Objectives: To evaluate the effectiveness of adalimumab in patients with psoriatic arthritis (PsA) and identify predictors of good clinical response for joint and skin lesions. Methods: Patients received adalimumab 40 mg every other week in addition to standard therapy in this prospective, 12-week, open-label, uncontrolled study. Four definitions of good clinical response were used: >= 50% improvement in American College of Rheumatology response criteria (ACR50), good response according to European League Against Rheumatism (EULAR) guidelines, a >= 3-grade improvement in Physician Global Assessment of psoriasis (PGA) and a >= 50% improvement in the Nail Psoriasis Severity Index (NAPSI). Response predictors were determined by logistic regres...
Objectives: To compare efficacy and safety of ixekizumab (IXE) to adalimumab (ADA) in biological dis...
Adalimumab is a human, antitumour necrosis factor (TNF) monoclonal antibody with a high specificity...
Background: Few studies have evaluated the effectiveness of adalimumab in the real-life setting in p...
Objectives: To evaluate the effectiveness of adalimumab in patients with psoriatic arthritis (PsA) a...
Objective. Adalimumab, a fully human, antitumor necrosis factor monoclonal antibody, was evaluated f...
Background: Few studies have compared the efficacy of switching to adalimumab in the real-life setti...
Objective. Adalimumab (ADA) was evaluated for its efficacy in patients with moderate to severely act...
Objective: To evaluate the long-term effectiveness and tolerability of adalimumab in the treatment o...
There is much evidence to show the efficacy of adalimumab, a human monoclonal antibody targeting tum...
ABSTRACT. Objective. This posthoc analysis evaluated the percentage of patients with psoriatic arthr...
Introduction: The aim of this work is to assess the effect of upadacitinib versus adalimumab and pla...
Objectives: To evaluate the efficacy and safety of adalimumab in psoriatic arthritis (PsA) patients ...
AbstractBackground/ObjectiveThe incidence of psoriasis vulgaris in Asians is estimated at 0.05–0.30%...
Objectives: To compare efficacy and safety of ixekizumab (IXE) to adalimumab (ADA) in biological dis...
Adalimumab is a human, antitumour necrosis factor (TNF) monoclonal antibody with a high specificity...
Background: Few studies have evaluated the effectiveness of adalimumab in the real-life setting in p...
Objectives: To evaluate the effectiveness of adalimumab in patients with psoriatic arthritis (PsA) a...
Objective. Adalimumab, a fully human, antitumor necrosis factor monoclonal antibody, was evaluated f...
Background: Few studies have compared the efficacy of switching to adalimumab in the real-life setti...
Objective. Adalimumab (ADA) was evaluated for its efficacy in patients with moderate to severely act...
Objective: To evaluate the long-term effectiveness and tolerability of adalimumab in the treatment o...
There is much evidence to show the efficacy of adalimumab, a human monoclonal antibody targeting tum...
ABSTRACT. Objective. This posthoc analysis evaluated the percentage of patients with psoriatic arthr...
Introduction: The aim of this work is to assess the effect of upadacitinib versus adalimumab and pla...
Objectives: To evaluate the efficacy and safety of adalimumab in psoriatic arthritis (PsA) patients ...
AbstractBackground/ObjectiveThe incidence of psoriasis vulgaris in Asians is estimated at 0.05–0.30%...
Objectives: To compare efficacy and safety of ixekizumab (IXE) to adalimumab (ADA) in biological dis...
Adalimumab is a human, antitumour necrosis factor (TNF) monoclonal antibody with a high specificity...
Background: Few studies have evaluated the effectiveness of adalimumab in the real-life setting in p...