The purpose of this study is to evaluate safety, tolerability, pharmacokinetics and pharmacodynamics of orally administrated DWP05195 in healthy male volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
80
tablets, oral administration, single and multiple administrations
Seoul National University Hospital
Seoul, South Korea
Assessment of Safety & tolerability: Adverse events, vital signs, 12-Lead ECG, laboratory safety variables and physical examination
Time frame: 72hr after drug administration
Pharmacokinetics: Cmax, tmax, AUC, and t½ in plasma / amount of drug, fraction, and CLr in urine Pharmacodynamics: Thermal NeuroSensory Analyser
Time frame: 72 hr after drug administration
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.