Updates
** Shares of therapy maker Sarepta Therapeutics SRPT.O fall 6.7% to $119.42
** Company says it will discontinue development of its new experimental drug, SRP-5051, that was being studied to treat patients with a type of Duchenne muscular dystrophy
** Duchenne muscular dystrophy is a condition that causes skeletal and heart muscle weakness that quickly gets worse with time
** In a small number of patients, company saw persistent hypomagnesemia-a condition where the level of magnesium in the blood is below normal-despite treatment discontinuation
** Co in its conference call said it is discontinuing its entire peptide conjugated PMO drugs franchise- that were in development to treat Duchenne muscular dystrophy
** Co says the decision to stop the program was based on "information available to date, including the risk-benefit of the program, feedback from the FDA, and the evolving therapeutic landscape for Duchenne"
** Company also reports Q3 revenue of $467.2 mln, beating analysts' estimate of $409.30 mln - LSEG data
** Q3 net product revenue for Elevidys, its gene therapy for Duchenne muscular dystrophy, at $181 mln
** Up to last close, stock up ~32% YTD
(Reporting by Sriparna Roy and Sneha S K in Bengaluru)
((Sriparna.Roy@thomsonreuters.com;))
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