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Adventures in Biotechnology

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Title: Adventures in Biotechnology


1
Adventures in Biotechnology Boro Dropulic PhD,
MBA
2
Overview
  • Background
  • Decision to Start a Biotech
  • Biotech Business Models
  • Financing of Biotech Companies
  • Modes of Productivity Relationship to Business
    Models
  • The relationship between Business Models and
    Investment
  • Case Study Lentigen Business Presentation

3
Background
  • PhD in Australia (University of Western
    Australia)
  • Fogarty Fellow at NIH Bld 10 then Bld 4
  • Embryonic Stem Cells
  • Gene Therapy
  • Johns Hopkins University
  • HIV vectors targeted to HIV infected cells (new
    IP)
  • VIRxSYS
  • First group to initiate and complete Lentiviral
    vector clinical trial (gene therapy for HIV
    infection)
  • MBA (Johns Hopkins University)
  • Lentigen
  • Broad business Model

4
Starting a Biotech Company
  • Defining the technology
  • Can the technology be used for multiple uses?
  • Licensing strategy vs starting a biotech company
  • If decision to start a company then
  • What are the objectives?
  • Sell the company to large biotech or pharma
  • Grow the company and license out products
  • Organization and focus of the company
  • Single product focus ? short term exit strategy
  • Multiple products ? long term exit strategy

5
Therapeutic Biotech Business Model
6
Milestone driven value - technology
7
Financing of Biotech
8
Financing of Biotech
OR Derive revenue streams from the sale of
product or services (research tools products
services) Smaller market potential - more
difficult to attract investors - revenue streams
are much smaller than the therapeutic or
vaccine markets - requires organic growth
strategies
9
The Very High Risk Nature of the Conventional
Biotech Business Model
  • High risk high failure rate
  • Especially true for biotech focused upon
    development of biologics
  • Failure not always related to science
  • Investor understanding of the technology and
    product development cycle time is very important
  • Financing strategy must match product development
    cycle time

10
Potential Saving Graces
  • Government Grants (SBIR etc)
  • Private Foundation Grants
  • Contracts (Government or Private/Foundation)
  • Out-license portions of the technology
  • Other financing models

11
Chimeric Business Models for High Risk
Technologies
Long Lead Times to Therapeutic Markets Gene
Therapy Cellular Therapies Stem Cell
Therapy Vaccines (viral vector) RNAi (viral
vector shRNAi)
Therapeutics
Therapeutics
Validation / Growth
Service / Research Products
Service / Research Products
Decreased Risk vs. Lack of Focus
12
Models of productivity
Geoff Race CFO Pangenetics Index Forum
2007 Stresa, Italy
Young Genius
Old Master
Femme à la resille (Woman in a hairnet), 1938,
by Pablo Picasso.
Still Life with Carafe, Sugar Bowl, Bottle,
Pomegranates, and Watermelon, 1906, by Paul
Cezanne
value
Paintings most valuable early work
Paintings most valuable late-in-life work
13
Comparison of Productivity Models
  • Young Genius
  • Innovation
  • Non-linear concept
  • Short term horizon
  • Rapid, immediate
  • Low of objectives
  • Single focus
  • Singularity of Purpose
  • Virtual simplicity
  • High Risk
  • No track record
  • Old Master
  • Experimentation
  • Process driven
  • Long term view
  • Quality mindset
  • Higher of goals
  • Competing priorities
  • Complexity/ Integrated
  • infrastructure
  • Low Risk
  • Track record

14
Comparison of Business Models
  • Single product Biotech Company
  • Innovation
  • Short term horizon
  • Low of objectives
  • Singularity of Purpose
  • High Risk
  • Concept Based Value Growth
  • Multiple product Biotech Company
  • Experimentation
  • Long term view
  • Higher of goals
  • Complexity/ Integrated
  • Low Risk
  • Linear Value Growth

15
Comparison of Business Models
  • Single Product Biotech
  • Innovation
  • Short term horizon
  • Low of objectives
  • Singularity of Purpose
  • Multiple Phases
  • High Risk
  • Concept Based Value Growth
  • ACQUIRED
  • Multi Product Biotech
  • Experimentation
  • Long term view
  • Higher of goals
  • Complexity/ Integrated
  • Lifes Work
  • Low Risk
  • Linear Value Growth
  • IPO - ALLIANCES

BOTH ARE VALID GROWTH STRATEGIES
16
Growth Strategy Needs to Match Investor Strategy
  • Investor Strategies
  • Large number of singly focused companies vs few
    technological platform companies
  • Shorter exit time for singly focused companies,
    but high risk
  • Longer exit time for technological platform
    companies, but lower risk
  • Investor Sophistication Important
  • Choice of Investor Critical for ultimate success

17
  • Company Presentation

January 2008
18
Safe Harbor and Confidentiality
  • The following information is confidential and
    should not be distributed without the permission
    of Lentigen Corporation. This presentation
    contains certain forward looking statements based
    on Lentigens current beliefs and expectations
    about future events. These statements are
    subject to numerous risks, uncertainties and
    assumptions and are not necessarily predictive of
    future results. Actual results may differ
    materially from those anticipated in this
    presentation depending upon a variety of factors
    including development of manufacturing
    procedures, market size and revenues, potential
    competition, regulatory compliance, operating
    effectiveness and other factors that may not be
    currently considered as material.

