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NCT00454740 · ClinicalTrials.gov registry record · Phase 3
Efficacy & Safety Study of VESIcare® (Solifenacin Succinate) in Patients Wishing to Switch From Detrol LA® for Treatment of Overactive Bladder
A Phase 3 study, sponsored by Astellas Pharma.
- Completed
- Registry status
- Phase 3
- Development phase
- 441
- Enrollment target
NCT00454740: Completed Phase 3 study, sponsored by Astellas Pharma.
NCT00454740 is a Phase 3 study that has completed, run by Astellas Pharma. The registered enrollment target is 441 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (43% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00454740, a Phase 3 study, has completed, sponsored by Astellas Pharma.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 441 participants
- Enrollment target
Study Summary
To evaluate the efficacy of 5 and10mg solifenacin succinate in patients with urgency who have OAB syndrome (urgency, with or without urge incontinence, usually with frequency and nocturia) and wish to switch from tolterodine tartrate extended release to solifenacin succinate due to lack of sufficient improvement in urgency episodes
Interventions
- DRUG solifenacin succinate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 441 participants |
| Start Date | 2004-06 |
| Est. Completion | 2005-08 |
| Phase | Phase 3 |
What the finished NCT00454740 record still lists
NCT00454740 is an interventional study that assigns participants to a tested intervention. The registered 441 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (43% lower).
The record links to 0 conditions, and to 1 intervention - of which solifenacin succinate is the first listed.
NCT00454740 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00454740 about?
NCT00454740 is a clinical study titled "Efficacy & Safety Study of VESIcare® (Solifenacin Succinate) in Patients Wishing to Switch From Detrol LA® for Treatment of Overactive Bladder". To evaluate the efficacy of 5 and10mg solifenacin succinate in patients with urgency who have OAB syndrome (urgency, with or without urge incontinence, usually with frequency and nocturia) and wish to switch from tolterodine tartrate extended release to solifenacin succinate due to lack of sufficien...
What is the current status of trial NCT00454740?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 441 participants. The study started on 2004-06. Estimated completion is 2005-08.
What interventions are being tested in trial NCT00454740?
The interventions under investigation include: solifenacin succinate (DRUG).
Who is sponsoring clinical trial NCT00454740?
This trial is sponsored by Astellas Pharma, which has 165 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00454740's enrollment target sits among peer trials
441 867th of 2000 higher than 1,134 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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