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T2 Biosystems Announces Extension of Multi-Year Capital Equipment Supplier Agreement With Vizient, Inc.

T2 Biosystems Announces Extension of Multi-Year Capital Equipment Supplier Agreement With Vizient, Inc.

T2 Biosystems宣佈延長與Vizient公司的多年資本設備供應商協議
T2 Biosystems ·  03/28 00:00

LEXINGTON, Mass., March 28, 2024 (GLOBE NEWSWIRE) -- T2 Biosystems, Inc. (NASDAQ:TTOO), a leader in the rapid detection of sepsis-causing pathogens and antibiotic resistance genes, today announced that its multi-year capital equipment supplier agreement with Vizient, Inc., the largest member-driven health care performance improvement company in the United States, has been extended through March 31, 2025. The products covered under the contract with Vizient include the T2Dx Instrument, the T2Bacteria Panel and the T2Candida Panel, which detect sepsis-causing bacterial and fungal pathogens directly from whole blood.

馬薩諸塞州列剋星敦,2024年3月28日(GLOBE NEWSWIRE)——敗血症致病原體和抗生素耐藥基因快速檢測領域的領導者T2 Biosystems, Inc.(納斯達克股票代碼:TTOO)今天宣佈,其與美國最大的成員驅動型醫療保健績效改善公司Vizient公司的多年資本設備供應商協議已延長至2025年3月31日。與Vizient簽訂的合同涵蓋的產品包括T2Dx 儀器,T2Bertia 小組和 T2Candida 小組,直接從全血中檢測出引起敗血症的細菌和真菌病原體。

"We are pleased to extend our multi-year agreement with Vizient, the nation's largest group purchasing organization. This reiterates the continued value that our products offer to patients suspected of sepsis," stated John Sperzel, Chairman and CEO of T2 Biosystems. "We believe there is a strong need for hospitals to have more effective rapid diagnostics that enable faster targeted therapy and this contract with Vizient improves hospitals' access to our life-saving technology."

“我們很高興延長與美國最大的團體採購組織Vizient的多年協議。這再次證實了我們的產品爲疑似敗血症患者提供的持續價值。” T2 Biosystems董事長兼首席執行官約翰·斯佩爾澤爾說。“我們認爲,醫院迫切需要更有效的快速診斷,以實現更快的靶向治療,而與Vizient簽訂的這份合同改善了醫院獲得我們救生技術的機會。”

Through the extended contract, Vizient members will continue to have access to broader exposure and contracted pricing for the T2Dx Instrument, the T2Bacteria Panel and the T2Candida Panel, the only FDA-cleared products able to detect sepsis-causing pathogens directly from blood.

通過延期合同,Vizient成員將繼續獲得T2Dx的更廣泛風險敞口和合同定價 儀器,T2Bertia 小組和 T2Candida Panel,唯一獲得美國食品藥品管理局批准的能夠直接從血液中檢測出引起敗血症的病原體的產品。

Vizient serves a wide range of health care organizations that represent a combined purchasing volume of approximately $100 billion annually and includes more than 50 percent of the nation's acute care hospitals, 95 percent of all academic medical centers, and 20 percent of the country's ambulatory market.

Vizient爲各種醫療保健組織提供服務,這些組織每年的總採購量約爲1000億美元,其中包括全國50%以上的急診醫院,95%的學術醫療中心和該國20%的門診市場。

About T2 Biosystems
T2 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 include the T2Dx Instrument, the T2Bacteria Panel, the T2Candida Panel, the T2Resistance Panel, and the T2Biothreat Panel, and are powered by the proprietary T2 Magnetic Resonance (T2MR) technology. T2 Biosystems has an active pipeline of future products, including the U.S. T2Resistance Panel, the Candida auris test, and the T2Lyme Panel. For more information, please visit www.t2biosystems.com.

關於 T2 生物系統
T2 Biosystems是快速檢測誘發敗血症的病原體和抗生素耐藥基因領域的領導者,致力於通過幫助臨床醫生比以往任何時候都更快地有效治療患者來改善患者護理和降低護理成本。T2 Biosystems 的產品包括 T2Dx 儀器,T2Bertia 小組,T2Candida 面板,T2Restance 面板和 T2Biothreat Panel,由專有的 T2 磁共振 (T2MR) 提供動力) 技術。T2 Biosystems擁有一系列活躍的未來產品,包括美國T2抗藥小組、耳念珠菌測試和T2Lyme試劑盒。欲了解更多信息,請訪問 www.t2biosystems.com

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 regarding the likelihood that Vizient members will adopt the Company's products, 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, 2022, filed with the U.S. Securities and Exchange Commission, or SEC, on March 31, 2023, 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.

前瞻性陳述
本新聞稿包含1995年《私人證券訴訟改革法》所指的前瞻性陳述。本新聞稿中包含的所有與歷史事實無關的陳述均應被視爲前瞻性陳述,包括但不限於關於Vizient成員採用公司產品的可能性的陳述,以及包含 “期望”、“可能”、“應該”、“預期” 等字樣的陳述以及具有未來或前瞻性質的類似陳述。這些前瞻性陳述基於管理層當前的預期。這些陳述既不是承諾也不是保證,但涉及已知和未知的風險、不確定性和其他重要因素,這些因素可能導致實際結果、業績或成就與前瞻性陳述所表達或暗示的任何未來業績、業績或成就存在重大差異,包括但不限於:(i) 無法 (a) 實現承諾、合同或產品的預期收益;(b) 成功執行戰略優先事項;(c) 將產品推向市場;(d) 擴大產品的使用或採用率;(e) 獲取客戶證言;(f)準確預測增長假設;(g)實現預期收入;(h)產生預期的運營支出水平;或(i)增加客戶設施的高風險患者人數;(ii)早期數據無法預測最終結果;(iii)未能在預期的時間範圍內或根本沒有提交或獲得預期的FDA申請或許可;或(iv)第1A項下討論的因素。公司於2023年3月31日向美國證券交易委員會(SEC)提交的截至2022年12月31日年度的10-K表年度報告中的 “風險因素”,以及公司不時向美國證券交易委員會提交的其他文件,包括我們的10-Q表季度報告和8-K表最新報告。這些因素和其他重要因素可能導致實際業績與本新聞稿中前瞻性陳述所示的結果存在重大差異。任何此類前瞻性陳述均代表管理層截至本新聞稿發佈之日的估計。儘管除非法律要求,否則公司可能會選擇在未來的某個時候更新此類前瞻性陳述,但它不承擔任何更新此類前瞻性陳述的義務,即使隨後發生的事件導致其觀點發生變化。因此,任何人都不應假設公司在一段時間內的沉默意味着實際事件是按照此類前瞻性陳述中明示或暗示的方式發生的。不應將這些前瞻性陳述視爲本新聞稿發佈之日後任何日期的公司觀點。

Investor Contact:
Philip Trip Taylor, Gilmartin Group
ir@T2Biosystems.com
415-937-5406

投資者聯繫人:
菲利普·特里普泰勒,吉爾馬丁集團
ir@T2Biosystems.com
415-937-5406

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Source: T2 Biosystems, Inc.

來源:T2 Biosystems, Inc.

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