{"id":10306,"date":"2025-07-09T09:02:31","date_gmt":"2025-07-09T07:02:31","guid":{"rendered":"https:\/\/syva.es\/vmd-grants-marketing-authorisation-for-syvazul-btv3-in-united-kingdom\/"},"modified":"2025-07-09T13:20:20","modified_gmt":"2025-07-09T11:20:20","slug":"vmd-grants-marketing-authorisation-for-syvazul-btv3-in-united-kingdom","status":"publish","type":"post","link":"https:\/\/syva.es\/en\/vmd-grants-marketing-authorisation-for-syvazul-btv3-in-united-kingdom\/","title":{"rendered":"VMD grants marketing authorisation for Syvazul\u00ae BTV3 in Great Britain"},"content":{"rendered":"<p><b>Syvazul\u00ae BTV 3 has obtained marketing authorisation in Great Britain for use in cattle and sheep, with a reduced dose in cattle.<\/b><\/p>\n<p><b>Le\u00f3n, 8 July 2025<\/b> \u2013 Syva is pleased to announce that <b>Syvazul\u00ae BTV 3 has obtained marketing authorisation (Vm 31592\/5006) in Great Britain,<\/b> allowing its use<b> in cattle and sheep<\/b> to combat <b>bluetongue virus serotype 3 (BTV-3)<\/b>. The authorisation, effective from <b>3 July 2025<\/b>, is <b>valid indefinitely.<\/b> <\/p>\n<p><b>A major update for cattle: reduced dose<\/b><\/p>\n<p>A key breakthrough in this new authorisation is that <b>the dose for cattle has been reduced from 4 ml to 2 ml<\/b>, improving convenience and aligning with the latest regulatory data.<\/p>\n<p><b>Reminder Indications and administration<\/b><\/p>\n<p><b>-&gt; Cattle<\/b><\/p>\n<ul>\n<li>For active immunisation to reduce viraemia caused by BTV-3.<\/li>\n<li><b>Onset of immunity<\/b>: 3 weeks after completing the primary vaccination course.<\/li>\n<\/ul>\n<p>Dosage (intramuscular):<\/p>\n<ul>\n<li>From 2 months of age in na\u00efve animals, or from 3 months if born to immune dams.<\/li>\n<li><b>Primary vaccination:<\/b> 2 doses of 2 ml, 3 weeks apart.<\/li>\n<\/ul>\n<p><b>-&gt; Sheep<\/b><\/p>\n<ul>\n<li>For active immunisation to reduce viraemia, mortality, clinical signs and lesions caused by BTV-3.<\/li>\n<li><strong>Onset of immunity<\/strong>: 4 weeks after completing the primary vaccination course.<\/li>\n<\/ul>\n<p>Dosage (subcutaneous)<\/p>\n<ul>\n<li>From 3 months of age.<\/li>\n<li><b>Primary vaccination<\/b>: 1 single dose of 2 ml.<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Syvazul\u00ae BTV 3 has obtained marketing authorisation in Great Britain for use in cattle and sheep, with a reduced dose in cattle. A key breakthrough in this new authorisation is that the dose for cattle has been reduced from 4 ml to 2 ml, improving convenience and aligning with the latest regulatory data<\/p>\n","protected":false},"author":4,"featured_media":10302,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[789,791,797,793,2176,805],"tags":[],"class_list":["post-10306","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-animal-welfare","category-corporate-en","category-export","category-in-focus","category-press-release","category-syva-in-the-world"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.6 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>VMD grants marketing authorisation for Syvazul\u00ae BTV3 in Great Britain - Syva<\/title>\n<meta name=\"description\" content=\"A key breakthrough in this new authorisation is that the dose for cattle has been reduced from 4 ml to 2 ml, improving convenience and aligning with the latest regulatory data\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/syva.es\/en\/vmd-grants-marketing-authorisation-for-syvazul-btv3-in-united-kingdom\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"VMD grants marketing authorisation for Syvazul\u00ae BTV3 in Great Britain - 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