Hello GBSN $$$ fans, wake up .... interesting research from other board ...>
... The 2 FDA approvals should - bring up to 300 million $$$ annual turnover ...
2) In addition to two already-approved tests, Great Basin has initiated clinical trials in preparation for FDA 510(k) marketing clearance: A) Staph blood infections (Staph ID/R), a potential $100- $150 million annual market in the US, and B) Shiga Toxin Producing E. Coli (STEC) test, also an approximate $100-$150 million US market. Marketing approvals for these next two diagnostic assays are expected to be filed in 2015 with potential clearance sometime this year or next. In addition, the Company has identified three additional assays for next-step clinical trials, including two in the higher-revenue multiplex panel category, with the other for the large-market size Staph aureus pre-surgical screening assay. 3) After completing a somewhat smaller-size IPO last year, Great Basin management can finally breathe easier regarding its longterm business plan following a recent, much larger equity raise earlier this year. In addition to the $21.7 million in approximate gross proceeds garnered from the February 2015 preferred stock offering, the Company has been able to raise additional funds through the subsequent exercise of warrants, and may continue to do so in the future depending on share price and volume. This additional cash is key to the Company’s growth going forward, fueling not only greater sales and marketing budgets, but increased inventories of both analyzer instruments (provided free of charge to customers) and disposable cartridges, as customer usage of Great Basin’s proprietary molecular diagnostic tests increase.
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