This trial is conducted in Europe. The aim of this trial is to investigate liraglutide in subjects with mild, moderate and severe degrees of hepatic impairment compared with subjects with normal hepatic function.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Single dose of 0.75 mg injected subcutaneously (under the skin)
Unnamed facility
Warsaw, Poland
Area under the Curve (0-infinity)
Area under the Curve (0-t)
Cmax, maximum concentration
tmax, time to maximum concentration
t½, terminal half-life
Adverse events
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