A Phase 1 Study to Evaluate the Safety and Pharmacodynamic/Pharmacokinetic Characteristics of HIP2101 in Healthy Volunteers
A Randomized, Open-label, Multiple-dose, Crossover Phase 1 Clinical Trial to Evaluate the Safety and Pharmacodynamic/Pharmacokinetic Characteristics after Oral Administration of HIP2101 in Healthy Adult Volunteers
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
32
Chungbuk University Hospital
Cheongju-si, South Korea
Duration time with integrated gastric pH>4 / 24hr
Time frame: 0-24hours
Median 24 hr gastric pH
Time frame: 0-24hours
Percent decrease from baseline in integrated gastric acidity for 24-hour interval after dose
Time frame: 0-24hours
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