This is a study to evaluate safety, tolerability, PK and PD effects of orally administered AZD7325 after single and repeated ascending doses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
48
Oral
Research Site
Philadelphia, Pennsylvania, United States
To assess the safety and tolerability of multiple ascending oral doses of AZD7325 compared to placebo by assessment of adverse events, vital signs, physical examinations, laboratory parameters, and ECGs
Time frame: Alssessments are made at each visit, at least daily, during the study.
Evaluation and characterization of the pharmacokinetics of AZD7325 when given orally in multiple ascending doses
Time frame: Blood samples will be taken during the study.
Evaluation of the pharmacodynamic effects of AZD7325
Time frame: Test batteries will be performed at specified times both before and following study drug administration.
Identification of genes that influence the disposition, efficacy, safety and tolerability of AZD7325.
Time frame: A single blood sample will be obtained.
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