快公司:2016年最具创新力的10家生物科技企业

  • 快公司,2016年,最具创新力,生物科技
  • 生物探索



2016年年初,《快公司》评估了上千家企业的创新表现,发现能够改变未来的观点、创意、人物、设计及技术的元素,从中挑选出拥有伟大想法以及强烈愿景的公司,推出了“2016年中国最佳创新公司”。其中在生物科技领域,评选出了10家最具有创新力的公司。


01 Novocure——For attacking tumors with electricity

Novocure开发了一种便携式(重约2.7 kg)、电池供电的装置,可在大脑中形成电场,从而治疗化疗后复发的成人多形性胶质母细胞瘤患者。


02 Bristol-Myers Squibb——For treating tumors with T cells

百时美施贵宝(BMS)开发的PD-1免疫疗法Opdivo(nivolumab)喜获欧盟批准治疗晚期黑色素瘤,使其成为首个撬开欧洲市场的PD-1免疫疗法,同时也是首个成功拿下日本、美国、欧盟3大主要市场的PD-1免疫疗法。


03 Amgen——For making cancer therapy go viral

安进公司的T-Vec是适用于首次手术后复发的黑色素瘤患者的局部治疗,是国际上首个被批准的溶瘤病毒疗法。


04 Emerald Therapeutics——For building a testing lab in the cloud

祖母绿治疗(Emerald Therapeutics)的模式是让生物科技创业公司摆脱一些初级工作的负担——一个个地数细胞,或分离蛋白质——将研究人员解放出来去做一些更复杂的工作,对结果进行分析。为了控制大量的实验室设备,祖母绿开发了自己的电脑语言和管理软件。


05 Enteromedics——For disrupting the signals between the brain and stomach to fight obesity

Enteromedics公司开发的Maestro Rechargeable System是FDA批准的首款食欲控制装置,可暂时阻滞大脑与胃之间的神经交通,从而减少饥饿感并增加饱食感,有望成为全世界胖人的福音。


06 Corgenix Medical Corp.——For speeding up the Ebola test

Corgenix Medical公司研发了一种可以快速检测埃博拉病毒和苏丹病毒的POCT设备,对全球公共卫生和防范生物恐怖主义威胁有重要的意义。


07 Oxford Performance Materials——For designing a better spine implant

牛津性能材料公司(Oxford Performance Materials)利用3D打印技术制作而成的头骨植入物由聚合物制成,意在促进骨骼生长,帮助植入物与周边骨骼的融合,且已经获得FDA批准。


08 Proteus Digital Health——For digitizing Abilify

Proteus Digital Health公司研发的电子药片(可消化微芯片)是这样的:当你吞下这种微芯片后,它们就会在身体里发挥作用,把所有重要的医疗数据直接传送到你的手机上。当然,这种芯片不会改造你的内脏,把你转变成一个机械人。


09 23andMe——For reinventing itself to get FDA approval



随着 23andMe不断向 FDA 证明自己的检测手段、用户教育方式以及后续服务,FDA 历经2年终于批准其布卢姆综合症基因携带者检测服务(一种隐性遗传病)。


10 Aprecia Pharmaceuticals——For creating the first 3-D-printed drug



Aprecia Pharmaceuticals公司使用改进型3D打印技术开发的新型速溶药片ZipDoses。是通过反复扩散由药物粉末结合水溶性粘合剂的使用制成,在该公司的测试中在仅仅4秒多的时间内就完全溶解了,是目前市场上首款3D打印药片。




This link:http://www.chemcd.com/news/25206.html

The ChemCD compiler finishing, shall not be reproduced without permission, for reprint please indicate the source。

comments powered by Disqus

Categories

Related News

Merck Announces FDA Acceptance of Biologics License Application for Bezlotoxumab, an Investigational Antitoxin for Prevention of Clostridium Difficile Infection Recurrence

Merck announced that the U.S. Food and Drug Administration (FDA) has accepted for review the Biologics License Application (BLA) for bezlotoxumab, an investigational antitoxin for prevention of Clostridium difficile (C. difficile) infection recurrence.

Sanofi and Regeneron Announce Sarilumab Biologics License Application Accepted for Review by US FDA

Sanofi and Regeneron Pharmaceuticals, Inc. today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the Biologics License Application (BLA) for sarilumab.

First data backs efficacy of BMS' novel HIV drug

A Bristol-Myers Squibb (BMS) drug that causes immature HIV particles to be released from cells early, interrupting their lifecycle, has cleared a proof-of-concept study.

EU Rules Could Restrict Genetic Testing

Genetic testing describes the application of laboratory methods to look at a person’s genes (the inherited DNA instructions). Genetic tests can be used to diagnose a genetic condition; screen for a risk of developing a particular health problems; for the selection of treatments; or to assess responses to treatments.

CHMP adopts positive opinion of Edurant in adolescents with HIV-1

The CHMP has adopted a positive opinion recommending a change to the terms of the marketing authorisation for Janssen’s Edurant (rilpivirine) in the EU to extend the indication to adolescent patients aged 12 to <18 years with human immunodeficiency virus-1 (HIV-1) infection

FDA finds mystery 'deficiencies' with Neos' long-acting Ritalin on the eve of approval

Neos Therapeutics got an ominous note from the FDA just weeks ahead of the expected approval date for its long-acting ADHD treatment, clouding the future of the company's lead asset.

Pfizer's once-failed cancer drug wins the FDA's 'breakthrough' tag

Pfizer has found new hope for a former pipeline standout, picking up the FDA's coveted breakthrough therapy designation for a Phase III reclamation project in oncology.