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Project Koenig

Information Memorandum June 2012. Project Koenig. Transaction Summary. Genesis of Project Koeing US: The Backdrop. The Backdrop. Company’s Formation.

eric-grimes
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Project Koenig

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  1. Information Memorandum June 2012 Project Koenig

  2. Transaction Summary

  3. Genesis of Project Koeing US: The Backdrop The Backdrop Company’s Formation • Over last few decades, global Pharma companies experience rising competition and costs related to conducting research on patented molecules. Thus, they increasingly resort to outsourcing this research or acquiring commercially attractive and ready molecules, esp. Biotech product patents • During the last over 8-10 years, the price of biotech molecules grew substantially ranging between US$ 0.5-16.0 bn. and several large transactions took place with Pharma companies buying or licensing out these molecules from biotech companies • However, the scientists responsible for developing these molecules were rarely sufficiently compensated, leading to a significant level of frustration in the scientist community, On the other hand, the biotech companies walked away with huge profits • Also, while the society was benefited with new innovative products, they came at a high cost • Given his extensive experience in the Pharma and medical field, the key promoter of Project Koeing US (PK US), identified a unique opportunity of creating a ‘platform’ for research scientists wherein they could internally develop patented molecules at effective costs and reap financial rewards for their efforts • With this background, PK US was formed in year 2003 • Many well renowned scientists from the U.S. and India joined PK US as equity holders in the Company and are currently on the Scientific Advisory Board, guiding the development of molecules they have themselves developed • The Company’s entire research team is not only fully dedicated to serving the society with their research contributions but is also focused on providing the same at more economical rates that would not have been possible otherwise

  4. Brief Description • Project Koeing India (PKI) is the Indian subsidiary ofPK US and is currently one of the fastest growing biotechnology companies in India • The Company’s vision is “ To improve the quality of human life by assisting in the detection and treatment of cancer and various abnormalities’ • PKI has a unique business model of acting as an incubator of various molecules and technology platforms during their development process • The Company has already in-licensed patented molecules and technology platforms in 5 areas related to Cancer and other diseases in India. All these molecules or platforms are fully validated by important authentic agencies from the U.S. and India • Currently, the Company owns 65 patents • CAD: Ready for Market today The CAD based technology for diagnosis of breast cancer and other types soft tissueof cancers. It is a validated technology in the sense that the company has already received Bionexus status from the Malaysian Biotechnology Corporation Sdn. Bhd. And has been tested in over 400 cases in the US and proven to have an accuracy of 95%. Project Koeing: A Snapshot

  5. The Company Structure Project Koeing 100% equity 100% equity 100% equity 30% equity Sub 1 • The Company has been created for the commercialisation of Manufacturing technology platform for manufacture of recombinant protein Sub 2 • The Company has been created for the commercialisation of a novel platform based on nucleic acid technology. • The 1st product has already been shown to be safe and efficacious in cancer in Phase II human clinical trials and is all set for Phase3 studies with all approvals in place Sub 3 • The Company has been created for the commercialisation of A Immune system boosting cytokine technology for breast cancer Products Sub 4 Malaysia • This division would undertake development of Biotechnology and Medical device projects In Malaysia – Currently a CAD Based Breast Cancer detection Project has been developed and is ready to market

  6. Project Koeing India: A Unique Business Model Various Stages Licensing out/Sale of the Developed Molecules In-house Value Add during the Development Process • Once the development process is complete, Project Koeing India plans to license out or sell the developed molecules to global Pharma company that will launch these drugs into the market • Incase of licensing out, Project Koeing India will continue to hold all the patents related to the molecules/technologies, which can be further used to develop new technologies in related areas • The upfront payment received from the Pharma companies and the periodic royalties etc will be main revenue generators, which will be shared with the original creators of molecules/technologies In-licensing of Molecules/Technology Platforms • The Company aims to: • Create cheaper and effective drugs to fight cancer. The Company is able to significant reduce the development costs of molecules as compared to Pharma Generic companies • Quick turnaround of the process • The Company enjoys the unique advantage of having various renowned scientists besides the original creator of the molecule/technology that provide extremely valuable insights during the development processes of these molecules/platforms • Project Koeing India licenses out new molecules or a technology platform from Pharma companies and takes over the remaining development process. The original creator (scientist) of the molecule typically takes an equity stake in Project Koeing India • Project Koeing India manages the entire development cycle of the molecule/platform in a more efficient & cost effective manner Typical Timeline – 3/4 Years

