Barbara Dalton United States

Pfizer Venture Investments (PVI) is the corporate venture capital arm of Pfizer and was founded in 2004. PVI has an annual investments budget of $50 million and invests up to $10M per investing round. The firm focuses mainly on U.S. startups but has global reach. PVI attempts to allocate 80% of its funding to U.S. based companies and utilizes the remaining 20% for international ventures. PVI provides equity funding for private companies in need of seed, growth, or venture financing. Remaining opportunistic, PVI focuses entirely on high growth prospects in all sectors and all phases of development. The ideal candidate has a potential for high growth and returns. Additionally, PVI will seek to in-license products and buyout companies if the opportunity arises.

Pfizer Venture Investments
Vice President 

John Davidson United States

Tangen Biosciences is an early stage diagnostic instrument company that has developed a group of novel technologies that together enable rapid, portable, lab-free, and very low cost molecular diagnostics at the point of care.   

The Tangen platform will amplify and detect specific nucleic acid sequences obtained from a variety of source samples, including clinical specimens such as blood, tissue and sputum, as well as environmental samples obtained from water, soil or food, for example.  The first application of the Tangen platform is the detection and diagnosis of Tuberculosis using DNA extracted from sputum samples, using the Tangen Sputum Processing assay kit

Year Founded
2012
Biotech Subsector
Indication
Biotech Phase of Development
Current Financing Needs

Additional $0.5-1M to close seed round

Tangen Biosciences
CSO 

Mr André de Fusco United States

Cynvenio has developed a new LiquidBiopsy technology to sequence the DNA of tumor cells isolated from peripheral blood. Key applications include longitudinal patient monitoring throughout the cancer care cycle, the detection of resistance mutations, and providing physicians with accurate molecular evidence to select the best targeted therapy for a given patient.

Cynvenio's technology can be accessed as a CLIA lab service, or  can be installed and operated inside hospital labs and cancer research centers. Cynvenio's lab has been CLIA certified since 2013 and LiquidBiopsy system deployments began in the second half of 2014.

Website:
www.cynvenio.com
Year Founded
2008
Biotech Subsector
Medtech Subsector
Biotech Phase of Development
Technology Overview
Sequencing tumor cells from whole blood
Alliance & Collaborations
Yes, US and International
Supporting Metrics or Evidence
CLIA/CAP accreditation, validations completed, generating revenue
Current Financing Needs
$15M
Current Timeline
Series C raise to scale commercial
Current Investors
Privately funded
IP Status
Core IP has issued
Recent Milestones
4 US deployments, 2 strategics
Management Team Highlights
Amgen, Nortel, Harvard, UCLA, McKinsey
Cynvenio Biosystems, Inc.
LinkedIn logo CEO 

Koen De Lombaert United States

Yuzu Labs, based in Silicon Valley, is a research startup that aims to make clinical, behavioral, and social research more accessible, easier, faster, and cheaper. We've recently launched a private beta of our initial product named StudyPages. Researchers can use this web application to quickly set up a dedicated webpage for their studies, share with target communities, and track signups. Please visit the site to learn more: https://studypages.com
Year Founded
2014
Service Provider Type
Koen De Lombaert
Yuzu Labs
LinkedIn logo Co-Founder 
BIO

Koen holds a MD (Catholic University Leuven, Belgium) and a MBA (Johns Hopkins University) and worked in lifesciences, bioinformatics, business development, marketing, and product management in academia, startups, and at Roche Pharmaceuticals. Koen enjoys technology and UX design and builds wireframes for new product ideas. His passion for science and entrepreneurshipmade him move stepwise from Belgium to the West and he calls Silicon Valley now his new home.

John De Michele United States

The HudsonAlpha Institute for Biotechnology

 

The HudsonAlpha Institute for Biotechnology is a Genomic focused Institute located on a 152-acre bio-medical research campus in Huntsville, Alabama whose mission is to translate scientific breakthroughs in the laboratory into real-world benefits that have a profound impact on people’s lives.

 

HudsonAlpha BioVentures Philanthropic Fund

•       Specific Philanthropic Fund - part of the HudsonAlpha Foundation a tax-exempt, 501(c) 3 non-profit organization.

•       All investments to the Fund are tax-deductible

•       Fund goal is $50 million

•       Targeted toward donors seeking to make a long-term impact in human health and make a difference for thousands, even millions, of people suffering from serious disease.

 

Option 1

HudsonAlpha Foundation invests funds in new or established companies and scientific discoveries. Foundation will have an equity stake and receive a ROI, as companies are successful. The return is reinvested into other companies and HudsonAlpha to further its mission and goals – the multiplier effect.

