85
Participants
Start Date
December 16, 2020
Primary Completion Date
December 16, 2023
Study Completion Date
December 16, 2023
Belimumab
The study will involve 80 adult patients diagnosed with SLE who will be started on belimumab (standard approved dose of i.v. 10 mg/kg or subcutaneous 200 mg/week) due to active disease. The intention to start belimumab will be made by the treating Rheumatologist(s), in accordance to the current standard of care, and on the basis of shared physician-patient decision making.
BRFAA, Athens
Collaborators (1)
Attikon Hospital
OTHER
University Hospital of Heraklion
UNKNOWN
GlaxoSmithKline
INDUSTRY
Biomedical Research Foundation, Academy of Athens
OTHER