The purpose of the study is to determine the efficacy, safety and pharmacokinetics of SC12267 (4SC-101, 35 mg) in combination with methotrexate in comparison to methotrexate alone in the treatment of patients suffering from Rheumatoid Arthritis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
266
MHAT "Kaspela" Department of Rheumatology
Plovdiv, Bulgaria
Efficacy of SC12267 (4SC-101) in combination with methotrexate in patients with RA
Time frame: 13 weeks
Evaluation of the safety of the combination of SC12267 (4SC-101) and methotrexate in patients with RA
Time frame: 13 weeks
Evaluation of the plasma concentration (trough value) of SC12267 (4SC-101) after once daily application in combination with methotrexate after once weekly administration.
Time frame: 13 weeks
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oral administration
Diagnostic Consulting Centre "Sv. Anna"
Sofia, Bulgaria
Military Medical Academy
Sofia, Bulgaria
National Multiprofile Transport Hospital "Tsar Boris III" Internal Clinic
Sofia, Bulgaria
UMHAT "Sveti Ivan Rilski"
Sofia, Bulgaria
Rheumatology Outpatient Clinic
Hlučín, Czechia
Diagnostic Center Mediscan
Prague, Czechia
Institute of Rheumatology
Prague, Czechia
Centrum Miriada, Prywatny Gabinet Specjalistyczny
Bialystok, Poland
Mazowieckie Centrum Badań Klinicznych s.c.
Grodzisk Mazowiecki, Poland
...and 17 more locations