The purpose of this study is to investigate the safety, tolerability and pharmacokinetics of MT-7117 in healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
144
Investigational center
United Kingdom, United Kingdom
Safety and Tolerability as measured by number of participants with adverse events
Time frame: up to Day56
Safety and Tolerability as measured by vital signs
Time frame: up to Day56
Safety and Tolerability as measured by physical examination
Time frame: up to Day56
Safety and Tolerability as measured by ECG
Time frame: up to Day21
Safety and Tolerability as measured by laboratory safety assessments
Time frame: up to Day21
Maximum plasma concentration (Cmax)
Time frame: 96 hours post dose
Area under the plasma concentration-time curve (AUC)
Time frame: 96 hours post dose
Time to maximum plasma concentration (Tmax)
Time frame: 96 hours post dose
Apparent elimination half-life in plasma
Time frame: 96 hours post dose
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