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Clinical trial

An Open-Label, Dose Escalating Study to Evaluate the Safety of Intravaginal Oxybutynin in Subjects With Urge Urinary Incontinence

NCT00749632 is registered in ClinicalTrials.gov with FemmePharma Global Healthcare, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
An Open-Label, Dose Escalating Study to Evaluate the Safety of Intravaginal Oxybutynin in Subjects With Urge Urinary Incontinence
Lead sponsor
FemmePharma Global Healthcare, Inc.
Phase
Phase 2
Overall status
Completed
Start date
July 31, 2007
Completion date
October 31, 2008
Enrollment
45 (actual)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.