TopoTargetTopoTarget A / S announced that a positive response from the FDA on a Special Protocol Assessment was a Phase III study for belinostat in PTCL received. This pivotal trial is included approximately 120 patients and is in the 4th Quarter of 2008 click to follow www.doxycyclinehyc.com . In June Fast Track designation was for the development of belinostat in this indication which supports TopoTarget granted rapid market entry strategy. There is currently no standard therapy for PTCL admitted. – This is very good news, we can now belinostat in a Phase III with the SPA in place we have on a design for our Phase III trial with the FDA to Q4 this year Q4 of this year agreed Additionally with Fast Track the FDA received designation in June for the PTCL indication we can with our strategy of rapid market entry for belinostat in an area to continue with a high unmet medical need Said Professor Peter Buhl Jensen, CEO of TopoTarget. – Design.
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