{"id":71907,"date":"2025-09-10T12:02:03","date_gmt":"2025-09-10T12:02:03","guid":{"rendered":"https:\/\/english.saigonbiz.com.vn\/2025\/09\/10\/jenavalve-announced-esc-guidelines-recognize-tavi-as-class-iib-recommendation-for-aortic-regurgitation\/"},"modified":"2025-09-10T12:02:03","modified_gmt":"2025-09-10T12:02:03","slug":"jenavalve-announced-esc-guidelines-recognize-tavi-as-class-iib-recommendation-for-aortic-regurgitation","status":"publish","type":"post","link":"https:\/\/english.saigonbiz.com\/vn\/jenavalve-announced-esc-guidelines-recognize-tavi-as-class-iib-recommendation-for-aortic-regurgitation\/","title":{"rendered":"JenaValve Announced ESC Guidelines Recognize TAVI as Class IIb Recommendation for Aortic Regurgitation"},"content":{"rendered":"<div>\n<p align=\"left\">IRVINE, Calif., Sept.  10, 2025  (GLOBE NEWSWIRE) &#8212; JenaValve Technology, Inc., developer and manufacturer of the Trilogy\u2122 Transcatheter Heart Valve (THV) System, today announced that the newly published guidelines from the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS) include transcatheter aortic valve implantation (TAVI) as a treatment option for patients with severe, symptomatic aortic regurgitation (AR) when ineligible for surgery. This decision marks the first formal recommendation for TAVI in AR guidelines.<\/p>\n<p>JenaValve is currently the only company with an approved transcatheter valve indicated for AR in Europe. The ALIGN-AR Pivotal Trial for the Trilogy THV System helped inform the updated guidelines with two papers using ALIGN-AR data cited in support of the recommendation.<\/p>\n<p>\u201cI\u2019m encouraged to see ESC and EACTS place renewed focus on aortic regurgitation, acknowledging the profound unmet need in this patient population,\u201d said John Kilcoyne, CEO of JenaValve. \u201cThe updated guidelines expand opportunities for intervention, providing a clear recommendation for imaging and diagnosis. This represents a meaningful advancement in patient care for those suffering from severe symptomatic, high risk aortic regurgitation.\u201d<\/p>\n<p>\u201cAs the only transcatheter valve indicated for aortic regurgitation, Trilogy\u2122 offers a lifeline to patients who until now had few viable options,\u201d said Duane Pinto, MD, MPH, Chief Medical Officer at JenaValve. \u201cThese updated guidelines mark a pivotal step in expanding access to care and affirm our mission: to ensure patients with AR, who have long been an underserved community, can finally receive the treatment they need and deserve.\u201d<\/p>\n<p>\u201cThe updated guidelines bring important focus to improving care for patients with aortic regurgitation,\u201d said Prof. Dr. Stephan Baldus, Cologne University Hospital \u201cAs interventional cardiologists, our priority is ensuring patients have access to therapies that can change and save their lives. It\u2019s encouraging to see these guidelines acknowledge such a vulnerable population, and Trilogy\u2019s dedicated indication is helping to advance the field and expand treatment options.\u201d<\/p>\n<p><strong>About JenaValve<\/strong><br \/>JenaValve Technology, Inc. is a medical device company focused on the design, development, and commercialization of innovative THV solutions for the treatment of patients suffering from heart valve disease. The Company&#8217;s Trilogy THV System is a TAVR system designed to treat patients with symptomatic, severe AR and symptomatic, severe aortic stenosis who are at high surgical risk. The Trilogy THV System received CE Mark approval, providing European physicians with the first TAVR device with true dual-disease treatment capabilities. In the US, the Trilogy THV System is limited to investigation use only.<\/p>\n<p>JenaValve is headquartered in Irvine, California, with additional locations in Leeds, United Kingdom, and Munich, Germany.<\/p>\n<p>JenaValve is backed by Bain Capital Life Sciences, Andera Partners, Valiance Life Sciences, Rosetta Capital, Cormorant Asset Management, Legend Capital, NeoMed Management, RMM, VI Partners, Pictet Alternative Advisors SA, Qatar Investment Authority (QIA), Innovatus Capital Partners, and Peijia Medical Limited.<\/p>\n<p>US: CAUTION \u2013 Investigational device. Limited by Federal (or United States) law to investigational use.<\/p>\n<p>Additional information is available at <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=DXuUMGYBCRjqYxUTADlv55DNOH-Z0gNBB2eYvi2dHApbL8wQ1T9GYwgKVhVi0AiLBavBgfl__RlCxU-8nBNfJ6_2IU-RTDHGb8wgXDhCScvkd-Qud9mY7ZjDW4NIpS-3-coDEH6Gu5CY7Gca2wxk2ZqduO5nnLdq-buVKS9Q-nrwzG3qWaoRFHWOhr30Peqr3HkvjzkH9fyvIfqeBGhf4coe7-ZMcPOv3q0-7tfwovYQJT3C6f2gz5dPtZWEMLHYwbEmwve6gsedG2JjGCopjhgbOrUdXeMI_vCgtFqK4ng-nnZtflxbOSzzg6fM-S52Vx0wQmiDAWTlMDGLc7mrGA0D-WOW3PNk2DpwxpA2vElitiz9n1fzaVNC2Kkl6Vh-\" rel=\"nofollow\" target=\"_blank\" title=\"www.jenavalve.com\">www.jenavalve.com<\/a>.<\/p>\n<p><strong>JenaValve Contact:<\/strong><br \/>Daniel Sun <br \/><a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fw89dpebvCT5IQAywMrOX-AtWQEFv9tpZl3BVmaPIrCexZBxl6iKoPhbJF_O5NmFaOjnRyEHZFD_LzLeZCPyqNEOn104b3yVMhybxEMH3Nc=\" rel=\"nofollow\" target=\"_blank\" title=\"dsun@jenavalve.com\">dsun@jenavalve.com<\/a><\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/ZDM1ZGFlMDctNTNmZi00M2RkLTkwMDMtNzA4YjRlMjE4N2QzLTEyMTUwNjItMjAyNS0wOS0xMC1lbg==\/tiny\/JenaValve-Technology-Inc-.png\" referrerpolicy=\"no-referrer-when-downgrade\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>IRVINE, Calif., Sept. 10, 2025 (GLOBE NEWSWIRE) &#8212; JenaValve Technology, Inc., developer and manufacturer of the Trilogy\u2122 Transcatheter Heart Valve (THV) System, today announced that the newly published guidelines from the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS) include transcatheter aortic valve implantation (TAVI) as a treatment option for [&#8230;]\n","protected":false},"author":1,"featured_media":71908,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-71907","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-pr-newswire"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v21.6 (Yoast SEO v21.6) - 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