Session » (1434–1466) Spondyloarthritis Including Psoriatic Arthritis – Treatment Poster II
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Abstract Number: 1436
Angiogenesis Markers in Difficult to Treat Psoriatic Arthritis Patients
- 10:30AM-12:30PM
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Abstract Number: 1449
Bimekizumab Demonstrated Comparable One-Year Efficacy in Male and Female Patients with Axial Spondyloarthritis: Results from Two Phase 3 Studies
- 10:30AM-12:30PM
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Abstract Number: 1439
Bimekizumab in Psoriatic Arthritis. A real-world prospective study. Comparison of its efficacy in bDMARD-naive and IL-17A-experienced patients
- 10:30AM-12:30PM
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Abstract Number: 1451
Bimekizumab was Efficacious Regardless of Age, BMI, CRP, or HLA-B27 Status: 1-Year Results from Two Phase 3 Studies
- 10:30AM-12:30PM
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Abstract Number: 1437
Characterization of ORKA-002, a Novel Extended Half-life Monoclonal Antibody Targeting IL-17A/F for the Treatment of Psoriasis and Other Indications
- 10:30AM-12:30PM
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Abstract Number: 1452
Clinical and Demographic Characteristics of Treatment-Refractory Axial Spondyloarthritis: Data from the Greek AxSpA Registry
- 10:30AM-12:30PM
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Abstract Number: 1458
Clinical Efficacy of Bimekizumab Treatment up to 2 Years Across Patients with Psoriatic Arthritis and Varying Baseline Joint Involvement: Results from a Post Hoc Analysis of Two Pooled Phase 3 Studies
- 10:30AM-12:30PM
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Abstract Number: 1440
Comparison of standard and tapered dose of biologic treatments in patients with axial spondyloarthritis
- 10:30AM-12:30PM
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Abstract Number: 1461
Digital Behavioral Therapy Improves Outcome in Patients With Axial Spondyloarthritis And Persistent Pain: Results From a Randomized Controlled Trial
- 10:30AM-12:30PM
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Abstract Number: 1460
Effect of Guselkumab and IL-17 Inhibitors on Work Productivity and Activity Impairment in Psoriatic Arthritis: 6-Month Results of the PsABIOnd Observational Study
- 10:30AM-12:30PM
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Abstract Number: 1463
Effective Prevention of Psoriatic Arthritis with Secukinumab: A 5-Year Observation from the SERENA Study
- 10:30AM-12:30PM
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Abstract Number: 1441
Efficacy and Safety of Vunakizumab in Patients with Active Ankylosing Spondylitis by Cigarette Smoking Status: A Post Hoc Analysis of a Randomized, Double-blind, Phase 2/3 Study
- 10:30AM-12:30PM
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Abstract Number: 1462
Five-Year Results of Secukinumab on Minimal Disease Activity (MDA) Components and the Impact of Biologic Treatment Status on Effectiveness and Safety in Patients With Psoriatic Arthritis: Real-World Data From the SERENA Study
- 10:30AM-12:30PM
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Abstract Number: 1459
Fungal Infections, Including Candida, in Patients With Active Psoriatic Arthritis (PsA) Treated With Secukinumab: A Pooled Analysis of 9 Phase 3 Trials
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Abstract Number: 1466
Impact of Bimekizumab on Spinal MRI Inflammation and Structural Lesions in Patients with Radiographic Axial Spondyloarthritis: 2-Year CANDEN Scoring Results from a Phase 3 Study and Its Open-Label Extension
- 10:30AM-12:30PM
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Abstract Number: 1435
Impact of Treatment With Upadacitinib on Non-Nociceptive Pain and Its Relevance for the Presence of Residual Symptoms in Axial Spondyloarthritis: Results from a Multicountry Observational Study
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Abstract Number: 1464
Incidence of Major Adverse Cardiovascular Events (MACE) in Psoriasis, Psoriatic Arthritis and Axial Spondyloarthritis Patients With and Without Cardiovascular Risk Factors Treated With Secukinumab: Five-Year Safety Data from the Real-World SERENA Study
- 10:30AM-12:30PM
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Abstract Number: 1448
Influence of Sex on the Therapeutic Persistence of Guselkumab in Psoriatic Disease: a Retrospective National Cohort Study
- 10:30AM-12:30PM
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Abstract Number: 1447
Long-term impact of secukinumab on the prevention of psoriatic arthritis in patients with psoriasis: a 5-year pooled analysis of the ERASURE, FIXTURE and SCULPTURE studies
- 10:30AM-12:30PM
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Abstract Number: 1443
Long-Term Safety and Efficacy of Upadacitinib in Patients With Psoriatic Arthritis: 5-Year Results From the Phase 3 SELECT-PsA 1 Study
- 10:30AM-12:30PM
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Abstract Number: 1454
Long-Term Safety and Tolerability of Bimekizumab Treatment Across Phase 2b and Phase 3 Studies in Patients with Axial Spondyloarthritis or Psoriatic Arthritis: 3-Year Update from the Phase 3 Studies
- 10:30AM-12:30PM
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Abstract Number: 1456
Long-Term Safety of Tildrakizumab Through Week 208 in Patients With Psoriatic Arthritis: Results From the Phase 2b Open-Label Extension Study
- 10:30AM-12:30PM
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Abstract Number: 1442
Modulation of Soluble Biomarkers of Cartilage and Bone Turnover and Inflammation by Zasocitinib (TAK-279), an Oral, Allosteric, Highly Selective and Potent TYK2 Inhibitor, is Associated with Clinical Response in Patients with Active Psoriatic Arthritis
- 10:30AM-12:30PM
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Abstract Number: 1445
Patient Characteristics, and Physician-Reported Treatment Effectiveness and Treatment Satisfaction with Bimekizumab for Axial Spondyloarthritis in the United States: Interim Analysis from a Real-World Study
- 10:30AM-12:30PM
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Abstract Number: 1446
Persistence of Second-line Treatment in Anti-TNF-experienced Axial Spondyloarthritis Patients: Comparing Cycling Anti–TNF vs Switching to a Different Mechanism of Action
- 10:30AM-12:30PM
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Abstract Number: 1444
Real-world comparative effectiveness of tofacitinib, tumor necrosis factor inhibitors, and interleukin-17 inhibitors among patients with axial spondyloarthritis
- 10:30AM-12:30PM
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Abstract Number: 1453
Real-World Comparative Effectiveness of Upadacitinib in Psoriatic Arthritis: Evaluation of Switching to Upadacitinib Versus Tumor Necrosis Factor Inhibitors or Interleukin-17 Inhibitors After First-Line Tumor Necrosis Factor Inhibitors
- 10:30AM-12:30PM
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Abstract Number: 1457
Real-world Patient Trajectories in Psoriasis and Psoriatic Arthritis: a Retrospective Study
- 10:30AM-12:30PM
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Abstract Number: 1434
Safety of Prescription NSAIDs in Adults with IBD: Data from a Large Administrative Claims Cohort
- 10:30AM-12:30PM
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Abstract Number: 1438
Similar Efficacy of Bimekizumab in Two Clinical Endotypes of Axial Spondyloarthritis: 2-Year Results from Two Phase 3 Studies and Their Open-Label Extension
- 10:30AM-12:30PM
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Abstract Number: 1455
Sonelokimab in Patients With Active Psoriatic Arthritis Who Are Naive to Biologic DMARDs: Phase 2 ARGO Analysis and Phase 3 IZAR-1 Study Design