Elusys Therapeutics

{{Infobox company

| name = Elusys Therapeutics

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| type = Private company

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| founded = 1998

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| hq_location = Pine Brook, New Jersey

| key_people = Dr. Elizabeth G. Posillico (Chief Executive Officer, President and Director)

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| website = {{URL|http://www.elusys.com/|elusys.com}}

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Elusys Therapeutics is a biopharmaceutical company founded in Pine Brook, New Jersey in 1998. The company specializes in the development of antibodies for the treatment infectious diseases.{{cite web|title=Company Overview of Elusys Therapeutics, Inc.|url=https://www.bloomberg.com/research/stocks/private/snapshot.asp?privcapId=92602|website=Bloomberg Business|accessdate=28 November 2015}} The antibodies are developed from protein complexes called heteropolymers which can bind to specific pathogens on one side and red blood cells on the other side.

The pathogens will be dragged to the liver where they will be destroyed.{{cite journal|last1=Sinha|first1=Gunjan|title=Kicking out killers|journal=Popular Science|date=February 2001|volume=258|issue=2|page=39|url=https://books.google.com/books?id=1nNGMLIL1cQC&pg=RA1-PA39|accessdate=28 November 2015|issn=0161-7370}} The antibodies have a potential to be used for the treatments of many blood-borne diseases. Currently, the company focuses on the late-stage clinical trials of Anthim (Obiltoxaximab) to be used for treatment and prevention of inhaled anthrax.{{cite web|title=Elusys Therapeutics Inc. Company Information|url=http://www.hoovers.com/company-information/cs/company-profile.ELUSYS_THERAPEUTICS_INC.7027d7663e00a047.html|website=Hoover's|accessdate=28 November 2015}}

History

Ronald P. Taylor, a professor of biochemistry and molecular genetics at the University of Virginia developed protein complexes called heteropolymers that mimic the natural process of white and red blood cells in clearing out the disease off the bloodstream.

The heteropolymers have specific binding that can bind to specific pathogens on one side and red blood cells on the other side. The red blood cells with the attached pathogens are delivered to the liver to be destroyed. In animal testing, the method can clear out pathogens within 2 hours.

Taylor's research were partially funded by the National Institutes of Health and the Defense Advanced Research Projects Agency{{cite news|title=Biochemist Ron Taylor Named Inventor Of The Year|url=http://www.virginia.edu/topnews/releases2000/inventor-may-3-2000.html|accessdate=28 November 2015|work=University of Virginia News|date=3 May 2000}} Additional funding was arranged by Seed-One Ventures, a venture capital company, through the formation of Elusys Therapeutics to raise several million dollars. Jeff Wolf, the founding CEO Elusys and Managing Partner of Seed-One, selected Stephen Sudovar as the CEO of Elusys. Sudovar was the former President of Roche Laboratories a division of Hoffmann-La Roche. Wolf also arranged to have Elusys' board of directors made up of people with prior experience from top global pharmaceutical companies and Food and Drug Administration (FDA).{{cite news|last1=Baard|first1=Erik|title=Inventing millionaires|url=http://www.villagevoice.com/news/inventing-millionaires-6417584|accessdate=28 November 2015|work=The Village Voice|date=29 August 2000}} As a startup, the company tested its first heteropolymers by using two chemically linked monoclonal antibodies for the treatment of lupus.{{cite journal|last1=Brower|first1=Vicki|title=Biotechnology to fight bioterrorism|journal=EMBO Reports|date=1 March 2003|volume=4|issue=3|pages=227–229|doi=10.1038/sj.embor.embor783|pmid=12634833|pmc=1315911}}

