share_log

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宣布延长与Vizient公司的多年资本设备供应商协议
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.

马萨诸塞州列克星敦,2024年3月28日(GLOBE NEWSWIRE)——败血症致病原体和抗生素耐药基因快速检测领域的领导者T2 Biosystems, Inc.(纳斯达克股票代码:TTOO)今天宣布,其与美国最大的成员驱动型医疗保健绩效改善公司Vizient公司的多年资本设备供应商协议已延长至2025年3月31日。与Vizient签订的合同涵盖的产品包括T2Dx 仪器,T2Bertia 小组和 T2Candida 小组,直接从全血中检测出引起败血症的细菌和真菌病原体。

"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."

“我们很高兴延长与美国最大的团体采购组织Vizient的多年协议。这再次证实了我们的产品为疑似败血症患者提供的持续价值。” T2 Biosystems董事长兼首席执行官约翰·斯佩尔泽尔说。“我们认为,医院迫切需要更有效的快速诊断,以实现更快的靶向治疗,而与Vizient签订的这份合同改善了医院获得我们救生技术的机会。”

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.

通过延期合同,Vizient成员将继续获得T2Dx的更广泛风险敞口和合同定价 仪器,T2Bertia 小组和 T2Candida Panel,唯一获得美国食品药品管理局批准的能够直接从血液中检测出引起败血症的病原体的产品。

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为各种医疗保健组织提供服务,这些组织每年的总采购量约为1000亿美元,其中包括全国50%以上的急诊医院,95%的学术医疗中心和该国20%的门诊市场。

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.

关于 T2 生物系统
T2 Biosystems是快速检测诱发败血症的病原体和抗生素耐药基因领域的领导者,致力于通过帮助临床医生比以往任何时候都更快地有效治疗患者来改善患者护理和降低护理成本。T2 Biosystems 的产品包括 T2Dx 仪器,T2Bertia 小组,T2Candida 面板,T2Restance 面板和 T2Biothreat Panel,由专有的 T2 磁共振 (T2MR) 提供动力) 技术。T2 Biosystems拥有一系列活跃的未来产品,包括美国T2抗药小组、耳念珠菌测试和T2Lyme试剂盒。欲了解更多信息,请访问 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.

前瞻性陈述
本新闻稿包含1995年《私人证券诉讼改革法》所指的前瞻性陈述。本新闻稿中包含的所有与历史事实无关的陈述均应被视为前瞻性陈述,包括但不限于关于Vizient成员采用公司产品的可能性的陈述,以及包含 “期望”、“可能”、“应该”、“预期” 等字样的陈述以及具有未来或前瞻性质的类似陈述。这些前瞻性陈述基于管理层当前的预期。这些陈述既不是承诺也不是保证,但涉及已知和未知的风险、不确定性和其他重要因素,这些因素可能导致实际结果、业绩或成就与前瞻性陈述所表达或暗示的任何未来业绩、业绩或成就存在重大差异,包括但不限于:(i) 无法 (a) 实现承诺、合同或产品的预期收益;(b) 成功执行战略优先事项;(c) 将产品推向市场;(d) 扩大产品的使用或采用率;(e) 获取客户证言;(f)准确预测增长假设;(g)实现预期收入;(h)产生预期的运营支出水平;或(i)增加客户设施的高风险患者人数;(ii)早期数据无法预测最终结果;(iii)未能在预期的时间范围内或根本没有提交或获得预期的FDA申请或许可;或(iv)第1A项下讨论的因素。公司于2023年3月31日向美国证券交易委员会(SEC)提交的截至2022年12月31日年度的10-K表年度报告中的 “风险因素”,以及公司不时向美国证券交易委员会提交的其他文件,包括我们的10-Q表季度报告和8-K表最新报告。这些因素和其他重要因素可能导致实际业绩与本新闻稿中前瞻性陈述所示的结果存在重大差异。任何此类前瞻性陈述均代表管理层截至本新闻稿发布之日的估计。尽管除非法律要求,否则公司可能会选择在未来的某个时候更新此类前瞻性陈述,但它不承担任何更新此类前瞻性陈述的义务,即使随后发生的事件导致其观点发生变化。因此,任何人都不应假设公司在一段时间内的沉默意味着实际事件是按照此类前瞻性陈述中明示或暗示的方式发生的。不应将这些前瞻性陈述视为本新闻稿发布之日后任何日期的公司观点。

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

投资者联系人:
菲利普·特里普泰勒,吉尔马丁集团
ir@T2Biosystems.com
415-937-5406

Primary Logo

Source: T2 Biosystems, Inc.

来源:T2 Biosystems, Inc.

声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
    抢沙发