The purpose of this study is to assess the safety and tolerability of AZD1656 after multiple repeated oral doses in Japanese patients with type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
24
Research Site
Fukuoka, Japan
Research Site
Tokyo, Japan
Safety by assessment of adverse events, BP, pulse rate, plasma glucose, safety laboratory variables and ECG
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions
Pharmacokinetic variables (AUC, Cmax, tmax, t½, CL/F, Ae and CLR).
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions
Pharmacodynamic variables (P-Glucose, S-Insulin and S-C-peptide).
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions
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