Wednesday, February 18, 2009
AMS get USA approval for Liquiband
HEALTHCARE technology company Advanced Medical Solutions (AMS) has reached a key milestone in its evolution by securing permission to market its products in America.The £16.9m turnover business, based in Winsford, Cheshire, has been given clearance for one of its major ranges of skin healing products called LiquiBand. The announcement opens AMS to a US market which is worth an estimated £140m a year, and the news prompted its shares to rise by 4.5 per cent or 1.5p to 35p. They later settled at 34.75p, a rise of 3.37 per cent.The deal also prompted analysts to predict a future target share price of 45p.While the LiquiBand range reduces the need for surgical stitches by `gluing' wounds together, some of its other products contain a derivative of seaweed to promote healing or silver to fight the spread of diseases.AMS is still seeking clearance for its other products in America which will ultimately provide it with an even stronger foothold in both accident and emergency departments and operating rooms.AMS chief executive Dr Don Evans said: "I am delighted that we have received this initial clearance on the back of which we will be finalising commercial arrangements for the introduction of our tissue adhesive technology to this key strategic market during 2009."AMS has already established a leading position in Britain and Europe with its LiquiBand range.Elizabeth Klein, of analyst Teathers, said: "We continue to highlight AMS as one of our top picks due to its good cash position - with no debt, its robust end markets, good relationships with partners and an expectation that new product approvals could additionally drive growth."
Nycomed's Tachosil receives expanded indication
•Surgical patch TachoSil® – first and only dual action patch for general tissue sealing
ZURICH, Switzerland, Feb. 17, 2009--Today Nycomed received an expanded indication for TachoSil®, its innovative surgical patch, from the European Medicines Agency (EMEA). To date, TachoSil was approved for haemostasis (control of bleeding) in surgery. With the new expanded indication, it becomes the first and only dual action patch approved for haemostasis, tissue sealing as well as for suture support in vascular surgery.
TachoSil is the key product in Nycomed’s tissue management portfolio and effectively fulfils the market need for a ready-to-use surgical patch, developed to assist surgeons in achieving fast and reliable bleeding control. Now, with the new expanded indication, Nycomed can offer a dual action patch approved for haemostasis, tissue sealing as well as for suture support in vascular surgery.
“With the expansion of TachoSil’s indication, Nycomed will bring the benefits of this unique product to surgical teams and those patients undergoing lung or other types of surgery requiring rapid air or body fluid sealing,” said Lone Nørgaard Andersson, International Brand Manager at Nycomed.
The new indication was filed with the EMEA in 2008, based on international clinical trial results on lung and cardiovascular surgery. TachoSil is currently available in Europe and Russia/CIS. In the United States, the product will be marketed by Baxter International Inc., while Nycomed will manufacture it and be responsible for the US regulatory filing.
ZURICH, Switzerland, Feb. 17, 2009--Today Nycomed received an expanded indication for TachoSil®, its innovative surgical patch, from the European Medicines Agency (EMEA). To date, TachoSil was approved for haemostasis (control of bleeding) in surgery. With the new expanded indication, it becomes the first and only dual action patch approved for haemostasis, tissue sealing as well as for suture support in vascular surgery.
TachoSil is the key product in Nycomed’s tissue management portfolio and effectively fulfils the market need for a ready-to-use surgical patch, developed to assist surgeons in achieving fast and reliable bleeding control. Now, with the new expanded indication, Nycomed can offer a dual action patch approved for haemostasis, tissue sealing as well as for suture support in vascular surgery.
“With the expansion of TachoSil’s indication, Nycomed will bring the benefits of this unique product to surgical teams and those patients undergoing lung or other types of surgery requiring rapid air or body fluid sealing,” said Lone Nørgaard Andersson, International Brand Manager at Nycomed.
The new indication was filed with the EMEA in 2008, based on international clinical trial results on lung and cardiovascular surgery. TachoSil is currently available in Europe and Russia/CIS. In the United States, the product will be marketed by Baxter International Inc., while Nycomed will manufacture it and be responsible for the US regulatory filing.
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