  7. The Technology Platform Five Technology Platforms • PKI currently has its four pillars of success in form of the following molecules: • A Platform technology for bio-manufacturing of recombinant proteins in yeast-based expression systems; Cost of production to be reduced to 20% of the current manufacturing cost • A Novel RNAi based Platform: Novel class award winning technology for the treatment of colorectal cancer; The product had already gone through Phase I / II studies in the US, and has been cleared by US FDA; Phase III studies to be conducted in India • Affinity based Drug delivery technology: Novel Class of molecules; The entire preclinical trials have been completed in US and application is being prepared for submission to the DCGI seeking approval to conduct Phase I/II clinical trials in India for liver cancer • Immunotherapy: A Cytokine Patent owned by the company and under further development in the Indian lab (at a preclinical stage); Very effective in Leukimia, Renal Cell carcinoma and other Cancers. • CAD: A Non invasive Medical device using AI based algorithms for detection of Breast cancer and automated biopsy plus drug delivery Put together, these molecules have a market potential of over US$ 50 Bn.; PKI’ first exit of a Molecule/Platform is expected to take place in the next 18-24 months; Prospective collaborators for these technologies include Merck, Roche, GSK, Pfizer etc PKI’ various projects such as these have strong technological validates from institutions including US FDA, DCGI (India), Dept. of Science & Technology (Govt. of India), Malaysian Biotechnology Corp. etc Project Koeing is consistently working on creating its future pipeline of molecules/platforms etc and currently is in process of acquiring/licensing another 5-7 technologies

  8. Five Key Projects in the Pipeline CAD Tech – 3 Months A Medical Device platform technology for not only detection of various types of abnormalities like cancer but also automated Biopsy and drug delivery RNAi – 12 to 18 months A Phase III-stage clinical candidate that belongs to a novel class of molecules called ribozymes, which work by destroying mRNA molecules of target proteins; This is for the treatment of colorectal cancer Manufacturing Tech. – 6 months A platform technology for bio-manufacturing of recombinant proteins in yeast-based expression systems Key Projects in the Pipeline Affinity based drug delivery – 24 to 36 months An early clinical stage candidate that belongs to a novel class of molecules that work by organ targeted drug delivery; This is for the treatment of liver cancer Immuno-therapy – 60 months An early-stage program to discover and develop a Immuno Therapy based cytokine which will be able to help boost the immune response to fight against melanoma, Lymphoma and Rena cell carcinoma etc.

  9. Enhanced Protein Expression Technology – Manufacturing Tech. • Platform for bio manufacturing of recombinant proteins in yeast based expression systems; • Eventually the platform will also be extended to mammalian systems like CHO cells • This platform enables 5-10 fold increase in yield per unit, thus cost of production of proteins can be reduced to 20% of the current manufacturing cost • It is also a platform which has varied applications • In house work has shown and increase in Yeast cell productivity by a factor of 2 fold. Description Benefits Current Status • Technology creator is SALK Institute for Biological Studies • Dr. Martin, who had originally patented this technology, is also a shareholder in PKI • INR 45 mn has been awarded From World Bank Technology Development Funds through ICICI • A total of around US$ 60 mn have been spent on the molecule so far • Time to market is around 1 year, with a total market potential of around US$ 30 bn Technology Investors & Funding Time to Market & Potential This is an interesting technology to increase the yield of fermented products and the yield is as much as 5-10 times more in fermentation of recombinant proteins, leading to substantial decrease in production cost

  10. RNAi • RNAi based products is a novel class prize winning technology for the treatment of colorectal cancer • The mechanism of action of RNAi based products is mediated through Ribozyme; The result of RNAi based products in patients with high VegFr1 in colonic cancer patients are very high • Besides colorectal cancer, RNAi based products can also be used in the treatment of other types of cancer including breast cancer ,and weight reduction • RNAi based products has already undergone Phase I & II trials in the U.S. and the Phase III are to begin in the next couple of months; the DCGI approval for the same has been received by PKI Benefits Current Status Description • 2 Major Biotech companies had initially worked on this molecule and invested over US$ 245 mn; KPI took over project when the the JV between the 2 companies split as a result of them being bought out by other major Pharma companie. • RNAi based products patent has been well acknowledged by the Govt. of India and thus has been granted US$ 4 mn from Dept. of Science & Technology for its development • Time to market is around 12- 18 months, with a total market potential of around US$ 15 bn • Potential collaborators post the clinical trials include Pfizer, J&J and Otsuka, Aventis, Taiho etc. (Discussion have already been initiated with them. Technology Investors & Funding Time to Market & Potential The DCGI has approved it for Phase III clinical trials in India at 20 cancer centers. RNAi based products will most likely be the first product to hit the market in the next 18-24 months with a high success rate and huge market potential

