SBIR-STTR Award

Lead Optimization of Crac Channel Inhibitors for the Treatment of Alzheimer's Disease
Award last edited on: 9/20/2022

Sponsored Program
SBIR
Awarding Agency
NIH : NIA
Total Award Amount
$4,408,145
Award Phase
2
Solicitation Topic Code
866
Principal Investigator
Milton L Greenberg

Company Information

Vivreon Biosciences LLC

??3210 Merryfield Row
San Diego, CA 92121
   (703) 244-3194
   N/A
   www.vivreonbiosciences.com
Location: Single
Congr. District: 50
County: San Diego

Phase I

Contract Number: 1R44AG055205-01
Start Date: 9/30/2016    Completed: 5/31/2017
Phase I year
2016
Phase I Amount
$222,453
Vivreon Biosciences is pleased to apply for NIA SBIR Solicitation #PA-16-091. Vivreon Biosciences is an innovative life sciences company that is developing a series of novel small molecule, Ca2+ channel inhibitors for the treatment of Alzheimer’s disease (AD). Our lead compound series achieves neuroprotection by an entirely new mechanism – inhibition of Ca2+ release-activated Ca2+ (CRAC) channels to block microgliosis. Vivreon seeks NIA funding to bridge the gap between discovery and development. We will optimize our promising lead compound series through medicinal chemistry. Upon successful completion of the program, our preclinical candidate will be the first to specifically target the CRAC pathway for neuroprotection in AD, thus comprising an entirely new tool in the battle against AD. Vivreon has discovered a lead compound series with oral bioavailability that penetrates into the central nervous system (CNS) very efficiently, shows no neurotoxicity in the Irwin test of CNS integrity, and demonstrates neuroprotection in a mouse model of microgliosis (experimental autoimmune encephalitis). The lead series inhibits microgliosis by blocking CRAC channel activity with nM potency; suppressing M1 NF-?B activity, while preserving M2 phagocytosis. We will improve on these favorable properties through medicinal chemistry lead optimization followed by biological screening. Our lead presents several routes for modification that could lead to improved drug-like properties, and these routes will be pursued to identify a preclinical candidate molecule suitable for future Investigational New Drug (IND)-enabling studies. The candidate will be identified using an animal model suitable for AD (5XFAD, Dr. Blurton- Jones, University of California, Irvine). The final aim for this proposal is synthesis and characterization of the first CRAC channel inhibitor for AD therapy.

Public Health Relevance Statement:
Vivreon Biosciences – NIA SBIR # PA-16-091 Project Narrative Current Alzheimer’s disease (AD) therapies act on neurons only to alleviate symptoms of the disease without slowing disease progression. Microglial-associated genes are risk factors for AD, and chronic microgliosis contributes to progressive neurodegeneration in AD. Vivreon Biosciences is developing neuroprotective therapeutics to block pathogenic microgliosis by inhibiting microglial Ca2+ release-activated Ca2+ (CRAC) channel activation for use in the treatment of AD.

Project Terms:
Adverse effects; Alzheimer's Disease; Amyloid; Animal Model; Award; Bioavailable; Biological; Biological Availability; Biological Sciences; Brain; California; candidate selection; Cell membrane; Cells; Chronic; Clinical; Development; Disease; Disease Progression; Doctor of Medicine; Doctor of Philosophy; drug discovery; Drug Targeting; Experimental Autoimmune Encephalomyelitis; Foundations; Funding; Future; Genes; Goals; Hematopoietic; improved; in vivo; Inflammation; Inflammatory; inhibitor/antagonist; innovation; Institution; Investigational Drugs; Lead; lead series; Mediating; Microglia; mid-career faculty; Mission; Modification; mouse model; Names; Nerve Degeneration; Neuraxis; Neuronal Injury; Neurons; neuroprotection; neurotoxic; neurotoxicity; novel; Nuclear; Oral; Pathway interactions; Phagocytosis; Pharmaceutical Chemistry; Pharmaceutical Preparations; pre-clinical; prevent; professor; programs; progressive neurodegeneration; Property; reduce symptoms; Research; research clinical testing; Risk Factors; Role; Route; screening; Series; Signal Transduction; Small Business Innovation Research Grant; small molecule; Testing; Therapeutic; TimeLine; tool; transcription factor; Universities

