The aims of this study are to assess the safety, tolerability and pharmacokinetics of single ascending oral doses of AZD5985 in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
72
Research Site
Gothenburg, Sweden
Safety variables (ECG, adverse events, blood pressure, pulse, body temp, safety lab)
Time frame: Frequent sampling occasions during study days
Pharmacokinetic variables
Time frame: Frequent sampling occasions during study days
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