Introduction: Improvements in both musculoskeletal and non-musculoskeletal manifestations are important treatment goals in psoriatic arthritis (PsA). Objective: These post hoc analyses determined whether additional benefits related to various PsA domains are observed in patients simultaneously achieving 50% improvement in American College of Rheumatology criteria (ACR50) and 100% improvement in Psoriasis Area Severity Index (PASI100), the primary endpoint of the SPIRIT-H2H study. Methods: Patients with active PsA and psoriasis in SPIRIT-H2H (N = 566) were categorised into two sets of four response groups irrespective of treatment allocation (approved dosages of ixekizumab or adalimumab): patients who simultaneously achieved ACR50 and PASI10...
Objective: To report patient-reported outcomes of patients with PsA treated with ixekizumab up to 52...
BACKGROUND: The International Dermatology Outcome Measures (IDEOM) established a set of core domains...
OBJECTIVES: To evaluate the efficacy through 52 weeks of guselkumab, an interleukin 23-p19 subunit i...
International audienceIntroductionImprovements in both musculoskeletal and non-musculoskeletal manif...
OBJECTIVE:Determine the contribution of joint and skin improvements to health-related quality of lif...
Introduction: Ixekizumab, a selective interleukin-17A antagonist, was compared with adalimumab in th...
OBJECTIVES: SPIRIT head-to-head (H2H) is a 52-week (Wk) trial comparing ixekizumab (IXE) with adalim...
OBJECTIVE: We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subj...
SPIRIT head-to-head (H2H) is a 52-week (Wk) trial comparing ixekizumab (IXE) with adalimumab (ADA) f...
Objective The Phase 3 DISCOVER-1 study of guselkumab is the first randomized controlled trial to us...
Objective The Phase 3 DISCOVER-1 study of guselkumab is the first randomized controlled trial to use...
INTRODUCTION: The aim of this work is to assess the effect of upadacitinib versus adalimumab and pla...
OBJECTIVE: To evaluate the efficacy and safety of ixekizumab (IXE), an interleukin 17A antagonist, i...
BACKGROUND/OBJECTIVE: The aim of this study was to evaluate relative performance of composite measur...
ObjectiveTo report patient-reported outcomes (PROs) of ixekizumab-treated patients with psoriatic ar...
Objective: To report patient-reported outcomes of patients with PsA treated with ixekizumab up to 52...
BACKGROUND: The International Dermatology Outcome Measures (IDEOM) established a set of core domains...
OBJECTIVES: To evaluate the efficacy through 52 weeks of guselkumab, an interleukin 23-p19 subunit i...
International audienceIntroductionImprovements in both musculoskeletal and non-musculoskeletal manif...
OBJECTIVE:Determine the contribution of joint and skin improvements to health-related quality of lif...
Introduction: Ixekizumab, a selective interleukin-17A antagonist, was compared with adalimumab in th...
OBJECTIVES: SPIRIT head-to-head (H2H) is a 52-week (Wk) trial comparing ixekizumab (IXE) with adalim...
OBJECTIVE: We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subj...
SPIRIT head-to-head (H2H) is a 52-week (Wk) trial comparing ixekizumab (IXE) with adalimumab (ADA) f...
Objective The Phase 3 DISCOVER-1 study of guselkumab is the first randomized controlled trial to us...
Objective The Phase 3 DISCOVER-1 study of guselkumab is the first randomized controlled trial to use...
INTRODUCTION: The aim of this work is to assess the effect of upadacitinib versus adalimumab and pla...
OBJECTIVE: To evaluate the efficacy and safety of ixekizumab (IXE), an interleukin 17A antagonist, i...
BACKGROUND/OBJECTIVE: The aim of this study was to evaluate relative performance of composite measur...
ObjectiveTo report patient-reported outcomes (PROs) of ixekizumab-treated patients with psoriatic ar...
Objective: To report patient-reported outcomes of patients with PsA treated with ixekizumab up to 52...
BACKGROUND: The International Dermatology Outcome Measures (IDEOM) established a set of core domains...
OBJECTIVES: To evaluate the efficacy through 52 weeks of guselkumab, an interleukin 23-p19 subunit i...