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肝胆相照论坛 论坛 学术讨论& HBV English [news]Roche Receives FDA Approval for Acute Hepatiti ...
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[news]Roche Receives FDA Approval for Acute Hepatitis B Test [复制链接]

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发表于 2011-11-1 13:42 |只看该作者 |倒序浏览 |打印
Roche Receives FDA Approval for Acute Hepatitis B Test                                Elecsys Anti-HBc IgM assay completes acute hepatitis test panel on cobas e 601 analyzer                                                                                                  
                                             
                           
                           

INDIANAPOLIS, Oct. 31, 2011 /PRNewswire via COMTEX/ --Roche (six:RO)(six:ROG)(otcqx:RHHBY) announced today that the U.S. Food and Drug Administration (FDA) granted Premarket Approval (PMA) for its IgM antibody to hepatitis B core antigen (Anti-HBc IgM) assay for use on the cobas e 601 analyzer, the immunoassay module of the cobas® 6000 analyzer series for mid-volume laboratories. The test represents the final component of the acute panel within the hepatitis test menu for the cobas 6000 series.                                                       

                           

The Anti-HBc IgM assay is used for the in-vitro qualitative determination of IgM antibodies to hepatitis B core antigen (anti-HBc IgM) in human serum or plasma.  The presence of anti-HBc IgM, in conjunction with other laboratory results and clinical information, is indicative of an acute or recent hepatitis B virus (HBV) infection.* The assay is intended for use with Roche's electrochemiluminescence (ECL) technology, a highly sensitive light detection system that provides excellent low-end sensitivity and broad dynamic measuring ranges.                                                       

                           

With this approval, Roche now offers a full selection of hepatitis tests in its immunoassay portfolio:  HBsAg, HBsAg Confirmatory, Anti-HBs, Anti-HCV, Anti-HAV, Anti-HAV IgM, Anti-HBc IgM (approved for cobas e 601 analyzer) and Anti-HBc (approved for MODULAR ANALYTICS E170 analyzer). The combination of full hepatitis menu with the lowest assay duration on the market, the broadest integrated menu and ECL technology allows the Roche total solution to inspire confidence in the laboratory environment. The Anti-HBc IgM assay is also pending FDA approval for use on Roche's cobas e 411 and MODULAR ANALYTICS E170 analyzers. Roche's current analyzer portfolio offers labs short assay duration (9 to 27 minutes) and the broadest test menu available on an integrated platform.                                                       

                           

About Roche                                                       

                           

Headquartered in Basel, Switzerland, Roche is a leader in research-focused healthcare with combined strengths in pharmaceuticals and diagnostics. Roche is the world's largest biotech company with truly differentiated medicines in oncology, virology, inflammation, metabolism and CNS. Roche is also the world leader in in-vitro diagnostics, tissue-based cancer diagnostics and a pioneer in diabetes management. Roche's personalized healthcare strategy aims at providing medicines and diagnostic tools that enable tangible improvements in the health, quality of life and survival of patients. In 2010, Roche had over 80,000 employees worldwide and invested over 9 billion Swiss francs in R&D. The Group posted sales of 47.5 billion Swiss francs. Genentech, United States, is a wholly owned member of the Roche Group. Roche has a majority stake in Chugai Pharmaceutical, Japan. For more information:  www.roche.com     or  www.roche-diagnostics.us    .                                                       

                           

*The Elecsys Anti-HBc Igm immunoassay's performance has not been established for the monitoring of HBV disease or therapy.                                                       

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发表于 2011-11-1 13:43 |只看该作者
罗氏公司获得美国FDA批准为急性乙型肝炎测试
Elecsys抗- HBc IgM抗体检测完成急性肝炎测试面板上COBAS发送601分析仪

印第安纳波利斯,2011年10月31日/美通社讯/ - 罗氏(六:反渗透)(SIX:ROG)(OTCQX:RHHBY)今天宣布,美国食品和药物管理局(FDA)批准其上市前批准(PMA) IgM抗体,乙肝核心抗原(抗- HBc IgM)的使用COBAS发送601,免疫分析模块的COBAS分析仪® 6000分析仪系列中体积实验室的检测。测试代表的急性肝炎COBAS 6000系列测试菜单面板内的最后一个组成部分。

抗- HBc IgM抗体检测是用于在体外定性测定人血清或血浆中的IgM抗体,乙肝核心抗原(抗- HBc IgM)的。抗- HBc IgM的存在,与其他化验结果和临床资料结合,是一种急性或最近乙型肝炎病毒(HBV)感染的指标.*检测使用罗氏电化学发光(ECL)技术,高度敏感的光检测系统,可提供出色的低端灵敏度和宽广的动态测量范围。

有了这个批​​准,罗氏现在提供了一个在其免疫法组合型肝炎测试选择:乙肝表面抗原,乙肝表面抗原验证,抗- HBs,抗- HCV,抗- HAV,抗- HAV IgM抗体,抗- HBc IgM抗体(COBAS发送601批准分析仪)和抗- HBc(E170分析仪模块化分析批准)。充分肝炎菜单与市场上最低的检测期限,最广泛的综合菜单和ECL技术相结合,允许罗氏整体解决方案,在实验室环境中激发信心。抗- HBc IgM的检测也正在等待FDA批准罗氏公司的COBAS发送411和模块化分析E170分析仪使用。目前罗氏公司的分析仪产品组合提供实验室检测期限短(9至27分钟)和一个集成平台上提供最广泛的测试菜单。

罗氏公司简介

总部设在瑞士巴塞尔的罗氏公司是在研究为重点的综合优势,在制药和诊断的医疗的领导者。罗氏公司是世界上最大的生物技术公司在肿瘤学,病毒学,炎症,代谢和中枢神经系统的真正差异化的药物。罗氏也是体外诊断的全球领导者,组织为基础的癌症诊断和糖尿病管理的先驱。罗氏的个性化医疗战略的目的是提供药品和诊断工具,使有形的健康,生活质量和患者的生存期的改善。 2010年,罗氏公司已超过80,000世界各地的员工和在R&D投资超过9亿瑞士法郎该集团的销售额为47.5亿瑞士法郎。美国基因泰克是罗氏集团的全资成员。罗氏制药公司已经在日本中外制药的多数股权。欲了解更多信息:www.roche.com或www.roche - diagnostics.us。

* Elecsys的抗- HBc IgM免疫的性能尚未建立监测乙肝疾病或治疗。
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