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AbbVie to Showcase New Data at the United European Gastroenterology Week Virtual 2021

AbbVie today announced new data on the investigational use of risankizumab  in Crohn's disease, upadacitinib in ulcerative colitis and HUMIRA ® in inflammatory bowel disease will be presented as live presentations and e-Posters at the United European Gastroenterology Week Virtual 2021, to be held October 3-5 . AbbVie is presenting a total of 13 abstracts, across a broad range of studies in IBD, including two ...
Chiedzo Mpofu Remo Panaccione Ann Gastroenterol Gastroenterol Hepatol Abbvie Ltd European Commission

Phase 3 Maintenance Results Show Patients with Crohn's Disease Receiving Risankizumab (SKYRIZI®) Achieved Endoscopic Response and Clinical Remission at One Year

Phase 3 Maintenance Results Show Patients with Crohns Disease Receiving Risankizumab (SKYRIZI®) Achieved Endoscopic Response and Clinical Remission at One Year - In Crohns disease patients with clinical response to risankizumab IV induction treatment, a significantly greater proportion of patients treated with risankizumab 360 mg SC achieved endoscopic response and clinical remission at one year (52 weeks) versus those who were withdrawn from risankizumab (control group)[1] - The overall safet...
United States Gastroenterol Hepatol Access Economics Pty Drug Administration Boehringer Ingelheim Exchange Commission

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Phase 3 Maintenance Results Show Patients with Crohn's Disease Receiving Risankizumab Achieved Endoscopic Response and Clinical Remission at One Year

ABBVie today announced positive top-line results from the Phase 3 maintenance study, FORTIFY, showing risankizumab 360 mg achieved the co-primary endpoints of endoscopic response and clinical remission at one year in adult patients with moderate to severe Crohn's disease. 1 In this study, patients who responded to 12 weeks of risankizumab intravenous induction treatment were re-randomized to receive risankizumab 180 ...
United States Region Flamande Marc Ferrante Michael Severino Gastroenterol Hepatol Access Economics Pty

AbbVie Showcases the Depth of its Rheumatology Portfolio with New Data Presented at the EULAR 2021 Virtual Congress of Rheumatology

AbbVie Showcases the Depth of its Rheumatology Portfolio with New Data Presented at the EULAR 2021 Virtual Congress of Rheumatology ABBVie today announced that it will present new data from a total of 41 abstracts covering its portfolio of immunology assets, including RINVOQ ® SKYRIZI ® HUMIRA ® and its pipeline across multiple rheumatic diseases at the EULAR 2021 Virtual Congress of Rheumatology, to be held virtually June 2-5 . Among the data presented will be new three-year and one-year ef...
United States Chiedzo Mpofu Corevita Ps Upadacitinib Pharmacokinetics Global Medical Affairs Abbvie Ltd

AbbVie : Presents New Late-Breaking Data Analyses Showing Risankizumab (SKYRIZI®) Achieves Clinical Remission and Endoscopic Response at Week 12 in Patients with Moderate to Severe Crohn's Disease

Message : Required fields NORTH CHICAGO, Ill., May 24, 2021 /PRNewswire/ -- Late-breaking data analyses presented by AbbVie (NYSE: ABBV) at Digestive Disease Week ® (DDW) Virtual Conference 2021 showed significantly greater proportions of patients with moderately to severely active Crohns disease treated with both doses of investigational risankizumab (600 mg or 1200 mg) met the co-primary endpoints of clinical remission and endoscopic response at week 12 compared to placebo (p
United States Remo Panaccione Gastroenterol Hepatol Access Economics Pty European Commission Drug Administration

AbbVie Presents New Late-Breaking Data Analyses Showing Risankizumab Achieves Clinical Remission and Endoscopic Response at Week 12 in Patients with Moderate to Severe Crohn's Disease

Late-breaking data analyses presented by ABBVie at Digestive Disease Week ® Virtual Conference 2021 showed significantly greater proportions of patients with moderately to severely active Crohn's disease treated with both doses of investigational risankizumab met the co-primary endpoints of clinical remission and endoscopic response at week 12 compared to placebo andor biologic therapy . The MOTIVATE trial ...
United States Remo Panaccione Gastroenterol Hepatol Access Economics Pty European Commission Drug Administration

AbbVie Submits Regulatory Applications for SKYRIZI® in Psoriatic Arthritis to FDA and EMA

ABBVie  today announced that it has submitted applications seeking approval for SKYRIZI ® to the U.S. Food and Drug Administration and for SKYRIZI ® to the European Medicines Agency  for the treatment of adults with active psoriatic arthritis. 1 The submissions were supported by two pivotal Phase 3 studies, KEEPsAKE-1 and KEEPsAKE-2, which evaluated SKYRIZI in adults with active psoriatic arthritis including … ABBVie (NYSE: ABBV) today announced that it has submitted applications seeking...
United States Midi Pyrees Ann Dermatol Venereol Clin Rheumatol Michael Severino Boehringer Ingelheim

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