www射-国产免费一级-欧美福利-亚洲成人福利-成人一区在线观看-亚州成人

Science and Health

US starts human blindness trial using stem cells

(Xinhua)
Updated: 2010-11-23 08:59
Large Medium Small

WASHINGTON - The US Food and Drug Administration (FDA) has approved Massachusetts-based Advanced Cell Technology's application for using retinal cells derived from human embryonic stem cells to treat patients with Stargardt's Macular Dystrophy (SMD), the company said Monday.

Related readings:
US starts human blindness trial using stem cells US court OKs US-funded stem cell research for now
US starts human blindness trial using stem cells US debates whether modified fish safe to eat
US starts human blindness trial using stem cells US appeals debate on embryonic stem cell research
US starts human blindness trial using stem cells Study shows progress with stem cell alternative

The case is the second human trial of human embryonic stem cells approved in the United States.

Stargardt's Macular Dystrophy causes progressive vision loss, usually starting in children between 10 and 20 years of age. Eventually, blindness results from photoreceptor loss associated with degeneration in the pigmented layer of the retina, called the retinal pigment epithelium (RPE).

"There is currently no treatment for Stargardt's disease," said Dr Robert Lanza, ACT's Chief Scientific Officer, in a statement. "Using stem cells, we can generate a virtually unlimited supply of healthy RPE cells, which are the first cells to die off in SMD and other forms of macular degeneration. We've tested these cells in animal models of eye disease. In rats, we've seen 100 percent improvement in visual performance over untreated animals without any adverse effects."

According to Lanza, the company's studies showed that the cells were capable of extensive rescue of photoreceptors in animals that otherwise would have gone blind. Near-normal function was also achieved in a mouse model of Stargardt's disease. The company hope to see a similar benefit in patients with various forms of macular degeneration.

The ACT's Phase I/II trial will be a prospective, open-label study that is designed to determine the safety and tolerability of the RPE cells following sub-retinal transplantation to patients with advanced SMD. A total of 12 patients will be enrolled in the study at multiple clinical sites.

Embryonic stem cells have been at the center of funding controversies in the United States because the research involves destroying the embryos, which some have argued is akin to abortion. But, many researchers consider embryonic stem cells the most versatile types of stem cells, as they can morph into any type of cell.

Last month, California-based Geron Corporation began using human embryonic stem cells to treat a patient with acute spinal cord injuries in the first authorized test of the technology in the United States.

主站蜘蛛池模板: 成网站在线观看人免费 | 亚洲午夜大片 | 美女美女大片黄a大片 | 一级aaaaa毛片免费视频 | 亚洲精品国产经典一区二区 | 亚洲成成品网站有线 | 欧美成人午夜影院 | 韩国在线精品福利视频在线观看 | 国产成人看片免费视频观看 | 欧美精品亚洲精品日韩 | aaaa欧美高清免费 | 精品成人一区二区三区免费视频 | 久久精品国产精品亚洲艾 | 国产精品激情丝袜美女 | 成人欧美一级毛片免费观看 | 成人a毛片高清视频 | 亚洲美女视频 | 欧美刺激午夜性久久久久久久 | 欧美成人免费观看国产 | 三级网址免费 | 亚洲精品国产综合99久久一区 | 中文字幕一二三四区2021 | 最新69成人精品毛片 | 日本加勒比视频 | 国产精品九九免费视频 | 成人自拍视频 | 国产精品毛片一区二区三区 | 亚洲精品成人久久久影院 | 国产手机在线国内精品 | 亚洲欧美一区二区三区综合 | 亚洲国产精品久久精品成人 | 国产视频高清在线 | 高清波多野结衣一区二区三区 | 亚洲 欧美 日韩中文字幕一区二区 | 中文国产成人精品久久一 | 日本一本黄 | 亚洲一区视频在线 | 国产网站91 | 亚洲福利精品一区二区三区 | 久草男人天堂 | 亚洲精品大片 |