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标题: 英国ReNeuron公司干细胞治疗RP最新进展 [打印本页]

作者: 雪山飞狐    时间: 2016-6-14 10:59     标题: 英国ReNeuron公司干细胞治疗RP最新进展

英国ReNeuron公司2016年3月份在美国哈佛大学附属麻省医院开始了2个阶段视网膜祖细胞(hrpc)治疗视网膜色素变性的临床试验.这次试验给每个病人注射的剂量都有所不同.

第一阶段主要是评估视网膜祖细胞治疗的安全性和耐受性以及效果.第一阶段给9名患者注射了视网膜祖细胞.预计在2017年初公布结果.

第二阶段给6名患者注射了视网膜祖细胞.预计会在2017年底公布结果.第二阶段主要评估治疗的有效性和长期的稳定性.

根据这两个阶段试验结果.英国ReNeuron公司预计在2017年底或者2018年初向美国FDA申请第三阶段临床试验.如果这三个阶段试验顺利英国ReNeuron将会获得美国和欧洲上市销售资格.

以上内容由病友金秋谷香从韩国RP网站获得.在此对她表示感谢!
作者: 海边    时间: 2016-6-14 11:20

如果是真的,这可是大好消息
作者: 742442837    时间: 2016-6-14 13:20

希望能有很好的效果
作者: 雄鹰    时间: 2016-6-14 14:15

谢谢楼主的分享
作者: 南国乞儿    时间: 2016-6-14 21:02

谢谢楼主的分享旭霰金秋谷香的转载,如果安全性没问题那么我们就可以放心了,期待着
作者: 雄鹰    时间: 2016-6-15 08:41

请共同卓绝地忍受着期待着,我们的天会变亮的!
作者: 城市乞丐    时间: 2016-6-15 18:23

谢谢楼主的分享
作者: 13583010813    时间: 2016-6-20 10:54

谢谢楼主的分享。
作者: flyeagle    时间: 2017-6-29 14:36

ReNeuron Group plc (the "Company") (AIM: RENE), a UK-based global leader in the development of cell-based therapeutics, provides an update on its cell therapy development programmes targeting degenerative diseases of the retina.  
We are delighted to report that the FDA has approved the cryopreserved formulation of our human retinal progenitor cell (hRPC) therapeutic candidate and that we have now started treating patients with this formulation in our ongoing US Phase I/II study clinical trial in retinitis pigmentosa (RP) patients.   
The new proprietary formulation enables the hRP cells to be frozen for shipping and storage and easily thawed at the point of clinical use.  This freeze-thaw modality provides a greatly enhanced shelf life for the product, lower prospective cost of goods and the capability to ship the cells for clinical and commercial application anywhere in the world.   
The new hRPC formulation has also facilitated an expansion of ReNeuron’s clinical programmes in ophthalmology.  As previously announced, we will shortly file an application with the FDA to expand the Phase II element of the ongoing Phase I/II clinical trial in RP from six to 20 patients.  The expanded study is designed to provide the depth and quality of data that, if positive, will allow subsequent progression to a Phase II/III pivotal study in this indication.  We also intend to file an application to start a new US Phase II clinical trial later this year in patients with cone-rod dystrophy, to be conducted alongside the Phase II part of the ongoing RP clinical trial.   
Olav Hellebø, Chief Executive Officer of ReNeuron, said:  
“We are delighted that the FDA has approved the use of the cryopreserved formulation of our hRPC retinal cell therapy candidate in our ongoing clinical development programmes.  This is a further significant milestone for ReNeuron, enabling an expansion of our clinical programmes in ophthalmology as well as providing ReNeuron with a significant commercial advantage in terms of prospective cost of goods and ease of use of a retinal disease therapy.”   
ENQUIRIES:   
ReNeuron +44 (0)20 3819 8400
Olav Hellebø , Chief Executive Officer  
Michael Hunt, Chief Financial Officer  
Buchanan +44 (0) 20 7466 5000
Mark Court, Sophie Cowles, Stephanie Watson  
Stifel Nicolaus Europe Limited +44 (0) 20 7710 7600
Jonathan Senior, Stewart Wallace, Ben Maddison (NOMAD and Broker)   
About ReNeuron ReNeuron is a leading, clinical-stage cell therapy development company.  Based in the UK, its primary objective is the development of novel cell-based therapies targeting areas of significant unmet or poorly met medical need.     
ReNeuron has used its unique stem cell technologies to develop cell-based therapies for significant disease conditions where the cells can be readily administered “off-the-shelf” to any eligible patient without the need for additional immunosuppressive drug treatments.  The Company has therapeutic candidates in clinical development for motor disability as a result of stroke, for critical limb ischaemia and for the blindness-causing disease, retinitis pigmentosa.      
ReNeuron is also advancing its proprietary exosome technology platform as a potential new nanomedicine targeting cancer and as a potential delivery system for gene therapy treatments.  
ReNeuron’s shares are traded on the London AIM market under the symbol RENE.L.  Further information on ReNeuron and its products can be found at www.reneuron.com.   
This announcement contains forward-looking statements with respect to the financial condition, results of operations and business achievements/performance of ReNeuron and certain of the plans and objectives of management of ReNeuron with respect thereto. These statements may generally, but not always, be identified by the use of words such as "should", "expects", "estimates", "believes" or similar expressions. This announcement also contains forward-looking statements attributed to certain third parties relating to their estimates regarding the growth of markets and demand for products. By their nature, forward-looking
statements involve risk and uncertainty because they reflect ReNeuron's current expectations and assumptions as to future events and circumstances that may not prove accurate.  A number of factors could cause ReNeuron's actual financial condition, results of operations and business achievements/performance to differ materially from the estimates made or implied in such forward-looking statements and, accordingly, reliance should not be placed on such statements.
作者: flyeagle    时间: 2017-6-29 14:37

