Title

A Study to Compare the Pharmacokinetic Profiles of DW224aa and DW224a
Clinical Trial to Compare the Pharmacokinetic Profiles of DW224aa (Aspartate) Tablet and DW224a (Hydrochloride) Capsule After a Single Oral Administration in Healthy Male Volunteers
  • Phase

    Phase 1
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    zabofloxacin ...
  • Study Participants

    32
The purpose of this study is to compare and explore pharmacokinetics of zabofloxacin, the main component of DW224aa(Test drug) and DW224a(Reference drug).
Study Started
Apr 30
2011
Primary Completion
May 31
2011
Last Update
Jul 18
2011
Estimate

Drug Experimental DW224aa

DW224aa tablet, single dose

Drug Experimental DW224a

DW224a capsule, single dose

DW224aa Experimental

DW224aa given by oral administration

DW224a Active Comparator

DW224aa given by oral administration

Criteria

Inclusion Criteria:

a healthy adult male within the range of 20 to 45 years old at the time of screening

one with weight of more than 55kg, in the range of IBW 20%

IBW(kg)={height(cm)-100}*0.9
one who understood completely about this study after the detailed explanation is given, decided to volunteer and gave written informed consent to participate in study in compliance with the requirement of the entire protocol.

Exclusion Criteria:

one with clinically significant disease in liver, kidney, nerve system, respiratory system, endocrine system, blood, tumor, urinary system, cardiovascular system, mental disease or with medical history
one with gastrointestinal disease or with gastrointestinal surgical history which can affect the absorption of the investigational drug.
one who is allergic or has clinically significant allergic history to the quinolone antibiotics, or to other drugs(Aspirin, antibiotics, etc)
one who shows the following result in clinical laboratory test: AST,ALT>1.25 times of the upper limit of normal range
one who has confirmed positive at serological tests (HBs antigen, HCV antibody and HIV antibody)
one who has drug abuse history or positive result at urine screening tests (cannabinoid, opioid, amphetamine, cocaine, barbiturate, benzodiazepine)
one who has taken any prescribed drugs, herbal agents or crude drugs within 2 weeks before study drug administration, or who has taken any over-the-counter (OTC) drugs or vitamins (Investigators will determine his eligibility by considering the effect of the drug on his safety or pharmacokinetic results in case other inclusion/exclusion criteria is satisfied.)
one who has participated in other clinical study within 2 months before study drug administration
one who donated whole blood within 2 months or component blood within 1 month or who are donated within 1 month before the treatment
one who drank Over 21 units/week of alcohol or subjects who would not be able to stop drinking alcohol during the hospitalization
one who are Heavy smoker more than 10 cigarettes/day within 3 months prior to screening or subjects who would not be able to stop smoking during the hospitalization
one who had a beverage containing caffeine, drank alcohol, or smoked within 48hrs before the hospitalization or who had a beverage containing grapefruits during the hospitalization
one with clinically significant observations considered as unsuitable based on medical judgment by investigators
No Results Posted