The GO-DACT is an investigator-initiated, multicentric randomized placebo-controlled double-blinded trial, that assesses dactylitis as primary endpoint. Psoriatic arthritis patients naïve to methotrexate and biologic disease modifying anti-rheumatic drugs, with at least one active dactylitis, were assigned to golimumab in combination with methotrexate or placebo in combination with methotrexate, for 24 weeks. Both clinical (dactylitis severity score and the Leeds dactylitis index) and imaging (high resolution magnetic resonance imaging), among others, were assessed as outcomes. The main objective of GO-DACT is to provide evidence to improve the treatment algorithm and care of psoria - tic arthritis patients with active dactylitis. In this m...
OBJECTIVE: We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subj...
Introduction: Adalimumab is normally prescribed with methotrexate (MTX) in rheumatoid arthritis give...
Objective: Golimumab, administered subcutaneously every 4 weeks, has been shown to be effective in r...
The GO-DACT is an investigator-initiated, national, multicentric randomized placebo-controlled doubl...
The GO-DACT is an investigator-initiated, national, multicentric randomized placebo-controlled doubl...
Objectives To assess the efficacy of golimumab in combination with methotrexate (MTX) versus MTX mon...
Psoriatic arthritis (PsA) is a chronic inflammatory arthritis which impacts significantly on the qu...
Objectives: Early initiation of effective treatment favours remission in rheumatoid arthritis, but i...
Objective: Methotrexate (MTX) is a commonly used disease-modifying antirheumatic drug in psoriatic a...
BACKGROUND: Clinical trials have demonstrated the efficacy of golimumab (GLB) in improving the s...
Objective: To evaluate the efficacy of etanercept and methotrexate as monotherapies and as combinati...
Introduction: Randomised controlled trials (RCTs) have compared biological and targeted systemic dis...
Methotrexate (MTX) is widely used in the treatment of psoriatic arthritis (PsA) despite the evidence...
Objectives To determine the effectiveness of golimumab (GLM) in improving joint, periarticular struc...
Psoriatic arthritis (PsA) causes inflammation in and around the joints and usually affects people wh...
OBJECTIVE: We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subj...
Introduction: Adalimumab is normally prescribed with methotrexate (MTX) in rheumatoid arthritis give...
Objective: Golimumab, administered subcutaneously every 4 weeks, has been shown to be effective in r...
The GO-DACT is an investigator-initiated, national, multicentric randomized placebo-controlled doubl...
The GO-DACT is an investigator-initiated, national, multicentric randomized placebo-controlled doubl...
Objectives To assess the efficacy of golimumab in combination with methotrexate (MTX) versus MTX mon...
Psoriatic arthritis (PsA) is a chronic inflammatory arthritis which impacts significantly on the qu...
Objectives: Early initiation of effective treatment favours remission in rheumatoid arthritis, but i...
Objective: Methotrexate (MTX) is a commonly used disease-modifying antirheumatic drug in psoriatic a...
BACKGROUND: Clinical trials have demonstrated the efficacy of golimumab (GLB) in improving the s...
Objective: To evaluate the efficacy of etanercept and methotrexate as monotherapies and as combinati...
Introduction: Randomised controlled trials (RCTs) have compared biological and targeted systemic dis...
Methotrexate (MTX) is widely used in the treatment of psoriatic arthritis (PsA) despite the evidence...
Objectives To determine the effectiveness of golimumab (GLM) in improving joint, periarticular struc...
Psoriatic arthritis (PsA) causes inflammation in and around the joints and usually affects people wh...
OBJECTIVE: We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subj...
Introduction: Adalimumab is normally prescribed with methotrexate (MTX) in rheumatoid arthritis give...
Objective: Golimumab, administered subcutaneously every 4 weeks, has been shown to be effective in r...