GlobeNewswire Inc | Jan 11, 2022 09:00AM EST

January 11, 2022

LEXINGTON, Mass., Jan. 11, 2022 (GLOBE NEWSWIRE) -- T2 Biosystems, Inc. (NASDAQ:TTOO), a leader in the rapid detection of sepsis-causing pathogens, today announced the initiation of a U.S. multi-site clinical trial evaluating the performance of its T2Resistance Panel designed to support a submission to the U.S. Food and Drug Administration (FDA).

The T2Resistance Panel, which runs on T2 Biosystems T2Dx Instrument, is a direct-from-blood test panel that detects 13 antibiotic resistance genes from both Gram-positive and Gram-negative bacterial pathogens, which are known to cause antibiotic-resistant infections that may lead to sepsis, and provides results in 3-5 hours without the need to wait for blood culture. The T2Resistance Panel is commercially available in Europe under a CE mark and was granted Breakthrough Device designation from the FDA, which provides for a prioritized FDA review process.

The Company plans to file the FDA submission for the T2Resistance Panel in 2022 following completion of the clinical trial, which will include up to 1,500 patients across 10 U.S. hospitals. The trial is estimated to cost T2 Biosystems $2,500,000.

We are pleased to have initiated the U.S. clinical trial for the T2Resistance Panel ahead of schedule, which should provide a path to file the FDA submission during 2022, said John Sperzel, Chairman and CEO at T2 Biosystems. We believe the detection of antibiotic resistant genes directly from whole blood in 3-5 hours would be a game changer in the U.S., as data show that each hour of delayed targeted treatment increases mortality risk by up to 8%. The T2Resistance Panel enables rapid detection of the common antibiotic resistance genetic markers and aids clinicians in targeting appropriate antimicrobial therapy for their patients when time is most critical. We intend to expand our sepsis product portfolio of culture independent diagnostic tests through the addition of the T2Resistance Panel in the U.S. market, and we thank BARDA for its continued support to address the growing threat of antimicrobial resistance.

Antimicrobial resistance is considered one of the greatest threats to global health. The U.S. Centers for Disease Control and Prevention estimates at least 2.8 million people are infected with antimicrobial-resistant bacteria or fungi in the U.S. each year, and more than 35,000 die as a result. Prudent use of antimicrobials reduces the risk of developing antimicrobial resistance and leads to a positive public health impact. Current standard of care therapy, blood culturing and the use of broad spectrum antibiotics, contributes to the overuse of antimicrobials and drives increases in global drug resistance rates. A culture-independent diagnostic would save critical time, improve therapeutic decision making by clinicians and improve patient outcome.

This project has been funded in whole or in part with federal funds from the U.S. Department of Health and Human Services, Office of the Assistant Secretary for Preparedness and Response, Biomedical Advanced Research and Development Authority (BARDA), under Contract No. 75A50119C00053.

About T2 BiosystemsT2 Biosystems, a leader in the rapid detection of sepsis-causing pathogens, is dedicated to improving patient care and reducing the cost of care by helping clinicians effectively treat patients faster than ever before. T2 Biosystems products include the T2Dx Instrument, T2Candida Panel, the T2Bacteria Panel, the T2Resistance Panel, and the T2SARS-CoV-2 Panel and are powered by the proprietary T2 Magnetic Resonance (T2MR) technology. T2 Biosystems has an active pipeline of future products, including the T2Cauris Panel, and T2Lyme Panel, as well as additional products for the detection of bacterial and fungal pathogens and associated antimicrobial resistance markers, and biothreat pathogens.

Forward-Looking StatementsThis press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding the ability of T2s culture-independent diagnostics to allow clinicians to achieve appropriate targeted therapy for their patients, faster than is possible with blood culture, the current standard of care, as well as statements that include the words expect, intend, plan, believe, project, forecast, estimate, may, should, anticipate, and similar statements of a future or forward looking nature. These forward-looking statements are based on management's current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, (i) any inability to (a) realize anticipated benefits from commitments, contracts or products; (b) successfully execute strategic priorities; (c) bring products to market; (d) expand product usage or adoption; (e) obtain customer testimonials; (f) accurately predict growth assumptions; (g) realize anticipated revenues; (h) incur expected levels of operating expenses; or (i) increase the number of high-risk patients at customer facilities; (ii) failure of early data to predict eventual outcomes; (iii) failure to make or obtain anticipated FDA filings or clearances within expected time frames or at all; or (iv) the factors discussed under Item 1A. "Risk Factors" in the Company's Annual Report on Form 10-K for the year endedDecember 31, 2020, filed with theU.S. Securities and Exchange Commission, orSEC, onMarch 31, 2021, and other filings the Company makes with theSECfrom time to time. These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While the Company may elect to update such forward-looking statements at some point in the future, unless required by law, it disclaims any obligation to do so, even if subsequent events cause its views to change. Thus, no one should assume that the Companys silence over time means that actual events are bearing out as expressed or implied in such forward-looking statements. These forward-looking statements should not be relied upon as representing the Company's views as of any date subsequent to the date of this press release.

Media Contact:Meagan Dominick, Vault Communicationsmdominick@vaultcommunications.com 773-369-4255

Investor Contact:Philip Trip Taylor, Gilmartin Groupphilip@gilmartinIR.com 415-937-5406