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NCT00205322 · ClinicalTrials.gov registry record · Phase 2
Oxaliplatin, 5-FU and Leucovorin in Combination With Oral Capecitabine for Metastatic Colorectal Cancer
A Phase 2 study, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- Phase 2
- Development phase
- 45
- Enrollment target
NCT00205322: Completed Phase 2 study, sponsored by University of Wisconsin, Madison.
NCT00205322 is a Phase 2 study that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 45 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00205322, a Phase 2 study, has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 45 participants
- Enrollment target
Study Summary
The combination of oxaliplatin, 5-FU, leucovorin, and capecitabine is hypothesized to retain and potentially improve upon the activity of the FOLFOX regimens. Additionally, the use of an oral rather than an infusional 5-fu regimen represents a clear advantage in terms of both patient convenience and lack of associated catheter-related complications.
Interventions
- DRUG chemotherapy (capecitabine, oxaliplatin, 5-FU, leucovorin)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2004-04 |
| Est. Completion | 2007-10 |
| Phase | Phase 2 |
What the finished NCT00205322 record still lists
NCT00205322 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% lower).
The record links to 0 conditions, and to 1 intervention - of which chemotherapy (capecitabine, oxaliplatin, 5-FU, leucovorin) is the first listed.
NCT00205322 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00205322 about?
NCT00205322 is a clinical study titled "Oxaliplatin, 5-FU and Leucovorin in Combination With Oral Capecitabine for Metastatic Colorectal Cancer". The combination of oxaliplatin, 5-FU, leucovorin, and capecitabine is hypothesized to retain and potentially improve upon the activity of the FOLFOX regimens. Additionally, the use of an oral rather than an infusional 5-fu regimen represents a clear advantage in terms of both patient convenience and...
What is the current status of trial NCT00205322?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 45 participants. The study started on 2004-04. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00205322?
The interventions under investigation include: chemotherapy (capecitabine, oxaliplatin, 5-FU, leucovorin) (DRUG).
Who is sponsoring clinical trial NCT00205322?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00205322's enrollment target sits among peer trials
45 1296th of 2000 higher than 679 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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