A study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending dose of ASP0456 in non-elderly healthy subjects. Two dosing condition, pre-prandial and postprandial administrations, is compared.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
TRIPLE
Enrollment
44
Unnamed facility
Kantou, Japan
Pharmacokinetics (such as Cmax, AUC and t1/2 etc.) of ASP0456 assessed by its plasma concentration change
Time frame: For 48 hours after dosing
Safety assessed by the incidence of adverse events, vital signs, 12-lead ECGs and labo tests
Time frame: For 48 hours after dosing
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