Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/2374
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dc.contributor.authorAkhmedov Khalmurad Sadullayevich, . Khojanazarov Ilkhom Eshkulovich,. Mullokulov Javohir Jamshid ugli,. Anorboyev Maruf Kholbuta ugli.-
dc.date.accessioned2025-11-13T15:08:29Z-
dc.date.available2025-11-13T15:08:29Z-
dc.date.issued2025-
dc.identifier.citationToshkenten_US
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/2374-
dc.description.abstractRheumatoid arthritis (RA) is a systemic autoimmune disease that has undergone a therapeutic revolution over the past two decades. Conventional synthetic DMARDs remain foundational, but the introduction of biologic and targeted synthetic DMARDs has transformed outcomes. This article reviews pivotal randomized controlled trials, comparative efficacy and safety data, and evolving treatment algorithms. Quantitative comparisons including absolute risk reduction (ARR), relative risk (RR), and number needed to treat (NNT) are provided for head-to-head studies, alongside safety analyses from ORAL Surveillance and regulatory guidance. A treat -to-target approach, precision medicine, and risk stratification remain essential for optimizing outcomes in 2025 and beyond.en_US
dc.language.isoenen_US
dc.subjectUpadacitinib, bDMARDs, tofacitinib, baricitiniben_US
dc.titleRHEUMATOID ARTHRITIS: NEW TREATMENT APPROACHES - A COMPARATIVE EVIDENCE REVIEWen_US
dc.typeArticleen_US
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