{"id":2930,"date":"2024-06-20T10:24:50","date_gmt":"2024-06-20T02:24:50","guid":{"rendered":"https:\/\/flcube.com\/?p=2930"},"modified":"2024-10-17T18:18:18","modified_gmt":"2024-10-17T10:18:18","slug":"abbvies-skyrizi-secures-fda-approval-for-ulcerative-colitis-expands-treatment-portfolio","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=2930","title":{"rendered":"AbbVie’s Skyrizi Secures FDA Approval for Ulcerative Colitis, Expands Treatment Portfolio"},"content":{"rendered":"\n

AbbVie (NYSE: ABBV<\/a>) has announced that the U.S. Food and Drug Administration (FDA) has approved a new indication for Skyrizi (risankizumab), marking it for use in treating adults with moderate to severely active ulcerative colitis (UC). This approval positions Skyrizi as the first IL-23 specific inhibitor to be approved for both UC and moderate to severe Crohn\u2019s disease, representing its fourth indication overall.<\/p>\n\n\n\n

For the ulcerative colitis indication, the treatment regimen involves three 1,200mg doses of Skyrizi administered every 4 weeks over a 12-week induction period, followed by maintenance therapy with either 180mg or 360mg doses given every 8 weeks. The FDA’s decision was supported by data from two studies: the INSPIRE study, which evaluated Skyrizi as an induction therapy over 12 weeks, and the COMMAND study, which assessed the lower-dosage maintenance regimen over 52 weeks.- Flcube.com<\/a><\/p>\n\n\n\n

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AbbVie (NYSE: ABBV) has announced that the U.S. Food and Drug Administration (FDA) has approved…<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,11],"tags":[234,622,853,15],"class_list":["post-2930","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-abbvie","tag-gastroenterology","tag-nyse-abbv","tag-product-approvals"],"yoast_head":"\nAbbVie's Skyrizi Secures FDA Approval for Ulcerative Colitis, Expands Treatment Portfolio - Insight, China's Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"AbbVie (NYSE: ABBV) has announced that the U.S. Food and Drug Administration (FDA) has approved a new indication for Skyrizi (risankizumab), marking it for use in treating adults with moderate to severely active ulcerative colitis (UC). 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