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BioTime’s Subsidiary ReCyte Therapeutics, Inc. Provides Update on Preclinical Development of Vascular Progenitors for …

Posted: Published on April 24th, 2012

ALAMEDA, Calif.--(BUSINESS WIRE)-- BioTime, Inc. (NYSE Amex: BTX) announced today that Steven Kessler, Ph.D., Vice President of Research at BioTimes subsidiary ReCyte Therapeutics, Inc. will provide and update on the development of reprogramming technologies and the generation of patient-specific vascular endothelial cells with essentially 100% purity using proprietary ACTCellerateTM technology. Dr. Kessler will also describe the use of ACTCellerateTM cell lines to manufacture specific secreted biologically active proteins, and will show animal preclinical data on the use of particular ACTCellerateTM lines as a potential means of improving recovery after stroke. Also presenting will be ReCytes collaborator Shahin Rafii, M.D., the Arthur B. Belfer Professor of Genetic Medicine and Director of the Ansary Stem Cell Institute at Cornell Weill Medical College. Drs. Kessler and Rafii will describe the wide array of age-related degenerative diseases potentially addressed by novel vascular cell therapies, including coronary heart disease afflicting an estimated 82 million Americans, and stroke that caused one out of every 18 deaths in the United States in 2007. Drs. Kesslers and Rafiis presentation will be available for viewing on BioTimes web site http://www.biotimeinc.com as well as ReCyte Therapeutics web site at http://www.recytecorp.com. About ReCyte Therapeutics ReCyte Therapeutics, Inc. is a majority-owned privately-held … Continue reading

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BioTime and its Subsidiary OrthoCyte Corporation Provides Update on Preclinical Development of OTX-CP07

Posted: Published on April 24th, 2012

ALAMEDA, Calif.--(BUSINESS WIRE)-- BioTime, Inc. (NYSE Amex: BTX) announced today that BioTimes CEO Michael West, Ph.D. will provide and update the development of OTX-CP07 by BioTimes subsidiary OrthoCyte Corporation at an investor meeting in New York City. OTX-CP07 is a combination product with human embryonic cartilage progenitors manufactured from human embryonic stem cells formulated with BioTimes proprietary cell delivery device ReneviaTM. Dr. West will describe studies underway at OrthoCyte that have currently identified progenitors to eight diverse cartilage types of the human body, as well as diverse tendon, bone, and muscle progenitors that may be useful in orthopedic research and the development of novel regenerative therapeutics. Dr. West will also show a video presentation from OrthoCytes Chief Scientific Officer, Arnold Caplan, Ph.D., who is also Director of the Skeletal Research Center at Case Western Reserve University. In the video, Dr. Caplan discusses the significance of the potential use of definitive progenitors of human cartilage for the repair of osteoarthritis, a disease afflicting an estimated 27 million Americans. Dr. Wests presentation as well as the video of Dr. Caplans presentation will be available for viewing on BioTimes web site http://www.biotimeinc.com as well as OrthoCyte Corporations web site at http://www.orthocyte.com. About OrthoCyte … Continue reading

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BioTime’s Subsidiary Cell Cure Neurosciences, Ltd. Provides Update on OpRegen® Product Development

Posted: Published on April 24th, 2012

ALAMEDA, Calif.--(BUSINESS WIRE)-- BioTime, Inc. (NYSE Amex: BTX) announced today that Charles S. Irving, Ph.D., the CEO of BioTimes subsidiary Cell Cure Neurosciences, Ltd. will provide an update on the development of OpRegen at an investor meeting in New York City. In his presentation, Dr. Irving will describe the unmet medical needs and markets for the treatment of the dry form of age-related macular degeneration (AMD), and the advantages of Cell Cures OpRegen which has been produced from human embryonic stem cells in culture conditions free of animal products, eliminating the need for designating the product as a xenotransplantation therapeutic. Dr. Irving will also discuss Cell Cures collaboration with Teva Pharmaceutical Industries Ltd., under which Teva has the option to develop and commercialize both OpRegen and OpRegen-Plus. Dr. Irving will describe the nature of the ongoing preclinical studies which are expected to lead to regulatory filings for the initiation of human clinical trials in 2013. Dr. Irvings presentation will be available on BioTimes web site http://www.biotimeinc.com as well as Cell Cure Neurosciences web site at http://www.cellcureneurosciences.com. Background. Age-related macular degeneration is the leading cause of blindness in an aging population. It is widely believed that the loss or dysfunction of … Continue reading

