The purpose of this study is to establish whether RA patients with moderate to severe disease activity with unsustainable response to infliximab 3 mg/kg every 8 weeks have better efficacy with adalimumab 40 mg s.c. eow compared to infliximab 3 mg/kg i.v. every 6 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
112
Remicade
Humira
Hvidovre Hospital
Copenhagen, Denmark
RECRUITINGBispebjerg Hospital
Copenhagen, Denmark
RECRUITINGGentofte Amtssygehus
Copenhagen, Denmark
RECRUITINGProportion of patients achieving combined good or moderate EULAR responses at week 24
Time frame: six months
ACR20/50/70 response at week 2, 6, 12, 18 and 24
Time frame: six months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Glostrup Hospital
Copenhagen, Denmark
RECRUITINGRigshospitalet
Copenhagen, Denmark
RECRUITINGGraasten Gigthospital
Gråsten, Denmark
RECRUITING