EFTA00506107.pdf

DACART CAPITAL LLC San Francisco, California: Where Biotechnology Was Born EFTA00506107  ED.Z..ART CAPITAL LLC DaCart Life Science DaCart Cleantech INVEST IN ENDURING INVESTMENT THEMES - HEALTH OF HUMANS - HEALTH OF THE PLANET EFTA00506108 DaCart Investment Charter Focused on funding Humanitarian Projects that are based on breakthrough technologies designed for the benefit of human health, and the health of the planet. DACAR C_APII AL LL, EFTA00506109 Investing in High Technology • Russian wealth needs investments in stable economies & access to centers of innovation (Silicon Valley) • European economies remain vulnerable • Investors need diversification • Various economies • Different industries • Mix of risk levels • Demand for life science and cleantech independent from economic growth DACAR C_AF'11AL LL, EFTA00506110 DaCart Capital $160 - $210M USA Life Science European Life Science Fund #1 Fund #1 $75M - $100M $50M - $75M ■ $75M Institutional ■ $30M Institutional ■ 10 Units @ $2.5M/Unit ■ 8 Units @ $2.5M/Unit ■ Available/Optional ■ Available USA Cleantech Fund #1 (USivt ■ $25M Institutional ■ 16 Units @ $625K/Unit ■ Available DAGAR C_APII AL LL, EFTA00506111  David Carter, Managing Director • 25+ years executive-level experience • Chairman, CEO/President - 7 companies • Co-founder - 3 companies • 3 , 1 IPO • >$500M raised • Vision - Leadership - • Track record • r I have the ability to aisringuisn " interesting science from a good investment. DACAR I C API JAL LLC7 EFTA00506112 The Case for Investment ■ Investment opportunities identified ■ First 4 investments are teed up • Short time & limited capital to profit/liquidity ■ Managing Director's hands-on involvement • Competitive fees - 2%/20% DACARTGAPIIAL LLC, EFTA00506113 The Case for Investment • Biotechnology • Big markets - big valuations • Big need - big pharma • Modern medicine • Clean Technology • Green chemistries - here now • Clean power - next generation batteries/solar are coming DACAR I CAPI IAL LL, EFTA00506114 DAC AR T C: API JAL L LC2, EFTA00506115  Maji Therapeutics Intra-op Post-op (8 months) EDA.GART IAL LLC7 EFTA00506116  Maji Therapeutics Sham Control Treated Mag x4 Mag x40 DACAR I CAPI TAL LLC:. EFTA00506117 Normal Vein Structure -5 4M. ••=.• a•In. aNIMP ••=i• aNIMP Lumen Endothelial cells Intima E c aNIMP MIN• 711.• ,<_•■••• •■•• •111.• a<- Media 110 .Mi• aNIMP MIND laminae Pratm Adventitia 1 111 DAGART,APITAL LLC, EFTA00506118 Injury to the Vessel During Surgery ., ,. •• C 4.1•• -->, aN•P , >, > 4•1I•P .'"' .C_________, .•IM. , , ••••• , csdol-helial cells E,astc .11.• dr° lon, ce Adventitio DAGAR I ,AVIIAL EFTA00506119 Growth factors, cytokines leading to smooth muscle cell proliferation MQ > <sic> ilINIP _> ______41INIP __≤.___; 4WD ________> ilINIP __________4i ----- a <- CIMP ,.> C., °o o 0 0 o o o Lumen Endothelial cells Intima Growth factors, cytokines 0 0 0 0 00 00 Elastic: 4=D laminc: 4IMMID IMP 4IMIP Fibroblasts, fat cells, interstitial matrix Adventitia DACART CAPITAL LLC7 EFTA00506120 Mechanism of Neointimal Thickening Medial SMC proliferation () 0 0 0 0 0 0 0 Lumen Endothelial cells Intima Growth factors, cit6b%-- oc) 00 la IMP Fibroblasts, fat cells, interstitial Adventitia IDACART CAP' JAL LLC7 EFTA00506121 SMC migration and neointimal lesion development and graft failure Fibroblasts, fat cells, interstitial matrix Adventitia DACART CAP' LLC: EFTA00506122 Delivery of Virus IMP ONE& <ism - <sm. etEc, Lumen Endothelial cells Intima Growth factors, cytokines Adventitia DACAR I C.APIIAL LLC7 EFTA00506123 Virally mediated prevention of SMC proliferation Elastic IaminaF Aaventrria DACART CAPITAL LLC:. EFTA00506124 Prevention of Graft Failure DAGART CAPITAL LLC EFTA00506125 Clinical Objective Lumen Endothelial cells Intima imilliglio < ,....____44m. il i um. 4mi. Media 411110. C .