19
Summary
  • Lentiviral Vector (LV) gene delivery technology
  • Four phase I/II clinical trials in 2008/9
  • Eight NIH/DOD grants supporting future
    therapeutic pipeline
  • Alliance with ThermoFisher - LV RNAi research
    tools
  • Dominant Intellectual Property Position
  • Experienced management team and board of
    directors
  • Upcoming Milestones

20
Lentigen Overview
  • Established 2004
  • Location
  • Gaithersburg, Maryland 2008Q1
  • 25,000 ft2 multi-product GMP facilities
  • Employees 40
  • Technology platform focus
  • Lentiviral vector mediated gene delivery
  • Areas of application
  • Vaccines Therapeutics
  • Research and Drug Discovery Tools

21
Lentiviral vector (LV) gene delivery
  • Most efficient, stable gene delivery system known
  • LentiMax LV system
  • High titer, low toxicity
  • Scalable manufacturing process
  • Bench to clinic translatability

22
Efficient stable gene delivery with LV-GFP
(Green Fluorescent Protein)
Cells before addition of LV-GFP
98.7
Cells after gene delivery with LV-GFP
Human kidney cells
23
Vaccine Therapeutic Pipeline
INDICATION GLIOBLASTOMA CANCER
(GVHD) INFLUENZA VACC. ANEMIA HEPATITIS
C LEUKEMIA (CLL) COR. ARTERY DIS. LYMPHOMA
(EBV) HEMOPHILIA MELANOMA
24
Glioblastoma
  • 18,000 per year (USA) cases with comparable
    market in Europe
  • 50 malignant with 40 week survival
  • Market size estimate - 300 million
  • Easily addressable patient population
  • Patients concentrated at surgical centers
  • Limited sales force
  • Targeted physicians
  • No good current treatment available
  • Treatments limited by toxicity Temezolomide (TMZ)
    effectively treats disease
  • but prolonged TMZ treatment results in severe
    lymphopenia and thrombocytopenia ? death

25
Glioblastoma therapy using LV-MGMT
  • Protection of stem cells from TMZ toxicity
  • ? longer TMZ treatment
  • ? better outcomes for patients
  • LV-MGMT can protect stem cells from effects of
    TMZ
  • Proof of concept shown in dogs and monkeys
  • Clinical trial endpoints are short 3 weeks
  • CWRU (Dr S. Gerson)
  • Broadly applicable
  • CML, AML, HIV etc
  • IP exclusively licensed

TEMEZOLOMIDE
LV MGMT
KILLTUMOR
PROTECT STEM CELLS
STEM CELLS
Bone Marrow Transplantation
26
Graft versus Host Disease (GVHD)
  • In 2005 7,250 allogenic transplants in USA and
    10,000 worldwide
  • 50 develop chronic GvHD
  • Market size estimate - 300M to 500M
  • Potential for huge savings to healthcare system
  • Easily addressable patient population
  • Patients concentrated at transplant centers
  • Limited sales force
  • Targeted physicians
  • No good current treatment available

27
GVHD therapy using LV-TMPK
  • Two technological advances
  • LV efficient gene delivery
  • TMPK human safety gene
  • Proof of concept shown in primary human T cells
  • Short clinical trial endpoints 3 weeks to 3
    months
  • CRADA with NIH 2 sites Drs Gress, Fowler,
    others
  • Broadly applicable to other diseases cancer,
    HIV etc
  • IP exclusively licensed

DONOR
28
Pandemic Seasonal Influenza
  • Influenza infects 10-20 of the population every
    year and causes 500,000 deaths
  • Approximately 300 million doses produced globally
  • Market Size 1B in 2004, rapidly expanding
    market
  • Need for vaccine MFG efficiencies
  • Egg manufacturing not cost effective
  • Cell culture with L.A. virus is limiting
  • Need for development of a rapid and efficient
    cell culture based vaccine manufacturing platform

29
LV-IFVX Influenza VLP vaccine
Synthesized gene cloned into LV 1 week
  • Rapid manufacturing platform
  • weeks not months MFG time
  • Virus Like Particles (VLP)
  • highly immunogenic
  • Exact strain match
  • no genetic drift during production
  • Continuous production of VLP
  • advantage over batch production
  • Safe
  • VLPs are genetically inactive
  • IP protected

