{"id":537934,"date":"2021-09-14T08:33:38","date_gmt":"2021-09-14T12:33:38","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\/"},"modified":"2021-09-14T08:33:38","modified_gmt":"2021-09-14T12:33:38","slug":"sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\/","title":{"rendered":"Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress"},"content":{"rendered":"<div class=\"mw_release\">\n<p align=\"justify\">CAMBRIDGE, Mass., Sept.  14, 2021  (GLOBE NEWSWIRE) &#8212; Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, will present at the World Muscle Society 2021 Virtual Congress (WMS 2021), taking place Sept. 20-24, 2021. This year\u2019s presentations at WMS 2021 highlight scientific leadership and innovation from across Sarepta\u2019s deep, multi-platform portfolio and reflect the Company\u2019s continued commitment advancing life-changing therapies to those with rare genetic diseases.<\/p>\n<p align=\"justify\">Presented research will include data from the Company\u2019s gene therapy and RNA platforms, in addition to new research into the prevalence of pre-existing antibodies to the AAVrh74 vector, which is used in several of Sarepta\u2019s gene transfer therapy programs.\u00a0\u00a0 All posters are available on-demand throughout the Congress beginning on Monday, Sept. 20, 2021 at 7:00 am E.T. The full WMS 2021 program is available at <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=_e1BgvAM6Ch_Vs0lzordmaW8ClhyFTdrrlctAvMlSH83QEbo6tNsW8uuTADU_BKaRWQaULDR-WMbadH-HNJx--CBTPKCxkjZetzlYtEtCJgqy4jWOAY9q0NIASm6vIjo6g05m0MM0pUh6wnK9a7cvw==\" rel=\"nofollow noopener\" target=\"_blank\">https:\/\/www.wms2021.com\/page\/programme<\/a>.<\/p>\n<p>\n        <strong><br \/>\n          <em>Poster Presentations <\/em><br \/>\n        <\/strong>\n      <\/p>\n<table style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;border-collapse: collapse;width:100%;border-collapse:collapse\">\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">\n            <strong>Poster #\u200b<\/strong>\n          <\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">\n            <strong>Title\u200b<\/strong>\n          <\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.096\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Micro-dystrophin gene therapy delivery and therapeutic plasma exchange in nonhuman primates\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.139\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Phase 1\/2a trial of SRP-9001 in patients with Duchenne muscular dystrophy: 3-year safety and functional\u00a0outcomes (SRP-9001-101)\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.149\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Delay in Duchenne muscular dystrophy progression with eteplirsen: Longer time to loss of ambulation\u00a0versus standard of care<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.150\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Casimersen\u00a0in patients with Duchenne muscular dystrophy amenable to exon 45 skipping: Interim results\u00a0from the Phase 3 ESSENCE trial\u00a0\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.151\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Evaluation of total binding antibodies against rAAVrh74 in patients with Duchenne muscular dystrophy\u00a0\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.152\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">ENDEAVOR: A gene delivery study to evaluate the safety of and expression from SRP-9001 in Duchenne\u00a0muscular dystrophy (SRP-9001-103)\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.185\u00a0\u200b<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Safety,\u00a0\u03b2-sarcoglycan\u00a0expression, and functional outcomes from systemic gene transfer of rAAVrh74.MHCK7.SGCB in limb\u00a0girdle muscular dystrophy type 2E\/R4\u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">EP.254<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">A Phase 2 clinical trial evaluating the safety and efficacy of SRP-9001 for treating patients with Duchenne\u00a0muscular dystrophy (SRP-9001-102) \u200b<\/td>\n<\/tr>\n<tr>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">LBP.22<\/td>\n<td style=\"border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: middle;text-align: left;padding-left: 10.0px;vertical-align: top\">Safety, tolerability, and pharmacokinetics of eteplirsen in patients 6-48 months old with Duchenne muscular dystrophy amenable to exon 51 skipping<\/td>\n<\/tr>\n<\/table>\n<p align=\"justify\">Presentations will be archived on the events and presentations page in the Investor Relations section of <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=uUY1rArsP46F4bPs-ju8NuG-vm-VHT82QifGOtCvzlq-cDAlxOmDsWmD4nge7gmQGhJjdV-0pF-2bjIC8HL0YA==\" rel=\"nofollow noopener\" target=\"_blank\">www.sarepta.com<\/a> for one year following their presentation at WMS 2021.<\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>About Sarepta Therapeutics<\/em><br \/>\n        <\/strong><br \/>\n        <br \/>Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing. For more information, please visit\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=uUY1rArsP46F4bPs-ju8NhjNkN1b2p0H-m6i_LvzLrUNRwqtvlzZGi80vtR-fkXGc1Jcynz3bUb7TtfF6yKJwQ==\" rel=\"nofollow noopener\" target=\"_blank\">www.sarepta.com<\/a> or follow us on <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=TB1nGkTwP6jfpIq9JbBHtgEFAPLavC9jt3jLbdnMkQiTpEIOVJyS72wstO4lHhN0IpwBEK7mbZ3lK7Teb2u1EQ==\" rel=\"nofollow noopener\" target=\"_blank\">Twitter<\/a>, <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=BzE7zk9QbDum7BBI8YUXJWK4vq1XoW4Oh01UxiB9zW3OTYMFQhSRYU5Jv90MTzwGmPLkBhFYT8e-UqwV9IuYCPXQKxpd9jrefTFNGHHUeOJ4sN8mObwifE1ekFXRoMAH\" rel=\"nofollow noopener\" target=\"_blank\">LinkedIn<\/a>, <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fkwyAYX0iKRa1mMat5HFUhrLjxiCmvFx-23bkBvKtOEDY4PgHmSFcwDF0zxVzX8meJxYKXorZ5OFNk62YOT3tDxWo9RBepwvmCNgkkM7VAk=\" rel=\"nofollow noopener\" target=\"_blank\">Instagram<\/a> and <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=BCMsaSTr4JZW4Eb14iPzg3Xic4wtVzjyCmbMqtLfgvKrGj8r9oswL15h0BUqsFiOFmFagbHCOVLhR4WstZZDvq5aJVW-fMUrGd-wklB78Jawo9P6aGV5qn8JOiqgU7Jc\" rel=\"nofollow noopener\" target=\"_blank\">Facebook<\/a>.