OBJECTIVES: To evaluate the relationship between radiographic progression and disease activity in subjects with PsA treated with adalimumab (ADA) or placebo (PBO) and the impact of concomitant MTX. METHODS: This was a post hoc analysis of the randomized, double-blind, PBO-controlled ADEPT trial. Subjects were categorized according to time-averaged (TA) disease activity (remission, low, moderate or high) based on Disease Activity Score of 28 joints with CRP [DAS28(CRP)], Disease Activity Index for Psoriatic Arthritis (DAPSA) or Psoriatic Arthritis Disease Activity Score (PASDAS), and achievement of minimal disease activity (MDA) at week 24. Radiographic progression was assessed as change in modified total Sharp score (ΔmTSS) from baseline to...
Objective. Adalimumab, a fully human, antitumor necrosis factor monoclonal antibody, was evaluated f...
OBJECTIVE: To determine which of the changes in synovial tissue correlates best with clinical respon...
Background: Psoriatic arthritis (PsA) patient data from two phase 3 secukinumab trials (FUTURE 1, 5)...
Objectives To evaluate the relationship between radiographic progression and disease activity in sub...
OBJECTIVE: Evaluate relationship between radiographic progression and clinical outcomes in post hoc ...
BACKGROUND: In the GO-VIBRANT trial of intravenous golimumab in psoriatic arthritis (PsA), golimumab...
Abstract Introduction To identify independent predict...
Introduction: To identify independent predictors of radiographic progression in psoriatic arthritis ...
Objective Evaluate relationship between radiographic progression and clinical outcomes in post hoc a...
Objective: Evaluate ustekinumab, an anti-interleukin (IL)-12 and IL-23 antibody, effects on radiogra...
OBJECTIVE: To compare achievement of Disease Activity Index in Psoriatic Arthritis (DAPSA) remission...
BACKGROUND: Guselkumab, a fully human monoclonal antibody targeting the interleukin (IL)-23p19 subun...
Objective. Adalimumab (ADA) was evaluated for its efficacy in patients with moderate to severely act...
Objectives: The purpose of this study was to compare radiographic outcomes according to the magnitud...
Objective: The aim of this study was to evaluate minimal disease activity (MDA) assessments in patie...
Objective. Adalimumab, a fully human, antitumor necrosis factor monoclonal antibody, was evaluated f...
OBJECTIVE: To determine which of the changes in synovial tissue correlates best with clinical respon...
Background: Psoriatic arthritis (PsA) patient data from two phase 3 secukinumab trials (FUTURE 1, 5)...
Objectives To evaluate the relationship between radiographic progression and disease activity in sub...
OBJECTIVE: Evaluate relationship between radiographic progression and clinical outcomes in post hoc ...
BACKGROUND: In the GO-VIBRANT trial of intravenous golimumab in psoriatic arthritis (PsA), golimumab...
Abstract Introduction To identify independent predict...
Introduction: To identify independent predictors of radiographic progression in psoriatic arthritis ...
Objective Evaluate relationship between radiographic progression and clinical outcomes in post hoc a...
Objective: Evaluate ustekinumab, an anti-interleukin (IL)-12 and IL-23 antibody, effects on radiogra...
OBJECTIVE: To compare achievement of Disease Activity Index in Psoriatic Arthritis (DAPSA) remission...
BACKGROUND: Guselkumab, a fully human monoclonal antibody targeting the interleukin (IL)-23p19 subun...
Objective. Adalimumab (ADA) was evaluated for its efficacy in patients with moderate to severely act...
Objectives: The purpose of this study was to compare radiographic outcomes according to the magnitud...
Objective: The aim of this study was to evaluate minimal disease activity (MDA) assessments in patie...
Objective. Adalimumab, a fully human, antitumor necrosis factor monoclonal antibody, was evaluated f...
OBJECTIVE: To determine which of the changes in synovial tissue correlates best with clinical respon...
Background: Psoriatic arthritis (PsA) patient data from two phase 3 secukinumab trials (FUTURE 1, 5)...