The purpose of this study is to investigate features of radioligand \[11C\]AZ12807110 and how much AZD5213 displaces radioligand from histamine receptors when given together.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
13
Radioligand
Research Site
Uppsala, Sweden
Distribution volume (VT)
Time frame: Venous blood samples for determination of concentrations of AZD5213 in plasma will be taken on many occasions from pre-dose until 48 h post-dose. Single PET measurement will take maximum 2 hours.
Estimation of the plasma concentration resulting in 50% receptor occupancy (Ki, pl).
Each healthy volunteer in the main panel will complete 3 PET measurements using radioligand; one at baseline and 2 after treatment with AZD5213.
Time frame: Venous blood samples for determination of concentrations of AZD5213 in plasma will be taken on many occasions from pre-dose until 48 h post-dose.
Adverse events
Time frame: Collected from Day 1 to follow-up
Vital signs (body temperature, BP and pulse)
Time frame: Measured at screening, study days -1 to day 3 and at follow-up
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