The primary objectives of the study are: * To evaluate the safety and tolerability of MT-1303 in subjects with moderate to severe active Crohn's Disease(CD) * To evaluate the clinical efficacy of MT-1303 in subjects with moderate to severe active CD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
78
Investigational site
City Name, Czechia
Investigational site
City Name, France
Investigational Site
City Name, Germany
Investigational site
City Name, Hungary
Proportion of subjects who achieve a 100-point decrease from Baseline in CDAI(Crohn's Disease Activity Index) score (i.e., CDAI 100) at Visit 6 (Week 12)
Time frame: 14 weeks
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Investigational site
City Name, Israel
Investigational site
City Name, Italy
Investigational site
City Name, Japan
Investigational site
City Name, Netherlands
Investigational site
City Name, Poland
Investigational site
City Name, Slovakia
...and 1 more locations