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NCT00695201 · ClinicalTrials.gov registry record · Phase 1

Hepatic Arterial Infusion With Floxuridine and Dexamethasone in Combination With Intravenous Oxaliplatin Plus Irinotecan in Patients With Unresectable Hepatic Metastases From Colorectal Cancer

A Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
Phase 1
Development phase
52
Enrollment target

NCT00695201: Completed Phase 1 study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00695201 is a Phase 1 study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 52 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00695201, a Phase 1 study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
52 participants
Enrollment target

Study Summary

The purpose of this study is to see how well patients tolerate the side effects of treatment with Floxuridine, Oxaliplatin and Irinotecan. We also want to know if these methods used together are a useful way of treating cancer. We have studied these drugs and know the best doses of each when they are used alone. We do not yet know how well the drugs work with each other. This study will tell us the best doses of each drug when they are given over the same period of time.

Interventions

  • DRUG Floxuridine, Oxaliplatin, CPT-11

Trial Details

FieldValue
Enrollment Target 52 participants
Start Date 2000-08
Est. Completion 2021-06-28
Phase Phase 1
Memorial Sloan Kettering Cancer Center

1,884 total trials

What the finished NCT00695201 record still lists

NCT00695201 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (13% lower).

The record links to 0 conditions, and to 1 intervention - of which Floxuridine, Oxaliplatin, CPT-11 is the first listed.

NCT00695201 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00695201 about?

NCT00695201 is a clinical study titled "Hepatic Arterial Infusion With Floxuridine and Dexamethasone in Combination With Intravenous Oxaliplatin Plus Irinotecan in Patients With Unresectable Hepatic Metastases From Colorectal Cancer". The purpose of this study is to see how well patients tolerate the side effects of treatment with Floxuridine, Oxaliplatin and Irinotecan. We also want to know if these methods used together are a useful way of treating cancer. We have studied these drugs and know the best doses of each when they ar...

What is the current status of trial NCT00695201?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 52 participants. The study started on 2000-08. Estimated completion is 2021-06-28.

What interventions are being tested in trial NCT00695201?

The interventions under investigation include: Floxuridine, Oxaliplatin, CPT-11 (DRUG).

Who is sponsoring clinical trial NCT00695201?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00695201's enrollment target sits among peer trials

52 956th of 2000 higher than 1,032 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 NCT00695201, the US trial registry maintained by the National Library of Medicine. NCT00695201 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.