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1
“Microbiome-Sparing Solutions for Alzheimer’s
& Cardiovascular Disease.”
2
AdVax is...
Advax is developing first-of-kind vaccines and a new suite of diagnostics,
therapeutics, and monoclonal antibodies in the multi-billion-dollar arena of
Alzheimer’s prevention and cure.
3
AdVax Founders
Garth Ehrlich, PhD, FAAAS
Systemic Microbiology & Genomics
Developer of the Mucosal Biofilm Paradigm,
Distributed Genome Hypothesis, & Rubric
of Bacterial Plurality.
Executive Director, Center for Genomic
Sciences, Allegheny-Singer Research
Institute.
Peter Nara, MSc, DVM, PhD, FAAAS
Vaccinology
Discoverer, Deceptive Imprinting
Inventor, Immune Refocusing Technology.
CEO, President, Chairman & co-founder
of Biological Mimetics, Inc.
Mentored by Jonas Salk
Daniel L. Sindelar, DMD
Periodontics & Oral Systemic Biology
Co-founder & recent president of the
American Academy for
Oral Systemic Health (AAOSH)
Founder and director of Oral Genomics.
Preceptorship in prevention of heart
attacks, strokes, & diabetes
Judith Miklossy, MD, PhD, DSc
Neuropathology, Neurology, & Psychiatry
Founder & Director of the Alzheimer’s
Prevention International Foundation
Director of the International Alzheimer’s
Research Center in Switzerland.
4
Scientific Advisory Board
Marc Penn, MD, PhD
• Former Medical Director,
Cardiac ICU, Cleveland
Clinic
• Former Director, Bakken
Heart-Brain Institute
• Chief Medical Officer,
Cleveland Heartlab
• Professor of Integrative
Medical Sciences,
Northeast Ohio Medical
University
StJohn Crean, PhD
• Executive Dean of
College of Clinical and
Biomedical Sciences,
University of Central
Lancashire
• Robert Bradlaw advisor,
Faculty of Dental Surgery
at the Royal College of
Surgeons of England
• Editor-in-Chief, Faculty
Dental Journal
W. Sue T. Griffin, PhD
• Editor-in-Chief, Journal
of Neuroinflammation
• Dillard Professor & Vice
Chairman, Donald W.
Reynolds Dept. of
Geriatrics, University of
Arkansas for Medical
Sciences
• Director of Research,
Geriatric Research,
Education and Clinical
Center, VAMC/CAVHS
Angela Kamer, DDS
• Research Scientist, NYU
School of Medicine
Center for Brain Health
• Associate Professor of
Periodontology &
Implant Dentistry, New
York University
Sim K. Singhrao, PhD
• Senior Research Fellow,
University of Central
Lancashire School of
Medicine & Dentistry
5
Our Vision
NEXT-GENERATION SALIVARY
DIAGNOSTICS to identify risk for
Alzheimer’s disease, multiple
cardiovascular diseases, and
neurodegenerative diseases.
LICENSING AGREEMENTS utilizing AdVax
IP, co-developing therapeutics for
Alzheimer’s disease, multiple
cardiovascular diseases, and
neurodegenerative diseases.
MICROBIOME-SPARING VACCINES
for keystone pathogen strains directly
involved in the pathogenesis of
Alzheimer’s disease, multiple
cardiovascular diseases, and
neurodegenerative diseases.
6
Recent Advances
Completed Phase I of Research & Development
AdVax has identified the most virulent strains of a keystone pathogen.
Initiated Development of a First-in-Man Diagnostic
First-of-kind salivary diagnostics performed by physicians to determine microbial burden & subsequent risk for
inflammatory disease
Engineered IRT Mutations into Bacterial Targets
(n= 2-4 targets with 5-10 IRT mutations per target)
Now an active member of the Alzheimer’s Association Small Company Consortium
The mission of the AASCC is to advance Alzheimer’s disease (AD) research and innovation in small, start-up
biotechnology, diagnostic and contract research organizations
7
Science & Technology
AdVax has sequenced and developed supragenome
modeling for the most pathogenic strains of two
unique pathogens of oral origin involved in the
pathogenesis of Alzheimer’s and cardiovascular
diseases:
• Treponema denticola
• Porphyromonas gingivalis
AdVax uses our existing patented technology,
developing diagnostics, monoclonal antibodies, and
first-in-man vaccines for P. gingivalis & T. denticola
AdVax, in partnership with BMI, brings market-
leading technologies currently being used in
advanced-stage development of a human rhinovirus
vaccine.