- 41INNIP _c - 4410110 V Adventitia u DACART C:API JAL LLC7 EFTA00506126 Maji Therapeutics • Modified to reduce systemic infectivity • Positive clinical safety data established • CMO protocols developed • History of successful large scale GMP production • Strong patent position • Pharmaceutical margins NV1020 vein graft saline solution permeable tube inserted into vein DIACAR I C:API IAL LLC7 EFTA00506127  Maji Therapeutics • High failure rate of bypass grafts • —45 % at 12 mo. — CABG • Novel, ex vivo HSV-1 therapy • Strong value proposition, very low COGS • 850,000+ annual procedures worldwide • $6.5 billion worldwide • Little to no competition et, "-kr. I et, A.'S A A 4)231V1 needed to reach 4)23UM enterprise value in 5 years DACARI CIAPI I AL LL, EFTA00506128 Maji Therapeutics ■ What Is It? A unique and patented method for preventing the failure of coronary artery bypass grafts. ■ How Does It Work? The genetically engineered therapeutic virus, with which the veins are perfused (prior to transplant), stops the rapid, smooth muscle cell growth on the interior walls of transplanted veins. This rapid growth of smooth muscle cells (called neointimal hyperplasia) occurs because the transplanted veins are not used to the hydrodynamic pressures they are subjected to when they are converted from veins to arteries . ■ Why Is It Important? 46.3% of all CABG procedures will experience at least one vein graft failure within the first year of surgery, principally due to neointimal hyperplasia. CABG patients who experience _ vein . graft failure have a dramatically higher . . incidence . . . of myocardial infarction, death, revascularizations and hospital readmissions. Reducing vein graft failure in CABG patients by 33% saves the payor at least $10,000 per procedure. DACART CAPITAL LLC EFTA00506129 Maji Therapeutics • Investment Thesis • CABG failure is "an unmet medical need". ▪ We have the intellectual property. • We have compelling preclinical data. • We can make a compelling pharmco-economic case for reimbursement. We can save more than the therapy will cost the payor. • The market potential for the therapeutic is $7.6B per year. • We can generate "pharmaceutical margins". THERE IS LITTLE TO NO COMPETITION. DACAR C:API IF•L LLC EFTA00506130  Prediction BioSciences • Over 2 million strokes in EU and the US alone each year (85% ischemic) Ischemic Stroke Occurs when oxygen-nch blood flow to the brain — $1 10 billion annual costs is restricted by a blood clot or other blockage. • Only one FDA/EMA approved clot buster -tissue plasminogen activator (t-PA) - $1.4 billion WW sales (2014) — $2 billion est. (2018) • t-PA causes fatal bleeding for 6 - 1 1% of treated patients • Presently, there is no reliable way to predict if a patient will suffer a significant bleed following t-PA therapy EDAGART C:API JAL LLC7 EFTA00506131 Prediction BioSciences First-to-Market Combination Diagnostic/Therapeutic For Ischemic Stroke Biosimilar of t-PA Producing t-PA in lab Biosimilar t-PA Clinical program is developed COGS: 12% of dose Screens 100% of bleeders Point of Care FDA/EMA approved platform Companion Results <15 min Diagnostic 5 patents; expiring 2032 (c-Fn) COGS: $10/test DAGART C:API 'AL LLC7 EFTA00506132  Prediction BioSciences • One approved product (off-patent t-PA) to treat -1.7 M ischemic stroke episodes annually (US & EU only). • 30 - 50% of patients treated with t-PA will experience bleeding events, 6 - 1 1% are fatal. • First-to-market therapeutic-diagnostic combination that eliminates the significant risks and liabilities associated with t-PA therapy. • Improved safety profile with similar efficacy drives rapid penetration of existing t-PA patient base and opens new opportunities for market expansion. • Strategic investor in place to cover $17.5 - 24.5 M (65 - 90%) of r-nnitnl rp,ni iir rnPntc thrni inh ('YE 9n1R $9.3 M needed to reach $150 M enterprise value in 2 years, $25.9 M needed to reach $500M enterprise value in 4 years. DACAR I CAPI IAL LLC EFTA00506133 Prediction BioSciences • What Is It? A biosimilar to t-PA and companion diagnostic for the prevention of bleeding episodes in ischemic stroke patients. • How Does It Work? Prediction BioSciences' proprietary "theranostic" approach employs a proprietary, rapid diagnostic that selects only those stroke patients with the highest safety profile for treatment, and then treats them with a proprietary biosimilar to t-PA. • Why Is It Important? Lack of effective patient screening results in less-than-desirable safety profile for t- PA, the only approved acute treatment for the -1.7 M ischemic stroke episodes occurring annually. .