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NCT00207129 · ClinicalTrials.gov registry record · Phase 1

Effect of Capecitabine on the Pharmacokinetics of BMS-247550 and BMS-247550 on the Pharmacokinetics of Capecitabine and Its Metabolites in Patients With Advanced Malignancies

A Phase 1 study, sponsored by R-Pharm.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00207129: Completed Phase 1 study, sponsored by R-Pharm.

NCT00207129 is a Phase 1 study that has completed, run by R-Pharm. The registered enrollment target is 25 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00207129, a Phase 1 study, has completed, sponsored by R-Pharm.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

The purpose of this study is to test how BMS-247550 (ixabepilone) affects the removal of capecitabine from the body and how capecitabine affects the removal of BMS-247550 from the body.

Interventions

  • DRUG Capecitabine
  • DRUG Ixabepilone

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2004-10
Est. Completion 2005-12
Phase Phase 1
R-Pharm

19 total trials

What the finished NCT00207129 record still lists

NCT00207129 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 2 interventions - of which Capecitabine is the first listed.

NCT00207129 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00207129 about?

NCT00207129 is a clinical study titled "Effect of Capecitabine on the Pharmacokinetics of BMS-247550 and BMS-247550 on the Pharmacokinetics of Capecitabine and Its Metabolites in Patients With Advanced Malignancies". The purpose of this study is to test how BMS-247550 (ixabepilone) affects the removal of capecitabine from the body and how capecitabine affects the removal of BMS-247550 from the body.

What is the current status of trial NCT00207129?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2004-10. Estimated completion is 2005-12.

What interventions are being tested in trial NCT00207129?

The interventions under investigation include: Capecitabine (DRUG), Ixabepilone (DRUG).

Who is sponsoring clinical trial NCT00207129?

This trial is sponsored by R-Pharm, which has 19 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00207129's enrollment target sits among peer trials

25 1495th of 2000 higher than 481 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00207129, the US trial registry maintained by the National Library of Medicine. NCT00207129 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.