AQUALUNG THERAPEUTICS ADVANCES ITS INVESTIGATIONAL MONOCLONAL ANTIBODY INTO IND-ENABLING STUDIES OF ACUTE RESPIRATORY DISTRESS SYNDROME (ARDS) AND VENTILATOR-INDUCED LUNG INJURY (VILI)

COVID-19 and exposure to mechanical ventilation increase unchecked inflammation and ARDS mortality(ARDS) AND VENTILATOR-INDUCED LUNG INJURY (VILI)

Key Takeaways

  • ARDS (Acute Respiratory Distress Syndrome), with a mortality rate of 35-40%, occurs in  patients with severe lung inflammation, low levels of oxygen in the blood (hypoxemia) and respiratory failure that requires mechanical ventilation as a life-saving intervention but which also contributes to lung inflammation and ARDS mortality
  • There were dramatic increases in virally-induced ARDS cases during the rise of two species-jumping coronaviruses, SARS (severe acute respiratory syndrome) and MERS (Middle East respiratory syndrome), and now with the novel coronavirus -COVID-19- pandemic
  • There are no FDA–approved treatments for ARDS or for ARDS-inducing stimuli such as COVID-19.

TUCSON, AZ., March 18, 2020 -- Aqualung Therapeutics Corporation is developing ALT-100, a therapeutic monoclonal antibody, to combat serious unchecked inflammation. The initial application aims to reduce the mortality of Acute Respiratory Distress Syndrome (ARDS) and Ventilator-Induced Lung Injury (VILI). This offers a potential option in the treatment of COVID-19, which causes severe pneumonia and respiratory failure and can be compounded by mechanical ventilation, resulting in multi-organ failure and death.

The Company is actively engaged with government agencies such as the National Institutes of Health & the Department of Defense for additional funding opportunities and has begun required testing as part of the Investigational New Drug (IND) regulatory package for the FDA.

“Antibacterial agents, antiviral agents and methylprednisolone to date have been largely ineffective in viral-induced ARDS and according to early reports, in NCIP-induced ARDS,” said Joe G.N. Garcia MD, CEO and Founder of Aqualung Therapeutics (ALT) and globally-recognized expert on ARDS. “There is a serious and ongoing unmet therapeutic need for COVID-19 therapies with a case fatality rate estimated to be ~2-3% as well as for the nearly 500,000 ARDS patients in the U.S. alone who annually develop ARDS from sepsis, trauma and a myriad of diverse stimuli and experience 30-40% mortality.”

Specifically, Aqualung Therapeutics is developing eNamptor™, a Next Gen platform comprised of:

1)      ALT-100, a humanized eNAMPT-neutralizing monoclonal antibody (ALT-100);

2)      eNAMPT-Plex, a plasma-based biomarker panel comprised of cytokines, including eNAMPT, which predicts ARDS mortality; and

3)      NAMPT-Gene, a genotyping assay that identifies individuals with NAMPT genetic variants at increased risk for ARDS death.

“We hope to quickly finalize our manufacturing agreements and get ALT-100 into the Emergency Room and ICU to address this significant unmet medical need as soon as possible, during not only this current COVID-19 crisis but in the future”, states Stan Miele, President of Aqualung Therapeutics.”

Aqualung Therapeutics identified an upstream protein, extracellular nicotinamide phosphoribosyltransferase (eNAMPT) and its receptor, Toll-like receptor 4 (TLR4) which are important in regulating the upstream inflammatory cascade that contributes to ARDS morbidity and mortality. Supported by strong preclinical and human data, combining the elements of the eNamptor™ platform technology has the potential to define high risk ARDS individuals as well as identify patients most likely to respond to ALT-100 and reduce downstream inflammation that contributes to death from COVID-19 infection and NCIP-induced ARDS.

In December 2019, a novel coronavirus, SARS-CoV-2, was found to produce COVID-19 infection in humans with clusters of acute respiratory illness in Wuhan, China, now known as novel coronavirus–infected pneumonia (NCIP).

Deaths due to coronavirus COVID-19 infection primarily occur in patients transferred to the ICU with NCIP. These patients have or develop severe respiratory distress, respiratory failure and full blown ARDS. In such cases, treatment requires placement on a ventilator and mechanical ventilation for respiratory failure.

Patients with NCIP-induced ARDS often succumb to multi-organ failure due to two life-threatening mechanisms. First, the organ failure that occurs is a direct result of unremitting inflammation generated by the virus-activated innate immunity pathways designed to contain the viral infection. A second and very important threat is the activation of inflammatory pathways by exposure to the increased mechanical stress to the lung created by exposure to mechanical ventilation.

