share_log

T2 Biosystems | 8-K: T2 Biosystems Receives Fda Approval to Market T2candida Panel to Paediatric Patients

T2 Biosystems | 8-K: T2 Biosystems Receives Fda Approval to Market T2candida Panel to Paediatric Patients

T2 Biosystems | 8-K:T2 Biosystems獲得FDA批准向兒科患者銷售T2Candida面板
美股SEC公告 ·  2024/09/16 21:21

Moomoo AI 已提取核心訊息

T2 Biosystems announced FDA clearance to market its T2Candida Panel for pediatric patients on September 16, 2024. The T2Candida Panel is the only FDA-cleared diagnostic test that can detect sepsis-causing Candida species directly from blood in 3-5 hours, without waiting for blood culture results. The panel detects five Candida species that account for up to 95% of all Candida bloodstream infections in the U.S.Clinical studies demonstrate significant advantages of the T2Candida Panel in pediatric applications. A 2022 study at Bambino Gesù hospital showed results 121.8 hours faster than blood culture, with higher detection rates. Additionally, a prospective study in Clinical Infectious Diseases found the T2Candida Panel had the highest sensitivity and specificity among four pre-blood culture tests.The expansion allows immediate marketing to over 200 children's hospitals in the U.S., addressing a critical healthcare need. According to research, children with invasive candidiasis face extended hospital stays averaging 21 days and approximately $92,000 in excess hospital costs. The panel is expected to improve outcomes through faster targeted antifungal treatment for pediatric patients.
T2 Biosystems announced FDA clearance to market its T2Candida Panel for pediatric patients on September 16, 2024. The T2Candida Panel is the only FDA-cleared diagnostic test that can detect sepsis-causing Candida species directly from blood in 3-5 hours, without waiting for blood culture results. The panel detects five Candida species that account for up to 95% of all Candida bloodstream infections in the U.S.Clinical studies demonstrate significant advantages of the T2Candida Panel in pediatric applications. A 2022 study at Bambino Gesù hospital showed results 121.8 hours faster than blood culture, with higher detection rates. Additionally, a prospective study in Clinical Infectious Diseases found the T2Candida Panel had the highest sensitivity and specificity among four pre-blood culture tests.The expansion allows immediate marketing to over 200 children's hospitals in the U.S., addressing a critical healthcare need. According to research, children with invasive candidiasis face extended hospital stays averaging 21 days and approximately $92,000 in excess hospital costs. The panel is expected to improve outcomes through faster targeted antifungal treatment for pediatric patients.
T2 Biosystems於2024年9月16日宣佈獲得FDA批准,將其T2Candida檢測面板用於兒科患者。T2Candida面板是唯一獲得FDA批准的診斷測試,可以在3-5小時內直接從血液中檢測引起敗血症的念珠菌屬,而無需等待血培養結果。該面板檢測五種念珠菌種類,這些種類佔美國所有念珠菌血流感染的95%。臨牀研究表明T2Candida面板在兒科應用方面具有顯著優勢。2022年在Bambino Gesù醫院的研究顯示,結果比血培養快121.8小時,且檢測率更高。此外,臨牀感染疾病雜誌中的一項前瞻性研究發現,在四種血培養前測試中,T2Candida面板具有最高的靈敏度和特異性。此次擴展使得在美國超過200家兒童醫院進行即時營銷,以滿足關鍵的醫療需求。研究表明,患有侵襲性念珠菌病的兒童住院時間平均延長21天,額外住院費用約爲92,000美元。預計該面板將通過更快的針對性抗真菌治療來改善兒科患者的治療效果。
T2 Biosystems於2024年9月16日宣佈獲得FDA批准,將其T2Candida檢測面板用於兒科患者。T2Candida面板是唯一獲得FDA批准的診斷測試,可以在3-5小時內直接從血液中檢測引起敗血症的念珠菌屬,而無需等待血培養結果。該面板檢測五種念珠菌種類,這些種類佔美國所有念珠菌血流感染的95%。臨牀研究表明T2Candida面板在兒科應用方面具有顯著優勢。2022年在Bambino Gesù醫院的研究顯示,結果比血培養快121.8小時,且檢測率更高。此外,臨牀感染疾病雜誌中的一項前瞻性研究發現,在四種血培養前測試中,T2Candida面板具有最高的靈敏度和特異性。此次擴展使得在美國超過200家兒童醫院進行即時營銷,以滿足關鍵的醫療需求。研究表明,患有侵襲性念珠菌病的兒童住院時間平均延長21天,額外住院費用約爲92,000美元。預計該面板將通過更快的針對性抗真菌治療來改善兒科患者的治療效果。
声明:本內容僅用作提供資訊及教育之目的,不構成對任何特定投資或投資策略的推薦或認可。 更多信息