetics, toxicology, and safety pharmacology will be studied to de-risk full IND studies. Completion of Aims 1&2 and Aim 3 will provide persuasive evidence of prospective efficacy and safety, respectively.

Public Health Relevance

Alzheimer's disease (AD) occurs in one out of eight Americans of age 65 and affects 43% of the elderly over 85. Current FDA-approved drugs provide short-term symptomatic relief of AD. The proposed research will lead to development of new disease-modifying medications.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Small Business Technology Transfer (STTR) Grants - Phase II (R42)
Project #
5R42AG044024-04
Application #
9354283
Study Section
Special Emphasis Panel (ZRG1-ETTN-M (11)B)
Program Officer
Refolo, Lorenzo
Project Start
2016-09-30
Project End
2018-05-31
Budget Start
2017-06-01
Budget End
2018-05-31
Support Year
4
Fiscal Year
2017
Total Cost
$697,279
Indirect Cost
Name
Revivo Therapeutics, Inc.
Department
Type
Domestic for-Profits
DUNS #
080255348
City
Durham
State
NC
Country
United States
Zip Code
27707