The purpose of this study is to compare the absorption of four different inhalation products with the reference product in healthy volunteers.
Healthy subjects will be enrolled and will receive single doses of 4 test inhalation products and two reference inhalation products according to a five-period cross-over design. Plasma tiotropium levels will be measured pre-dose and over 48 hours post-dose.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
38
Cmax
maximum plasma concentration
Time frame: 48 hours
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