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NCT00417209 · ClinicalTrials.gov registry record · Phase 3

Larotaxel Compared To Continuous Administration of 5-FU in Advanced Pancreatic Cancer Patients Previously Treated With A Gemcitabine-Containing Regimen

A Phase 3 study, sponsored by Sanofi.

Completed
Registry status
Phase 3
Development phase
408
Enrollment target

NCT00417209: Completed Phase 3 study, sponsored by Sanofi.

NCT00417209 is a Phase 3 study that has completed, run by Sanofi. The registered enrollment target is 408 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00417209, a Phase 3 study, has completed, sponsored by Sanofi.

COMPLETED
Registry status
Phase 3
Development phase
408 participants
Enrollment target

Study Summary

The purpose of this study is to compare the efficacy and the safety Larotaxel administered as single agent every 3 weeks to continuous administration of 5-FU every 3 weeks, in patients with advanced pancreatic cancer (non operable in a curative intent, locally recurrent or metastatic) previously treated with gemcitabine based therapy.

Interventions

  • DRUG Capecitabine
  • DRUG 5-Fluorouracil
  • DRUG Larotaxel (XRP9881)

Trial Details

FieldValue
Enrollment Target 408 participants
Start Date 2006-12
Est. Completion 2009-11
Phase Phase 3
Sanofi

713 total trials

What the finished NCT00417209 record still lists

NCT00417209 is an interventional study that assigns participants to a tested intervention. The registered 408 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (47% lower).

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

NCT00417209 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00417209 about?

NCT00417209 is a clinical study titled "Larotaxel Compared To Continuous Administration of 5-FU in Advanced Pancreatic Cancer Patients Previously Treated With A Gemcitabine-Containing Regimen". The purpose of this study is to compare the efficacy and the safety Larotaxel administered as single agent every 3 weeks to continuous administration of 5-FU every 3 weeks, in patients with advanced pancreatic cancer (non operable in a curative intent, locally recurrent or metastatic) previously tre...

What is the current status of trial NCT00417209?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 408 participants. The study started on 2006-12. Estimated completion is 2009-11.

What interventions are being tested in trial NCT00417209?

The interventions under investigation include: Capecitabine (DRUG), 5-Fluorouracil (DRUG), Larotaxel (XRP9881) (DRUG).

Who is sponsoring clinical trial NCT00417209?

This trial is sponsored by Sanofi, which has 713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00417209's enrollment target sits among peer trials

408 911th of 2000 higher than 1,088 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00417209, the US trial registry maintained by the National Library of Medicine. NCT00417209 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.