Phase II

Contract Number: 4R44AG055205-02
Start Date: 9/30/2016    Completed: 5/31/2019
Phase II year
2017
(last award dollars: 2021)
Phase II Amount
$4,185,692

Vivreon Biosciences is pleased to apply for NIA SBIR Solicitation #PA-16-091. Vivreon Biosciences is an innovative life sciences company that is developing a series of novel small molecule, Ca2+ channel inhibitors for the treatment of Alzheimer’s disease (AD). Our lead compound series achieves neuroprotection by an entirely new mechanism – inhibition of Ca2+ release-activated Ca2+ (CRAC) channels to block microgliosis. Vivreon seeks NIA funding to bridge the gap between discovery and development. We will optimize our promising lead compound series through medicinal chemistry. Upon successful completion of the program, our preclinical candidate will be the first to specifically target the CRAC pathway for neuroprotection in AD, thus comprising an entirely new tool in the battle against AD. Vivreon has discovered a lead compound series with oral bioavailability that penetrates into the central nervous system (CNS) very efficiently, shows no neurotoxicity in the Irwin test of CNS integrity, and demonstrates neuroprotection in a mouse model of microgliosis (experimental autoimmune encephalitis). The lead series inhibits microgliosis by blocking CRAC channel activity with nM potency; suppressing M1 NF-?B activity, while preserving M2 phagocytosis. We will improve on these favorable properties through medicinal chemistry lead optimization followed by biological screening. Our lead presents several routes for modification that could lead to improved drug-like properties, and these routes will be pursued to identify a preclinical candidate molecule suitable for future Investigational New Drug (IND)-enabling studies. The candidate will be identified using an animal model suitable for AD (5XFAD, Dr. Blurton- Jones, University of California, Irvine). The final aim for this proposal is synthesis and characterization of the first CRAC channel inhibitor for AD therapy.

Public Health Relevance Statement:
Current Alzheimer’s disease (AD) therapies act on neurons only to alleviate symptoms of the disease without slowing disease progression. Microglial-associated genes are risk factors for AD, and chronic microgliosis contributes to progressive neurodegeneration in AD. Vivreon Biosciences is developing neuroprotective therapeutics to block pathogenic microgliosis by inhibiting microglial Ca2+ release-activated Ca2+ (CRAC) channel activation for use in the treatment of AD.

Project Terms:
Adverse effects; Alzheimer's Disease; Amyloid beta-Protein; Animal Model; Award; Bioavailable; Biological; Biological Availability; Biological Sciences; Brain; California; candidate selection; Cell membrane; Cells; Chronic; Clinical; clinical candidate; clinical development; Development; Disease; Disease Progression; drug discovery; Drug Targeting; Experimental Autoimmune Encephalomyelitis; Foundations; Funding; Future; Goals; Hematopoietic; improved; in vivo; Inflammation; Inflammatory; inhibitor/antagonist; innovation; Investigational Drugs; Lead; lead series; Mediating; Microglia; Mission; Modification; mouse model; Nerve Degeneration; Neuraxis; Neuronal Injury; Neurons; neuroprotection; neurotoxic; neurotoxicity; novel; Nuclear; Oral; Pathogenicity; Pathway interactions; Phagocytosis; Pharmaceutical Chemistry; Pharmaceutical Preparations; Pharmacology; pre-clinical; prevent; programs; progressive neurodegeneration; Property; reduce symptoms; Research; research clinical testing; Risk Factors; risk variant; Route; screening; Series; Signal Transduction; Small Business Innovation Research Grant; small molecule; Testing; Therapeutic; TimeLine; tool; transcription factor; Universities