8
AdVax Science & Technology
AdVax has discovered that cardiovascular disease and neurodegenerative diseases
such as Alzheimer's have a common pathogenic etiology:
Specific strains of P. gingivalis.
9
Percentage of People with Pathogenic Bacteria Over Threshold
P. Gingivalis Infects…
40% 61% 70% 77%
Age
<30
83%
Age
30-40
Age
40-50
Age
50-60
Age
>60
Data accumulated from over
200,000 salivary diagnostic samples
10
to P. gingivalis & T. denticola
The Body’s Response
WHEN THESE BACTERIA ARE IN THE
MOUTH
• Oral/systemic vascular and organ
inflammation
• Chronic active/silent infection
• Biofilm formation
• Bleeding gums
• Bone loss
• Loose/lost teeth
• Cavities
WHEN THESE BACTERIA ARE
PRESENT IN THE HEART
• Foam cells
• Ox-LDL
• hs-CRP
• Lp-PLA2
• MPO
WHEN THESE BACTERIA ARE
PRESENT IN THE BRAIN
• Focal and disseminated neuro-
inflammation
• Amyloid beta/Tau activation
• Broad slow cognitive decline
• Pre-AD and Alzheimer’s
disease
• Breakdown of BBB
A rubric of genetic inflammatory traits
determines where and how the body
responds to these pathogens.
11
Lifestyle Triggers
Traditional lifestyle triggers such as stress, nutritional deficiencies, diet, and sleep:
• Increase the systemic burden of P. gingivalis and T. denticola
• Decrease the host response to these pathogens
A person can have healthy looking gums, but still have a very high bioburden. This silent infection
can have grave impacts systemically, in the absence of traditional signs of periodontal disease,
triggering both bacterial spread and inducing inflammation at distant sites resulting in Alzheimer’s
disease, as well as a host of cardiovascular diseases. These relationships are not linear—
stress/cortisol, genetics, diet, and obstructive sleep apnea play confounding roles.
12
MMP-9/TIMP-1 imbalance induced in human dendritic cells by
Porphyromonas gingivalis.
Monocytes may be used as a vehicle for transporting PG. PG can
stimulate cytokine production and survive in monocytes.
Microbial Hijacking of Complement–Toll-Like Receptor Crosstalk:
Pathogens may not simply undermine complement or TLRs as
separate entities, but may also exploit their crosstalk pathways.
Oral administration of P. gingivalis induces dysbiosis of gut
microbiota and impairs barrier function leading to
dissemination of enterobacteria to the liver
Copper exhibits antimicrobial activity against PG by
reducing planktonic & biofilm growth & invasion of host
epithelial cells.
Porphyromonas gingivalis Infection Reduces Regulatory
T Cells in Infected Atherosclerosis Patients.
MMP-9/TIMP-1imbalance induced in human dendritic cells
by Porphyromonas gingivalis. Blood-brain barrier dysfunction
by regulation of the MMP-9/TIMP-1 balance.
PG exacerbates brain amyloid deposition and triggers brain
inflammation, leading to enhanced cognitive impairment.
Immune-Altering & Manipulating
Microbiome-Disrupting
Immune response deposits Cu
Alters Regulatory T-Cells
Breaks Down Blood Brain Barrier
Initiates Neuroinflammation
Promotes Monocyte Migration by Activating MMP-9
Immune-Evading & Translocating
P. gingivalis
13
P. gingivalis initiates neuroinflammatory diseases,
specifically Alzheimer's
“The data from the human brains and that from the in
vivo mouse study suggested specific associations of P.
gingivalis with AD inflammatory pathology.”
