A study to investigate the effect on safety, pharmacokinetics and pharmacodynamics when ASP1941 is administered as add-on therapy to metformin.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
36
Unnamed facility
Balatonfüred, Hungary
Unnamed facility
Budapest, Hungary
Unnamed facility
Groningen, Netherlands
Unnamed facility
Warsaw, Poland
Unnamed facility
Bratislava, Slovakia
Safety assessed by incidence of adverse events, vital signs, 12-lead ECG and glucose monitoring
Time frame: 5 weeks
Pharmacodynamics assessed by serum glucose change
Time frame: 5 weeks
Pharmacokinetics assessed by metformin plasma concentration change
Time frame: 5 weeks
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