T2 Biosystems Announces Preliminary Fourth Quarter and Full Year 2024 Financial Results
TTOO 01.07.2025

About Gravity Analytica
Full Year 2024 and Recent Commercial Highlights (unaudited)
- Achieved record product revenues of
$2.3 million for the fourth quarter of 2024 and$8.3 million for the full-year 2024, representing increases of 37% and 23% respectively, compared to the prior year period, driven by record sepsis test sales. - Executed contracts for 27 T2Dx® Instruments in 2024, including 23 T2Dx Instruments for outside the
U.S. and 4 T2Dx Instruments for theU.S. - Entered into a multi-year exclusive U.S. agreement with Cardinal Health, granting Cardinal exclusive rights to sell the T2Dx Instrument, the T2Bacteria Panel, and the T2Candida® Panel, the only FDA-cleared products able to detect sepsis-causing pathogens directly-from-blood.
- Announced co-marketing collaboration with Prxcision, to market the Company’s rapid direct-from-blood diagnostics with Prxcision’s real-time AI-powered decision support platform to combat the escalating crisis of antibiotic resistance.
- Expanded international distribution network to include
the Netherlands ,Belgium ,Qatar ,Vietnam ,Malaysia , andIndonesia , and re-enteredSwitzerland . - Extended multi-year capital equipment supplier agreement with Vizient, Inc., the largest member-driven health care performance improvement company in the US, through March 31, 2026.
- Converted
$30 million of the Company’s term loan with entities affiliated withCRG Servicing, LLC (“CRG”) into T2 Biosystems’ common stock, reducing the Company’s debt and quarterly interest payments by approximately 80% over the past year. - Cash and cash equivalents were
$1.7 million as ofDecember 31, 2024 .
Full Year 2024 and Recent Pipeline and Clinical Highlights
- Announced plans to license the Company’s proprietary technology to expand its leadership in direct-from-whole-blood detection of sepsis-causing bacterial and fungal pathogens.
- Received FDA 510(k) clearance to expand the pathogen detection capabilities of the FDA-cleared T2Bacteria® Panel to add detection ofAcinetobacter baumannii.
- Received FDA 510(k) clearance to expand the use of the FDA-cleared T2Candida® Panel to include pediatric testing.
- Advanced the
T2Resistance Panel towardU.S. FDA 510(k) submission, expected to occur during the first quarter of 2025. - Successfully defended against an opposition filed against a key patent for its direct-from-whole blood detection method in the European Union
- Announced the publication of a new study highlighting the clinical benefits and performance of real-world use of the T2Resistance® Panel in The
Journal of Clinical Microbiology .
“We made considerable progress across the business during 2024, increasing our global installed base of T2Dx Instruments, and generating record sales for our sepsis test panels, including record
About T2 Biosystems
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, the likelihood that the exclusive
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Source: T2 Biosystems, Inc.