以上是该公司2017年6月19日发布的消息,请高手翻译。
作者: zane    时间: 2017-6-29 16:52

本帖最后由 zane 于 2017-6-29 16:56 编辑

就算是2018年开始第三期,那也要到2019年才能出结果,然后再申请FDA批准,估计真正能上市最快也需要等到2020年。那时候我们的视力还能剩下多少
作者: 心潮澎湃    时间: 2017-6-30 10:25

位于英国的基于细胞的治疗剂开发的全球领先公司ReNeuron Group plc(“公司”)(AIM:RENE)提供了针对视网膜退行性疾病的细胞治疗发展计划的更新。
我们很高兴地报告,FDA已经批准了人类视网膜祖细胞(hRPC)治疗候选物的低温保存制剂,我们现在已经在我们持续的美国I / II期临床试验中开始治疗患有这种制剂的患者, RP)患者。
新的专有配方使hRP细胞能够被冻结用于运输和储存,并在临床使用时容易解冻。这种冻融方式为产品提供了大大提高的保质期,降低了商品的预期成本以及将细胞运送到世界任何地方的临床和商业应用的能力。
新的hRPC制剂也促进了ReNeuron临床眼科项目的扩大。如前所述,我们将很快向FDA提交申请,将RP中正在进行的I / II期临床试验的第二阶段成分扩大到六至二十名患者。扩展的研究旨在提供数据的深度和质量,如果为正,将允许随后进行II / III期关键研究。我们还打算在今年晚些时候向锥状营养不良患者提交新的美国II期临床试验申请,并与正在进行的RP临床试验的II期临床试验一起进行。
ReNeuron首席执行官Olav Helleb&oslash表示:
“我们很高兴FDA正在批准在我们正在进行的临床开发计划中使用我们的hRPC视网膜细胞治疗候选人的冷冻保存制剂。这是ReNeuron的另一个重要里程碑,可以扩展我们的眼科临床项目,并为ReNeuron在商品的预期成本和易于使用视网膜疾病治疗方面提供重要的商业优势。
作者: flyeagle    时间: 2017-6-30 16:34

13# 心潮澎湃

谢谢您的翻译,辛苦了。
作者: 雄鹰    时间: 2017-6-30 20:23

感谢翻译与分享。总有一天我们也可以飞翔。




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