This study is designed to investigate the food-effects on FDC(gemigliptin/metformin HCl sustained release) 50/1000mg(25/500mg x 2tablets)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Enrollment
24
Asan Medical Center
Seoul, South Korea
AUClast
To evaluate AUClast of gemigliptin and metformin
Time frame: up to 48 h post-dose
Cmax
TO evaluate Cmax of gemigliptin and metformin
Time frame: up to 48 h post-dose
AUCinf
To evaluate AUCinf of gemigliptin,metformin and LC15-0636(active metabolite of gemigliptin)
Time frame: up to 48 h post-dose
Tmax
To evaluate Tmax of gemigliptin, metformin and LC15-0636(active metabolite of gemigliptim)
Time frame: up to 48h post-dose
t1/2
To evaluate t1/2 of gemigliptin, metformin and LC15-0636(active metabolite of gemigliptim)
Time frame: up to 48 h post-dose
Cmax
To evaluate Cmax of LC15-0636(active metabolite of gemigliptim)
Time frame: up to 48h post-dose
AUClast
To evaluate AUClast of LC15-0636(active metabolite of gemigliptim)
Time frame: up to 48h post-dose
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