Objective : To study acceptance rate and factors influencing acceptance of the switch from originator etanercept (Enbrel©) to biosimilar etanercept (SB4, Bénépali©) in patients with rheumatic disease.Methods : Patients with a well-controlled rheumatic disease consulting in our rheumatology department were offered the switch for SB4. After oral and written information concerning biosimilar, free choice to accept the switch was left to the patients. The main outcome was primary switch acceptance rate defined by switch acceptance during the initial consult. Real switch adherence, socio-cultural factors and beliefs influencing switch acceptance rate were retrieved during a telephonic interview at distance from the consultation.Results : Fifty-t...
Background: Patients in clinical practice are transitioned from originator etanercept (OR-ETA) to bi...
Biosimilars are broadly available for the treatment of several diseases including inflammatory arthr...
Objective Biosimilars are approved as an alternative treatment to their originators. We compared the...
International audienceObjective : To study acceptance rate and factors influencing acceptance of the...
Aims: Switching from originator to biosimilar is part of current practice in inflammatory rheumatic ...
Objective. To evaluate the effects of non-mandatory transitioning from the originator biologic drug ...
Objective. To evaluate the effects of non-mandatory transitioning from the originator biologic drug ...
Despite several studies proving the efficacy and safety of biosimilars compared with original drugs,...
Fabrizio Cantini,1 Maurizio Benucci2 1Department of Rheumatology, Hospital of Prato, Prato, Italy; 2...
Background: To describe the uptake and system-level effects of the introduction of biosimilars in a ...
OBJECTIVES: To compare treatment retention between biosimilars and their originator products among f...
Background: Although Inflectra, biosimilar infliximab, has been approved by the EMA since September ...
John Waller,1 Emma Sullivan,1 James Piercy,1 Christopher M Black,2 Sumesh Kachroo2 1Adelphi Real Wo...
objective: to compare etanercept and adalimumab biosimilars (SB4 and ABP501) and respective biorigin...
Background: Patients in clinical practice are transitioned from originator etanercept (OR-ETA) to bi...
Biosimilars are broadly available for the treatment of several diseases including inflammatory arthr...
Objective Biosimilars are approved as an alternative treatment to their originators. We compared the...
International audienceObjective : To study acceptance rate and factors influencing acceptance of the...
Aims: Switching from originator to biosimilar is part of current practice in inflammatory rheumatic ...
Objective. To evaluate the effects of non-mandatory transitioning from the originator biologic drug ...
Objective. To evaluate the effects of non-mandatory transitioning from the originator biologic drug ...
Despite several studies proving the efficacy and safety of biosimilars compared with original drugs,...
Fabrizio Cantini,1 Maurizio Benucci2 1Department of Rheumatology, Hospital of Prato, Prato, Italy; 2...
Background: To describe the uptake and system-level effects of the introduction of biosimilars in a ...
OBJECTIVES: To compare treatment retention between biosimilars and their originator products among f...
Background: Although Inflectra, biosimilar infliximab, has been approved by the EMA since September ...
John Waller,1 Emma Sullivan,1 James Piercy,1 Christopher M Black,2 Sumesh Kachroo2 1Adelphi Real Wo...
objective: to compare etanercept and adalimumab biosimilars (SB4 and ABP501) and respective biorigin...
Background: Patients in clinical practice are transitioned from originator etanercept (OR-ETA) to bi...
Biosimilars are broadly available for the treatment of several diseases including inflammatory arthr...
Objective Biosimilars are approved as an alternative treatment to their originators. We compared the...