{"id":982,"date":"2025-03-05T08:57:52","date_gmt":"2025-03-05T07:57:52","guid":{"rendered":"https:\/\/www.francecoag.org\/projects\/emhira\/"},"modified":"2025-03-07T18:01:42","modified_gmt":"2025-03-07T17:01:42","slug":"emhira","status":"publish","type":"projects","link":"https:\/\/www.francecoag.org\/en\/projects\/emhira\/","title":{"rendered":"EMHIRA"},"content":{"rendered":"<h2>Non-interventional, descriptive, retrospective study using data from the FranceCoag system in hemophilia A patients with anti-factor VIII inhibitors treated with Hemlibra\u00ae.<\/h2>\n<p>&nbsp;<\/p>\n<h3>Progress<\/h3>\n<p>Inclusions closed on 10\/29\/2021<br \/>\nAnalyses finalized on 07\/25\/2022<br \/>\nArticle in submission<\/p>\n<h3><\/h3>\n<h3>Presentation and objectives<\/h3>\n<p>The aim of this study is to describe the characteristics of the patients, their therapeutic management, their clinical course (occurrence of bleeding events and bleeding requiring treatment), and the events that occurred from the initiation of Hemlibra\u00ae prophylaxis.<\/p>\n<p>&nbsp;<\/p>\n<h3>Persons concerned<br \/>\nType of data collected<br \/>\n(*data excluding FranceCoag)<\/h3>\n<p>Severe hemophilia A with inhibitor<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<h3>Regulatory approvals<br \/>\nInformation note<\/h3>\n<p>Favourable opinion from FranceCoag&#8217;s Scientific Committee<br \/>\nMR004 declared to the CNIL<\/p>\n<p>NI Children<br \/>\nNI Adolescents<br \/>\nNI ParentsFavorable opinion of the FranceCoag Scientific Committee<br \/>\nMR004 declared to the CNIL<\/p>\n<p>NI Adults and Parents<\/p>\n<p>&nbsp;<\/p>\n<h3>Project sponsor (financier)<\/h3>\n<p>Roche Laboratory<\/p>\n","protected":false},"parent":0,"template":"","etat-projet":[80],"class_list":["post-982","projects","type-projects","status-publish","hentry","etat-projet-projects-completed"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - 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