“The keystone hypothesis of Hajishengallis et al. helps
to explain the contribution that P. gingivalis may cause
the early development of a neurodegenerative
condition such as Alzheimer’s disease. In our view, P.
gingivalis (highly virulent strains) access the CNS during
healthy stages but only those individuals with
inflammatory susceptibility traits are likely to develop
progressive inflammatory component representing
neurodegenerative disease processes.”
Sim K. Singhrao, Alice Harding, Sophie Poole, Lakshmyya Kesavalu, and StJohn Crean, “Porphyromonas gingivalis Periodontal Infection and Its Putative Links with
Alzheimer’s Disease,” Mediators of Inflammation, vol. 2015, Article ID 137357, 10 pages, 2015. doi:10.1155/2015/137357
14
Oral pathogens found at
the site of beta amyloid
deposits in 98% of
Alzheimer’s brains and
non-existent in all but
7% of the non-
Alzheimer’s brains.
ORAL ORIGIN
OLFACTORY BULB
(First sign of AD is loss of smell)
ENTORHINAL CORTEX
(First site of AD destruction & AB)
Miklossy J. Alzheimer's disease - a neurospirochetosis.
Analysis of the evidence following Koch's and Hill's
criteria. J Neuroinflammation. 2011;8(1):90.
15
AdVax Targets: Class II Pathogens
Class II pathogens are resistant to current
vaccine and monoclonal antibody
technologies due to their ability to use
molecular decoys, mutate and exist in
numerous strains
Vaccines are the only known medical product
that can be given to prevent infection by Class
II pathogens.
Unmet and completely open multi-Billion
dollar markets exist for multiple pathogens.
16
AdVax, in partnership with BMI, has the exclusive
technology to overcome deceptive imprinting.
How do Class II Pathogens
Accomplish this Feat?
DECEPTIVE IMPRINTING
17
BMI holds background and genus species specific patents for target vaccine proteins
in infectious diseases areas for humans and animal health.
BMI has exclusive worldwide license for Immune Refocusing Technology from the
National Institutes of Health.
BMI and AdVax co-own new identified Red Complex oral pathogens
(Initial immune refocused P. gingivalis and T. denticola patents pending.)
Biological Mimetics, Inc.
AdVax Intellectual Property
in Partnership with BMI
Biological Mimetics, Inc. (“BMI”) was formed in 1996 to commercialize innovative pharmaceutical products that will improve the quality of life and
overall state of public health by combating resistant and emerging diseases in human and veterinary medicine.
18
AdVax Solutions
6 mos. – 1 year
ORAL
GENOMICS
2 years
DIAGNOSTICS &
THERAPEUTICS
3-6 years
VACCINES
First-of-kind salivary
diagnostics performed by
physicians to determine
microbial burden &
subsequent risk for
inflammatory disease
REVENUE:
$25 - $50 million per year
Early detection &
prevention of disease
Paradigm-changing
diagnostics, medical
devices, and monoclonal
antibody-based
therapeutics
REVENUE:
$100 million/year
& a solution for prevention
& early detection of
Alzheimer’s disease
Next-generation
prophylactic,
microbiome-sparing
vaccines
REVENUE:
$1 - 2 billion/year
& a cure for one cause of
Alzheimer’s disease
19
Vaccine, Nanobody, & Monoclonal Antibody
Development Timeline
Acquisition of a broad array of
clinical strains of each species
(N = 10) of periodontal
pathogen associated with AD
Map IDNPE’s on bacterial
targets (n=1-2 bacterial sp.)
Sequence a minimum of 20
strains of each periodontal
pathogen (N = 200)
Engineer IRT mutations into
bacterial targets (n= 2-4
targets with5-10 IRT
mutations per target)
Perform comparative
genomics on each species
including supragenome
modeling, identify core
genes, identify core gene
subset under immune
selection for each species
Express IRT bacterial
proteins in commercially
licensable systems/
Prepare recombinant
proteins for at least 4
candidate core genes for
each species and collect
human sera from AD and
periodontal patients.
