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AbbVie Presents New Data Analyses for Growing Dermatology Portfolio at the 30th European Academy of Dermatology and Venereology (EADV) Congress

AbbVie Presents New Data Analyses for Growing Dermatology Portfolio at the 30th European Academy of Dermatology and Venereology (EADV) Congress
prnewswire.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from prnewswire.com Daily Mail and Mail on Sunday newspapers.

Stefan florentinusGlobal medical affairsEuropean academy of dermatologyAbbvie ltdBoehringer ingelheimFree communications in atopic dermatitisImprovements in healthEuropean unionFree communications in psychodermatologyAbbvie deutschland gmbh coEuropean commissionExchange commissionMaintenance of healthCohort study using clinical practice research datalinkEuropean academyVie data

Aktien New York Ausblick: Erholungsversuch nach Kursrutsch

Aktien New York Ausblick: Erholungsversuch nach Kursrutsch
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

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MÄRKTE USA/Uneinheitlich - Fed-Sitzung im Fokus

MÄRKTE USA/Uneinheitlich - Fed-Sitzung im Fokus
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

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AbbVie to Present Analysis Evaluating Continuous RINVOQ® (upadacitinib) Treatment in Psoriatic Arthritis for More Than One Year at EULAR 2021 Virtual Congress

AbbVie to Present Analysis Evaluating Continuous RINVOQ® (upadacitinib) Treatment in Psoriatic Arthritis for More Than One Year at EULAR 2021 Virtual Congress - In SELECT-PsA 2, 29 percent of bDMARD-IR patients treated with continuous RINVOQ (upadacitinib, 15 mg, once daily) achieved minimal disease activity at 56 weeks, which was consistent with improvements from baseline seen at week 24[1],[2] - The safety results of RINVOQ 15 mg were consistent with previously reported results in rheumatoid arthritis, with no new significant safety risks identified[1],[3] - Full results to be presented at the EULAR 2021 Virtual Congress - RINVOQ is the first oral, once-daily, selective and reversible JAK inhibitor approved for three adult rheumatic indications in the European Union: rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis[2]

Clin rheumatolPhilip measeMudra kapoorPrnewswire abbvieExchange commissionJoseph healthEuropean commissionAbbvie deutschland gmbh coVirtual congressAmerican college of rheumatologyResults observedDisease activityLeeds enthesitis indexAmerican collegeRheumatology research divisionSwedish medical

AbbVie to Present Analysis Evaluating Continuous RINVOQ® Treatment in Psoriatic Arthritis for More Than One Year at EULAR 2021 Virtual Congress

ABBVie today announced results of an analysis from the Phase 3 SELECT-PsA 2 clinical trial, showing that continuous treatment with RINVOQ ® resulted in sustained improvements in disease activity for more than one year among patients with active psoriatic arthritis who have responded inadequately to one or more biologic disease modifying anti-rheumatic drugs . 1 At week 56, 29 percent of patients treated with .

Clin rheumatolPhilip measeMudra kapoorExchange commissionJoseph healthEuropean commissionAbbvie deutschland gmbh coVirtual congressAmerican college of rheumatologyResults observedDisease activityLeeds enthesitis indexAmerican collegeRheumatology research divisionSwedish medicalAllergan aesthetics