Prosensa announces commencement of re-dosing of drisapersen in North America in patients with Duchenne muscular dystrophy

Prosensa Holding N.V. (NASDAQ: RNA), the biopharmaceutical company focusing on RNA-modulating therapeutics for rare diseases with high unmet need, today announced that a comprehensive program of re-dosing has commenced, with the first patients now re-dosed in the United States. All dosing in the drisapersen clinical program had been placed on hold by GSK on September 20, 2013, upon announcement of the DEMAND III study results.

Prosensa announces Lancet Neurology publication of an exploratory phase II study (DEMAND II) demonstrating efficacy and safety of drisapersen in patients with Duchenne muscular dystrophy

Prosensa Holding N.V. (NASDAQ: RNA), the biopharmaceutical company focusing on RNA-modulating therapeutics for rare diseases with high unmet need, today announced that the full data from its exploratory, double-blind, placebo-controlled Phase II study (DEMAND II/ DMD114117/ NCT01153932) of drisapersen in patients with Duchenne muscular dystrophy (DMD) have been published in Lancet Neurology https://bit.ly/1rSMpeJ.

CureDuchenne Launches “Dollar 4 Duchenne” Campaign Today for World Duchenne Awareness Day

CureDuchenne launched the Ì¢‰âÒDollar 4 DuchenneÌ¢‰âÂÌ_ campaign today during World Duchenne Awareness Day to fund research to find a cure for Duchenne muscular dystrophy. The Ì¢‰âÒDollar 4 DuchenneÌ¢‰âÂÌ_ campaign encourages people to donate one dollar to help fund Duchenne research. Ì¢‰âÒDollar 4 DuchenneÌ¢‰âÂÌ_ is part of a comprehensive CureDuchenne fundraising campaign to raise $7 million to fund a Duchenne research project.