Immunogenicity studies in
2 lab animal species
Determine which of the
candidate core proteins
react with human serum
from patients with
periodontal disease
creating an active target list
4 months 6 months 2 months 6 months 3 months
Quarter 1 Quarter 2 Quarter 3 Quarter 4
COMPLETED
Ehrlich DGH Studies – Sequencing &
Molecular Cataloguing
Nara IRT Vaccine
& Monoclonal Antibody Development
20
Diagnostics Timeline
6 month time frame
TEST 1: SALIVARY DIAGNOSTICS
First-of-kind salivary diagnostics performed by
physicians to determine microbial burden &
subsequent risk for CVD, Alzheimer’s, RA, Diabetes,
Glaucoma, etc.
TEST 2: BUCCAL INFLAMMATORY TESTING
Determines inflammatory risk for Alzheimer’s
disease.
MARKET-READY
DIAGNOSTICS
RESEARCH & DEVELOPMENT
RESEARCH & DEVELOPMENT
COMPLETED
21
Product Launch Timeline
Year 1 Year 2 Year 3 Year 4 Year 5 Year 6
Salivary Diagnostics &
Advanced Inflammation Testing
Value Inflection Point
Salivary Diagnostic Revenues
Value Inflection &
Exit Point*
Animal Ready, First-in-Man Vaccines
& mAb Therapeutics for AD & CVD
causing pathogens.
First-in-Man Vaccines &
mAb Therapeutics for AD & CVD
causing pathogens. Full body scan
for early detection of AD
Value Inflection
& Exit Point*
Value Inflection
& Exit Point*
Value Inflection
& Exit Point*
*Capitalizing on existing relationships with Big Pharma
Value Inflection
& Exit Point*
22
Multiple exits: Phase 1, Phase 2a/2b
Value Inflection Points: Discovery,
IND Filing, Phase 1, Phase 2
THE RETURN
Seed Bridge Funding: $500,000 MET
Series A Funding: $2-5M
Series B Funding: $10-15M
CAPITAL NEEDS
Series A/B funding opportunities are being sought for the company's
financing of both the development of novel point of care diagnostics worth
$100s of millions per year and monoclonal antibodies and vaccines worth
more than $1-2 billion per year.
INVESTMENT OPPORTUNITIES
23

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AdVax Summary Slide Deck

  • 1. 1 “Microbiome-Sparing Solutions for Alzheimer’s & Cardiovascular Disease.”
  • 2. 2 AdVax is... Advax is developing first-of-kind vaccines and a new suite of diagnostics, therapeutics, and monoclonal antibodies in the multi-billion-dollar arena of Alzheimer’s prevention and cure.
  • 3. 3 AdVax Founders Garth Ehrlich, PhD, FAAAS Systemic Microbiology & Genomics Developer of the Mucosal Biofilm Paradigm, Distributed Genome Hypothesis, & Rubric of Bacterial Plurality. Executive Director, Center for Genomic Sciences, Allegheny-Singer Research Institute. Peter Nara, MSc, DVM, PhD, FAAAS Vaccinology Discoverer, Deceptive Imprinting Inventor, Immune Refocusing Technology. CEO, President, Chairman & co-founder of Biological Mimetics, Inc. Mentored by Jonas Salk Daniel L. Sindelar, DMD Periodontics & Oral Systemic Biology Co-founder & recent president of the American Academy for Oral Systemic Health (AAOSH) Founder and director of Oral Genomics. Preceptorship in prevention of heart attacks, strokes, & diabetes Judith Miklossy, MD, PhD, DSc Neuropathology, Neurology, & Psychiatry Founder & Director of the Alzheimer’s Prevention International Foundation Director of the International Alzheimer’s Research Center in Switzerland.
