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A Study to Characterize the Pharmacokinetics of DA-8031 in Healthy Male Subjects

Phase 1
Completed
Conditions
Premature Ejaculatory Dysfunction
Interventions
Drug: Placebo
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
GroupInterventionDescription
PlaceboPlacebo-
DA-8031DA-8031-
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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

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