Sarepta therapeutics announces presentations at the 19th international congress of the world muscle society

Cambridge, mass.--(business wire)--sarepta therapeutics, inc. (nasdaq:srpt), a developer of innovative rna-based therapeutics, today announced that it will give one oral presentation and two poster presentations on data from its ongoing phase ii and preclinical trials evaluating exon-skipping therapies for the treatment of duchenne muscular dystrophy (dmd) at the international congress of the world muscle society (wms), being held from october 7-11, 2014, in berlin, germany. the oral presentation will include additional detail about the 144-week, 6-minute walk test (6mwt) and safety data from the phase iib study of eteplirsen, as well as other information including 144-week pulmonary function test results and information on individual mip and mep results. details of sarepta’s presentations at wms are as follows: oral presentation : eteplirsen in duchenne muscular dystrophy (dmd): 3 year update on six-minute-walk test (6mwt) and safety poster presentations: session title: safety and pharmacokinetic profile of eteplirsen, srp-4045, and srp-4053, threephosphorodiamidate morpholino oligomers (pmos) for the treatment of patients withduchenne muscular dystrophy (dmd) pulmonary function is stable through 120 weeks in patients with duchenne musculardystrophy (dmd) treated with exon-skipping drug eteplirsen in phase 2b study the oral presentation will be archived under the events and presentations section of the sarepta therapeutics website at www.sarepta.com following the presentation for 90 days. about sarepta therapeutics sarepta therapeutics is focused on developing first-in-class rna-based therapeutics to improve and save the lives of people affected by serious and life-threatening rare and infectious diseases. the company's diverse pipeline includes its lead program eteplirsen, for duchenne muscular dystrophy, as well as potential treatments for some of the world's most lethal infectious diseases. sarepta aims to build a leading, independent biotech company dedicated to translating its rna-based science into transformational therapeutics for patients who face significant unmet medical needs. for more information, please visit us at www.sarepta.com.
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