(EU & US). This results in only 40% and 25% of eligible Patients receiving treatment in the EU and US, respectively. A prealcTive screen forbleeding episodes in stroke patients would capture _ _ • _ • _ _I _ • significant share of the existing $1.4 B WW (12% AGR) market, and further expand this market opportunity by 2x and 3x in the EU and US, respectively. DACAR I CAPIIAL LLC7 EFTA00506134 Prediction BioSciences ■ Investment Thesis • Strong market need - 30-50% of ischemic stroke patients treated with t-PA will experience bleeding episodes, 6-1 1% of which are fatal. • Highly differentiated product (better safety profile, only proprietary, bundled offering) in an large ($1 .4 B) and growing (12% AGR) market. • Short path to commercialization (42 - 48 months) due to advanced state of development & low regulatory hurdle. • Experienced management team with successful track record commercializing biosimilars and companion diagnostics. • Strong patent protection through 2032. • Commitments from strategic partner and other non-dilutive funding sources limit dilution. • Other applications for anti-coagulants in cardiovascular disease I epleel I I JICy..I III IC.UI II UpJlUe. DACART CAPITAL LLC EFTA00506135 OvationBio DAC :ARi CArt !AL LLC2 EFTA00506136 Products Deposited in Eggs DAGAI,T,APITAL LLC EFTA00506137 Polyclonal Antibodies Monoclonal Polyclonal • In Di.Cnar Cnrirni ttc in k Multivalency Increased avidity ncrea sed p eoe frtectnocry 4 function EFTA00506138 OvationBio We can produce entirely novel molecules in several multi-billion dollar markets. • Huge market opportunity • Enzyme Replacement Therapy - $15.0 B • Polyclonal Antibodies: c. difficile, MRSA - $10.0 B • Factor VII Deficiency - $5.8 B $25M needed to reach $200M enterprise value in 3 years DACAR1 C: API I AL LL, EFTA00506139 OvationBio Avian facility Cell Culture Facility Facility cost Facility cost $22.5 M (@$450/sf) $625 M (@ $25K/L) 15,000 chickens 25,000 L (1g/L) 1000 kg per year 25 Kg X 40 runs $50/g for therapy 1000 kg per year $50/g for therapy Revenue $50.0 M Revenue $50.0 M Opex 3.4 M Opex 17.5 M EBITDA $46.6 M EBITDA $32.5 M Net Income $26.9 M Net Income ($55.5 M) Payback period <12 months Payback period D"ClART CIAPIIAL EFTA00506140 OvationBio • What Is It? The egg - a novel bioreactor. A patented manufacturing platform, with proprietary genes and novel manufacturing methods for the production of therapeutic enzymes, and human sequence monoclonal and polyclonal antibodies. • How Does It Work? OvationBio selects the most active and effective protein for our application. By using our proprietary transgenesis technology, we introduce the gene for this protein into primordial germ cells to create transgenic chicken strains. These transgenic chicken strains produce these proteins in the eggs they lay. The protein is then purified from the eggs for therapeutic applications. %AIL... I.. It WY ily iz II IIIIF.JVIIlJl I1. OvationBio technologies enable the development of completely novel, pLA ICI IllAL/IG I I IUICk.-UIG II IU I UUI I I.JG IJILJUUUCLA II I IUUIIIIIG3 UI I /...)U VI I I IC l_,UpllUI cost and 1/7'h of the operating costs associated with current production technologies. DACAR I C:API IAL LLC: EFTA00506141 OvationBio Investment Thesis ■ Our patented manufacturing platform yields significant reductions in capital (30x) and operating costs (7x). ■ Current market opportunity for enzyme replacement therapy, polyclonal antibodies, and factor VIII deficiency is >$30 B. ■ We already have a significant investor/strategic partners willing to participate, and non-dilutive funding is available. ■ We have experienced scientific and management teams that have successfully done this before. ........ DACAR I ("API I AL LLC7 EFTA00506142 C ncentRx TARGETED BIOTHERAPY DACAR T C 'AL I Lc EFTA00506143  ConcentRx T-Cells Ready to Infuse O (Day 15) og T-cells Target Autologous Blood Oncolytic Agent Tumor Activated to (vvDD) into And Release Express T-cell T-cells Agent To Tumor targeting tumor antigens NkG2D C Cell (48 hrs) Tumor Blood Vessels Tumor Eradication (4 - 8 hrs) DAC AR T C API IAL LLC EFTA00506144  ConcentRx A cell-based therapy platform that is fully automated, high throughput, scalable, and lower cost that allows a patient's cells to be activated and propagated at the point of care with specific and optimized therapeutic function. Cell Propagation/Concentration incubator GMP 11.--L or Oncolytic Reagents agent Introduced I_ ntroduced ipatient Cell Activation Incubator Infusion Preparation DACARI CIAPI I AL LL, EFTA00506145 ConcentRx Clinical studies (e.g. Dendreon, Juno) have unequivocally shown that combining an appropriate autologous immune cell with an appropriate tumor cell antigen can achieve a demonstrable oncolytic effect in humans. The ConcentRx technology platform further advances the state of the art in autologous immune cell cancer therapies by: • Employing the patient's own enriched, activated T cells as a delivery vehicle to protect the oncolytic agent from the patient's immune system prior to reaching its target. • Highly efficient targeting by employing an abundant and specific tumor cell antigen (NkG2D). • Conferring long term to tumor post therapy • Incorporating simplified, cost-effective, and scalable immunotherapy production at the point of care. DACAR 1 C:API JAL LLC7 EFTA00506146 ConcentRx ■ What Is It? A proprietary technology platform that adds critical therapeutic function to a patient's own cells, and allows the formulation of specific strategies to treat disease with a precision medicine approach. The platform enables simplified, scalable and cost-effective therapeutic production at the point of care. ■ How Does It Work? In the ovarian cancer application, autologous blood cells are drawn from the patient, these cells are activated to express molecules that target tumor antigens (NkG2D). An oncolytic agent (vaccinia virus) is incorporated into the targeting T- cells, the T-cells are injected into the patient, where they then target the tumor cells, release the oncolytic agent into the tumor cells, and eradicate the tumor cells via lysis. ■ Why Is It Important? The technology platform produces oncolytic agents that are highly tumoricidal, and after therapy there is sustained immunity against the cancer type that was Treatea. ine piarrorm nas me potential To Target an Tumor Types, ana IT can conrer sustained immunity to all tumor cells (both bulk tumors and metastatic disease). DACART CAPITAL LLC.L' EFTA00506147 ConcentRx Investment Thesis • Poised to quickly file IND with unprecedented preclinical data in an area of high unmet medical need - ovarian cancer. ▪ Both components of the dual biotherapy (CIK cells, vaccinia virus) have been extensively vetted by the scientific and regulatory community, and have both been FDA approved for human therapy. ▪ Platform technology play in autologous cell-based immune therapy • production of therapy for other partners in the space • joint development deals with companies seeking to develop autologous therapies • own product portfolio ▪ Scientific and managemetR-t team has a proven track record. DAC ART C_ API JAL LLC: EFTA00506148 ConcentRx Broadly enabling technology platform in autologous cell- based immunotherapy. • Next generation cancer immunotherapy • Regenerative medicine for organs & joints • Immune system prophylaxis and restoration $5 M needed to reach $40M enterprise value in 18 months. $25M need to reach $300M enterprise value in 4 years. DACARI CAPI I AL LL, EFTA00506149 Summary • Investment opportunities identified • 4 projects teed up • We are hunting "big game" • Short time & limited capital to profit/liquidity • I have hands-on experience doing this successfully • Competitive fees — 2%/20% Target >25% ROI for the portfolio. 