The study is carried out in order to investigate safety, tolerability and pharmacokinetics after administrating single and fractionated doses of AZD3241 to healthy volunteers
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
64
Research Site
Stockholm, Sweden
General tolerability and safety variables
Time frame: 2 weeks
pk
Time frame: approximately 48 hour
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