The primary objectives of the study are: * To evaluate the effects of three oral doses of MT-1303 compared to placebo given for a period of 24 weeks in subjects with relapsing-remitting multiple sclerosis (RRMS) on MRI parameters * To evaluate the safety and tolerability of three oral doses of MT-1303 compared to placebo given for a period of 24 weeks in subjects with RRMS.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
415
Research Site
Brussels, Belgium
Research Site
Sofia, Bulgaria
Research Site
Edmonton, Canada
The total number of MRI Gd-enhanced T1-weighted lesions
Time frame: Weeks 24
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site
Zagreb, Croatia
Research Site
Prague, Czechia
Research Site
Vantaa, Finland
Research Site
Berlin, Germany
Research Site
Budapest, Hungary
Research Site
Roma, Italy
Research Site
Kaunas, Lithuania
...and 8 more locations