  11. Affinity based Drug delivery • The Ligand technology is a mechanism by which the active drug molecule can be delivered to the targeted organ depending on the nature of the disease • The technology enables the specific Anti-Cancer drug needed to treat the tumor for focused delivery into the tumor • The first application targets liver cancer and comprises the cancer drug 5FdU linked to a second molecule that directs it selectively to the liver • The FDA awarded Orphan Drug Status to the same that puts the drug on a fast track for approval • An IND application has been prepared and is ready for submission to the DCGI seeking approval to conduct Phase I/II clinical trials of LIV-1 in India for liver cancer Description Benefits Current Status • Technology creator was a Maryland based Biotech company under a JV with John Hopkins and as mentioned above, it has been validated by US FDA • A total of around US$ 40 mn have been spent on the molecule so far • Time to market is around 3 years, with potential market collaborators including Pfizer • Market potential is around US$ 3 bn Technology Investors & Funding Time to Market & Potential LIV1 is an early clinical stage candidate that belongs to a novel class of molecules that work by organ targeted drug delivery and is targeted at treating Liver related cancers

  12. Immuno Therapy • The Immunotherapy, is an early-stage program to discover and develop a Cytokine based product for treating various immune based cancers like Myloma, Lymphoma and Renal Cell Carcinoma • While the product is at an early stage of development, it is believed to be very beneficial for breast and other kinds of cancers • The tech works in threeways: • Blocking tumour angiogenesis (new blood vessel formation) • Inhibiting tumour cell proliferation by sequestering the growth factors • Limiting tumour metastasis by inhibiting tumour cell migration across semi-permeable barriers Description Benefits & Current Status How it works • Technology creator is researchers at NIH and PK US • The funding of INR 94 mn has been provided by grants and soft loan from the Department of Biotechnology, Government Of India • Time to market is around 6 to 7 years, with a total market potential of around US$ 2 bn • Potential collaborators include Novartis and GSK Technology Investors & Funding Time to Market & Potential Cytokine Technology is an early clinical stage gene therapy product that is targeted at treating Renal Cell Carcinoma, Myloma/ Lymphoma and other kinds of cancer

  13. CAD Technology • The CAD based technology for diagnosis of breast cancer and other types soft tissueof cancers. It is a validated technology in the sense that the company has already received Bionexus status from the Malaysian Biotechnology Corporation Sdn. Bhd. The Company in Malaysia will go intoproduction as soon as funding can be obtained. In Studies involving over 400 patients the technology has shown to have an accuracy of 95% with less than 1 false positive in 4 films. CAD Ready for Market today • Project Koeing has acquired an interesting technology for use in various asthmatic conditions. where the new spacers patented, developed, approved by US FDA can be of tremendous use in delivering much higher quantity of drug into the lungs as compared to the current traditional inhalers Spacer for Inhalation

  14. The Promoter Team • Graduate in Engineering from the US • Over 23 years of experience in Biotechnology- both in the US & India • Founder and Executive Vice President of a CMO [worked in using Mammalian and Yeast Cell lines]. Subsequently, founded a BioInstruments company [Nasdaq quoted company], which was involved in the marketing of sophisticated equipments for Biotech R&D. Prior to this he was associated with a Medical device company- a CAD based diagnostic Tech company • Founder, Managing Director of PK US and its associate companies in India and Malaysia Founder • Has spent over 40 years in the pharmaceutical industry • Commenced at age 19 in Schering AG; Grew up to the level of All India No. 2, at the age of 27 • Joined The UB Group as General Manager [Corporate Management div.]; Grew to the level of President Life Science Division, and was running 7 group companies in India and Africa • Was a member of Hoechst AgrEvo board, Aventis AgrEvo, and several other UB Group companies • Was responsible for bringing pain killer “Combiflam“in India, and several other successful brands of the group • President Project Koeing India for last four years. Also Director, of a leading Neutraceutical company. Co Founder

