The purpose of this study is to compare the absorption of a test inhalation product with the reference product in healthy volunteers.
Healthy subjects will be enrolled and will receive doses of a test inhalation product and a reference inhalation product for 28 days according to a crossover design. Plasma tiotropium levels will be measured predose and over 24 hours postdose on days 1 and 28.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
40
inhalation
3M Health Care
Loughborough, United Kingdom
Peak Plasma Concentration (Cmax)
noncompartmental analysis
Time frame: 24 hours
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