The purpose of this study is to evaluate the safety, tolerability, and PK of single oral doses of JTT-252 and the effect of food on the PK of JTT-252 in healthy subjects, and to evaluate the safety, tolerability, PK and PD of single oral doses of JTT-252 in type 2 diabetes mellitus subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
85
Subjects will receive JTT-252 or Placebo
Subjects will receive JTT-252
Unnamed facility
Overland Park, Kansas, United States
Unnamed facility
Austin, Texas, United States
Number of subjects with adverse events
Time frame: 22 days
Vital signs and 12 lead ECGs
Time frame: 22 days
Cmax (maximum concentration)
Time frame: 22 days
t1/2 (elimination half-life)
Time frame: 22 days
AUC (area under the concentration-time curve)
Time frame: 22 days
fe(total) (fraction of systemically available drug excreted into the urine over entire collection interval)
Time frame: 3 days
Plasma glucose
Time frame: 22 days
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