3x return in 5 years, 5x return in 7 years DACARI CAPI I AL LL, EFTA00506150 Return on Investment Xenogen Jan-98 Aug-06 Nov-1 1 Series C Calper acq. Perkin Elmer acq. $14 M $62 M $210 M $1.00 18.8% IRR $4.31 $1.00 21.1% IRR $14.58 Cobalt Biofuels Mar-07 ,„„-13 II Series B Series E $17M $1 17M cr nn 4)O& / nn 4) 1 .UU 36.2% IRR .OO DiNGART C_APIIAL LL, EFTA00506151 Advisory Board Thomas Shenk, • Dr. Shenk is the Elkins Professor in the Department of Molecular Biology at Princeton University. Professor Shenk is the recipient of the Eli Lilly Award from the American Society of Microbiology, an American Cancer Society Professorship and an Investigatorship from the Howard Hughes Medical Institute. He is a past president of the American Society for Virology and a past president of the American Society for Microbiology. He is currently a member of the National Science Advisory Board for Biosecurity, and a member of the Board of Directors of CV Therapeutics, and Merck and Company. Robert Dow, BSc MBChB FRCP (Edin) Dr. Dow's current position is as Vice President of Strategic Product Development for PPD, a global Contract Research Organization. Previously, Dr. Dow served as Chief Medical Officer and Senior Vice President of medical affairs at Cell Genesys. He oversaw all clinical, regulatory and medical affairs activities associated with Cell Genesys' product portfolio. Prior to Cell Genesys, he was Chief Executive Officer of Biolitec Pharma Ltd., a U.K.-based biotechnology company, and also previously held senior executive positions with Quantanova and Scotia Holdings, plc. Prior to that, Dr. Dow was head of Global Drug Development with Hoffman-La Roche in Basel, Switzerland and previously was with Syntex Corporation for over 10 years in various senior positions in drug development. Dr. Dow holds a B.Sc. in Medical Science from the University of St. Andrews and his medical qualification, an MBChB degree, from the University of Dundee in Scotland. He also is Fellow of the Royal College of Physiciansof Edinburgh and a Fellow of the Faculty of Pharmaceutical Physicians. DACAR I CAPITAL LLC7 EFTA00506152 Advisory Board Pamela R. Contag, Dr. Contag most recently served as Founder and CEO of Cobalt Technologies, Inc. a venture- backed biofuels company, and raised $40M dollars and placed Cobalt in the top 20 clean tech companies in the US in 2008. Prior to Cobalt, she served as Founder and President of Xenogen Corporation from 1995-2006, with an IPO in 2004 and a merger with Caliper Life Sciences in 2006. She has 36 issued patents and over 65 publications in the field of Microbiology and Engineering and she is a founding Board Member of the Startup America Foundation. Howard Pien Mr. Pien most recently served as Chairman of the Board and CEO of Medarex, Inc. from 2007 to its acquisition by Bristol Myers Squibb Company in September 2009. Prior to that, he was a private consultant from 2006 to 2007. Prior to that he served as President and CEO of Chiron Corporation from 2003 to its acquisition by Novartis AG in 2006. Prior to that he served in various executive capacities for GlaxoSmithKline plc (GSK) and its predecessor companies, culminating in his tenure as President of GSK's International Pharmaceuticals business from 2000 to 2003. Prior to joining SmithKline Beecham plc Mr. Pien worked for six years at Abbott Laboratories and for five years at Merck & Co. Mr. Pien is also a director of Vanda Pharmaceuticals and ViroPharma Incorporated. DACAR 1 CAPIIAL LLC EFTA00506153 References • Michael Eisenson - Charlesbank, Managing Partner • Alan Salzman - VantagePoint, Managing Partner • Kevin Hrusovsky - Perkin Elmer, President of Life Sciences & Technology • Dan Junius - Immunogen, CEO • Al Sommers - JHU, Former Dean, School of Public Health 111 • Chris Jones - J Walter Thompson, former CEO • Bill Halter - Lt. Governor, Arkansas DAC .ART C:APITAL EFTA00506154  DACART CAPITAL LLC San Francisco, California: Where Biotechnology Was Born EFTA00506155