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NuvOx Pharma utilizes nanotechnology to develop oxygen therapeutics for various medical applications, including brain cancer, stroke, and hemorrhagic shock. The company, led by a team of experienced professionals, has a robust pipeline of innovative solutions backed by FDA-approved drugs and cutting-edge technology.
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NuvOxPharma Saves Lives with Nanotechnology Oxygenation Evan Unger, MD, FACR President and CEO NuvOx Pharma
Management Team has developed 15 FDA approved drugs! • Evan Unger, MD, CEO • 1st Company Sold 20x Return • 2nd Company Went Public • >100 US Pharma Patents Issued • Betty Weaver,CFO • Financial expert • Assists Biotech company expansion • Rajan Ramaswami, PhD, COO • Chemistry, Manufacturing, and Controls • Gordon Brandt, MD • VP Regulatory Affairs • Experienced in US and Intl. drug product approval
Board of Directors • Richard Carmona, MD – Trauma Surgeon , 17th Surgeon General of US • Jennifer Johnson, PhD – Co-Founder, Formulation Scientist, Inventor • Michael Sember– 40 years in Pharma, 100+ Licensing Transactions/Acquisitions • Marvin Slepian, MD – Inventor, founded 8 biotech start-ups • Jonathan Schilling – Schilling Robotics was acquired by FMC for $400M • Evan Unger, MD – Co-Founder
Scientific Advisory Board & Collaborators • Paul August, PhD, 20 years + experience in drug development R&D • Minesh Mehta, MD, Deputy Director and Chief of Radiation Oncology, Miami Cancer Institute • Solomon Ofori-Acquah, PhD, Associate Professor of Medicine, Director, Center of Translational and International Hematology, University of Pittsburgh • William Culp, MD, Distinguished Chair of Stroke Research, University of Arkansas, PI of current stroke trial
NuvOx Company • Employees • 4 PhDs, 2 MDs, 1 MS, 1 MBA, 3 BS Chem. • Clean room for clinical product manufacturing • Aseptic filling system • Manufacturing capacity to support Phase I and Phase II clinical trials. • 5 fully equipped laboratories • 5 active R&D programs
NuvOx’s Oxygen Therapeutics Dodecafluoropentane emulsion (DDFPe) • Terminal half-life 90 minutes • Clears via exhalation • Used as an oxygen therapeutic • Carries > 100x more O2 than other fluorocarbons (FCs) • Required dose < 0.5% of other FCs 250 nm
Competitive Advantages and Intellectual Property • Reduced Development Risk • $100 million spent by licensor developing DDFPe • Used safely in 2,200 patients • Approved in Europe as an ultrasound contrast agent • 5 patents issued, 12 pending
DDFPe Delivers Oxygen to Hypoxic Tissue In-human BeforeInjection AfterInjection • These MRIs show the oxygen level of a patient with a hypoxic solid brain tumor. • Tumor oxygenation increases significantly (p=0.015) • Healthy brain tissue oxygenation does not change significantly (p=0.65)
Pre-Treatment with NVX-208 Diminishes Stroke in Animals Treated with tPA A = control, B = animal treated with t-PA at 9 hours, and C = animal pre-treated with NVX-208 prior to t-PA.
DDFPe vs. Volume Expander Standard of care – Stop the bleeding and give 500 mL Volume Expander • DDFPe was tested at less than 1/10th the volume of volume expanders – lighter weight. • DDFPe could be carried in patent pending pre-loaded syringes for field use.
DDFPe Protects Against Fatal Anemia Rats’ blood slowly replaced with Volume Expander, then given either DDFPe or Blank Vehicle • Control rats see 0% survival (n = 16) • DDFPe rats see 100% survival (n = 16) • DDFPe rats survive with about half the hemoglobin level that was fatal in controls
Hemorrhagic Shock Model, Part 1 Pigs anesthetized, given fractured femur bone, and ~50% blood loss. • Controls had 30% survival (n=19) • Pigs given Volume Expander had 80% survival (n=10) • Pigs given DDFPe had 100% survival (n=6)
Hemorrhagic Shock Model, Part 2 Pigs sedated and bled ~50% of their blood volume, then given treatment 1 hr later • Volume expander had 86% survival (n=7). • DDFPe had 100% survival (n=7) at 14 days. Pigs grow and act normally. • DDFPe pigs had increased arterial O2 (p<0.01).
Conclusion • Researchers concluded: “DDFPe is a better resuscitation fluid than volume expander.”
Going Forward • Technology Out-licensed for Peri-Operative Blood Loss and Hemorrhagic Shock in China. • Partner will fund clinical studies, NuvOx will supply the drug. NuvOx gets data and retains rights to all other countries. • Manufacturing not transferred until drug launched in China.
DDFPe in Rat TBI Model Hypoxia is a Secondary Injury Mechanism • DDFPe significantly increases brain tissue oxygen tension (p < 0.05)
NuvOx is Seeking: • Collaborators for its programs to develop battle-field ready products to prevent combat death due to traumatic injury associated with hemorrhagic shock and TBI.
Thank you • Clinical stage biotechnology company - substantially reduced risk • Actively seeking investors and corporate partners NuvOxPharma,1635E.18th St.,Tucson,AZ,85719,USAeunger@nuvoxpharma.com office:+1520-624-6688www.nuvoxpharma.com