Great Basin Receives FDA 510(k) Clearance for First Multiplex Panel
Staph ID/R Blood Culture Panel detects blood sepsis caused by MRSA and other Staph species;; expands molecular diagnostics company’s menu with high-value panel
Salt Lake City, March 28, 2016 – Great Basin Scientific, Inc. (NASDAQ: GBSN), a molecular diagnostics company, has received U.S. Food & Drug Administration (FDA) 510(k) clearance for its Staph ID/R Blood Culture Panel, following submission in August 2015. The Company received notification of clearance from the FDA on March 25, 2016. This is Great Basin’s first multiplex panel to receive FDA clearance, adding to the value and versatility of the company’s analyzer, which is capable of performing low-plex, multiplex and direct-from-specimen assays.
Great Basin’s Staph ID/R Blood Culture Panel is a sample-to-result, automated, DNA multiplex assay for simultaneous identification of Staphylococcus aureus and Staphylococcus species directly from positive blood cultures in about 2 hours. The panel also detects the mecA gene, a major drug resistance marker that confers resistance to methicillin and other beta-lactams and creates the superbug MRSA. The assay workflow maintains Great Basin’s dedication to ease of use with less than one minute of hands-on time and no results interpretation due to the electronic results reporting.
The multiplex panel is run on the Great Basin Analyzer, which also performs the company’s commercially available low-plex tests for Clostridium difficile (C. diff) and Group BStreptococcus (GBS), as well as the company’s stand-alone molecular test for Shiga toxin- producing E. coli (STEC) detection.
Patients with a positive blood culture are generally treated with broad-spectrum antibiotics. However, according to the Centers for Disease Control, 20 to 50 percent of all positive blood cultures are likely false positives due to contamination caused by Coagulase-negative staphylococci (CoNS), many of which — like S. epidermidis— are part of the normal flora of human skin and are not dangerous. The Great Basin Staph ID/R Blood Culture Panel clearly identifies CoNS, giving care providers the data they need to quickly and more effectively manage patient treatment and reduce the unnecessary use of broad-spectrum antibiotics. A more complete diagnostic test drives disease-appropriate treatment that supports antimicrobial
stewardship, saving this last line of defense in the battle against antibiotic resistance and also helping lower treatment cost to patients, the hospital, and the healthcare system.
“Receiving FDA clearance for our Staph ID/R Blood Culture Panel — our second FDA clearance this month — marks a major milestone in our growth as a Company,” said Ryan Ashton, co- founder and Chief Executive Officer of Great Basin Scientific. “This menu expansion to four products, along with the five tests we plan to bring to clinical trial in 2016, will add further value for our customers who rely on our analyzer system to perform a greater variety of tests. The customer feedback we’ve received is that we are truly meeting the needs of the small and mid- sized hospital labs with our superior menu versatility, cost efficiency and customer service.”
Great Basin expects to offer the panel at a significantly lower cost than other molecular blood panels on the market today, making fast, easy diagnosis of staph-caused blood sepsis affordable for the small to medium hospitals the Company serves.
About Great Basin Scientific
Great Basin Scientific is a molecular diagnostics company that commercializes breakthrough chip-based technologies. The Company is dedicated to the development of simple, yet powerful, sample-to-result technology and products that provide fast, multiple-pathogen diagnoses of infectious diseases. The Company’s vision is to make molecular diagnostic testing so simple and cost-effective that every patient will be tested for every serious infection, reducing misdiagnoses and significantly limiting the spread of infectious disease. More information can be found on the company’s website at www.gbscience.com.
This press release includes forward-looking statements regarding the Company’s continuing business efforts related to its products, including but not limited to, statements regarding the Staph ID/R Blood Culture Panel benefits, planned tests to be brought to clinical trial in 2016, expected price for Staph ID/R Blood Culture Panel, target customer group and related statements. Forward-looking statements involve risk and uncertainties, which could cause actual results to differ materially, and reported results should not be considered as an indication of future performance. These risk and uncertainties include, but are not limited to: (i) our limited operating history and history of losses;; (ii) our ability to develop and commercialize new products and the timing of commercialization;; (iii) our ability to obtain capital when needed;; and (iv) other risks set forth in the Company’s filings with the Securities and Exchange Commission, including the risks set forth in the company’s Annual Report on Form 10-K for the fiscal year ended December 31, 2015. These forward-looking statements speak only as of the date hereof
and Great Basin Scientific specifically disclaims any obligation to update these forward-looking statements, except as required by law.
Kate Ottavio Kent
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