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美国StemCells公司得到FDA批准开始干细胞治疗干性黄斑变性临床试验

与先进细胞公司不同的是,StemCells公司用的是来自人的神经干细胞HuCNS-SC,此外他们把目标定位在保存视网膜光感细胞功能方面,而不是再生出新的光感细胞
NEWARK, Calif., Feb. 2, 2012 (GLOBE NEWSWIRE) -- StemCells, Inc. (Nasdaq:STEM - News) today announced that the U.S. Food and Drug Administration (FDA) has authorized the initiation of a Phase I/II clinical trial of the Company's proprietary HuCNS-SC(R) product candidate (purified human neural stem cells) in dry age-related macular degeneration (AMD), the most common form of AMD. AMD is the leading cause of vision loss and blindness in people over 55 years of age, and approximately 30 million people worldwide are afflicted with the disease. There are no approved treatments for dry AMD.'
"With the approval of this trial, we have accomplished something truly unique in the stem cell field, which is the extension of clinical testing of our proprietary human neural stem cell platform to all three elements of the central nervous system: the brain, spinal cord and eye," said Martin McGlynn, President and CEO of StemCells, Inc. "The preclinical data supporting our IND is particularly compelling and we look forward to getting this trial underway."
The Phase I/II trial will evaluate the safety and preliminary efficacy of HuCNS-SC cells as a treatment for dry AMD. The trial will be an open-label, dose-escalation study, and is expected to enroll a total of 16 patients. The HuCNS-SC cells will be administered by a single injection into the space beneath the retina. Patients' vision will be evaluated using conventional methods of ophthalmological assessment at predetermined intervals over a one-year period. Patients will then be followed for an additional four years in a separate observational study.
Preclinical data submitted as part of the Company's Investigative New Drug application demonstrated that HuCNS-SC cells protect host photoreceptors and preserve vision in a well-established animal model of retinal disease that is relevant to dry AMD. HuCNS-SC transplants significantly protect against the degeneration of photoreceptors, the key cells of the eye involved in vision. Moreover, the number of cone photoreceptors, which are responsible for central vision, remain constant over an extended period, consistent with the sustained visual acuity and light sensitivity observed. In humans, degeneration of the cone photoreceptors account for the unique pattern of visual loss in dry AMD. A summary of the Company's preclinical data was published in the February issue of the international peer-reviewed European Journal of Neuroscience, and is available online at http://onlinelibrary.wiley.com/d ... 1.07970.x/abstract.
We have published the preclinical evidence demonstrating that our human neural stem cells might offer a safe, effective and simple approach to treating AMD and other retinal diseases," said Stephen Huhn, MD, FACS, FAAP, Vice President and Head of the CNS Program at StemCells, Inc. "Our approach is to provide durable protection of photoreceptors, thereby preserving vision, as opposed to approaches that aim to replace photoreceptors or the retinal pigmented epithelial cells. Furthermore, our preclinical data supports our hypothesis that we can achieve clinical benefit with a single transplant in AMD patients."
About StemCells, Inc.
Inc. is engaged in the research, development, and commercialization of cell-based therapeutics and tools for use in stem cell-based research and drug discovery. The Company's lead therapeutic product candidate, HuCNS-SC(R) cells (purified human neural stem cells), is currently in development as a potential treatment for a broad range of central nervous system disorders. Clinical trials are currently underway in spinal cord injury and in Pelizaeus-Merzbacher disease (PMD), a fatal myelination disorder in children, and the Company expects to initiate a Phase I/II clinical trial in dry AMD in the near future. In addition, the Company is pursuing preclinical studies of its HuCNS-SC cells in Alzheimer's disease. StemCells also markets stem cell research products, including media and reagents, under the SC Proven(R) brand, and is developing stem cell-based assay platforms for use in pharmaceutical research, drug discovery and drug development. Further information about StemCells is available at http://www.stemcellsinc.com.

