This trial is conducted in Oceania. The aim of this trial is to test for bioequivalence between each of the two new liraglutide formulations at pH 7.9 and 8.15 and the planned Phase 3 formulation at pH 7.7.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
24
One single dose of 0.75 mg administered on three different dosing occasions with a 14-day wash-out period between each dosing. Injected subtaneously
Novo Nordisk Investigational Site
Adelaide, Australia
Area under the Curve (0-t)
Cmax, maximum concentration
Area under the curve (0-infinity)
tmax, time to reach Cmax
t½, terminal half-life
Terminal elimination rate constant
Adverse events
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