The purpose of this study is to evaluate the pharmacokinetics of different extended-release formulations of AZD1305 when given as single and multiple oral doses to healthy male volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
24
Research Site
Harrow, United Kingdom
Pharmacokinetic variables of AZD1305 by assessment of drug concentrations in plasma
Time frame: From predose until 48 hours post last dose
Adverse Events, ECG variables, vital signs, physical examination, laboratory variables and weight
Time frame: Frequent safety measurements during the study, from screening period to follow-up
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