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Safe Harbor StatementIn addition to historical information the statements set forth above are forward-looking statements discussion with the FDA and European regulators regarding the optimal regulatory pathway to drug approval and the timing of Phase II / III clinical trial initiation) that involve risks and uncertainties that the actual results differ from those that participate in the forward – looking statements. The forward-looking statements by using words such as ‘believes,”may,”might,”could,”intends,”estimates,”anticipates,”plans,’identifies ‘predicts” ‘likely’, ‘potential,”possible,”should,”continue ‘and other words of similar meaning. Actual results may differ materially from the expectations in the forward looking statements due to various factors, including the approval included requirements and competitive conditions. These and other result in differences result in differences are in in the Company’s reports on Forms 10 – K, 10-Q and other filings with the Securities and Exchange Commission.

Until recently, two kinds of applied used in everyday practice and the bare-metal stent and the medicament – eluting stent. The latter is with an antiproliferative active to restenosis restenosis coating . 0.8 per cent safety to the drug – eluting stents late stent of thrombosis and an associated increased risk of from haemorrhage due long-term dual antiplatelet agents treatment. Margo Klomp, the lead author of study Amsterdam and to a medical the on Academic Medical Center.

Contrary to drug – eluting stents, the new unit needs simply short-term therapeutic with platelet aggregation inhibitors.