The purpose of this study is to evaluate the safety, tolerability, and PK (Pharmacokinetics) of single oral doses of JTT-251 in healthy and type 2 diabetes mellitus subjects and to evaluate the effect of food on the PK of JTT-251 in healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
94
Subjects will receive JTT-251 or Placebo
Unnamed facility
Orlando, Florida, United States
Number of subjects with adverse events
Time frame: 1 week
Vital signs and 12 lead ECGs
Time frame: 1 week
Cmax (maximum concentration)
Time frame: 1 week
t1/2 (elimination half-life)
Time frame: 1 week
AUC (area under the concentration-time curve)
Time frame: 1 week
fe(total) (fraction of systemically available drug excreted into the urine over entire collection interval)
Time frame: 1 week
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