  • 4. 4 Scientific Advisory Board Marc Penn, MD, PhD • Former Medical Director, Cardiac ICU, Cleveland Clinic • Former Director, Bakken Heart-Brain Institute • Chief Medical Officer, Cleveland Heartlab • Professor of Integrative Medical Sciences, Northeast Ohio Medical University StJohn Crean, PhD • Executive Dean of College of Clinical and Biomedical Sciences, University of Central Lancashire • Robert Bradlaw advisor, Faculty of Dental Surgery at the Royal College of Surgeons of England • Editor-in-Chief, Faculty Dental Journal W. Sue T. Griffin, PhD • Editor-in-Chief, Journal of Neuroinflammation • Dillard Professor & Vice Chairman, Donald W. Reynolds Dept. of Geriatrics, University of Arkansas for Medical Sciences • Director of Research, Geriatric Research, Education and Clinical Center, VAMC/CAVHS Angela Kamer, DDS • Research Scientist, NYU School of Medicine Center for Brain Health • Associate Professor of Periodontology & Implant Dentistry, New York University Sim K. Singhrao, PhD • Senior Research Fellow, University of Central Lancashire School of Medicine & Dentistry
  • 5. 5 Our Vision NEXT-GENERATION SALIVARY DIAGNOSTICS to identify risk for Alzheimer’s disease, multiple cardiovascular diseases, and neurodegenerative diseases. LICENSING AGREEMENTS utilizing AdVax IP, co-developing therapeutics for Alzheimer’s disease, multiple cardiovascular diseases, and neurodegenerative diseases. MICROBIOME-SPARING VACCINES for keystone pathogen strains directly involved in the pathogenesis of Alzheimer’s disease, multiple cardiovascular diseases, and neurodegenerative diseases.
  • 6. 6 Recent Advances Completed Phase I of Research & Development AdVax has identified the most virulent strains of a keystone pathogen. Initiated Development of a First-in-Man Diagnostic First-of-kind salivary diagnostics performed by physicians to determine microbial burden & subsequent risk for inflammatory disease Engineered IRT Mutations into Bacterial Targets (n= 2-4 targets with 5-10 IRT mutations per target) Now an active member of the Alzheimer’s Association Small Company Consortium The mission of the AASCC is to advance Alzheimer’s disease (AD) research and innovation in small, start-up biotechnology, diagnostic and contract research organizations
  • 7. 7 Science & Technology AdVax has sequenced and developed supragenome modeling for the most pathogenic strains of two unique pathogens of oral origin involved in the pathogenesis of Alzheimer’s and cardiovascular diseases: • Treponema denticola • Porphyromonas gingivalis AdVax uses our existing patented technology, developing diagnostics, monoclonal antibodies, and first-in-man vaccines for P. gingivalis & T. denticola AdVax, in partnership with BMI, brings market- leading technologies currently being used in advanced-stage development of a human rhinovirus vaccine.
  • 8. 8 AdVax Science & Technology AdVax has discovered that cardiovascular disease and neurodegenerative diseases such as Alzheimer's have a common pathogenic etiology: Specific strains of P. gingivalis.
  • 9. 9 Percentage of People with Pathogenic Bacteria Over Threshold P. Gingivalis Infects… 40% 61% 70% 77% Age <30 83% Age 30-40 Age 40-50 Age 50-60 Age >60 Data accumulated from over 200,000 salivary diagnostic samples
  • 10. 10 to P. gingivalis & T. denticola The Body’s Response WHEN THESE BACTERIA ARE IN THE MOUTH • Oral/systemic vascular and organ inflammation • Chronic active/silent infection • Biofilm formation • Bleeding gums • Bone loss • Loose/lost teeth • Cavities WHEN THESE BACTERIA ARE PRESENT IN THE HEART • Foam cells • Ox-LDL • hs-CRP • Lp-PLA2 • MPO WHEN THESE BACTERIA ARE PRESENT IN THE BRAIN • Focal and disseminated neuro- inflammation • Amyloid beta/Tau activation • Broad slow cognitive decline • Pre-AD and Alzheimer’s disease • Breakdown of BBB A rubric of genetic inflammatory traits determines where and how the body responds to these pathogens.