Option 2

HudsonAlpha Foundation will fund promising intellectual property emanating from HudsonAlpha laboratories.

Option 3

HudsonAlpha Foundation provides grant funding to companies who are relocating to or expanding on the HudsonAlpha campus.

 

All investors/donors will have an opportunity to invest in the future in any and all companies and will be informed regularly on the progress of these companies

Year Founded
2008
Biotech Subsector
Management Team Highlights
Richard M. Meyers Ph.D President and Director of Science •Internationally recognized thought leader in genomics and genetics •Leads scientific collaborations in 18 countries with over 700 researchers and clinicians •Scientific expertise in cancer research including breast, kidney, prostate; neurological disorders including ALS, Parkinson’s disease; psychiatric disorders including schizophrenia, bipolar disorder and major depression. •Former Chair of the Department of Genetics at Stanford University and Director of the Stanford Human Genome Center •Dr. Myers and his lab contributed 11% of the data in the Human Genome Project’s efforts to sequence the first human genome. •Ph.D. in Biochemistry, University of California Berkeley •Performed doctoral work at Harvard University with Dr. Tom Maniatis
HudsonAlpha Institute for Biotechnology
Vice President for Advancement 
BIO
JohnDeMicheleJohn De Michele

Vice President for Advancement

John De Michele came to HudsonAlpha in June 2014 from San Diego, bringing with him 30 years of fundraising leadership and nonprofit executive experience. His diverse background ranges from Tufts University to Northwestern University Medical Center Foundation, from the National Jewish Medical and Research Center to the San Diego Symphony, where he mobilized the largest single gift in its history: $125 million. De Michele understands the challenges facing nonprofit leaders today and acts strategically, and tirelessly on behalf of the Institute.

Steve DeNelsky United States

Life Sciences Alternative Funding (LSAF) founded in 213 is a direct investment firm based in White Plains New York. The firm focuses exclusively on providing debt capital for commercial-stage medical technology companies. The firm can allocate between USD 1M-5M per investment. The firm looks to provide flexible ?tailor-made? financing solution to companies. The firm can invest globally and is currently seeking new investment opportunities.

Life Sciences Alternative Funding
President 

Eric Desai United States

Greenhouse Capital Partner is a venture capital firm that was founded in 2006 and is based in Sausalito, California. The firm selectively makes equity investments into life science companies in seed stage and series A financing round, but it also provides growth equity to highly capital efficient companies that can achieve cash flow break-even within two years. The typical investment size ranges from $0.25 million to $2 million.The firm focuses on investments in US based companies.

Greenhouse Capital Partners
Principal 

Cornelius Diamond United States

Website:
www.predict.net
Year Founded
2010
Biotech Subsector
Biotech Phase of Development
Technology Overview
Assay to predict bleeding; paired with various cardiovascular drugs, also developed by the company, to displace existing therapeutics from a safety perspective
Alliance & Collaborations
Glycotope GmbH, Cellonic SA, Qualigen Inc.
Supporting Metrics or Evidence
7 published papers on c-Fn predicting bleeding in various neurological indications
Current Financing Needs
$1.5M
Current Timeline
on-market 2018
Current Investors
NACP, Private Offices
IP Status
3 granted patents on main technology; several more in various WW phases
Recent Milestones
Private investment of more than $1Mio to progress first therapeutic/companion Dx assay to market
Management Team Highlights
Divestment of oncology Dx business
Prediction BioSciences
Founder & CEO 

Mr Kurt Dieck United States

Biosortia has opened the door to a new frontier of fascinating compounds that have the potential to materially impact the direction of various chronic diseases.  We are dedicated to discovering new chemical entities for the management of critical chronic disease states such as cancer, neuroscience, infectious disease, and inflammatory disorders to ultimately improve the lives of others.

Value Proposition

Pharma is looking for 3 key things:

1. Novel, never seen before, chemistry from new environments to fight chronic disease

2. Higher levels of potency (nano to Pico molar) to reduce the impact of side-effects

3. New mechanisms of action to fight chronic disease in new and more effective manner

It is well known that micro-organism consortia (not macro) are one of the most biologically active and chemically diverse plant/fungi that are rich in what we call “Defense Mechanism Chemistry”.  Defense Mechanism Chemistry is key in developing drugs for cancer, infectious disease and inflammation.  The problem is no one has been able to get access to this unique chemistry at scale and have the natural products expertise to identify the unique compounds…until now.  