<\/p>\n<p align=\"justify\">\n        <strong><br \/>\n          <em>Internet Posting of Information<\/em><br \/>\n        <\/strong><br \/>\n        <br \/>\n        <em>We routinely post information that may be important to investors in the &#8216;For Investors&#8217; section of our website at\u00a0<\/em><br \/>\n        <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=uUY1rArsP46F4bPs-ju8NpvndMG_AM6Aqf53ukwaxh2yrp3JG3SMP7jYegCoBU7BJdHU9TEq850xXq2vdP2qKA==\" rel=\"nofollow noopener\" target=\"_blank\"><br \/>\n          <em><br \/>\n            <u>www.sarepta.com<\/u><br \/>\n          <\/em><br \/>\n        <\/a><br \/>\n        <em>. We encourage investors and potential investors to consult our website regularly for important information about us.<\/em>\n      <\/p>\n<p>Source: Sarepta Therapeutics, Inc.<\/p>\n<p>\n        <strong><br \/>\n          <em>Investor Contact: <\/em><br \/>\n        <\/strong><br \/>\n        <br \/>Ian Estepan, 617-274-4052<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=oo1PwxFSM05ou7uCuQv8PURxVbN8tubzRvU2ORzZhDh_soLUrJwkDkABz0MXXag-qBOXZRhT3ELvi9xhXUTAfgFpNt3yU-aL19fD_QALH9g=\" rel=\"nofollow noopener\" target=\"_blank\">iestepan@sarepta.com<\/a><\/p>\n<p>\n        <strong><br \/>\n          <em>Media Contact: <\/em><br \/>\n        <\/strong><br \/>\n        <br \/>Tracy Sorrentino, 617-301-8566<br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=G_QdGtNbm2cO4P4PPcUP9SWK5sTeigtCfYUcC0TqeHXTd9pgys3UmVYKIMwdsddhhBqzfHbTWVtaj-PPC6pdiaCwNntrSfaHJPRelprhLQQ=\" rel=\"nofollow noopener\" target=\"_blank\">tsorrentino@sarepta.com<\/a><\/p>\n<p>      <img decoding=\"async\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODMyNTU5OSM0NDAzNjc3IzIwMDcxNTc=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" src=\"https:\/\/ml.globenewswire.com\/media\/NmJkYTRjMjktNTA1NC00MWY2LTgxNmYtMzBhZmFlMjdjNjQ3LTEwMTg3MzA=\/tiny\/Sarepta-Therapeutics-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>CAMBRIDGE, Mass., Sept. 14, 2021 (GLOBE NEWSWIRE) &#8212; Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, will present at the World Muscle Society 2021 Virtual Congress (WMS 2021), taking place Sept. 20-24, 2021. This year\u2019s presentations at WMS 2021 highlight scientific leadership and innovation from across Sarepta\u2019s deep, multi-platform portfolio and reflect the Company\u2019s continued commitment advancing life-changing therapies to those with rare genetic diseases. Presented research will include data from the Company\u2019s gene therapy and RNA platforms, in addition to new research into the prevalence of pre-existing antibodies to the AAVrh74 vector, which is used in several of Sarepta\u2019s gene transfer therapy programs.\u00a0\u00a0 All posters are available on-demand throughout the Congress beginning on Monday, &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-537934","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"CAMBRIDGE, Mass., Sept. 14, 2021 (GLOBE NEWSWIRE) &#8212; Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, will present at the World Muscle Society 2021 Virtual Congress (WMS 2021), taking place Sept. 20-24, 2021. This year\u2019s presentations at WMS 2021 highlight scientific leadership and innovation from across Sarepta\u2019s deep, multi-platform portfolio and reflect the Company\u2019s continued commitment advancing life-changing therapies to those with rare genetic diseases. Presented research will include data from the Company\u2019s gene therapy and RNA platforms, in addition to new research into the prevalence of pre-existing antibodies to the AAVrh74 vector, which is used in several of Sarepta\u2019s gene transfer therapy programs.\u00a0\u00a0 All posters are available on-demand throughout the Congress beginning on Monday, &hellip; Continue reading &quot;Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2021-09-14T12:33:38+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=ODMyNTU5OSM0NDAzNjc3IzIwMDcxNTc=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress\",\"datePublished\":\"2021-09-14T12:33:38+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/\"},\"wordCount\":504,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=ODMyNTU5OSM0NDAzNjc3IzIwMDcxNTc=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/sarepta-therapeutics-to-showcase-data-from-its-gene-therapy-and-rna-platforms-at-world-muscle-society-2021-virtual-congress\\\/\",\"name\":\"Sarepta Therapeutics to Showcase Data from its Gene Therapy and RNA Platforms at World Muscle Society 2021 Virtual Congress - 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(NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, will present at the World Muscle Society 2021 Virtual Congress (WMS 2021), taking place Sept. 20-24, 2021. This year\u2019s presentations at WMS 2021 highlight scientific leadership and innovation from across Sarepta\u2019s deep, multi-platform portfolio and reflect the Company\u2019s continued commitment advancing life-changing therapies to those with rare genetic diseases. 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