APosted on the OSN SuperSite February 2, 2012
NEWARK, Calif. — StemCells Inc. has received authorization from the U.S. Food and Drug Administration to begin a phase 1/2 clinical trial of the company's purified human neural stem cell product candidate for treating dry age-related macular degeneration, according to a company press release.
The trial is expected to enroll 16 patients in an open-label, dose-escalation study to analyze the safety and efficacy of the company's proprietary HuCNS-SC cells in treating dry AMD, the release said. After a single injection of the cells into the subretinal space, vision will be evaluated over a 1-year period before being followed for 4 additional years in a separate observational study.8
"With the approval of this trial, we have accomplished something truly unique in the stem cell field, which is the extension of clinical testing of our proprietary human neural stem cell platform to all three elements of the central nervous system: the brain, spinal cord and eye," Martin McGlynn, president and CEO of StemCells, said in the release. "The preclinical data supporting our [investigative new drug] is particularly compelling, and we look forward to getting this trial under way."
  Preclinical data submitted as part of the application showed the HuCNS-SC cells were capable of preserving vision and protecting host photoreceptors in animals, the release said.8 F6 t4 a5 g. M  
"We have published the preclinical evidence demonstrating that our human neural stem cells might offer a safe, effective and simple approach to treating AMD and other retinal diseases," Stephen Huhn, MD, FACS, FAAP, vice president and head of the CNS program at StemCells, said in the release. "Our approach is to provide durable protection of photoreceptors, thereby preserving vision, as opposed to approaches that aim to replace photoreceptors or the retinal pigmented epithelial cells. Furthermore, our preclinical data supports our hypothesis that we can achieve clinical benefit with a single transplant in AMD patients."
谢谢楼主的分享
生命不息,战斗不止。
英文版 阅读有难度啊
希望明天会更好!
以下为谷歌翻译
纽瓦克,加利福尼亚州,2012年2月2日(中国商业电讯) - StemCells公司(纳斯达克:干 - 新闻)今天宣布,美国食品和药物管理局(FDA)已经批准启动的I / II期临床阶段试用该公司专有的HuCNS-SC的(R)的候选产品(纯化的人类神经干细胞)在干燥的年龄相关性黄斑变性(AMD)AMD的最常见的形式。 AMD是人在55岁以上的视力减退和失明的首要原因,全世界大约有30万人患有此病折磨。有没有批准的干性AMD治疗。
“随着这项试验的批准,我们已经完成了真正独特的东西,在干细胞领域,这是我们的一种特有的人类神经干细胞中枢神经系统的所有三个要素平台的临床试验的延伸:脑,脊髓和眼睛,说:“StemCells公司总裁兼首席执行官马丁·麦格林,”临床数据支持我们的实业格外引人注目,我们期待得到这个试验正在进行中。“
第一阶段的I / II期临床试验将评估HuCNS-SC细胞作为干性AMD的治疗的安全性和初步疗效。审判将是一个开放标签,剂量递增研究,预计招收共16例。 HuCNS-SC细胞,将管理由单一注射到视网膜下的空间。患者的视力将在预定的时间间隔超过一年的时间内使用常规的眼科评估方法进行评估。然后将一个额外的4年在一个单独的观察研究应遵循的患者。
作为公司的调查新药申请的一部分提交的临床数据表明HuCNS-SC细胞保护主机感光和保存在视网膜疾病行之有效的动物模型是相关的干性AMD的愿景。 HuCNS-SC移植显着防止感光细胞变性,眼视力的关键细胞。此外,锥感光细胞的数量,这是负责中央视力,保持不变,在一个长时期内,持续的视力和光线的敏感性观察相一致。在人类中,占锥感光细胞退化为干性AMD的视力丧失的独特模式。公司的临床数据的摘要发表在同行评审的国际欧洲神经科学杂志二月号,是在http://onlinelibrary.wiley.com/d可在网上... 1.07970.x/abstract。
斯蒂芬Huhn,医师,流式细胞仪,访谈中,副总统和中枢神经系统的项目负责人说,“我们已发表的临床证据表明,我们人类的神经干细胞可能提供一种安全,有效和简单的方法来治疗AMD和其他视网膜疾病StemCells公司“我们的做法是提供持久的感光保护,从而保护视力,而不是旨在取代感光细胞的视网膜色素上皮细胞的方法。此外,我们的临床数据支持我们的假设,我们可以实现在单一的AMD患者移植的临床受益。“
关于StemCells公司
公司正在从事的研究,开发和商品化基于细胞疗法和干细胞基础研究和药物发现中使用的工具。公司的主导治疗的候选产品,HuCNS-SC(R)的细胞(纯化的人类神经干细胞),是目前发展为一种中枢神经系统疾病的范围广泛的潜在的治疗。在脊髓损伤和致命髓鞘障碍在儿童Pelizaeus Merzbacher病(PMD),目前正在进行临床试验,该公司预计将发起一个阶段I / II期临床试验,在不久的将来在干性AMD。此外,该公司正在寻求HuCNS-SC细胞在阿尔茨海默氏病的临床前研究。干细胞也是市场的干细胞研究,包括媒体和试剂产品,SC证明(R)品牌下,并正在开发基于干细胞的实验平台,用于中医药研究,药物发现和药物开发。关于干细胞的进一步信息是在http://www.stemcellsinc.com提供。

