{"id":2544,"date":"2025-10-25T11:47:44","date_gmt":"2025-10-25T11:47:44","guid":{"rendered":"https:\/\/network.rvrising.com\/?p=2544"},"modified":"2025-10-25T11:47:44","modified_gmt":"2025-10-25T11:47:44","slug":"cardiovalve-completes-target-study-enrollment-for-ce-registration-study-for-tricuspid-valve-replacement","status":"publish","type":"post","link":"https:\/\/www.rvrising.com\/news\/business\/cardiovalve-completes-target-study-enrollment-for-ce-registration-study-for-tricuspid-valve-replacement\/","title":{"rendered":"Cardiovalve Completes TARGET Study Enrollment for CE Registration Study for Tricuspid Valve Replacement"},"content":{"rendered":"<p><b><span id=\"spanHghlt87a9\">The Company Advances Toward European CE Mark Submission with 150 Patients Enrolled; On Track for 2027 Commercial Launch<\/span><\/b><\/p>\n<div>\n<p><span class=\"legendSpanClass\">HANGZHOU, China<\/span>, <span class=\"legendSpanClass\">Oct. 25, 2025<\/span> \/PRNewswire\/ &#8212;\u00a0Venus\u00a0Medtech (Hangzhou) Inc. (2500.HK, hereinafter referred to as the &#8220;Company&#8221;) today announced the successful completion of patient enrollment in the <b>Cardiovalve TARGET study<\/b> for Transcatheter Tricuspid Valve Replacement (TTVR), with a total of <b>150 patients enrolled<\/b>. The completion of enrollment marks a major milestone toward European regulatory approval for Cardiovalve&#8217;s <b>Transcatheter Tricuspid Valve Replacement (TTVR) system<\/b>, the company&#8217;s flagship solution for treating tricuspid regurgitation.<\/p>\n<p>With enrollment now complete, the company is preparing to submit its <b>CE Mark application<\/b> to European regulators later this year. Pending approval, <b>commercial launch of the Cardiovalve TR system in Europe is projected for 2027<\/b>.<\/p>\n<p>Building on this achievement, Cardiovalve is also preparing to initiate its <b>AHEAD study<\/b>, which will evaluate the safety and performance of Cardiovalve&#8217;s <b>mitral valve replacement system<\/b> in patients suffering from significant mitral regurgitation (MR). The AHEAD study is designed to support a future <b>CE Mark application<\/b> for the mitral system.<\/p>\n<p><b>Cardiovalve Participation at TCT 2025<\/b><\/p>\n<p>Cardiovalve will present preliminary data for its mitral regurgitation (MR) system at <b>TCT 2025<\/b>.<\/p>\n<p>The presentation, titled &#8220;Transcatheter Mitral Valve Replacement Using the New Generation Cardiovalve System,&#8221; will be led by <b>Dr. Christian Frerker.<\/b><\/p>\n<p><b>Session Details<\/b>:<\/p>\n<ul type=\"disc\">\n<li><b>Session<\/b>: Innovation Session 17 \u2014 New Generation Transcatheter Mitral Technologies: Case-in-a-Box Demonstrations<\/li>\n<li><b>Date<\/b>: Tuesday, October 28, 2025<\/li>\n<li><b>Time<\/b>: 12:25\u201312:30 PM<\/li>\n<li><b>Location<\/b>: Moscone Center, North, Exhibition Level, Hall E- Innovation Theatre<\/li>\n<\/ul>\n<p><b>About Cardiovalve<\/b><\/p>\n<p>A subsidiary of <b>Venus Medtech<\/b>, <b>Cardiovalve<\/b> is a pioneer in transcatheter valve replacement technology, standing at the forefront of innovation in structural heart therapy. With more than <b>150 approved patents<\/b>, a highly experienced team, and a <b>state-of-the-art manufacturing facility<\/b>, Cardiovalve is dedicated to providing physicians with next-generation solutions that improve patient outcomes and quality of life\u2014without the need for open-heart surgery.<\/p>\n<p><b>About Venus Medtech<\/b><\/p>\n<p><b>Venus Medtech (Hangzhou) Inc. (2500.HK)<\/b> is a leading innovator in transcatheter heart valve solutions for structural heart disease. The company has developed a comprehensive product pipeline covering all four heart valves \u2014 <b>TAVR, TPVR, TMVR, and TTVR<\/b> \u2014and related accessory products. With global R&amp;D centers in China, the United States, and Israel, The company is committed to providing effective treatment solutions for life-threatening diseases.<\/p>\n<p>SOURCE Venus Medtech (Hangzhou) Inc.<\/p>\n<\/div>\n<p><b>This release is auto-published via PR Newswire; our journal is not responsible for the content.<\/b><\/p>\n<p><a href=\"https:\/\/www.prnewswire.com\/news-releases\/cardiovalve-completes-target-study-enrollment-for-ce-registration-study-for-tricuspid-valve-replacement-302593458.html\">Source link <\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Company Advances Toward European CE Mark Submission with 150 Patients Enrolled; On Track for 2027 Commercial Launch<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8,92],"tags":[705],"class_list":["post-2544","post","type-post","status-publish","format-standard","hentry","category-business","category-pr-newswire","tag-venus-medtech-hangzhou-inc"],"_links":{"self":[{"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/posts\/2544","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/comments?post=2544"}],"version-history":[{"count":1,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/posts\/2544\/revisions"}],"predecessor-version":[{"id":2564,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/posts\/2544\/revisions\/2564"}],"wp:attachment":[{"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/media?parent=2544"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/categories?post=2544"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.rvrising.com\/news\/wp-json\/wp\/v2\/tags?post=2544"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}