The purpose of this study is to evaluate the systemic exposure to ibuprofen after single oromucosal administration of the test product V0498 and single oral administration of a reference product.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Single oromucosal administration
Single oral administration
Unnamed facility
Liège, Belgium
Maximum Plasma Concentration (Cmax)
Time frame: 11 time points up to 10h after administration
Time of Maximum Concentration
Time frame: 11 time points up to 10h after administration
Area Under Curve (AUC0-72)
Time frame: 11 time points up to 10h after administration
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