(Nasdaq:RNA), the Dutch biopharmaceutical companyfocusing on RNA-modulating therapeutics for rare diseases with high unmet need,today reported financial results for the first quarter ending March 31, 2014and provided an update on the next steps for its exon-skipping platform for thetreatment of Duchenne Muscular Dystrophy (DMD). Hans Schikan, CEO of Prosensa said, 'We have made excellent progress duringthis period, and are very pleased that we are now in a position to commencere-dosing with drisapersen of boys that have previously participated indrisapersen trials beginning in the third quarter of 2014. In addition, our250-patient Natural History study, designed to better understand the diseaseprogression of DMD, has almost completed enrollment.' 'We are encouraged by our ongoing interactions with the regulatory authorities,in both the United States and Europe, and remain on track to communicating apotential regulatory path forward for drisapersen by the end of June,' headded. 'Prosensa is dedicated to enabling long term patient access todrisapersen and its follow-on candidates as novel treatments for DMD. We aredetermined to accomplish this as soon as possible.' Recent Corporate Highlights-- Updates on the Drisapersen Development Program -- On January 13, we announced that we regained the rights to drisapersen from GSK and retained the rights to all other programs … Continue reading
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