Upadacitinib versus placebo or adalimumab with background methotrexate in patients with rheumatoid arthritis and an inadequate response to methotrexate: a subgroup analysis of a phase III randomized controlled trial in Central and Eastern European patients

التفاصيل البيبلوغرافية
العنوان: Upadacitinib versus placebo or adalimumab with background methotrexate in patients with rheumatoid arthritis and an inadequate response to methotrexate: a subgroup analysis of a phase III randomized controlled trial in Central and Eastern European patients
المؤلفون: Daina Andersone, Tzvetanka Petranova, Matija Tomšič, Orsolya Nagy, Branimir Anić, Tiina Veldi, Karel Pavelka, Nemanja Damjanov, Roy Fleischmann, Jerzy Świerkot, Zoltán Szekanecz, Mazurov Vi, Marija Maksimovic, Asta Baranauskaitė, Catalin Codreanu
المصدر: Drugs in Context, Vol 9, Pp 1-15 (2020)
بيانات النشر: BioExcel Publishing Ltd, 2020.
سنة النشر: 2020
مصطلحات موضوعية: musculoskeletal diseases, rheumatoid arthritis, safety, medicine.medical_specialty, Placebo, law.invention, 03 medical and health sciences, 0302 clinical medicine, Randomized controlled trial, treatment efficacy, law, Internal medicine, Post-hoc analysis, medicine, Adalimumab, 030212 general & internal medicine, 030203 arthritis & rheumatology, Pharmacology, business.industry, eastern europe, lcsh:RM1-950, General Medicine, medicine.disease, Rheumatology, upadacitinib, 3. Good health, Eastern european, lcsh:Therapeutics. Pharmacology, Rheumatoid arthritis, Molecular Medicine, Methotrexate, business, medicine.drug
الوصف: Background: In the randomized, phase III, global SELECTCOMPARE study, upadacitinib 15 mg demonstrated efficacy at week 12 versus placebo and adalimumab with methotrexate (MTX) in patients with rheumatoid arthritis and inadequate response to MTX, which was maintained over 48 weeks. This post hoc analysis of SELECT-COMPARE reports the efficacy and safety of upadacitinib in Central and Eastern European (CEE) patients. Methods: Patients were randomized 2:2:1 to upadacitinib 15 mg once daily, placebo, or adalimumab 40 mg every other week, and continued MTX. Efficacy and safety were assessed through 48 weeks. Primary endpoints were the achievement of ≥20% improvement in American College of Rheumatology response criteria and Disease Activity Score in 28 joints with C-reactive protein
اللغة: English
تدمد: 1740-4398
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3de042c830d34df20d08bd6ee9927953
https://www.drugsincontext.com/upadacitinib-versus-placebo-or-adalimumab-with-background-methotrexate-in-patients-with-rheumatoid-arthritis-and-an-inadequate-response-to-methotrexate
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....3de042c830d34df20d08bd6ee9927953
قاعدة البيانات: OpenAIRE