The purpose of this study is to assess safety and tolerability of AZD6714 after single ascending oral doses in healthy male subjects and type 2 diabetic patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
26
Research Site
Gothenburg, Sweden
Safety variables (AE, BP, pulse, plasma glucose, laboratory variables and ECG)
Time frame: AEs will be collected during the whole study period (1-3 months). The other variables will be measured repeatedly during 24 hours on the study day sessions
Pharmacokinetic variables
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions.
Pharmacodynamic variables (P-Glucose, S-Insulin and C-peptide)
Time frame: Blood samples taken repeatedly during 24 hours on study day sessions.
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Oral single doses d and g suspension