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Former Alabama football players get stem cell injections from Gulf Shores doctor

Posted: Published on April 24th, 2012

MOBILE, Alabama -- At the end of this past season with the Oakland Raiders, an aching Rolando McClain gave an assignment to his agent: Find out more about stem cell therapies for injuries, like other athletes are trying. Ive been having two seasons of nagging pain in my knee, the former University of Alabama standout said. Not long afterward, McClain was on his way to Gulf Shores. There, radiologist Jason R. Williams performed liposuction on McClain and then injected stem cells from the linebackers own fat cells into his knee and into the area of a high ankle sprain. It feels a lot better, McClain said in an interview last week, adding that hes working out four days a week with the Raiders, running, lifting weights, doing squats and even sprinting with hardly any pain at all. About three months ago, Williams, 38, began the new procedure in which he injects patients -- two of them being McClain and former University of Alabama receiver Marquis Maze -- with their own stem cells in an effort to repair damaged joints and muscles. This is going to be the future of medicine, said Williams, who owns Precision StemCell, which includes a diagnostic … Continue reading

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BioTime Demonstrates Efficient Method for the Manufacture of Cartilage-Producing Cells from Human Embryonic Stem Cells

Posted: Published on April 24th, 2012

ALAMEDA, Calif.--(BUSINESS WIRE)-- BioTime, Inc. (NYSE Amex: BTX) and its wholly owned subsidiary OrthoCyte Corporation reported today a means of manufacturing cartilage from human embryonic stem cells that is suited for industrial scale-up of a product for the treatment of osteoarthritis. The paper, published online (ahead of print) in the peer-reviewed journal Regenerative Medicine, characterizes a progenitor cell line produced from human embryonic stem (hES) cells using proprietary ACTCellerate technology. The study reports that the cells are capable of regenerating cartilage with long sought-after identification markers. The study also shows that the cells can be directly expanded on a scale needed for industrial manufacture, which will be necessary in order to make transplantable cells available in commercial quantities. In todays publication, BioTime scientists reported on one ACTCellerate line designated 4D20.8. This proprietary cell line is the cellular component of OrthoCytes product in development, OTX-CP07. The scientific publication demonstrates that 4D20.8 cells possess site-specific markers of craniofacial mesenchyme, in particular, markers of proximal mandibular mesenchyme. This tissue is of significance in that it naturally produces one of the strongest joint cartilages of the body. The study documented conditions in which the cells can be propagated on a large scale, conditions in … Continue reading

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Raiders' Rolando McClain: Stem-cell therapy worked well

Posted: Published on April 24th, 2012

Oakland Raiders linebacker Rolando McClain turned to stem-cell therapy to deal with the aches and pains that come with being a professional football player, the Mobile Press-Register reported Sunday. Reuter: Impact LB prospects According to the newspaper, McClain, who missed only one game last season but was hampered by knee pain and an ankle injury, had stem cells taken from his own fat and injected into his knee and leg. McClain credits the procedure for helping him do what he needs to do to prepare for the 2012 season. "It feels a lot better," McClain told the newspaper, adding he has been able to work out "with hardly any pain at all." Jason R. Williams, the radiologist who performed the procedure in Alabama, called the experimental therapy "the future of medicine." However, the newspaper also reported that the FDA has warned consumers about the possible pitfalls of stem-cell treatments. "There is a potential safety risk when you put cells in an area where they are not performing the same biological function as they were when in their original location in the body," said Stephanie Simek, deputy director of the FDA's Office of Cellular, Tissue and Gene Therapies, in a statement. … Continue reading

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Regenerative Medicine Institute, Mexico Presents Summary of Clinical Data at the International Society of Stem Cell …

