Abstract Background This multicenter, open-label, prospective, single cohort study evaluated the effectiveness and safety of adalimumab in a clinical setting reflecting the Canadian standard of care for the treatment of patients with rheumatoid arthritis (RA). Methods Patients ≥ 18 years of age with a history of active RA ≥ 3 months and fulfilling Canadian requirements for biological therapy received adalimumab 40 mg subcutaneously every other week for 12 weeks. Pre-study DMARD treatment regimens, corticosteroids, or NSAIDs were allowed throughout the study. The primary effectiveness outcome measure was the mean change in 28-joint disease activity score (DAS28) from baseline to Week 12. Secondary measures included the proportion of patients...
Objectives: To observe the choices of conventional disease modifying antirheumatic drugs (cDMARDs) a...
INTRODUCTION: Current recommendations for the management of rheumatoid arthritis (RA) focus on a tre...
OBJECTIVES: To evaluate efficacy, dose response, safety, and tolerability of adalimumab (D2E7...
International audienceINTRODUCTION: Patients with active rheumatoid arthritis who had failed at leas...
Objective: To evaluate the safety and effectiveness of adalimumab alone or in combination with stand...
The purpose of the study was to estimate the clinical profile of naïve biological patients with rheu...
Background: The aim of this study was to assess the real-world effectiveness and safety of certolizu...
The purpose of the study was to estimate the clinical profile of naïve biological patients with rheu...
BACKGROUND: Discontinuation of rheumatoid arthritis (RA) treatment for lack or loss of initial resp...
Adalimumab (ADA) is a monoclonal antibody. Published studies indicate that its use in patients with ...
OBJECTIVES: To evaluate efficacy, dose response, safety, and tolerability of adalimumab (D2E7) in di...
The purpose of the study was to estimate the clinical profile of na\uefve biological patients with r...
AIMS: To assess the effectiveness of biologic disease-modifying anti-rheumatic drugs (bDMARDs) as mo...
Abstract Background Long-term clinical registries are essential tools to evaluate new therapies in ...
The purpose of the study was to estimate the clinical profile of na\uefve biological patients with r...
Objectives: To observe the choices of conventional disease modifying antirheumatic drugs (cDMARDs) a...
INTRODUCTION: Current recommendations for the management of rheumatoid arthritis (RA) focus on a tre...
OBJECTIVES: To evaluate efficacy, dose response, safety, and tolerability of adalimumab (D2E7...
International audienceINTRODUCTION: Patients with active rheumatoid arthritis who had failed at leas...
Objective: To evaluate the safety and effectiveness of adalimumab alone or in combination with stand...
The purpose of the study was to estimate the clinical profile of naïve biological patients with rheu...
Background: The aim of this study was to assess the real-world effectiveness and safety of certolizu...
The purpose of the study was to estimate the clinical profile of naïve biological patients with rheu...
BACKGROUND: Discontinuation of rheumatoid arthritis (RA) treatment for lack or loss of initial resp...
Adalimumab (ADA) is a monoclonal antibody. Published studies indicate that its use in patients with ...
OBJECTIVES: To evaluate efficacy, dose response, safety, and tolerability of adalimumab (D2E7) in di...
The purpose of the study was to estimate the clinical profile of na\uefve biological patients with r...
AIMS: To assess the effectiveness of biologic disease-modifying anti-rheumatic drugs (bDMARDs) as mo...
Abstract Background Long-term clinical registries are essential tools to evaluate new therapies in ...
The purpose of the study was to estimate the clinical profile of na\uefve biological patients with r...
Objectives: To observe the choices of conventional disease modifying antirheumatic drugs (cDMARDs) a...
INTRODUCTION: Current recommendations for the management of rheumatoid arthritis (RA) focus on a tre...
OBJECTIVES: To evaluate efficacy, dose response, safety, and tolerability of adalimumab (D2E7...