{"id":24946,"date":"2024-02-05T14:00:00","date_gmt":"2024-02-05T14:00:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4328368_CN28368_0"},"modified":"2024-02-05T14:00:00","modified_gmt":"2024-02-05T14:00:00","slug":"genesis-medtech-completes-enrollment-in-its-united-states-early-feasibility-study-utilizing-the-j-valve-transfemoral-system-for-patients-with-severe-aortic-regurgitation","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=24946","title":{"rendered":"Genesis MedTech Completes Enrollment in its United States Early Feasibility Study Utilizing the J-Valve\u2122 Transfemoral System for Patients with Severe Aortic Regurgitation"},"content":{"rendered":"\n<p><i>JC Medical reports milestone accomplishment with its TAVR device <\/i><\/p>\n<p><span class=\"legendSpanClass\"><span class=\"xn-location\">BURLINGAME, Calif.<\/span><\/span>, <span class=\"legendSpanClass\"><span class=\"xn-chron\">Feb. 5, 2024<\/span><\/span> \/PRNewswire\/ &#8212; Genesis&nbsp;MedTech, a leading medical device company, today announced the completion of enrollment in its United States Early Feasibility Study (EFS) using its dedicated transcatheter aortic valve replacement (TAVR) system, J-Valve\u2122 Transfemoral (TF) System. Finalizing the EFS&nbsp;marks another significant milestone for Genesis MedTech and its U.S.-based subsidiary JC Medical.<\/p>\n<p>The FDA approved&nbsp;EFS trial involved patient enrollment at five centers across <span class=\"xn-location\">the United States<\/span>. The trial focused on evaluating symptomatic individuals with severe Aortic Regurgitation. The last patient was successfully enrolled by <b>Drs. <span class=\"xn-person\">Ron Waksman<\/span> and <span class=\"xn-person\">Lowell Satler<\/span><\/b>, MedStar Washington Hospital <span class=\"xn-location\">Center, Washington<\/span>, DC. The EFS Co-Principal Investigators were <b>Dr. <span class=\"xn-person\">Dean Kereiakes<\/span><\/b>, President of the Christ Hospital Heart and Vascular Institute, <span class=\"xn-location\">Cincinnati, OH<\/span>. and <b>Dr. <span class=\"xn-person\">Michael Reardon<\/span><\/b>, Professor of Cardiothoracic Surgery, Allison Family Distinguished Chair of Cardiovascular Research at Houston Methodist Hospital, <span class=\"xn-location\">Houston, TX.<\/span> Patients meeting the inclusion criteria received treatment using the J-Valve\u2122 TF system. The outcomes of this clinical experience will be presented later this year.<\/p>\n<p>&quot;TAVR has proven results for patients with Aortic Stenosis. An unmet need remains for patients with Aortic Regurgitation,&quot; Dr. Reardon <span id=\"spanHghlt6c5c\">commented. &quot;<\/span>The J-Valve\u2122 being a dedicated TAVR design has shown promise in treating patients with aortic regurgitation. We are pleased with our findings to date from our EFS and look forward to the successful initiation of the pivotal trial.&quot;<\/p>\n<p>Developed by&nbsp;JC Medical, the J-Valve\u2122 TF System has been granted Breakthrough Device designation for the proposed indication of&nbsp;treating severe native aortic regurgitation (AR) and AR-dominant mixed aortic valve disease. Patients are assessed by a heart team to be eligible for the device and at high risk for surgical aortic valve replacement. The procedure is performed through a minimally invasive transfemoral approach, without the need for open-heart procedure or extracorporeal circulation. The innovative design and features of the J-Valve\u2122 TF System can potentially help patients that suffer from aortic valve regurgitation, currently lacking approved treatment options in <span class=\"xn-location\">the United States<\/span>.<\/p>\n<p>&quot;This accomplishment would not have been possible without the dedicated efforts of the investigators and research teams involved,&quot; stated&nbsp;<b>Dr. <span class=\"xn-person\">Mark A. Turco<\/span><\/b>, CEO&nbsp;of JC Medical&nbsp;and President of Vascular Intervention North America at Genesis MedTech. &quot;We look forward to the data and learnings as well as the initiation of our upcoming Pivotal Trial.&quot;<\/p>\n<p>The&nbsp;J-Valve \u2122 TF System is an investigational device in <span class=\"xn-location\">the United States<\/span> and <span class=\"xn-location\">Canada<\/span>.<\/p>\n<p><b>ABOUT GENESIS MEDTECH &amp; JC MEDICAL<\/b><\/p>\n<p>Based in&nbsp;Burlingame California, JC Medical Inc., under Genesis MedTech Group, is a transcatheter based cardiovascular company that is primarily engaged in the design and development of transcatheter valve replacement products for the minimally invasive treatment of structural heart diseases.<\/p>\n<p>Genesis&nbsp;MedTech Group is a medical device company headquartered in <span class=\"xn-location\">Singapore<\/span>. Founded by a group of professionals and entrepreneurs with MedTech experience globally, the company&#8217;s product portfolio focuses on multi-therapy medical device products for emerging markets with sales and distribution through its established commercial network. Genesis MedTech Group covers the entire industry value chain of research and development, production, quality management, supply chain, marketing, and sales.<\/p>\n<p>For more information, visit&nbsp;<b><a href=\"http:\/\/www.genesismedtech.com\/\" target=\"_blank\" rel=\"nofollow noopener\">http:\/\/www.genesismedtech.com<\/a><\/b>&nbsp;&amp;&nbsp;<b><u><a href=\"https:\/\/j-valve.com\/\" target=\"_blank\" rel=\"nofollow noopener\">https:\/\/j-valve.com<\/a><\/u><\/b><\/p>\n","protected":false},"excerpt":{"rendered":"<p>JC Medical reports milestone accomplishment with its TAVR device BURLINGAME, Calif., Feb. 5, 2024 \/PRNewswire\/ &#8212; Genesis&nbsp;MedTech, a leading medical device company, today announced the completion of enrollment in its United States Early Feasibility Study (EFS) using its dedicated transcatheter aortic valve replacement (TAVR) system, J-Valve\u2122 Transfemoral (TF) System. Finalizing the EFS&nbsp;marks another significant milestone [&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-24946","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>Genesis MedTech Completes Enrollment in its United States Early Feasibility Study Utilizing the J-Valve\u2122 Transfemoral System for Patients with Severe Aortic Regurgitation - 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=24946\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Genesis MedTech Completes Enrollment in its United States Early Feasibility Study Utilizing the J-Valve\u2122 Transfemoral System for Patients with Severe Aortic Regurgitation - My Blog\" \/>\n<meta property=\"og:description\" content=\"JC Medical reports milestone accomplishment with its TAVR device BURLINGAME, Calif., Feb. 5, 2024 \/PRNewswire\/ &#8212; Genesis&nbsp;MedTech, a leading medical device company, today announced the completion of enrollment in its United States Early Feasibility Study (EFS) using its dedicated transcatheter aortic valve replacement (TAVR) system, J-Valve\u2122 Transfemoral (TF) System. 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