  • 11. 11 Lifestyle Triggers Traditional lifestyle triggers such as stress, nutritional deficiencies, diet, and sleep: • Increase the systemic burden of P. gingivalis and T. denticola • Decrease the host response to these pathogens A person can have healthy looking gums, but still have a very high bioburden. This silent infection can have grave impacts systemically, in the absence of traditional signs of periodontal disease, triggering both bacterial spread and inducing inflammation at distant sites resulting in Alzheimer’s disease, as well as a host of cardiovascular diseases. These relationships are not linear— stress/cortisol, genetics, diet, and obstructive sleep apnea play confounding roles.
  • 12. 12 MMP-9/TIMP-1 imbalance induced in human dendritic cells by Porphyromonas gingivalis. Monocytes may be used as a vehicle for transporting PG. PG can stimulate cytokine production and survive in monocytes. Microbial Hijacking of Complement–Toll-Like Receptor Crosstalk: Pathogens may not simply undermine complement or TLRs as separate entities, but may also exploit their crosstalk pathways. Oral administration of P. gingivalis induces dysbiosis of gut microbiota and impairs barrier function leading to dissemination of enterobacteria to the liver Copper exhibits antimicrobial activity against PG by reducing planktonic & biofilm growth & invasion of host epithelial cells. Porphyromonas gingivalis Infection Reduces Regulatory T Cells in Infected Atherosclerosis Patients. MMP-9/TIMP-1imbalance induced in human dendritic cells by Porphyromonas gingivalis. Blood-brain barrier dysfunction by regulation of the MMP-9/TIMP-1 balance. PG exacerbates brain amyloid deposition and triggers brain inflammation, leading to enhanced cognitive impairment. Immune-Altering & Manipulating Microbiome-Disrupting Immune response deposits Cu Alters Regulatory T-Cells Breaks Down Blood Brain Barrier Initiates Neuroinflammation Promotes Monocyte Migration by Activating MMP-9 Immune-Evading & Translocating P. gingivalis
  • 13. 13 P. gingivalis initiates neuroinflammatory diseases, specifically Alzheimer's “The data from the human brains and that from the in vivo mouse study suggested specific associations of P. gingivalis with AD inflammatory pathology.” “The keystone hypothesis of Hajishengallis et al. helps to explain the contribution that P. gingivalis may cause the early development of a neurodegenerative condition such as Alzheimer’s disease. In our view, P. gingivalis (highly virulent strains) access the CNS during healthy stages but only those individuals with inflammatory susceptibility traits are likely to develop progressive inflammatory component representing neurodegenerative disease processes.” Sim K. Singhrao, Alice Harding, Sophie Poole, Lakshmyya Kesavalu, and StJohn Crean, “Porphyromonas gingivalis Periodontal Infection and Its Putative Links with Alzheimer’s Disease,” Mediators of Inflammation, vol. 2015, Article ID 137357, 10 pages, 2015. doi:10.1155/2015/137357
  • 14. 14 Oral pathogens found at the site of beta amyloid deposits in 98% of Alzheimer’s brains and non-existent in all but 7% of the non- Alzheimer’s brains. ORAL ORIGIN OLFACTORY BULB (First sign of AD is loss of smell) ENTORHINAL CORTEX (First site of AD destruction & AB) Miklossy J. Alzheimer's disease - a neurospirochetosis. Analysis of the evidence following Koch's and Hill's criteria. J Neuroinflammation. 2011;8(1):90.
  • 15. 15 AdVax Targets: Class II Pathogens Class II pathogens are resistant to current vaccine and monoclonal antibody technologies due to their ability to use molecular decoys, mutate and exist in numerous strains Vaccines are the only known medical product that can be given to prevent infection by Class II pathogens. Unmet and completely open multi-Billion dollar markets exist for multiple pathogens.