  15. Senior Management Team

  16. Knowledge Quotient of the Team

  17. Scientific Advisory Board The Scientific Board plays a key role in maintaining a strong product pipeline for the Company by continuously searching for and acquiring new technologies/products for Project Koeing India to work upon in the future; Most of the Board members are part owners of the technologies/products, thus are shareholders in the Company

  18. Clinical Advisory Board The Clinical Board plays an active role in the development and testing of products by guiding the entire process from acquisition till the clinical trials of the products

  19. The R&D Lab at Mumbai Project Koeing India has an 18,000 sq ft Research and Development laboratories in Mumbai.  This state of the art DSIR approved R&D labs will be used to develop products.  A larger pilot plant and manufacturing center on 11 acres will be setup in Khapoli. Lab Facilities include • State of the art of Recombinant, Mammalian and Bacterial yeast based cGLP Laboratories • State of the art level 2t, Gene Therapy Labs with incineration at exhaust points to contain any virus spillage and positive pressure Corridors • Labs for development of cytokine based Immunotherapy  • The common infrastructure is set aside with easy access for all labs • All the labs are in a clean zone environment and accessible only with appropriate access using electronic keys and electronic air lock system The lab facility at Mumbai is the cornerstone infrastructure for all the ongoing R&D efforts at PKI and is a state of the art facility serving all requirements of the various technologies/products under development

  20. Key Features of the Lab • These labs are used for preparation of DNA, RNA and plasmids, banking of plasmids in E. coli bacteria, and analysis of DNA by restriction enzyme mapping, polymerase chain reaction (PCR) and gel electrophoresis. The major equipment here is as follows: • Biocontainment hood • Incubators • Bench-top refrigerated centrifuges and microfuges • PCR Thermocyclers • Electrophoresis systems • Gel documentation system (for electronic capture and recording of data) Microbiology & Molecular Biology • These labs are used for yeast fermentation and application of VFF2 technology to produce recombinant bio-therapeutic proteins such as human insulin, human growth hormone, G-CSF, etc. The major equipment here is as follows: • Biocontainment hood • Incubators • Five-liter Fermentors • Chiller and compressor units • Bench-top refrigerated centrifuges and microfuges • Floor model centrifuges • PCR Thermocyclers • Electrophoresis systems • HPLC • Chromatography systems (Radial and Axial) Fermentation & Protein Purification

  21. Key Features of the Lab (contd.) • These labs are used for discovery, production and analysis of lentiviral-based gene therapy products using MSP36. Since lenti-viruses can be pathogenic, the gene therapy lab has been specially designed to provide Level II containment with an independent HVAC system, negative pressure and burn-out unit. The major equipment here is as follows: • Biocontainment hoods • CO2 Incubators • Microscope • Two-way autoclave for biohazard waste decontamination • Ultra-centrifuge Gene Therapy & RCL Assay • They include labs for Media Preparation, Analytical and Cell Culture. The major equipment here is as follows: • Water purification system • Autoclaves • Freezers: -80oC and -20oC • UV/VIS Spectrophotometer • ELISA Reader • Biocontainment hoods • CO2 Incubators Ancillary Labs

  22. The Pilot Plant • Pilot Plant for Recombinant Proteins (being equipped): This has been built to be “almost” GMP specifications, incorporating separate HVAC systems, uni-directional flow of personnel, labs for QC/QA, Media Prep Room, and various suites for Fermentation, Clarification and Downstream. The major equipment here are as follows: • 10- and 30-liter Fermentors • Autoclaves • Boiler (steam generation), chiller and compressor unit • Floor model centrifuges • Tangential flow filtration systems • Low pressure and High Performance Chromatography systems • Analytical lab instrumentation Pilot Plat for Recombinant Proteins

  23. SWOT Analysis Strengths Weaknesses • Only company in India with a drug in Phase III stage • Owner of unique Manufacturing technology • High IPR value • Validated and recognized by International Research Institutes and Governments Agencies • Wide spectrum Of operations • High Precision Value Chain • Currently, an Indian Government subsidized organization, however with minimal incentive from the Govt. • Infancy stage of the biotech sector and the lack of significant awareness in India • Lack of super specialist manpower • Slightly complex legal structures Opportunities Threats • US$30 bn Orphan Drug Market to be tapped • Opportunity to generate very high networth worth US$100 bn worldwide • Huge Potential of value creation • Opportunity to generate higher IPR value • Opportunity to improve the quality of life by creating new improved treatments for cancer • Opportunity to improve Biotech research status in India & abroad • Brain Drain • Infringement of IPR • Sustention of Continuous R&D Investment • Technology obsolesce of the technical equipment used • Volatility of global economic conditions • High lead time in Infrastructure Development

