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NCT00005991 · ClinicalTrials.gov registry record · Phase 2

Gemcitabine and Liposomal Doxorubicin in Treating Women With Metastatic Breast Cancer

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
76
Enrollment target

NCT00005991: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00005991 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 76 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00005991, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
76 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of gemcitabine and liposomal doxorubicin in treating women who have metastatic breast cancer.

Interventions

  • DRUG pegylated liposomal doxorubicin hydrochloride
  • DRUG gemcitabine hydrochloride

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 1997-08-25
Est. Completion 2003-02-14
Phase Phase 2

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT00005991

The ClinicalTrials.gov registry entry for NCT00005991 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which pegylated liposomal doxorubicin hydrochloride is the first listed.

NCT00005991 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00005991 about?

NCT00005991 is a clinical study titled "Gemcitabine and Liposomal Doxorubicin in Treating Women With Metastatic Breast Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of gemcitabine and liposomal doxorubicin in treating women who have meta...

What is the current status of trial NCT00005991?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 76 participants. The study started on 1997-08-25. Estimated completion is 2003-02-14.

What interventions are being tested in trial NCT00005991?

The interventions under investigation include: pegylated liposomal doxorubicin hydrochloride (DRUG), gemcitabine hydrochloride (DRUG).

Who is sponsoring clinical trial NCT00005991?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 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.