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NCT00602329 · ClinicalTrials.gov registry record · Phase 2

MRI in Predicting Response in Patients Receiving Combination Chemotherapy and Bevacizumab For Advanced or Metastatic Colorectal Cancer

A Phase 2 study, sponsored by Abramson Cancer Center at Penn Medicine.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT00602329 is a Phase 2 study that was terminated before completion, run by Abramson Cancer Center at Penn Medicine. The registered enrollment target is 5 participants.

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The verdict

NCT00602329, a Phase 2 study, was terminated before completion, sponsored by Abramson Cancer Center at Penn Medicine.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as fluorouracil, leucovorin, and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving bevacizumab together with combination chemotherapy may kill more tumor cells. Diagnostic procedures, such as MRI, may help doctors predict a patient's response to treatment and help plan the best treatment. PURPOSE: This randomized phase II trial is studying how well MRI works in predicting response to combination chemotherapy given together with bevacizumab in treating patients with advanced or metastatic colorectal cancer.

Interventions

  • DRUG oxaliplatin
  • DRUG fluorouracil
  • DRUG leucovorin calcium
  • BIOLOGICAL bevacizumab

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2006-02
Est. Completion 2009-10
Phase Phase 2

What the Registry Record Tells You About NCT00602329

The ClinicalTrials.gov registry entry for NCT00602329 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abramson Cancer Center at Penn Medicine, which has 402 total studies on file at ClinicalTrials.gov.

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

NCT00602329 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00602329 about?

NCT00602329 is a clinical study titled "MRI in Predicting Response in Patients Receiving Combination Chemotherapy and Bevacizumab For Advanced or Metastatic Colorectal Cancer". RATIONALE: Drugs used in chemotherapy, such as fluorouracil, leucovorin, and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Som...

What is the current status of trial NCT00602329?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2006-02. Estimated completion is 2009-10.

What interventions are being tested in trial NCT00602329?

The interventions under investigation include: oxaliplatin (DRUG), fluorouracil (DRUG), leucovorin calcium (DRUG), bevacizumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00602329?

This trial is sponsored by Abramson Cancer Center at Penn Medicine, which has 402 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.