The purpose of this study is to investigate the efficacy, safety, tolerability and pharmacokinetics of multiple oral administration of MT-3995 in patients with NASH.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
48
Investigational site
Kanagawa, Japan
Investigational site
Osaka, Japan
Percent change from baseline in ALT
Time frame: 24 weeks
Change from baseline in ALT
Time frame: 24 weeks
Adverse events
Time frame: From baseline to 72 weeks
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