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ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response

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Last updated 27 dezembro 2024
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
PDF] ASAS40 and ASDAS clinical responses in the ABILITY-1 clinical trial translate to meaningful improvements in physical function, health-related quality of life and work productivity in patients with non-radiographic axial spondyloarthritis
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Long-Term Safety and Efficacy of Ixekizumab in Patients With Axial Spondyloarthritis: 3-year Data From the COAST Program
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Disease Control Data, Ankylosing Spondylitis
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
The Brazilian Society of Rheumatology guidelines for axial spondyloarthritis – 2019, Advances in Rheumatology
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
A and B, Percentages of patients in the golimumab (GLM) and placebo
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Translating Improvements with Ixekizumab in Clinical Trial Outcomes into Clinical Practice: ASAS40, Pain, Fatigue, and Sleep in Ankylosing Spondylitis
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Safety Profile, Axial Spondyloarthritis
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Table 6, Details of Included Studies - Upadacitinib (Rinvoq) - NCBI Bookshelf
ASAS-HI improvement ≥30%, ASDAS LDA status and ASAS40 response
Disease Control Data, Ankylosing Spondylitis
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