APosted上的专题报道,到2012年2月2日
加利福尼亚州纽瓦克 - StemCells公司已收到来自美国食品和药物管理局的授权,开始阶段该公司的纯化人类神经干细胞治疗干的年龄相关性黄斑变性的候选产品的1/2期临床试验,根据公司新闻稿。
发布的消息说,审判预计招收16例,在一个开放标签,剂量递增研究,分析该公司专有的HuCNS-SC的细胞的安全性和治疗干性AMD疗效。进入视网膜下腔细胞单次注射后,视力将评估前额外4年超过1年的时间在一个单独的观测study.8
“随着这项试验的批准,我们已经完成了真正独特的东西,在干细胞领域,这是我们的一种特有的人类神经干细胞中枢神经系统的所有三个要素平台的临床试验的延伸:脑,脊髓和眼睛,StemCells公司总裁兼首席执行官马丁·麦格林说:“在释放。 “支持我们调查的新药物的临床前数据]是特别引人注目的,和我们期待着这次审判正在进行。”
  作为应用程序的一部分提交的临床数据表明HuCNS-SC细胞能够保护视力和保护动物的主机的感光细胞,释放said.8 F6 T4 A5Ğ。中号
“我们已发表的临床证据表明,我们人类的神经干细胞可能会提供一个安全,有效和简单的方法来治疗AMD和其他视网膜疾病,”斯蒂芬Huhn,医师,流式细胞仪,访谈中,副总裁和中枢神经系统的计划主管干细胞,在新闻稿中说。 “我们的做法是,以提供持久的感光保护,从而保护视力,反对旨在取代感光细胞的视网膜色素上皮细胞的方法。此外,我们的临床数据支持我们的假设,我们可以实现用一个移植的临床受益AMD患者。“
谢谢楼主的分享
谢谢楼主的分享!

美国的干细胞都是治疗黄斑变性,什么时候开始治疗RP才是真正的好消息。
又是治疗黄斑变性的消息,谢谢楼主的分享,希望好消息越来越多
也希望治疗RP的好消息越来越多
有消息总比没有消息强!顶一下!希望治疗RP的办法快点做临床实验!
本帖最后由 chinatiger 于 2012-2-8 22:39 编辑

正式的中文翻译版本已经在生物谷刊登出来了,里面提到了对RP有用:
视网膜变性的一个突破性治疗将成为第二个进入Ⅰ/Ⅱ期临床试验的干细胞疗法。StemCells 公司(SCI)已获得美国食品和药物管理局授权对患干性-年龄相关性黄斑变性(AMD)病人开展神经干细胞治疗的临床试验。

在先进细胞技术(ACT)之后10天,SCI发布这此消息,其中ACT发布了2011年视网膜变性的首个干细胞治疗临床试验,并宣布干性AMD和Stargardt病这两个首个研究参与者的鼓舞人心的安全与效能研究结果。SCI正计划开展干性AMD的临床试验,此临床试验由16家医院参与。此研究的其他细节即将出现。

SCI的神经干细胞疗法被设计成通过保护提供视力的视锥视杆细胞免于变性而维持视力。将在位于视网膜中心区域的黄斑下注射的治疗细胞被设计成持续释放保持视锥视杆细胞健康的蛋白。

在一篇发表于期刊 European Journal of Neuroscience的2012年1月30日版上的论文中, 研究人员报道了神经干细胞治疗方法在视网膜变性哺乳动物模型上的长期安全性与有效性。干细胞预防视力丧失,不引起任何免疫性反应或其他安全问题。

美国抗盲基金会首席研究专家Stephen Rose博士说,SCI治疗方法不同于ACT疗法的关键一点是:SCI的神经干细胞以它们天然的形式被移植以发挥保护作用。相反,ACT则从胚胎干细胞衍生视网膜色素上皮细胞(RPE)。新的RPE细胞被移植并替代、补充病人自身的RPE细胞,它是受如黄斑退行性变性一样的情况影响的。

"SCI的干细胞象一个药物工厂样发挥作用,这个工厂提供连续的蛋白递送以来保持视网膜健康并保持视力",他说,"另一方面,ACT则以替代疾病丧失的RPE为目标。RPE在视网膜中发挥关键性的支持与维持作用,为视锥视杆细胞提供营养与废物处理,ACT希望它的移植的RPE提供这些功能。希望两种方法都起作用。他们对治疗宽范围视网膜疾病有影响,包括视网膜色素变性和Usher综合症。俄勒冈健康与科学大学名誉教授、RSCI啮齿动物研究的研究人员Raymond Lund博士说,"如果没有美国抗盲基金会对我和我的团队的直接支持,将什么也不会发生,也就是说,美国抗盲基金会创造了一个环境,这个环境就是激励科学家们了解人们和他们的因视网膜疾病丧失视力的家人的需要。我很乐观,这项努力将给出视力获救的结果。"

近二十年来美国抗盲基金会资助各种项目,Lund博士在视网膜疾病的干细胞研究中是一名知名专家,在帮助ACT将其疗法推入临床试验中也起主导作用。

SCI在旧金山加利福尼亚大学进行一种胎儿神经疾病佩-梅病(Pelizaeus-Merzbacher disease)神经干细胞治疗方法的临床试验,并在瑞士开展脊髓损伤的临床研究。它也在从事阿尔茨海默症治疗方法的临床前研究。

美国抗盲基金会将公布SCI公司干性AMD临床试验包括招募信息、选入与淘汰标准在内的其他信息,一旦可用便会公布在网页上。(生物谷bioon.com)
希望RP的治疗早日到来!
希望明天会更好!
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