T2 Biosystems Announces Exclusive U.S. Agreement with Cardinal Health to Sell its FDA-Cleared Direct-From-Blood Diagnostics for Rapid Detection of Sepsis-Causing Pathogens
08 October 2024 - 12:05AM
T2 Biosystems, Inc. (NASDAQ: TTOO) (the “Company”), a leader in the
rapid detection of sepsis-causing pathogens and antibiotic
resistance genes, today announced that it has entered into a
multi-year exclusive U.S. agreement with Cardinal Health (NYSE:
CAH),. Under the agreement, Cardinal Health will have exclusive
rights to sell T2 Biosystems’ FDA-cleared direct-from-blood
diagnostics for the rapid detection of sepsis-causing pathogens,
including the T2Dx® Instrument, the T2Bacteria® Panel, and the
T2Candida® Panel.
“We are thrilled to have entered into a
distribution agreement with Cardinal Health that will make them the
exclusive distributor of our FDA-cleared direct-from-blood
diagnostics in the United States which will dramatically increase
our representation with hospital customers who are eager to add
culture-independent diagnostics to strengthen their sepsis clinical
care,” stated John Sperzel, Chairman and CEO of T2 Biosystems.
“We expect this collaboration to greatly expand our access to the
U.S. hospital market as Cardinal Health has an extensive commercial
and distribution infrastructure that includes capital equipment
specialists who will sell the T2Dx Instrument.”
Despite the widespread use of blood
culture-based diagnostics to detect sepsis-causing pathogens and
antibiotic susceptibility, sepsis remains the leading cause of
death in U.S. hospitals and claims the lives of approximately
350,000 Americans annually.1 Sepsis also represents the leading
cost of U.S. hospitalization, costing our healthcare system an
estimated $62 billion annually.2 Lastly, sepsis is the leading
cause of 30-day hospital readmission in the U.S., with 19% of
sepsis survivors re-hospitalized within 30 days and 40% within 90
days,3,4,5 which underscores the need for advanced technologies in
sepsis detection.
A September 2024 article which appeared in The
Lancet, titled “The Culture of Blood Culture,” described the
weakness of blood culture, including poor sensitivity (i.e., missed
infections), slow time to result (i.e., typically 2-3 days);
vulnerability to contamination; reduced effectiveness in patients
who have received antibiotics; and a labor-intensive process
requiring skilled technicians.
T2 Biosystems has developed the only FDA-cleared
diagnostics able to detect sepsis-causing bacterial and fungal
pathogens directly-from-blood, in just 3-5 hours, without the need
to wait days for a positive blood culture. The T2Bacteria Panel
runs on the FDA cleared T2Dx Instrument and detects six pathogens
which account for nearly 75% of U.S. bacterial bloodstream
infections, with 90% sensitivity and 98% specificity, including E.
faecium, S. aureus, K. pneumoniae, A. baumannii, P.
aeruginosa, and E. coli. The T2Candida Panel runs on the
FDA-cleared T2Dx Instrument and detects five Candida species which
account for up to 95% of U.S. Candida blood stream infections, with
91% sensitivity and 99% specificity, including C. albicans, C.
tropicalis, C. parapsilosis, C. krusei, and C. glabrata.
The T2 Biosystems test panels are not affected by prior
antimicrobial treatment.
About Cardinal HealthCardinal
Health is a distributor of pharmaceuticals, a global manufacturer
and distributor of medical and laboratory products, and a provider
of performance and data solutions for healthcare facilities. With
more than 50 years in business, operations in more than 30
countries and approximately 48,000 employees globally, Cardinal
Health is essential to care. Information about Cardinal Health is
available at cardinalhealth.com.
About T2 BiosystemsT2
Biosystems, a leader in the rapid detection of sepsis-causing
pathogens and antibiotic resistance genes, 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 are powered by the proprietary T2 Magnetic
Resonance (T2MR®) technology and include the T2Dx® Instrument, the
T2Bacteria® Panel, the T2Candida® Panel, the T2Resistance® Panel,
and the T2Biothreat™ Panel. T2 Biosystems has an active pipeline of
future products, including the U.S. T2Resistance Panel, the T2Lyme™
Panel, and the expended T2Candida Panel to add the detection of
Candida auris. For more information, please visit
www.t2biosystems.com.
- Centers for Disease Control
https://www.cdc.gov/mmwr/volumes/72/wr/mm7234a2.htm
- Buchman, T. G., Simpson, S. Q., Sciarretta, K. L., Finne, K.
P., Sowers, N., Collier, M., ... & Kelman, J. A. (2020). Sepsis
among medicare beneficiaries: 3. The methods, models, and forecasts
of sepsis, 2012–2018. Critical care medicine, 48(3),
302-318.
https://journals.lww.com/ccmjournal/FullText/2020/03000/Sepsis_Among_Medicare_Beneficiaries__3__The.4.as
- Fingar K, Washington R. HCUP Statistical Brief #196. November
2015. Agency for Healthcare Research and Quality, Rockville, MD.
https://www.hcup-us.ahrq.gov/reports/statbriefs/sb196-Readmissions-Trends-High-Volume-Conditions.jsp
- Gadre SK, et al. Chest. 2019;155(3):483-490.
https://journal.chestnet.org/article/S0012-3692(18)32895-2/abstract
- Prescott H and Angus D. JAMA. 2018;319(1):91.
https://jamanetwork.com/journals/jama/fullarticle/2667724
Forward-Looking Statements
This 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 the likelihood that this collaboration will
greatly expand our access to the U.S. hospital market and the
potential that hospitals will complement the standard of care with
new culture-independent diagnostic technology, as well as
statements that include the words “expect,” “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 ended December 31, 2023, filed with the U.S. Securities and
Exchange Commission, or SEC, on April 1, 2024, and other filings
the Company makes with the SEC from time to time, including our
Quarterly Reports on Form 10-Q and Current Reports on Form 8-K.
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 Company’s 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.
Investor Contact:Philip Trip Taylor, Gilmartin
Groupir@T2Biosystems.com 415-937-5406
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