A Study to Characterize the Pharmacokinetics of DA-8031 in Healthy Male Subjects
- Registration Number
- NCT01104948
- Lead Sponsor
- Dong-A Pharmaceutical Co., Ltd.
- Brief Summary
This is a dose block-randomized, double-blind, placebo-controlled, single/multiple dosing, dose-escalation study. The study is designed to describe the relationship between multiple doses and pharmacokinetic parameters of DA-8031 as well as safety profile.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 106
Inclusion Criteria
- 20-45 years healthy male subjects
- Body weight :60-90kg, BMI between 18.5-25
Exclusion Criteria
- show SBP(Systolic Blood Pressure) =<100mmHg or >=140mmHg, or DBP(Diastolic Blood Pressure)=<60mmHg or >=90mmHg, or tachycardia (PR(Pulse Rate)>=100times/min)
- have a history of drug abuse or show positive for drug abuse or cotinine at urine screening
- smokers
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Placebo - DA-8031 DA-8031 -
- Primary Outcome Measures
Name Time Method To characterize the pharmacokinetic parameters such as AUC(Area under concentration-time curve), Cmax, Tmax, T1/2, fe, and CL/F of DA-8031 by as assessment of plasma and urine concentration
- Secondary Outcome Measures
Name Time Method To evaluate the safety and tolerance of DA-8031 by assessment of vital signs, clinical laboratory tests, physical examinations, ECG findings, and adverse events collected by investigator questionnaire and subjects spontaneous report
Trial Locations
- Locations (1)
Clinical Research Institute, Seoul National University Hospital
🇰🇷Seoul, Chongno-Gu, Yon-Gon Dong 28, Korea, Republic of