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NCT00215982 · ClinicalTrials.gov registry record · Phase 2

Study of Capecitabine With Irinotecan and Oxaliplatin (Eloxatin) in Advanced Colorectal Cancer

A Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

Completed
Registry status
Phase 2
Development phase
24
Enrollment target

NCT00215982: Completed Phase 2 study, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

NCT00215982 is a Phase 2 study that has completed, run by H. Lee Moffitt Cancer Center and Research Institute. The registered enrollment target is 24 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00215982, a Phase 2 study, has completed, sponsored by H. Lee Moffitt Cancer Center and Research Institute.

COMPLETED
Registry status
Phase 2
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to find out how effective the new combination of the drugs Capecitabine (Xeloda), Oxaliplatin (Eloxatin), and Irinotecan (Camptosar) are against colon and rectal cancer. All three of these drugs are approved by the Food and Drug Administration (FDA) for the treatment of colon or rectal cancer. This however is the first time that these three drugs have been combined in this schedule for the treatment of colon/rectal cancer.

Primary Outcome

To determine the radiographic response rate in patients with metastatic colorectal cancer treated with Oxaliplatin, Capecitabine and Irinotecan

Interventions

  • DRUG Oxaliplatin
  • DRUG Irinotecan
  • DRUG capecitabine

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2004-12
Est. Completion 2007-07
Phase Phase 2

What the finished NCT00215982 record still lists

NCT00215982 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 3 interventions - of which Oxaliplatin is the first listed.

NCT00215982 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00215982 about?

NCT00215982 is a clinical study titled "Study of Capecitabine With Irinotecan and Oxaliplatin (Eloxatin) in Advanced Colorectal Cancer". The purpose of this study is to find out how effective the new combination of the drugs Capecitabine (Xeloda), Oxaliplatin (Eloxatin), and Irinotecan (Camptosar) are against colon and rectal cancer. All three of these drugs are approved by the Food and Drug Administration (FDA) for the treatment of ...

What is the current status of trial NCT00215982?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 24 participants. The study started on 2004-12. Estimated completion is 2007-07.

What interventions are being tested in trial NCT00215982?

The interventions under investigation include: Oxaliplatin (DRUG), Irinotecan (DRUG), capecitabine (DRUG).

Who is sponsoring clinical trial NCT00215982?

This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00215982's enrollment target sits among peer trials

24 1756th of 2000 higher than 217 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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Source: ClinicalTrials.gov NCT00215982, the US trial registry maintained by the National Library of Medicine. NCT00215982 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.