{"id":76772,"date":"2016-05-23T14:05:26","date_gmt":"2016-05-23T14:05:26","guid":{"rendered":"http:\/\/healthmedicinet.com\/i\/fda-staff-question-utility-of-sanofi-diabetes-drugs\/"},"modified":"2016-05-23T14:05:26","modified_gmt":"2016-05-23T14:05:26","slug":"fda-staff-question-utility-of-sanofi-diabetes-drugs","status":"publish","type":"post","link":"http:\/\/healthmedicinet.com\/i\/fda-staff-question-utility-of-sanofi-diabetes-drugs\/","title":{"rendered":"FDA staff question utility of Sanofi diabetes drugs"},"content":{"rendered":"<p><span id=\"articleText\"><br \/>\n<span id=\"midArticle_start\" \/><\/p>\n<p><span class=\"focusParagraph\"><\/p>\n<p><span class=\"articleLocatio\/spann\">A preliminary review by the U.S. Food and Drug Administration questioned whether Sanofi SA&#8217;s experimental diabetes drug lixisenatide contributed any benefit to a fixed-dose combination product the company hopes to market.<\/span><\/p>\n<p><\/span><span id=\"midArticle_0\" \/><\/p>\n<p>The review comes ahead of a May 25 meeting of an FDA advisory panel that will discuss lixisenatide and a separate treatment, iGlarLixi, which delivers lixisenatide and Sanofi&#8217;s drug Lantus, known also as insulin glargine, in a fixed dose combination.    The FDA is not obliged to follow the recommendation of its advisory panels but typically does so.<\/p>\n<p><span id=\"midArticle_1\" \/><\/p>\n<p>Lixisenatide belongs to a class of diabetes treatments called GLP-1 agonists that also includes Novo Nordisk A\/S&#8217; Victoza and Bristol-Myers Squibb Co and AstraZeneca&#8217;s Byetta and Bydureon.<\/p>\n<p><span id=\"midArticle_2\" \/><\/p>\n<p>On May 24 the committee will consider a similar combination treatment made by Novo Nordisk that combines Victoza, known also as liraglutide, with another of the company&#8217;s drugs, Tresiba, or insulin degludec.<\/p>\n<p><span id=\"midArticle_3\" \/><\/p>\n<p>        <span class=\"first-article-divide\" \/><\/p>\n<p>The FDA&#8217;s preliminary review of Novo Nordisk&#8217;s drug, sold in Europe under the brand name Xultophy, questioned the interpretability of the company&#8217;s data and practical use of the treatment. The reviewers raised similar questions about Sanofi&#8217;s drug.<\/p>\n<p><span id=\"midArticle_4\" \/><\/p>\n<p>Lixisenatide was approved by regulators in Europe and Japan in 2013 and is sold under the brand name Lyxumia. A U.S. brand has not yet been announced. Sanofi licensed lixisenatide from Denmark&#8217;s Zealand Pharma A\/S.<\/p>\n<p><span id=\"midArticle_5\" \/><\/p>\n<p>        <span class=\"second-article-divide\" \/><\/p>\n<p>Novo Nordisk&#8217;s product was approved in Europe in 2014 under the brand name Xultophy (iDegLira).<\/p>\n<p><span id=\"midArticle_6\" \/><\/p>\n<p>        <span class=\"third-article-divide\" \/><\/p>\n<p>The companies&#8217; products, if approved, would be the first to combine a GLP-1 and a basal insulin in a single injection instead of two injections. The goal is to treat patients earlier with a combination drug rather than waiting for patients to lose control of their blood sugar on one drug before moving to another.<\/p>\n<p><span id=\"midArticle_7\" \/><\/p>\n<p \/><span id=\"midArticle_8\" \/><\/p>\n<p> (Reporting by Toni Clarke in Washington; Editing by Jeffrey Benkoe and Andrea Ricci)<\/p>\n<p><span id=\"midArticle_9\" \/><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>A preliminary review by the U.S. Food and Drug Administration questioned whether Sanofi SA&#8217;s experimental diabetes drug lixisenatide contributed any benefit to a fixed-dose combination product the company hopes to market. The review comes ahead of a May 25 meeting of an FDA advisory panel that will discuss lixisenatide and a separate treatment, iGlarLixi, which <a class=\"read-more-link\" href=\"http:\/\/healthmedicinet.com\/i\/fda-staff-question-utility-of-sanofi-diabetes-drugs\/\">Read More<\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-76772","post","type-post","status-publish","format-standard","hentry"],"_links":{"self":[{"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/posts\/76772","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/comments?post=76772"}],"version-history":[{"count":0,"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/posts\/76772\/revisions"}],"wp:attachment":[{"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/media?parent=76772"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/categories?post=76772"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/healthmedicinet.com\/i\/wp-json\/wp\/v2\/tags?post=76772"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}