Elusys is a member of the Alliance for Biosecurity.{{Cite web|url=https://www.allianceforbiosecurity.org/contact|title=Our Members|website=Alliance for Biosecurity|access-date=2017-02-13}}{{Dead link|date=August 2019 |bot=InternetArchiveBot |fix-attempted=yes }} The alliance is a group of companies and scholars that work to promote the development of vaccines and other measures that can be used in the case of a pandemic or bioterrorism attack.{{Cite web|url=https://www.allianceforbiosecurity.org/mission|title=Our Mission|website=Alliance for Biosecurity|access-date=2017-02-13}}{{Dead link|date=August 2019 |bot=InternetArchiveBot |fix-attempted=yes }}{{Cite web|url=https://www.allianceforbiosecurity.org/about2-c4nz|title=Our Work|website=Alliance for Biosecurity|archive-url=https://web.archive.org/web/20170214102551/https://www.allianceforbiosecurity.org/about2-c4nz|archive-date=2017-02-14|url-status=dead|access-date=2017-02-13}}

Treatment

Anthim is monoclonal antibody designed for the treatment of exposure to Bacillus anthracis spores (etiologic agent of anthrax).

Elusys initially collaborated with University of Texas at Austin and United States Army Medical Research Institute of Infectious Diseases (USAMRIID) in the development of Anthim. With the bioterrorism risk of anthrax, the United States Department of Health and Human Services awarded a five-year contract in 2010 valued at $143 million to develop IV-based drug to treat patients who are already infected by anthrax. In 2011, the company was awarded with an additional five-year contract valued at $68.9 million to develop intramuscular injection for anthrax prevention measure.{{cite news|title=Feds award Elusys $69 million to develop anthrax drug|url=http://www.njbiz.com/article/20110912/NJ0702/110919967/feds-award-elusys-69-million-to-develop-anthrax-drug|accessdate=28 November 2015|work=NJBIZ|date=12 September 2011}} In 2012, the company was awarded additional $50.2 million to test the efficacy of the treatment.{{cite news|last1=Todd|first1=Susan|title=Elusys forges ahead on anthrax treatment with $50.2 million in government funding|url=http://www.nj.com/business/index.ssf/2012/08/elusys_forges_ahead_on_anthrax.html|accessdate=28 November 2015|work=The Star-Ledger|date=2 August 2012}}

The Biologics License Application for both intravenous and intramuscular administrations was accepted by the FDA in June 2015 with efficacy data of animal models and safety data from human volunteers.{{cite news|title=FDA Accepts License Application For Anthrax Prevention Drug|url=http://www.hstoday.us/briefings/grants-funding/single-article/fda-accepts-license-application-for-anthrax-prevention-drug/1beb858ff2bd179a031d4941a2ffef5d.html|accessdate=28 November 2015|work=Homeland Security Today|date=1 June 2015}}{{Dead link|date=March 2024 |bot=InternetArchiveBot |fix-attempted=yes }} In March 2016, Anthim was approved to treat inhalational anthrax in conjunction with appropriate antibacterial drugs, also for prevention when alternative therapies are not available or appropriate.{{cite web|url=https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm491470.htm?mrkid=%7B%7Blead.Id%7D%7D&mkt_tok=3RkMMJWWfF9wsRokuKjMcO%2FhmjTEU5z17e8uX6S3lMI%2F0ER3fOvrPUfGjI4HSsdhPa%2BTFAwTG5toziV8R7LMKM1ty9MQWxTk|title=FDA approves new treatment for inhalation anthrax|author=News Release|publisher=FDA|date=21 March 2016}}{{dead link|date=May 2025|bot=medic}}{{cbignore|bot=medic}}

In November 2015, the company received a five-year contract of $44.9 million for the production and future delivery of Anthim to the Strategic National Stockpile.{{cite news|last1=O'Brien|first1=Kathleen|title=Anthrax drug wins $44.9 million contract for Morris firm|url=http://www.nj.com/healthfit/index.ssf/2015/11/morris_county_firm_wins_federal_contract_for_anthr.html|accessdate=28 November 2015|work=NJ.com|date=12 November 2015}}

References