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Session » RA – Treatments Poster I: Novel Treatments

Date: Sunday, November 10, 2019

Time: 9:00AM-11:00AM

Meeting: 2019 ACR/ARP Annual Meeting

9:00AM-11:00AM
Abstract Number: 542
‘BENEFIT’ Pan-European Observational Study to Evaluate the Real-world Effectiveness of SB4 Transition from Originator Etanercept (ETN) in Patients with Rheumatoid Arthritis or Axial Spondyloarthritis: A Switch Success Story
9:00AM-11:00AM
Abstract Number: 511
A Comparative Analysis of Upadacitinib Monotherapy and Upadacitinib Combination Therapy for the Treatment of Rheumatoid Arthritis from Two Phase 3 Trials
9:00AM-11:00AM
Abstract Number: 524
A Comparison of Upadacitinib Plus Methotrexate and Upadacitinib Plus Other CsDMARDs in Patients with Rheumatoid Arthritis: An Analysis of Two Phase 3 Studies
9:00AM-11:00AM
Abstract Number: 532
A Phase 2 Study of E6011, an Anti-Fractalkine Monoclonal Antibody, ㏌ Patients with Rheumatoid Arthritis Inadequately Responding to Biologics
9:00AM-11:00AM
Abstract Number: 503
A Pilot Phase 1, Randomized, Double-blind, Two-arm, Parallel Group, Single-dose Study to Evaluate the Safety and Pharmacokinetics of CT-P17 and Humira in Healthy Male Subjects
9:00AM-11:00AM
Abstract Number: 514
A Pooled Analysis of 1-year Clinical Outcomes Among 6-month Responders and Non-responders from Three Randomized Controlled Studies of TNF Inhibitor Biosimilars in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 539
A Randomized Double-Blind Study Comparing Pharmacokinetics (PK) and Pharmacodynamics (PD) of ABP 798 with Rituximab in Subjects with Moderate to Severe RA
9:00AM-11:00AM
Abstract Number: 517
A Subgroup Analysis of Clinical Efficacy Response and Quality of Life Outcomes from Phase 3 Study of Filgotinib in Patients with Inadequate Response to Biologic DMARDs
9:00AM-11:00AM
Abstract Number: 504
A Subgroup Analysis of the Efficacy of Filgotinib in Demographic and Clinical Subgroups of Patients with Refractory Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 528
Assessment of Bone and Cartilage Turnover Markers Following Treatment with Repository Corticotropin Injection in Patients with Persistently Active Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 546
Change in Rheumatoid Arthritis (RA)-Related Autoantibody Profile and Risk of Disease Flare After Withdrawal of Therapy in Patients with Early RA Treated with Abatacept and MTX
9:00AM-11:00AM
Abstract Number: 529
Characterization of Remission in Patients with Rheumatoid Arthritis Treated with Upadacitinib or Comparators
9:00AM-11:00AM
Abstract Number: 515
Clinical Responses in Patients with Inadequate Response to bDMARDs upon Treatment with Upadacitinib
9:00AM-11:00AM
Abstract Number: 540
Comparing Real-world Retention Rates in a Matched Cohort of Rheumatoid Arthritis Patients Who Either Remained on the Etanercept Originator or Switched to a Biosimilar
9:00AM-11:00AM
Abstract Number: 534
CXCL13 Serum Levels and Circulating Follicular Helper T-Cells Decrease After Co-stimulation Blockade with Abatacept in Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 543
Cytokine Signaling Pathways Inhibited by Different Biologics in Rheumatoid Arthritis Patients
9:00AM-11:00AM
Abstract Number: 521
Discontinuation of Disease Modifying Drugs Due to Inefficacy in Patients with Incident Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 548
Efficacy and Safety of a Novel Subcutaneous Formulation of CT-P13 over the 1-year Treatment Period and After Switching from Intravenous CT-P13 in Patients with Active Rheumatoid Arthritis: Results from Part 2 of Phase I/III Randomized Controlled Trial
9:00AM-11:00AM
Abstract Number: 506
Efficacy and Safety of Filgotinib for Patients with Rheumatoid Arthritis with Inadequate Response to Methotrexate: FINCH1 Primary Outcome Results
9:00AM-11:00AM
Abstract Number: 531
Efficacy and Safety of Gonadotropin-Releasing Hormone Antagonism in Severe Biologic Refractory Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 512
Efficacy and Safety of Upadacitinib Monotherapy in MTX-naïve Patients with Early Active RA Receiving Treatment Within 3 Months of Diagnosis: A Post-hoc Analysis of the SELECT-EARLY
9:00AM-11:00AM
Abstract Number: 520
Efficacy and Safety Results from a Phase 3 Study of Biosimilar Candidate ABP 710 in Subjects with Moderate to Severe RA
9:00AM-11:00AM
Abstract Number: 537
Efficacy and Safety Results from a Randomized Double-Blind Study That Compared the Proposed Biosimilar ABP 798 with Rituximab in Subjects with Moderate to Severe RA
9:00AM-11:00AM
Abstract Number: 519
Efficacy of Biosimilar Candidate ABP 710 in a Phase 3 Study in Subjects with Moderate to Severe RA: Additional Analysis Focusing on the ACR Individual Components
9:00AM-11:00AM
Abstract Number: 553