We will provide Pharma with new compounds, rich in “Defense Mechanism Chemistry” on a routine basis that could shorten the discovery cycle by 2-3 years and reduce the overall cost.  

Best Regards,

Kurt Dieck

President and CEO

kdieck@biosortia.com

(614) 296-7076

Year Founded
2008
Biotech Subsector
Biotech Phase of Development
Technology Overview
Mobile, scalable, technology that maintains the integrity of the cell. Biosortia has proprietary methods & technologies that allow us to harvest unique single cellular micro-organism consortia never before studied and in unprecedented quantities targeting 500-1,000kg dry weight solids (DWS). Our technologies and capabilities open up this rich environment of bioactive and chemically diverse compounds for research in the pharmaceutical space for the first time ever. Biosortia’s relationship with NOAA and our Cooperative Research and Development Agreement (CRADA) with them provides Biosortia with identification and access to distinctly qualified harvest locations.
Alliance & Collaborations
(Eli Lilly, AstraZeneca, Eisai and Cubist Pharmaceuticals) with more in the pipeline.
Supporting Metrics or Evidence
Promising Early Results with big pharma (Eli Lilly, AstraZeneca, Eisai and Cubist Pharmaceuticals) with more in the pipeline. • Eli Lilly’s OIDD To date, nearly 100% of Compounds of Interest submitted into Eli Lilly’s Open Innovation Drug Discovery (OIDD) program have been accepted for evaluation…compared to an average 50-60% rejection rate on all submissions. This unprecedented achievement has recently earned Biosortia the inaugural “Collaborator of the Year” award from Lilly. In addition, due to the success in the OIDD Program, Lilly asked to join our Pharma Direct Model and test our fraction library. Initial results across simple 2 assays have produced 10 leads that they desire to follow-up in December 2014. • Big Pharma Interest As of September 30, 2014 we have 4 Big Pharma companies in our Pharma Direct Model (Eli Lilly, AstraZeneca, Cubist and Eisai) with 3 others in the pipeline in various stages of discussions.
Current Financing Needs
Capital- Biosortia has raised 2 rounds of series A Preferred Shares; November 2012 of $1.1M ($29M pre-money valuation) and September 2013 of $3.9M ($35M pre money valuation). In addition, it secured $1 million loan (2% interest) from the State of Ohio, therefore meeting our original desired capital raise of $4-5 million. The current raise is for $3-$6 million dollar to provide the runway to our first licensing agreement in Q4 2015 and drive the scaling of science capability to support the volume from our fraction libraries to be launched in Q1 of 2015.
Current Timeline
Hit rates well in excess of expectations Through our Pharma Direct Partners and 8 academic collaborators, we have over 50% of our fractions active against various therapy areas. This demonstrates both the richness of our compounds and the diversity across multiple therapy areas. With one of our Big Pharma partners alone, we have 48 active fractions/wells, with 20 showing inhibition of cancer growth from 90-99.8%. • Clear pathway to first license event in 2015 We can share with you a clear pathway to a license event in 2015. AZ, Lilly and Eisai are all on schedule to complete their R&D efforts by Q3 of 2015 that will put them in position to determine which compounds of interest they would like to license.
Recent Milestones
To date, nearly 100% of Compounds of Interest submitted into Eli Lilly’s Open Innovation Drug Discovery (OIDD) program have been accepted for evaluation…compared to an average 50-60% rejection rate on all submissions. This unprecedented achievement has recently earned Biosortia the inaugural “Collaborator of the Year” award from Lilly.
Management Team Highlights
Experienced Leadership Team & Advisors Biosortia’s leadership team has over 135 years of healthcare and life science experience with expertise in both pharmaceutical research and the micro-organism aquatic environments with the capability to provide new chemistry in a research ready format and co-develop with Pharma to pre-clinical. -Kurt D. Dieck, President and CEO - Mr. Dieck has spent 30 years in healthcare, including 18 years at Arthur Andersen where he was a global equity partner. In 2002, Kurt joined Cardinal Health, a Fortune 20 public company as a senior executive; where over his tenure he had responsibilities for Strategy, Business Development and ultimately SVP of Business Execution for the $100B pharmaceutical distribution segment. There he worked with a broad spectrum of partners, including brand pharmaceutical manufacturers, throughout the supply chain. Kurt also sits on two other healthcare related boards that are owned by Private Equity firms. -Guy T. Carter, Ph.D., Chief Scientific Officer – Dr. Carter has over 30 years of experience working in Pharmaceutical R&D, primarily in the discovery and development of microbial products. In the course of his career in the pharmaceutical industry he worked as a natural products discovery scientist and advanced through levels of scientific management to the overall leadership of the Natural Products Discovery function at Wyeth Research (later acquired by Pfizer), as well as directing other elements of the Chemical Technologies Department. Guy received a doctorate in Biochemistry from the University of Wisconsin-Madison, and then pursued marine natural products research on an NIH-sponsored post-doctoral fellowship with Kenneth Rinehart at the University of Illinois. -Haiyin He, Ph.D., VP of Research – Dr. He has more than 20 years of experience in pharmaceutical R&D, specializing in discovery of drug leads from natural products and their semi-synthetic analogs in oncology, infectious disease, and other therapeutic areas. Haiyin worked as a principle scientist III and group leader at Wyeth Research and after the merger between Pfizer and Wyeth, he continued on to work at Pfizer World Wide Medicinal Chemistry as an associate research fellow in the area of antibody-drug conjugates for cancer chemotherapy. Haiyin received a doctorate in marine natural products at Scripps Institution of Oceanography with John Faulkner, and then acquired a postdoctoral experience at Chemistry Department, Cornell University with Jon Clardy.
Mr Kurt Dieck
Biosortia Pharmaceuticals
LinkedIn logo President and CEO 