Activation of these evolutionarily-conserved inflammatory pathways results in massive increases in the circulating levels of inflammatory cytokines which produce vascular leak, edema of multiple critical organs (lung, kidneys, heart, brain, liver, GI tract) and ultimately result in multi-organ dysfunction and death. The overall inflammatory burden produced by the virus and by use of the mechanical ventilation drives the occurrence of severe, and often fatal organ failure.

About Aqualung Therapeutics Corporation

Aqualung is an early stage biotech company developing immune-focused therapeutic antibodies for patients suffering from disorders characterized by acute and chronic lung and systemic inflammation. Founded in 2016 and led by a physician scientist, Aqualung’s science-driven approaches led them to the identification of nicotinamide phosphoribosyltransferase (NAMPT) and other key proteins expressed in both acute and chronic inflammatory diseases. The pipeline of ALT is designed to target a range of diseases, including ARDS, ventilator- and radiation-induced lung injury, prostate cancer, pulmonary hypertension and pulmonary fibrosis. These conditions all exhibit a significant unmet medical need with significant morbidity and mortality. For additional information about the company, please visit www.aqualungtherapeutics.com.

Aqualung Therapeutics Corporation   

Tel: +1-(312) 618-7337    

Joe GN “Skip” Garcia, MD, CEO & Founder        

skip@aqualungtherapeutics.com

Key Takeaways

  • ARDS (Acute Respiratory Distress Syndrome), with a mortality rate of 35-40%, occurs in  patients with severe lung inflammation, low levels of oxygen in the blood (hypoxemia) and respiratory failure that requires mechanical ventilation as a life-saving intervention but which also contributes to lung inflammation and ARDS mortality
  • There were dramatic increases in virally-induced ARDS cases during the rise of two species-jumping coronaviruses, SARS (severe acute respiratory syndrome) and MERS (Middle East respiratory syndrome), and now with the novel coronavirus -COVID-19- pandemic
  • There are no FDA–approved treatments for ARDS or for ARDS-inducing stimuli such as COVID-19.

Contacts

Stan Miele
Stan@aqualungtherapeutics.com
919-410-0504
President & Chief Business Officer

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Quotes

There is a serious and ongoing unmet therapeutic need for COVID-19 therapies with a case fatality rate estimated to be ~2-3% as well as for the n...
Joe "Skip" Garcia M.D.CEO & Founder

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Joe "Skip" G.N. Garcia, MD
Founder & Chief Executive Officer
University of Arizona Endowed Merlin K. DuVal MD Professor of Medicine and an elected member of the National Academy of Medicine. Dr. Garcia is a internationally recognized physician-scientist with over 30 years of research experience in pulmonary disease and has led multi-billion dollar academic organizations.
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Stan Miele, BA
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A recognized global executive with success in sales, marketing and P&L leadership in the pharmaceutical/medical device and biotech industries. Mr. Miele was formally the Chief Commercial Officer at bioLytical Laboratories and Sucampo Pharmaceuticals Inc. He was also President of Sucampo Pharma Americas for 6 years. He was instrumental on some key licensing agreements for Sucampo, inclusive of the agreement with Abbott Japan, and also Takeda Pharmaceuticals (now Shire). He is actively part of the team ensuring proper execution of clinical development, manufacturing, licensing, capital funding, alliances, and ensuring Aqualung meets all critical milestones. He will be helping the company move toward accelerating the pipeline/platform technology and moving eNamptor™ toward commercialization.
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Mariam Morris
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Ms. Morris serves as Aqualung’s CFO, since October 2018. Prior to Aqualung, she served as the Chief Financial Officer of Cerecor from May 2015 through August 2018. While at Cerecor, she completed the Company’s IPO and raised over $28 million in financings, in-licensed and out-licensed key assets, and completed two corporate acquisitions. She was responsible for the Company’s financial and corporation operations, investor relations, and served as the board’s secretary. Prior to joining Cerecor, Ms. Morris was the sole proprietor of Mariam Morris CPA, a full-service tax, accounting and business consulting firm, which she founded in January 2009 and operated until May 2015 where she served as an advisor to many private and public biotechnology companies. She served as the Chief Financial Officer of Sucampo Pharmaceuticals, Inc. from February 2004 to July 2009, where she completed the Company’s IPO and raised over $56 million in financings. From 1991 until 2001, Ms. Morris was and managing auditor for PricewaterhouseCoopers. Ms. Morris received her B.B.A. in Accounting from Texas Tech University and her M.S. in Taxation from Old Dominion University. Ms. Morris is a Certified Public Accountant in the State of Texas and a member of the TSCPA and AICPA.
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