Clinical trial

Study to Compare the Safety and Efficacy of Solifenacin With Oxybutynin for the…

NCT00431041 · Astellas Pharma Inc, Industry · Completed

Key facts

NCT number NCT00431041
Title Study to Compare the Safety and Efficacy of Solifenacin With Oxybutynin for the Treatment of Overactive Bladder (VECTOR)
Official title VECTOR: A Randomized Double-blind Study to Assess the Safety and Efficacy of Solifenacin (Vesicare®) in Comparison to Oxybutynin for Overactive Bladder Patients
Acronym VECTOR
Lead sponsor Astellas Pharma Inc, Industry
Collaborators Astellas Pharma Canada, Inc. Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Overactive Bladder
Intervention type Drug
Interventions solifenacin, oxybutynin immediate release
Enrollment 132
Start date Dec 1, 2006
Primary completion Feb 1, 2008
Completion Feb 1, 2008
First posted Feb 2, 2007
Last update posted Jun 8, 2010
Countries Canada

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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