{"id":27499,"date":"2024-06-28T15:55:00","date_gmt":"2024-06-28T15:55:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4451493_AE51493_0"},"modified":"2024-06-28T15:55:00","modified_gmt":"2024-06-28T15:55:00","slug":"pierre-fabre-laboratories-announce-granting-of-european-marketing-authorization-for-obgemsa-vibegron-in-overactive-bladder","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=27499","title":{"rendered":"Pierre Fabre Laboratories announce granting of European marketing authorization for OBGEMSA\u2122 (vibegron) in overactive bladder."},"content":{"rendered":"<table name=\"logo_release\" border=\"0\" cellspacing=\"10\" cellpadding=\"5\" align=\"right\">\n<tbody>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mma.prnasia.com\/media2\/2416854\/4789117\/Pierre_Fabre_Laboratories.jpg?p=medium600\" border=\"0\" alt title=\"logo\" hspace=\"0\" vspace=\"0\" width=\"118\"><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>CASTRES, <span class=\"xn-location\">France<\/span>, <span class=\"xn-chron\">June 28, 2024<\/span> \/PRNewswire\/ &#8212; The European Commission (EC) has authorized the marketing of OBGEMSA\u2122 (vibegron) by Pierre Fabre Laboratories for the symptomatic treatment of overactive bladder syndrome in adults, a particularly debilitating condition affecting over 70 million patients* in <span class=\"xn-location\">Europe<\/span>. In 2022, Pierre Fabre Laboratories acquired the exclusive license for vibegron from Urovant Sciences Gmbh for the registration and commercialization of this innovative treatment in the European Economic Area. The decision of the EC will be applicable to all EU member states as well as <span class=\"xn-location\">Iceland<\/span>, <span class=\"xn-location\">Liechtenstein<\/span>, and <span class=\"xn-location\">Norway<\/span>. OBGEMSA\u2122 is a trademark owned by Urovant Sciences.<\/p>\n<p>PDF &#8211; <a href=\"https:\/\/mma.prnewswire.com\/media\/2451098\/Pierre_Fabre.pdf\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/mma.prnewswire.com\/media\/2451098\/Pierre_Fabre.pdf<\/a><\/p>\n<p>&#8220;<i>We are delighted with this development, which will allow European patients to benefit from a new therapeutic option for overactive bladder syndrome and further strengthen our expertise of over 40 years in urology. This decision confirms Pierre Fabre Laboratories&#8217; commitment to offering patients innovative therapies that provide better management of chronic debilitating diseases,<\/i>&#8221;&nbsp;<b>said <span class=\"xn-person\">Eric Ducournau<\/span>, CEO of Pierre Fabre Laboratories.<\/b><\/p>\n<p>The decision of the EC follows the favorable opinion issued on <span class=\"xn-chron\">April 25<\/span> by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA). It is based on the results of two pivotal, multicenter, double-blind, randomized phase 3 studies in adults with overactive bladder symptoms. Study RVT-901-3003 (EMPOWUR) evaluated the efficacy, tolerability, and safety of vibegron (at a dose of 75 mg per day) over 12 weeks compared to placebo and with tolterodine as a positive control. Its extension, study RVT-901-3004 (EMPOWUR Extension), double-blindly evaluated the long-term safety, tolerability, and efficacy of vibegron over 52 weeks, with tolterodine as an active comparator. In these studies, vibegron, as a new selective agonist of beta-3 adrenergic receptors (AR), demonstrated a favorable benefit-risk profile in the symptomatic treatment of urgency, increased frequency of urination, and urge urinary incontinence (UUI) that can occur in patients with overactive bladder syndrome.<\/p>\n<p>Contact:<\/p>\n<p>Laurence MARCHAL<br \/><a href=\"mailto:laurence.marchal@pierre-fabre.com\" target=\"_blank\" rel=\"nofollow noopener\">laurence.marchal@pierre-fabre.com<\/a>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>CASTRES, France, June 28, 2024 \/PRNewswire\/ &#8212; The European Commission (EC) has authorized the marketing of OBGEMSA\u2122 (vibegron) by Pierre Fabre Laboratories for the symptomatic treatment of overactive bladder syndrome in adults, a particularly debilitating condition affecting over 70 million patients* in Europe. In 2022, Pierre Fabre Laboratories acquired the exclusive license for vibegron from [&hellip;]<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[20],"tags":[],"class_list":["post-27499","post","type-post","status-publish","format-standard","hentry","category-business-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Pierre Fabre Laboratories announce granting of European marketing authorization for OBGEMSA\u2122 (vibegron) in overactive bladder. - My Blog<\/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:\/\/transmediavictoria.net.au\/?p=27499\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pierre Fabre Laboratories announce granting of European marketing authorization for OBGEMSA\u2122 (vibegron) in overactive bladder. - My Blog\" \/>\n<meta property=\"og:description\" content=\"CASTRES, France, June 28, 2024 \/PRNewswire\/ &#8212; The European Commission (EC) has authorized the marketing of OBGEMSA\u2122 (vibegron) by Pierre Fabre Laboratories for the symptomatic treatment of overactive bladder syndrome in adults, a particularly debilitating condition affecting over 70 million patients* in Europe. 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