The purpose of this study is to determine how well tolerated and safe AZD8566 is at different dose levels. This study will also determine how AZD8566 is distributed around the body and how it leaves the body.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
108
Research Site
Nottingham, United Kingdom
Pharmacokinetic profile: concentration of AZD8566 in blood
Time frame: Samples taken during Visit 2 (residential period) at up to 16 defined timepoints pre-dose and post- dose
Safety and tolerability of AZD8566 by assessment of vital signs, laboratory variables, ECG and adverse events
Time frame: Assessments taken at Visit 1 (enrolment), defined timepoints pre-dose and post-dose during Visit 2 (residential period) and at Visit 3 (follow up). Volunteers will be monitored throughout the study from Visit 1 to Visit 3 for adverse events.
Pharmacokinetic profile: concentration of AZD8566 in urine
Time frame: Samples collected over 48 hours from pre-dose to 48 hours post-dose.
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