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NCT00084773 · ClinicalTrials.gov registry record · NA

Neoadjuvant Cetuximab, Fluorouracil, and Pelvic Irradiation in Treating Patients With Locally Advanced or Locally Recurrent Rectal Cancer

A NA study, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
NA
Development phase
28
Enrollment target

NCT00084773: Completed NA study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT00084773 is a NA study that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 28 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00084773, a NA study, has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
NA
Development phase
28 participants
Enrollment target

Study Summary

RATIONALE: Monoclonal antibodies such as cetuximab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy such as fluorouracil work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Giving cetuximab with fluorouracil and radiation therapy may kill more tumor cells.

Interventions

  • DRUG fluorouracil
  • BIOLOGICAL cetuximab
  • RADIATION radiation therapy
  • PROCEDURE neoadjuvant therapy

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2004-03
Est. Completion 2010-03
Phase NA

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT00084773

The ClinicalTrials.gov registry entry for NCT00084773 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

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

NCT00084773 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00084773 about?

NCT00084773 is a clinical study titled "Neoadjuvant Cetuximab, Fluorouracil, and Pelvic Irradiation in Treating Patients With Locally Advanced or Locally Recurrent Rectal Cancer". RATIONALE: Monoclonal antibodies such as cetuximab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy such as fluorouracil work in different ways to stop tumor cells from dividing so they stop growing or di...

What is the current status of trial NCT00084773?

This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2004-03. Estimated completion is 2010-03.

What interventions are being tested in trial NCT00084773?

The interventions under investigation include: fluorouracil (DRUG), cetuximab (BIOLOGICAL), radiation therapy (RADIATION), neoadjuvant therapy (PROCEDURE).

Who is sponsoring clinical trial NCT00084773?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 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, the data changelog, or report a data error.