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Big Pharma Eyeing Mesoblast?
Ninemsn - Jul 27, 2010 By Chris Shaw Southern Cross Equities analyst Stuart Roberts has picked up a recent trend in the global pharmaceutical sector: an increase in merger and acquisition activity. In particular the ...
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Mesoblast Receives TGA Regulatory Approval to Commercially Manufacture Adult Stem Cell Products
PR Newswire - Jul 21, 2010 MELBOURNE, Australia, July 21 /PRNewswire/ -- Australian regenerative medicine company, Mesoblast Limited (ASX:MSB; ADR:MBLTY), today announced that the Australian Therapeutic Goods Administration ...
Mesoblast Limited (ASX:MSB) Receives Australian Therapeutic Goods Administration Regulatory Approval To Commercially Manufacture Adult Stem Cell Products - Asia Business NewsMesoblast product gets TGA licence - Brisbane Times News-Medical.net - pharmabiz.com - PharmaLive.com |
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Mesoblast Ltd Receives TGA Regulatory Approval To Commercially Manufacture Adult Stem Cell Products
Reuters Key Development - Jul 21, 2010 |
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Phase 3 Meeting Scheduled With US FDA Following Positive Results of Bone Marrow Regeneration Trial
PR Newswire - Jul 12, 2010 MELBOURNE, Australia, July 11 /PRNewswire/ -- Australian regenerative medicine company, Mesoblast Limited (ASX: MSB; ADR: MBLTY), today announced that based on positive results from its bone ...
Mesoblast Limited (ASX:MSB) Phase 3 Meeting Scheduled With FDA Following Positive Results Of Bone Marrow Regeneration Trial - ABN NewswireMesoblast schedules formal meeting with FDA to discuss proposed Phase 3 clinical trial program - News-Medical.net |
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Mesoblast Limited (ASX:MSB) Featured At ASX Singapore Conference Highlighting Emerging Market Leaders
Asia Business News - May 28, 2010 Melbourne, May 28, 2010 (ABN Newswire) - Australia's regenerative medicine company, Mesoblast Limited (ASX:MSB) (ADR:MBLTY), was featured yesterday by the ASX at its inaugural Small to Mid Caps ...
Mesoblast Featured at ASX Singapore Conference, Highlighting Emerging Market Leaders - irasia.com |
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United States FDA Clears Mesoblast Limited (ASX:MSB) Phase 2 Trial For Cervical Spinal Fusion
Asia Business News - May 19, 2010 Melbourne, May 19, 2010 (ABN Newswire) - Australia's regenerative medicine company, Mesoblast Limited (ASX:MSB) (ADR:MBLTY), today announced that it has received clearance from the United States ...
United States FDA Clears Phase 2 Trial for Cervical Spinal Fusion - irasia.com |
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Company Profile
Cash position at June 30th 2009: $16, 526, 278
Revenue during 2008-09 was $890, 708
Mesoblast Limited (Mesoblast) is a biotechnology company committed to the development of adult stem cell products targeting a range of bone, cartilage and musculoskeletal conditions.
Cardiovascular stem cell therapy: The Company holds a 38.4% interest in Angioblast Systems, Inc. (Angioblast), a company developing the same platform technology for the treatment of cardiovascular diseases, including repair and regeneration of blood vessels and heart muscle. Mesoblast is developing an allogeneic or off-the-shelf cell product, called NeoFuse, to generate bony spinal fusion.
Revascor, their proprietary "off the shelf" adult stem cell product for heart failure, have continued to show sustained improvement in heart muscle function at six months. Interim results of the ongoing phase two trial of Revascor were presented at the annual conference of the American Heart Association currently underway in Orlando, Florida. The presenter, Dr Nabil Dib associate professor of medicine and director of cell therapy, University of California, San Diego and director of cardiovascular research, Mercy Gilbert and Chandler Medical Centers, Phoenix Arizona said at six months a single dose of Revascor was accompanied by a 22% mean increase in EF whereas controls had an 18% mean decrease in EF over the same period.
Stem cells for back/disc problems: In August 2009, the United States Food and Drug Administration cleared a Phase II clinical trial of its allogeneic adult stem cells for use in minimally invasive lumbar spinal fusion surgery. The 24-patient trial, based at multiple United States sites, is comparing the effectiveness and safety of two low doses, NeoFuse with autograft in minimally invasive surgery for fusion of the lumbar spine.
