Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00072514 · ClinicalTrials.gov registry record · Phase 2

Gemcitabine Hydrochloride, Carboplatin, Dexamethasone, and Rituximab in Treating Patients With Previously Treated Lymphoid Malignancies

A Phase 2 study, sponsored by Fred Hutchinson Cancer Center.

Completed
Registry status
Phase 2
Development phase
55
Enrollment target

NCT00072514 is a Phase 2 study that has completed, run by Fred Hutchinson Cancer Center. The registered enrollment target is 55 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00072514, a Phase 2 study, has completed, sponsored by Fred Hutchinson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
55 participants
Enrollment target

Study Summary

This pilot phase II trial studies the side effects and how well giving gemcitabine hydrochloride, carboplatin, dexamethasone, and rituximab together works in treating patients with previously treated lymphoid malignancies. Drugs used in chemotherapy, such as gemcitabine hydrochloride, carboplatin, and dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving more than one drug (combination chemotherapy) and giving monoclonal antibody therapy with chemotherapy may kill more cancer cells

Interventions

  • DRUG carboplatin
  • BIOLOGICAL rituximab
  • DRUG dexamethasone
  • DRUG gemcitabine hydrochloride

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2003-08
Est. Completion 2013-11
Phase Phase 2

Sponsor

Fred Hutchinson Cancer Center

483 total trials

What the Registry Record Tells You About NCT00072514

The ClinicalTrials.gov registry entry for NCT00072514 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 55 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Fred Hutchinson Cancer Center, which has 483 total studies on file at ClinicalTrials.gov.

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

NCT00072514 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00072514 about?

NCT00072514 is a clinical study titled "Gemcitabine Hydrochloride, Carboplatin, Dexamethasone, and Rituximab in Treating Patients With Previously Treated Lymphoid Malignancies". This pilot phase II trial studies the side effects and how well giving gemcitabine hydrochloride, carboplatin, dexamethasone, and rituximab together works in treating patients with previously treated lymphoid malignancies. Drugs used in chemotherapy, such as gemcitabine hydrochloride, carboplatin, a...

What is the current status of trial NCT00072514?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 55 participants. The study started on 2003-08. Estimated completion is 2013-11.

What interventions are being tested in trial NCT00072514?

The interventions under investigation include: carboplatin (DRUG), rituximab (BIOLOGICAL), dexamethasone (DRUG), gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00072514?

This trial is sponsored by Fred Hutchinson Cancer Center, which has 483 total clinical trials registered on ClinicalTrials.gov.

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

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.