Posted: Published on April 24th, 2012

TIJUANA, Mexico, April 23, 2012 (GLOBE NEWSWIRE) -- Regenerative Medicine Institute, Mexico (RMI) will be among top scientists and physicians presenting cutting edge data at the International Society of Stem Cell Research (ISSCR). The ISSCR's annual meeting has become the world's premier stem cell research event. The meeting serves as the largest forum for stem cell and regenerative medicine professionals from around the world. The ISSCR 10th Annual Meeting will be held June 13 - 16, 2012 at the Pacifico Yokohama in Yokohama, Japan. A summary of data on the use of adult stem cells from adipose tissue to treat heart failure and COPD will be presented by Kristin Comella, Chief Scientific Officer of Bioheart Inc. Bioheart is focused on the discovery, development, and commercialization of autologous cell therapies for the treatment of chronic and acute heart damage and peripheral vascular disease. RMI is currently running Phase I/II trials at the Hospital Angeles in collaboration with Bioheart and the Ageless Regenerative Institute. Dr. Javier Lopez, President and CEO of RMI and a member of ISSCR said that "We are proud to share our initial results with the scientific community at such a prestigious event." For more information on RMI, visit … Continue reading

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Starr Foundation Continues Support for Stem Cell Research in New York with $50 Million Gift

Posted: Published on April 24th, 2012

Tri-Institutional Stem Cell Initiative Pursues Cutting-Edge Stem Cell Research and Therapies Newswise NEW YORK (April 23, 2012) -- The Starr Foundation is continuing its historic commitment to stem cell research with a $50 million gift in support of the Tri-Institutional Stem Cell Initiative (Tri-SCI), which was established through a generous grant from the Foundation in 2005. The new gift, awarded to the original Tri-SCI members -- Memorial Sloan-Kettering Cancer Center, The Rockefeller University and Weill Cornell Medical College, all in New York City -- will support and enhance collaborative, pioneering stem cell research at the three adjacent Manhattan campuses. With support from The Starr Foundation, Tri-SCI laboratories are investigating the properties of embryonic stem cells, which have the potential to differentiate into any cell type in the body, and adult stem cells, which are found in various tissues and can give rise to specific cell types. These studies are opening new avenues for understanding a range of health conditions, including developmental disorders, neurodegenerative diseases and cancer. The knowledge gained through this research is also laying the groundwork for the design of regenerative therapies to replenish tissues lost to illness or injury. Under the Tri-Institutional Stem Cell Initiative, investigators work across … Continue reading

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Finding stem cell donor match warden’s ‘only hope’ for fighting cancer

Posted: Published on April 24th, 2012

If all goes according to plan in Gregory Sanborns life over the coming weeks, doctors find a matching stem cell donor for him and he undergoes an aggressive year of procedures and solitary recovery, he can return to work cancer-free. I let my immune system get strong, I come back to work a year from now, and I live to be old, fat and happy in my garden, Sanborn said. The alternative: a stem cell match is not found or a matching donation fails to produce the desired results. In that case, Sanborn knows what happens. The cutaneous T-cell lymphoma that is ravaging his body wins. And Sanborn dies. Basically, its my only hope, Sanborn said of the stem-cell transplant he has been left to hope for. If it works, Ill be cured. And if it doesnt, I wont be. Sanborn, a 46-year-old career game warden who now serves as the deputy chief of the Maine Warden Service, remains optimistic. He is also realistic. And after several months of treatment, Sanborn has learned that his self-reliance always one of his attributes of which he was proudest may stand in the way of his recovery. Thats why last Friday he was … Continue reading

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ACT Announces Third Dry AMD Patient Treated in Clinical Trial

Posted: Published on April 22nd, 2012

MARLBOROUGH, Mass.--(BUSINESS WIRE)-- Advanced Cell Technology, Inc. (ACT; OTCBB: ACTC), a leader in the field of regenerative medicine, announced today the dosing of the third patient in its Phase I/II trial for dry age-related macular degeneration (dry AMD) using retinal pigment epithelial (RPE) cells derived from human embryonic stem cells (hESCs). The outpatient transplantation surgery was performed successfully, and the patient is recovering uneventfully. Gary Rabin, chairman and CEO of ACT, commented, The completion of enrollment of the first cohort of patients in our dry AMD clinical trial is a significant step forward in our RPE clinical program. The first six patients in the U.S. trials have all been treated at UCLA, and as we have recently announced, the trials should soon expand to additional sites. As we have built our clinical team, we have been fortunate to have attracted the attention of some of the highest-caliber ophthalmologists and related institutions in the U.S. and Europe and recognize the huge value that their expertise provides us as we plan for the future of our therapeutic programs. With their guidance, we have also worked with the FDA to successfully expand the criteria of eligibility for patients to participate in our dry … Continue reading

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