The purpose of this study is to assess the effect of food on the pharmacokinetics of a single oral dose of mirabegron in healthy male and female subjects.
Subjects will be assigned in a random order to receive 3 dosing regimens: 1. a single oral dose under a fasting condition; 2. a single oral dose with food (low fat breakfast); 3. a single oral dose with food (high fat breakfast).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
76
oral tablet
Unnamed facility
Tacoma, Washington, United States
Assess the effects of food on the pharmacokinetics of a single oral dose of mirabegron
Time frame: 4-5 weeks
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