LV manufacture and QC testing 1 week
LV transduction 1 day
Scale Up cells 3 weeks
Vaccine Purification 1 day
30
Potent Immune Response in Mice
Strong immune response generated in mice against
Lentigens H5N1 VLP vaccine (blue) and vaccine
with adjuvant (purple) pre-bleed controls (red)
31
Biogenerics Proprietary Biologics
  • Biologics that are coming off-patent are worth
    30B
  • Erythropoietin, cytokines, coagulation factors,
    antigens, McAbs
  • COGS critically important for competing in the
    protein MFG markets
  • Efficiencies gained by decreasing time to market
  • Efficiencies gained by increasing yield from cell
    lines
  • LVs can reduce time to market and decrease COGS
  • High copy numbers in cells without gene
    amplification
  • Integration in areas of open chromatin ? higher
    expression

32
Erythropoietin production
  • Gold Standard
  • Efficient
  • Bulk CHO Cells 2.5 g/L
  • No cell cloning
  • No selection
  • No enhancement of cell growth conditions
  • Levels of 5 10 g/L attainable with isolation
    of cell clones

33
Research Drug Discovery Tools Pipeline
RESEARCH DEVELOPMENT
PRODUCT LAUNCHED
PRODUCT SMARTVECTOR RNAi CUSTOM
LVs LENTI-GFP, YFP, LUC LV MFG (GLP,
GMP) PROTEIN EXPRESSION LENTIKIT LENTI
PROMOTER LENTI cDNA LIBRARY LENTI RNAi
LIBRARY LENTI EXPRESS KIT LENTI CELL LINES
  • Alliance with ThermoFisher Scientific to market
    LV RNAi products

34
SMARTvector RNAi Effective gene silencing
GAPDH knockdown 9 days post-transduction with
SmartVector shRNAi Lentiviral vector particles
SHSY5Y neuronal cells Fixed and stained with
GAPDH antibody (red) and Hoechst (blue)
35
Effective gene silencing in a wide variety of
cells
Neuronal cells
Stem cells
Suspension cells
Suspension cells
75
Difficult-to-Transfect
36
Intellectual Property
  • Dominant patent estate for Lentiviral vectors
  • Lentigen (GBP IP) has acquired the entire Cell
    Genesys Lentiviral vector IP portfolio
  • Non-provisional patent coverage of
  • Novel LV compositions and methods
  • Use of LVs for Influenza VLP manufacturing
  • Use of Novel LVs for protein manufacturing
  • Lentigen has exclusively in-licensed several key
    payload technologies
  • TMPK LentiSafe technology
  • MGMT LentiSelect technology
  • Lentigen continues to develop and in-license
    additional key proprietary intellectual property

37
Grants
  • Seven (7) SBIR Grants from National Institutes of
    Health
  • Leading Clinical Centers Investigators
  • Oncology
  • Infectious Diseases
  • STTR Grant from Department of Defense
  • Efficient Manufacture of Monoclonal Antibodies in
    the National Stockpile
  • MIPS Grant
  • Development of new animal models for cancer

38
Experienced Management
  • Boro Dropulic, PhD, MBA - Founder and CEO
  • 19 years experience
  • Founder CSO of VIRxSYS, Johns Hopkins
    University, NIH
  • Sponsor Investigator of first Lentiviral Vector
    Clinical trial in humans
  • Adam Sachs, MSE President, Commercial
    Operations
  • 23 years experience
  • Life Technologies (now Invitrogen), Qiagen,
    Origene
  • Global Director for Manufacturing at Qiagen
  • Gregory Feulner, PhD, JD VP, Business
    Development
  • 19 years experience
  • NIH, Johns Hopkins, Gene Logic Inc., Galileo
    Genomics, 3M
  • Yung-Nien Chang, PhD VP, Vector Development
  • 22 years of experience
  • Johns Hopkins University, VIRxSYS, NIH, GTI (now
    Novartis)

39
Board of Directors
  • David Wetherell Chairman of the Board
  • Former Chairman, CMGI,
  • Founder, Greenwich Biotech Ventures
  • Boro Dropulic, PhD, MBA
  • Douglas Lind, MD
  • Managing Partner of Accendx Management LLC
  • Former Senior Biotech. Equity Analyst at Morgan
    Stanley PaineWebber
  • John McMullen, JD, MBA
  • Managing Principal of Cambridge Meridian Group
  • Republican Nominee for Senate, VT (2004)
  • Robert Breyer
  • Former President/COO of Alkermes
  • Former President and General Manager of Eli Lilly
    Italy
  • Barrie Carter, PhD
  • EVP and CSO of Targeted Genetics
  • Former Chief of the Lab. of Mol. Cell Biology
    at the NIH

40
Upcoming Milestones
  • Initiate phase I/II clinical trials for GVHD
    Glioblastoma
  • Complete pre-clinical studies for Influenza
    vaccine and Erythropoietin protein product
  • Continue development of pipeline for therapeutic
    vaccine products, leveraging grant funding
    mechanisms
  • Expand alliance with ThermoFisher and other
    partners
  • Certify Lentigens new GMP manufacturing
    facilities
  • Complete additional financing

41
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