Kevin Dillon United States

We have developed the CloSys Hemostatic Device (HD)  - a highly differentiated technology for vascular closure after an interventional cardiology or peripheral procedure.  CloSys HD is unique in that it facilitates rapid closure but leaves NO foreign material behind in the patient.  It does this using a patented technology that eliminates heparin (anti-coagulant) from a small amount of the patient's blood and re-infuses this back to the puncture site and around the entire artery.  The de-heparinized blood rapidly and safely forms a clot to seal the artery naturally.  There are several other unique attributes of this product.  First  - it is the only product that will also seal "backsticks" or inadvertant punctures that go through the other side of the artery.  Backsticks are a leading cause of retroperitoneal hemorrhage.  Second - it preserves immediate re-access at the same site in the advent of an emergency.  

There is also an important economic value proposition offered by CloSys HD.  It will have a very low cost of goods so it could be sold for a price that will allow high margins to the manufacturer and cost savings to the hospital.  

We are approximately 25% of the way through a US pivotal trial and to date all performance and safety endpoints have been met.  There is a highly experienced management team and exceptional Board of Directors now associated with the company.    

Year Founded
2005
Main Sector
Medtech Subsector
Indication
Medtech Phase of Development
Technology Overview
CloSys HD consists a simple to use two component system. One component is a "wall locater" that is deployed inside the artery to achieve temporary hemostasis. The other component is a syringe with a special "reactor" in the tip that contains glass beads coated with a proprietary polymer. Blood withdrawn through the sheath passes through the reactor in the syringe which instantaneously removes heparin from the blood. The de-heparinzed blood is re-infused and forms a clot at the puncture site and around the artery.
Alliance & Collaborations
Rex Healthcare (part of UNC) in Raleigh, NC. Cardiovascular Institute of the South in Lafayette, LA, Deborah Heart and Lung in Brown Mills, NJ, and Mt. Sinai Medical Center in Miami, FL
Supporting Metrics or Evidence
Early results from an IDE trial. In this key performance endpoints of time to hemostasis and time to ambulation are being met. Safety endpoint of no unanticipated adverse events being met too. Results from two earlier studies performed in Europe as well numerous GLP and bench test reports have demonstrated effectiveness and safety.
Current Financing Needs
$4 million to complete trial, submit, obtain regulatory approval
Current Timeline
Approximately 10 months to complete enrollment and follow up, 2 to 3 months to write report, tie up loose ends at study sites and submit to the FDA. Approval time and questions ranges from about 4 months to 9 months.
Current Investors
Mostly angel investors and several smaller institutions such as Iowa Lakes Capital, University of St. Thomas Norris Fund, and Blankney Group from Milwaukee
IP Status
10 issued patents in the US, 3 issued patents in Europe and Canada, one provisional patent filed in the US
Recent Milestones
New members adde to the Board of Directors, meeting with FDA to re-classify to a Class Ii device
Management Team Highlights
Kevin Dillon - CEO and Director, Mary Lach - CFO, Kelly Elliot - Clinical Study Director, John Erb - Director, Warren Watson - Director, Christopher Barys - Director, Steven Zenz - Director, Bruce Johnson - Chairman and Director
Kevin Dillon
CloSys Corporation
CEO