  • 16. 16 AdVax, in partnership with BMI, has the exclusive technology to overcome deceptive imprinting. How do Class II Pathogens Accomplish this Feat? DECEPTIVE IMPRINTING
  • 17. 17 BMI holds background and genus species specific patents for target vaccine proteins in infectious diseases areas for humans and animal health. BMI has exclusive worldwide license for Immune Refocusing Technology from the National Institutes of Health. BMI and AdVax co-own new identified Red Complex oral pathogens (Initial immune refocused P. gingivalis and T. denticola patents pending.) Biological Mimetics, Inc. AdVax Intellectual Property in Partnership with BMI Biological Mimetics, Inc. (“BMI”) was formed in 1996 to commercialize innovative pharmaceutical products that will improve the quality of life and overall state of public health by combating resistant and emerging diseases in human and veterinary medicine.
  • 18. 18 AdVax Solutions 6 mos. – 1 year ORAL GENOMICS 2 years DIAGNOSTICS & THERAPEUTICS 3-6 years VACCINES First-of-kind salivary diagnostics performed by physicians to determine microbial burden & subsequent risk for inflammatory disease REVENUE: $25 - $50 million per year Early detection & prevention of disease Paradigm-changing diagnostics, medical devices, and monoclonal antibody-based therapeutics REVENUE: $100 million/year & a solution for prevention & early detection of Alzheimer’s disease Next-generation prophylactic, microbiome-sparing vaccines REVENUE: $1 - 2 billion/year & a cure for one cause of Alzheimer’s disease
  • 19. 19 Vaccine, Nanobody, & Monoclonal Antibody Development Timeline Acquisition of a broad array of clinical strains of each species (N = 10) of periodontal pathogen associated with AD Map IDNPE’s on bacterial targets (n=1-2 bacterial sp.) Sequence a minimum of 20 strains of each periodontal pathogen (N = 200) Engineer IRT mutations into bacterial targets (n= 2-4 targets with5-10 IRT mutations per target) Perform comparative genomics on each species including supragenome modeling, identify core genes, identify core gene subset under immune selection for each species Express IRT bacterial proteins in commercially licensable systems/ Prepare recombinant proteins for at least 4 candidate core genes for each species and collect human sera from AD and periodontal patients. Immunogenicity studies in 2 lab animal species Determine which of the candidate core proteins react with human serum from patients with periodontal disease creating an active target list 4 months 6 months 2 months 6 months 3 months Quarter 1 Quarter 2 Quarter 3 Quarter 4 COMPLETED Ehrlich DGH Studies – Sequencing & Molecular Cataloguing Nara IRT Vaccine & Monoclonal Antibody Development
  • 20. 20 Diagnostics Timeline 6 month time frame TEST 1: SALIVARY DIAGNOSTICS First-of-kind salivary diagnostics performed by physicians to determine microbial burden & subsequent risk for CVD, Alzheimer’s, RA, Diabetes, Glaucoma, etc. TEST 2: BUCCAL INFLAMMATORY TESTING Determines inflammatory risk for Alzheimer’s disease. MARKET-READY DIAGNOSTICS RESEARCH & DEVELOPMENT RESEARCH & DEVELOPMENT COMPLETED
  • 21. 21 Product Launch Timeline Year 1 Year 2 Year 3 Year 4 Year 5 Year 6 Salivary Diagnostics & Advanced Inflammation Testing Value Inflection Point Salivary Diagnostic Revenues Value Inflection & Exit Point* Animal Ready, First-in-Man Vaccines & mAb Therapeutics for AD & CVD causing pathogens. First-in-Man Vaccines & mAb Therapeutics for AD & CVD causing pathogens. Full body scan for early detection of AD Value Inflection & Exit Point* Value Inflection & Exit Point* Value Inflection & Exit Point* *Capitalizing on existing relationships with Big Pharma Value Inflection & Exit Point*
  • 22. 22 Multiple exits: Phase 1, Phase 2a/2b Value Inflection Points: Discovery, IND Filing, Phase 1, Phase 2 THE RETURN Seed Bridge Funding: $500,000 MET Series A Funding: $2-5M Series B Funding: $10-15M CAPITAL NEEDS Series A/B funding opportunities are being sought for the company's financing of both the development of novel point of care diagnostics worth $100s of millions per year and monoclonal antibodies and vaccines worth more than $1-2 billion per year. INVESTMENT OPPORTUNITIES
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