Study To Evaluate The Effect Of Single Intravenous Doses Of Tigecycline On QTc Intervals In Healthy Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy
In brief
Administration of a single 50 mg or 200 mg dose of tigecycline will not cause a change in QT/QTc intervals.
Key facts
- Study ID
- NCT01287793
- Run by
- Pfizer
- People needed
- 48
- Starts
- 2011-01-01
- Expected to finish
- 2011-05-01
- Last updated by the study team
- 2011-05-24
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy
- Body mass index 17.5 - 30.5 kg
- Total body weight greater than 50 kg
You may not qualify if…
- Recent history of diarrhea
- Use of oral antibiotics in the last 2 weeks
- History of risk factors for QT prolongation pregnant females
- Nursing females
Where it is running
- Pfizer Investigational Site — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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