Efficacy and safety of MY-REPT capsule in primary, liver transplantation recipients
Open label, Multicenter, Non-comparative Study to evaluate the efficacy and safety of MY-REPT capsule in primary, liver transplantation
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
MY-REPT capsule 500\~1500mg/day, per oral, capsules twice a day with Tacrolimus, Corticosteroids, Basiliximab post liver transplantation
Asan medical center
Seoul, South Korea
RECRUITINGSamsung Medical Center
Seoul, South Korea
COMPLETEDSeoul ST Mary's Hospital
Seoul, South Korea
COMPLETEDRate of acute rejection
Rate acute rejection by liver biopsy
Time frame: up to 26weeks
Frequency, Time, Severity of acute rejection
Time frame: up to 26 weeks
Graft loss, Patient survival rate
Time frame: up to 26weeks
Kidney function test by e-GFR(Glomerular filtration rate)
Time frame: up to 26weeks
Questionnaire of gastrointestinal symptom assessment
Time frame: screening visit, closing visit
Questionnaire of gastrointestinal quality of life index
Time frame: screening visit, closing visit
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