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NCT00394173 · ClinicalTrials.gov registry record · Phase 2
Efficacy, Safety and Tolerability of DNK333 (25 mg Bid) in Women With Diarrhea-predominant Irritable Bowel Syndrome (IBS-D)
A Phase 2 study, sponsored by Novartis.
- Completed
- Registry status
- Phase 2
- Development phase
- 180
- Enrollment target
NCT00394173: Completed Phase 2 study, sponsored by Novartis.
NCT00394173 is a Phase 2 study that has completed, run by Novartis. The registered enrollment target is 180 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (35% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00394173, a Phase 2 study, has completed, sponsored by Novartis.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 180 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the efficacy of DNK333 compared to placebo for relieving symptoms of IBS-D in female patients.
Interventions
- DRUG Placebo
- DRUG DNK333
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2006-09 |
| Est. Completion | 2007-10 |
| Phase | Phase 2 |
What the finished NCT00394173 record still lists
NCT00394173 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (35% higher).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00394173 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00394173 about?
NCT00394173 is a clinical study titled "Efficacy, Safety and Tolerability of DNK333 (25 mg Bid) in Women With Diarrhea-predominant Irritable Bowel Syndrome (IBS-D)". The purpose of this study is to evaluate the efficacy of DNK333 compared to placebo for relieving symptoms of IBS-D in female patients.
What is the current status of trial NCT00394173?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 180 participants. The study started on 2006-09. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00394173?
The interventions under investigation include: Placebo (DRUG), DNK333 (DRUG).
Who is sponsoring clinical trial NCT00394173?
This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00394173's enrollment target sits among peer trials
180 365th of 2000 higher than 1,610 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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