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March 7, 2013
10:42 EDTSRPTSarepta DMD drug still has accelerated approval potential, says Piper Jaffray
Piper Jaffray said it still believes there is a 50/50 chance that Sarepta will be able to file for approval of its Duchenne Muscular Dystrophy drug eteplirsen with its existing data. Piper said that if the company is required to conduct a larger trial prior to filing, a slide in the stock would be likely but would present a buying opportunity. The firm maintains an Overweight rating and $35 price target on Sarepta.
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June 19, 2013
11:13 EDTSRPTSarepta rises after reporting clinical data
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09:54 EDTSRPTSarepta data supports accelerated approval, says Piper Jaffray
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08:39 EDTSRPTSarepta eteplirsen demonstrates benefit on walking test in Phase IIb study
Sarepta Therapeutics announced updated data from Study 202, a Phase IIb open-label extension study of eteplirsen in patients with Duchenne muscular dystrophy, or DMD. Results at 84 weeks showed a continued stabilization of walking ability in eteplirsen-treated patients evaluable on the 6-minute walk test. As previously reported, Study 202 met its primary endpoint of increased novel dystrophin as assessed by muscle biopsy at Week 48 and is now in the long-term extension phase in which patients continue to be followed for safety and clinical outcomes. Eteplirsen is Sarepta's lead exon-skipping compound in development for the treatment of patients with DMD who have a genotype amenable to skipping of exon 51.
June 17, 2013
12:20 EDTSRPTOptions with increasing implied volatility: WLT LNCO SRPT LINE
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June 14, 2013
11:23 EDTSRPTOptions with increasing implied volatility: TWO SRPT LNCO LINE DVA
06:15 EDTSRPTLeerink remains cautious on accelerated approval for Sarepta
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June 5, 2013
13:29 EDTSRPTOptions with decreasing implied volatility: INFI SRPT GES SUPN CPRT
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