Etanercept Biosimilar GP 2015 (Erelzi®) in Rheumatic Diseases: Interim Analysis of Real-World Data from COMPACT: A Multicentric, Prospective, Observational Cohort Study
9:00AM-11:00AM
Abstract Number: 554
Evidence to Guide Glucocorticoid Tapering Is Lacking in RA
9:00AM-11:00AM
Abstract Number: 535
Exploratory Analysis of a Phase 2b Study Confirms Substantial Pain Improvement with Anti-GM-CSF Monoclonal Antibody Otilimab (GSK3196165) in Patients (Pts) with Active RA
9:00AM-11:00AM
Abstract Number: 525
Factors Associated with Persistent Drug-free Remission in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 526
Factors Influencing Discontinuation in Long-term RA Treatment
9:00AM-11:00AM
Abstract Number: 516
Impact of Baseline Demographics and Disease Activity on Outcomes in Patients with Rheumatoid Arthritis Receiving Upadacitinib
9:00AM-11:00AM
Abstract Number: 533
Impact of Formulary Change on TNFi Treatment Patterns and Healthcare Utilization Costs in RA Patients
9:00AM-11:00AM
Abstract Number: 552
In the Real World Clinical Setting Etanercept Biosimilar SB4(BENEPAIL®) Demonstrates Equivalent Safety and Effectiveness in Biological Naïve as Well as with ENBREL® Pretreated RA,SPA, and PSA Patients
9:00AM-11:00AM
Abstract Number: 507
Inhibition of Joint Destruction in Patients with Rheumatoid Arthritis Treated with Peficitinib in Combination with Methotrexate: A Randomized, Double-Blind, Placebo-Controlled Trial in Japan
9:00AM-11:00AM
Abstract Number: 547
Inhibition of Structural Joint Damage with Upadacitinib as Monotherapy or in Combination with Methotrexate in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 538
Long-Term Safety and Efficacy of Upadacitinib in Patients with Rheumatoid Arthritis and an Inadequate Response to CsDMARDs: Results at 60 Weeks
9:00AM-11:00AM
Abstract Number: 508
Longer Term Safety and Efficacy of Peficitinib in Patients with Rheumatoid Arthritis After 22.7 Months Mean Treatment Exposure: Interim Data from a Long-Term, Open-Label Extension Study in Japan, Korea and Taiwan
9:00AM-11:00AM
Abstract Number: 505
Low-grade Total Rheumatoid Arthritis MRI Scoring System Can Predict Successful Half-dose Reduction of MTX in Patients with RA in Clinical Remission
9:00AM-11:00AM
Abstract Number: 545
Molecular Analysis of the Mode of Action of Upadacitinib in Rheumatoid Arthritis Patients: Whole Blood RNA Expression Data from the SELECT-NEXT Study
9:00AM-11:00AM
Abstract Number: 541
Multicenter, Evaluator-blinded, Randomized, Non-inferiority Study, to Assess the Efficacy, Safety and Immunogenicity of Etanercept Biosimilar (EtaBS) vs. Reference Etanercept (EtaRef) in Combination with Methotrexate for the Treatment of Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 536
PERFUSE: A French Prospective/Retrospective Non-interventional Cohort Study of Infliximab-naïve and Transitioned Patients Receiving Infliximab Biosimilar SB2; An Interim Analysis
9:00AM-11:00AM
Abstract Number: 530
Phase I Evaluation of the PDE4 Inhibitor LY2775240: Head to Head Comparison with Apremilast Using an Ex Vivo Pharmacodynamic Assay
9:00AM-11:00AM
Abstract Number: 550
Rheumatoid Arthritis Treatment with Filgotinib: Week 156 Safety and Efficacy Data from a Phase 2b Open-Label Extension Study
9:00AM-11:00AM
Abstract Number: 527
Safety and Effectiveness of Upadacitinib or Adalimumab in Patients with Rheumatoid Arthritis: Results at 48 Weeks
9:00AM-11:00AM
Abstract Number: 509
Safety Profile of Upadacitinib in Rheumatoid Arthritis: Integrated Analysis from the SELECT Phase 3 Clinical Program
9:00AM-11:00AM
Abstract Number: 523
The Impact of Upadacitinib versus Methotrexate or Adalimumab on Individual and Composite Disease Measures in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 544
Tolerance, Survival, and Adherence to Methotrexate Treatment in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 510
Treatment with Upadacitinib Is Associated with Improvements in Reverse Cholesterol Transport in Patients with Rheumatoid Arthritis: Correlation with Changes in Inflammation and HDL Levels
9:00AM-11:00AM
Abstract Number: 522
Treatment with Upadacitinib Results in the Normalization of Key Pathobiologic Pathways in Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 513
Upadacitinib as Monotherapy in Patients with Rheumatoid Arthritis: Results at 48 Weeks
9:00AM-11:00AM
Abstract Number: 518
Upadacitinib in Patients with Rheumatoid Arthritis and Inadequate Response or Intolerance to Biological DMARDs: Results at 60 Weeks
9:00AM-11:00AM
Abstract Number: 551
Upadacitinib Treatment and the Routine Assessment of Patient Index Data 3 (RAPID3) Among Patients with Rheumatoid Arthritis
9:00AM-11:00AM
Abstract Number: 549
US Rheumatologists’ Beliefs and Knowledge About Biosimilars – an Ongoing Survey

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