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[企业动态] 贝瑞和康与Illumina为CFDA获批 共同开发集成NGS系统

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发表于 2014-7-22 09:52 | 显示全部楼层 |阅读模式

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贝瑞和康与Illumina为CFDA获批 共同开发集成NGS系统
北京时间2014年7月22日,北京贝瑞和康生物技术有限公司与美国Illumina公司(NASDAQ: ILMN)在中国北京和美国圣迭戈同时宣布进行合作,选择使用Illumina领先的新一代基因测序技术作为贝瑞和康向中国食品药品监督管理局(CFDA)提交临床检测项目的注册申请的核心技术平台,在中国提供以高通量测序技术为基础的临床检测业务。

依据此份协议,合作双方已经共同开发出一款高性价比、易于操作的,用于无创DNA产前检测的新一代测序系统。目前,该系统的试剂盒以及测序设备在中国已经完成了临床验证,进入到CFDA医疗器械审批阶段的尾声。

这套全新的系统由两大部分组成。第一部分是贝瑞和康的贝比安TM无创DNA产前检测,由文库构建试剂盒、数据管理及分析系统组成;第二部分是全新的NextSeqTM CN500测序仪。贝比安TM检测运用独有的PCR-free文库构建技术和RUPATM快速分析系统,其性能已经得到超过20万例临床样本的检测验证。

“在中国,每年约有200万处于妊娠高危或高龄的孕妇,这一数字是美国的3倍。我们必须提供安全可靠的技术满足这些孕妇的临床需求。作为第一个也是唯一一个得到美国FDA(食品药品监督管理局)许可的高通量基因测序设备供应商,Illumina在测序领域具备丰富的经验,是非常理想的合作伙伴。”贝瑞和康CEO周代星博士说。

“贝瑞和康是中国无创DNA产前检测的领导者之一,Illumina公司对此次合作感到非常荣幸,将致力于支持贝瑞和康生产符合中国CFDA监管要求的高通量基因测序仪。” Illumina高级副总裁,体外诊断业务部主管Greg Heath说。“这一合作协议的签署,也体现了Illumina对于包括中国在内的全世界体外诊断公司的承诺,Illumina愿意与大家合作共同开发基于高通量基因测序技术的体外诊断新方法,并推进其商业化进程。”


关于贝瑞和康
北京贝瑞和康生物技术有限公司(www.berrygenomics.com)是中国生物技术公司的领导者之一。贝瑞和康以新一代高通量基因测序技术为核心,针对遗传疾病检测和肿瘤检测开发了一系列临床应用的整体解决方案,并成功推向市场。贝瑞和康在中国开创性的推广无创DNA产前检测技术(NIPT)并成为领先的NIPT服务机构。目前,贝瑞和康同样正在研发更多与NIPT同样先进的产品和技术,为了满足遗传疾病和肿瘤疾病检测的广泛市场需求。


关于Illumina
Illumina公司(www.illumina.com)是全球生命科学仪器领域顶级的开发商和制造商。为遗传变异研究及功能分析提供生命科学研究方法与集成系统。为基因分型、拷贝数变异分析、甲基化分析、基因表达谱、和DNA/RNA/蛋白质多重分析提供创新的测序技术和芯片技术解决方案。同时为客户提供推进基因组学及诊断学发展的研究工具和科研服务。Illumina公司的技术和产品,加速了遗传研究及其相关应用的发展,为分子医学的发展铺平道路,并最终提升医疗服务的质量。



BEIJING, CHINA and SAN DIEGO, CA, USA – July 21, 2014 –Berry Genomics Co. Ltd. announced today it has chosen IlluminaInc’s.(NASDAQ: ILMN)next generation sequencing (NGS) technology as the platform on which Berry will secure Chinese Food and Drug Administration (CFDA) regulatory approval for clinical applications, thereby expanding access to NGS-based tests in China.

Under the agreement, the companies co-developed an NGS system to provide a cost-effective, easy-to-use assay for non-invasive prenatal testing (NIPT). A working version of the new assay and instrument system has been validated in clinical settings in China, and is in late stage review under the CFDA’s medical device registration process.

The new system integrates Berry Genomics’ BambniTM assay, which includes a library preparation kit, analysis software, and a sequencing instrument based on Illumina’s NextSeqTM 500 Sequencing System. Berry’s proprietary BambniTM assay, which has been validated on more than 200,000 samples, utilizes a unique PCR-free library prep technology and the proprietary RUPATM analysis software.

“There are two million high-risk and advanced maternal age pregnancies a year in China, which is about three times the size of the U.S. market. We need to ensure we are addressing women’s needs by offering a safe and proven technology. As the first and only company with a U.S. FDA cleared next-generation sequencing instrument, Illumina is an ideal collaboration partner given their experience,” said Daixing Zhou, CEO of Berry Genomics.

“Berry is one of the leading providers of NIPT in China, and Illumina is excited to collaborate with them to customize the NextSeq under CFDA requirements,”said Greg Heath, Senior Vice President, IVD Development at Illumina. “This agreement is an example of our commitment to working with clinical companies in China and worldwide who want to develop and commercialize in vitro diagnostics based on next-generation sequencing.”


About Berry Genomics
Berry Genomics (www.berrygenomics.com) is a leading biotech company in China which develops and commercializes next generation sequencing based integrated solutions for clinical applications, primarily in genetic testing and oncology testing. Berry Genomics pioneered non-invasive prenatal testing (NIPT) in China and is the leading provider of NIPT in China. Like NIPT, the products and technologies under development at Berry Genomics will address unmet needs of other genetic diseases and cancer.


About Illumina
Illumina (www.illumina.com) is a leading developer, manufacturer, and marketer of life science tools and integrated systems for the analysis of genetic variation and function. We provide innovative sequencing and array-based solutions for genotyping, copy number variation analysis, methylation studies, gene expression profiling, and low-multiplex analysis of DNA, RNA, and protein. We also provide tools and services that are fueling advances in consumer genomics and diagnostics. Illumina’s technology and products accelerate genetic analysis research and its application, paving the way for molecular medicine and ultimately transforming healthcare.


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