  24. Milestones Achieved & Road Ahead Licensing/Sale of RNAi based products (First Exit) DCGI Approval for Phase III Trials for RNAi based products 18,000 sq.ft. R&D setup at Mumbai Production & Approvals for RNAi based products Acquired 5 acres of land for the new manufacturing plant Govt. Permissions/R&D Plant setup More than US$ 10 mn invested by PKI in the current pipeline Year 0-1 Year 1-2 Year 2-3 Achievements Till Date Expected Milestones

  25. Key Focus Areas for Growth Complete the ongoing development of the current product pipeline on schedule Key Focus areas for Project Koeing Create the planned Pilot manufacturing plant at Khopoli Focus on acquiring new technologies /products to maintain a strong product pipeline Currently, Project Koeing requires US$ 30 mn to pursue its growth strategy, which primarily includes continuing development activities for its four key products and bring them to conclusion

  26. Project Wise Fund Requirement The total fund requirement of US$ 30 mn is split across all the four key technologies/products with the Manufacturing and RNAi based products garnering the majority shares

  27. Prospective Clients Upon Product Maturity Typical Exit Potential Collaborators • Revenue generation at PKI will take place at the exit of a product/technology, which will most likely take place in form of the licensing out of the technology/product once it is ready for commercialization • A typical licensing deal includes an upfront payment to the technology owner and royalties/periodic payments over next 10-15 years • There could also be a sale of the technology/product for a large lump sum payment • All the major pharma companies in the world are prospective clients for Project Koeing, especially the ones doing significant research on cancer related drugs. Some such companies include Roche, GSK, Pfizer, J&J etc • Also, other companies such as UB Group, Shaw Wallace etc are also potential clients as they use fermentation technology as a basis of their operations Project Koeing has a large potential client base upon the maturity of its products/technologies

  28. Biotechnology: The Next Sunshine Sector The Global Biotechnology Sector The Indian Biotechnology Sector • The global biotechnology industry is over 30 years old and is generating almost US$ 100 bn in revenues. There are appr. 7,000 companies worldwide, less than 600 of which are public companies • There has also been a significant support from the Governments, given that almost US$ 150 bn worth Govt. funding has been granted to this sector • In last decade, the industry has made historic progress with strong product pipelines and product successes, record-breaking financing totals, unprecedented deal activity and impressive financial results. Further, according to an E&Y report, all the leading regions in the world have been recording a strong double digit growth • The sector is now beginning to understand disease 'globally' i.e., from a systems point of view, from gene or SNP to protein to networks to disease. In parallel, and conversely, the notion of 'one size fits all' is being replaced by medicine targeting the individual and the central tenet on which a huge biopharmaceutical industry has been built has to adjust to a new and evolving personalized medicine world • The Biotechnology sector in India, although nascent at the present time and accounting for a mere 2% of the global Biotechnology market, is poised for exponential growth over the next 5 years with an expected global market share of 10% • The total revenues of this sector stand at around US$ 1 bn. With a market cap of around US$ 2.5 bn. • The Indian biotechnology industry is gathering momentum, by leveraging its low cost scientific skill base in an imitative manner with which to build its capPK USlities • Today, the Indian biotech sector has attained critical mass in manufacturing as well as research services and has slowly built a market for biotech products and services Indian Biotechnology is now poised to leverage its scientific skills and technical experience to make a global impact on a strong innovation led platform • A vibrant pharmaceutical industry, and fast developing clinical capPK USlities collectively points to a promising biotechnology sector and has placed India favourably in the global market.

  29. Global Pharma Companies Focus on R&D Global Pharma companies are increasingly spending more money on their R&D efforts, which indicates the significant focus from their end on developing new drugs and technologies. As a result, these companies have also been partnering with Biotech companies to fulfill their need for new drug discovery & development through various means

  30. Deal Activity in Biotechnology Sector Pharma – Biotech Transactions Biotech – Biotech Transactions There has been significant deal activity in the Biotech sector in the past few years, indicating the various synergistic values both Pharma & Biotech companies are recognizing between themselves

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