The Effect Of Fluconazole On Pharmacokinetics Of Fesoterodine In Healthy Subjects
Completed · Phase 1
Conditions studied: Overactive Bladder With Symptoms of Frequency, Urgency, and Urge Urinary Incontinence
In brief
This study is designed to estimate the effect of fluconazole (200 mg BID for 2 days), a moderate CYP3A4 inhibitor on the pharmacokinetics of a single 8 mg oral dose of fesoterodine in healthy adult subjects.
Key facts
- Study ID
- NCT00911235
- Run by
- Pfizer
- People needed
- 28
- Starts
- 2009-05-01
- Expected to finish
- 2009-07-01
- Last updated by the study team
- 2011-06-01
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy subjects between the ages of 18 and 55 years
You may not qualify if…
- Not healthy subjects. subjects with acute or chronic medical or psychiatric condition or laboratory abnormality
Where it is running
- Pfizer Investigational Site — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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