{"id":63870,"date":"2026-05-12T06:17:56","date_gmt":"2026-05-12T06:17:56","guid":{"rendered":"https:\/\/www.europesays.com\/ch\/63870\/"},"modified":"2026-05-12T06:17:56","modified_gmt":"2026-05-12T06:17:56","slug":"roche-gets-second-european-approval-for-alzheimers-test","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ch\/63870\/","title":{"rendered":"Roche gets second European approval for Alzheimer&#8217;s test"},"content":{"rendered":"\n<p class=\"yf-1fy9kyt\">ZURICH, May 12 (Reuters) &#8211; Swiss drugmaker Roche has received the CE mark &#8211; a \u200cEuropean regulatory clearance allowing sale in \u200cthe region &#8211; for its second Elecsys blood test for \u200bAlzheimer&#8217;s disease, it said on Tuesday.<\/p>\n<p class=\"yf-1fy9kyt\">The test was developed with U.S. company Eli Lilly.<\/p>\n<p class=\"yf-1fy9kyt\">\u2022 Compared with its already approved pTau181 test, \u200cwhich mainly helps \u2060rule out Alzheimer&#8217;s-related amyloid pathology, the newer pTau217 test can both \u2060help confirm and exclude the disease. It is validated for use in both primary \u200band specialist \u200bcare.<\/p>\n<p class=\"yf-1fy9kyt\">\u2022 The test \u200bhas already received breakthrough \u200cdevice designation from the U.S. FDA.<\/p>\n<p class=\"yf-1fy9kyt\">\u2022 Blood tests could speed diagnosis and widen access to treatments such as Biogen and Eisai&#8217;s Leqembi and Eli Lilly&#8217;s Kisunla, as current \u200cdiagnostic methods are often \u200bcostly or uncomfortable.<\/p>\n<p class=\"yf-1fy9kyt\">\u2022 Roche \u200bsaid an estimated \u200b75% of people living with \u200cdementia remain undiagnosed.<\/p>\n<p class=\"yf-1fy9kyt\">\u2022 The test \u200bis expected \u200bto become available in CE-marked markets from July, Olivier Gillieron, life cycle leader \u200bin cardiometabolic \u200cand neurology at Roche told media \u200bin a call.<\/p>\n<p class=\"yf-1fy9kyt\">(Reporting by Marleen Kaesebier. \u200bEditing by Mark Potter)<\/p>\n","protected":false},"excerpt":{"rendered":"ZURICH, May 12 (Reuters) &#8211; Swiss drugmaker Roche has received the CE mark &#8211; a \u200cEuropean regulatory clearance&hellip;\n","protected":false},"author":2,"featured_media":63871,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[124],"tags":[13066,14442,216,134,15704],"class_list":{"0":"post-63870","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-roche","8":"tag-alzheimer39s-disease","9":"tag-blood-test","10":"tag-eli-lilly","11":"tag-roche","12":"tag-test"},"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@ch\/116560153971820290","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/63870","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/comments?post=63870"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/63870\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media\/63871"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media?parent=63870"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/categories?post=63870"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/tags?post=63870"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}