Pfizer Investigational Site
Tokyo, Japan
NCT Number: NCT01407016
The purpose of this study is to assess the safety, tolerability and pharmacokinetics of metronidazole following single and multiple intravenous infusion in healthy Japanese adult subjects.
Looking for future studies?
Notify Me20 year–55 year
All sexes
Interventional
Phase 1
Tokyo, Japan
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
On Day 1, subjects will receive a single dose of 500 mg metronidazole by intravenous infusion over 20 minutes. On Day 3 to Day 7, subjects will receive multiple doses of 500 mg metronidazole by intravenous infusion over 20 minutes 4 times a day (every 6 hours) for 5 days.
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: prior to Day 3 and Day 6-8 morning dose and 6 hours post morning dose on Day 8
Time frame: Day 8 to Day 9
Time frame: Day 8 to Day 9
Time frame: Day 8 to Day 9
Time frame: Day 8 to Day 9
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: Day 1 to Day 3
Time frame: prior to Day 3 and Day 6-8 morning dose and 6 hours post morning dose on Day 8
Time frame: Day 8 to Day 9
Time frame: Day 8 to Day 9
Time frame: Day 8 to Day 9
Looking for future studies?
Notify MePfizer
Industry
A Phase 1, Open Study To Assess The Safety, Tolerability And Pharmacokinetics Of Metronidazole Following Single And Multiple Intravenous Infusion In Healthy Japanese Adult Subjects
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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