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NCT01046864 · ClinicalTrials.gov registry record · Phase 1

Combination of Brivanib With 5-Fluorouracil/Leucovorin (5FU/LV) and 5-Fluorouracil/Leucovorin/Irinotecan (FOLFIRI)

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
49
Enrollment target

NCT01046864: Completed Phase 1 study, sponsored by Bristol-Myers Squibb.

NCT01046864 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 49 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01046864, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

The purpose of this study is to determine a safe and maximum tolerable dose of Brivanib when combined with standard dose 5FU/LV and FOLFIRI.

Interventions

  • DRUG Leucovorin
  • DRUG Irinotecan
  • DRUG 5-FU
  • DRUG Brivanib

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2010-02
Est. Completion 2014-06
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT01046864 record still lists

NCT01046864 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 49 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (18% lower).

The record links to 0 conditions, and to 4 interventions - of which Leucovorin is the first listed.

NCT01046864 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01046864 about?

NCT01046864 is a clinical study titled "Combination of Brivanib With 5-Fluorouracil/Leucovorin (5FU/LV) and 5-Fluorouracil/Leucovorin/Irinotecan (FOLFIRI)". The purpose of this study is to determine a safe and maximum tolerable dose of Brivanib when combined with standard dose 5FU/LV and FOLFIRI.

What is the current status of trial NCT01046864?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2010-02. Estimated completion is 2014-06.

What interventions are being tested in trial NCT01046864?

The interventions under investigation include: Leucovorin (DRUG), Irinotecan (DRUG), 5-FU (DRUG), Brivanib (DRUG).

Who is sponsoring clinical trial NCT01046864?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01046864's enrollment target sits among peer trials

49 1017th of 2000 higher than 976 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 NCT01046864, the US trial registry maintained by the National Library of Medicine. NCT01046864 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.