Clinical Update On TAMARIS Phase III Trial For NV1FGF
Sanofi-aventis announced that the Phase III TAMARIS trial evaluating the investigational angiogenic therapy NV1FGF (riferminogen pecaplasmid) did not meet its primary endpoint. The primary endpoint was to demonstrate the superiority of NV1FGF vs. placebo in the prevention of major amputation or death from any cause over 12 months, whichever came first, in critical limb ischemia patients who were not eligible for revascularization.
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iData Research has released a series of global reports that claim the U.S. market for vascular access devices and accessories was valued at just over $3 billion in 2009 and projects an estimated growth to $4.6 billion by the year 2016.