{"id":39377,"date":"2023-10-31T18:40:27","date_gmt":"2023-10-31T18:40:27","guid":{"rendered":"https:\/\/prosfunds.com\/investing\/sarepta-therapeutics-shares-plunge-as-gene-therapy-trial-falls-short-of-primary-goal\/"},"modified":"2023-10-31T18:40:28","modified_gmt":"2023-10-31T18:40:28","slug":"sarepta-therapeutics-shares-plunge-as-gene-therapy-trial-falls-short-of-primary-goal","status":"publish","type":"post","link":"https:\/\/prosfunds.com\/?p=39377","title":{"rendered":"Sarepta Therapeutics shares plunge as gene therapy trial falls short of primary goal"},"content":{"rendered":"<div id=\"js-article__body\" itemprop=\"articleBody\" data-sbid=\"WP-MKTW-0002674220\" role=\"document\">\n<p>Sarepta Therapeutics Inc. shares<br \/>\n        SRPT,<br \/>\n        <bg-quote field=\"percentchange\" format=\"0,000.00%\" channel=\"\/zigman2\/quotes\/206140855\/composite\" class=\"negative\">-38.71%<\/bg-quote><br \/>\n       dropped more than 40% premarket on Tuesday after the company said a trial of its gene therapy for Duchenne muscular dystrophy fell short of its main goal. <\/p>\n<p>The therapy, Elevidys, helped patients\u2019 movement and walking ability but failed to produce a statistically significant improvement versus placebo in an ambulatory assessment after 52 weeks of treatment, Sarepta said in a release Monday. <\/p>\n<div class=\"paywall\">\n<p>The trial involved patients age 4 through 7 years with Duchenne muscular dystrophy, a genetic disorder that can cause severe muscle weakness, with symptoms starting in early childhood. <\/p>\n<p>Based on the overall trial results, Sarepta said it plans to seek a label expansion so that Elevidys can treat all patients. The U.S. Food and Drug Administration in June approved Elevidys for treatment of patients age 4 through 5 years. The trial results support the conclusion that Elevidys \u201cmodifies the trajectory of Duchenne and benefits patients across age groups living with this ferociously degenerative disease,\u201d Doug Ingram, Sarepta\u2019s president and CEO, said in a statement. <\/p>\n<p>The trial data were \u201cextremely disappointing,\u201d Leerink Partners analysts wrote in a note Monday, but \u201cwe are not writing off the FDA\u2019s historical flexibility\u201d in Duchenne muscular dystrophy. The analysts maintained an outperform rating on Sarepta shares but cut their price target to $130, from $185. <\/p>\n<p>Sarepta stock is down 16.9% in the year to date, while the S&amp;P 500<br \/>\n        SPX<br \/>\n       has gained 8.5%. <\/p>\n<\/p><\/div>\n<\/div>\n<p>Read the full article <a href=\"https:\/\/www.marketwatch.com\/story\/sarepta-therapeutics-shares-plunge-as-gene-therapy-trial-falls-short-of-primary-goal-baf4734e?mod=investing\" target=\"_blank\" rel=\"noopener\">here<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Sarepta Therapeutics Inc. shares SRPT, -38.71% dropped more than 40% premarket on Tuesday after the company said a trial of its gene therapy for Duchenne muscular dystrophy fell short of its main goal. The therapy, Elevidys, helped patients\u2019 movement and walking ability but failed to produce a statistically significant improvement versus placebo in an ambulatory [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":3704,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"content-type":"","footnotes":""},"categories":[32],"tags":[],"class_list":{"0":"post-39377","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-investing"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Sarepta Therapeutics shares plunge as gene therapy trial falls short of primary goal | Prosfunds<\/title>\n<meta name=\"description\" content=\"Sarepta Therapeutics Inc. shares SRPT, -38.71% dropped more than 40% premarket on Tuesday after the company said a trial of its gene therapy for Duchenne\" \/>\n<meta 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