The purpose of this study is to assess safety and tolerability of AZD1656 after single ascending oral doses in Japanese healthy male subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
36
Dose escalation of oral single doses of AZD1656 to achieve maximal tolerated dose
Research Site
Glendale, California, United States
Safety variables (AEs, blood pressure (BP), pulse, safety laboratory variables and electrocardiography (ECG)
Time frame: Safety variables taken repeatedly during 24 hours on study day sessions
Pharmacokinetic variables
Time frame: Pharmacokinetic variables taken repeatedly during 24 hours on study day sessions
Pharmacodynamic variables
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions
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