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NCT00782379 · ClinicalTrials.gov registry record · Phase 2

Combination Chemotherapy, Donor Stem Cell Transplant, Tacrolimus, Mycophenolate Mofetil, and Cyclophosphamide in Treating Patients With Hematologic Cancer

A Phase 2 study, sponsored by Northside Hospital.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT00782379 is a Phase 2 study that has completed, run by Northside Hospital. The registered enrollment target is 20 participants.

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The verdict

NCT00782379, a Phase 2 study, has completed, sponsored by Northside Hospital.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

RATIONALE: Giving chemotherapy, such as fludarabine, busulfan, and cyclophosphamide, before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells and helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells. Giving high-dose cyclophosphamide together with tacrolimus and mycophenolate mofetil after transplant may stop this from happening. PURPOSE: This phase II trial is studying how well combination chemotherapy works when given together with a donor stem cell transplant, followed by tacrolimus, mycophenolate mofetil, and high-dose cyclophosphamide, in treating patients with high-risk hematologic cancer.

Interventions

  • DRUG cyclophosphamide
  • DRUG fludarabine phosphate
  • DRUG tacrolimus
  • DRUG busulfan
  • DRUG mycophenolate mofetil

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2008-10
Est. Completion 2012-04
Phase Phase 2

Sponsor

Northside Hospital

26 total trials

What the Registry Record Tells You About NCT00782379

The ClinicalTrials.gov registry entry for NCT00782379 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northside Hospital, which has 26 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which cyclophosphamide is the first listed.

NCT00782379 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00782379 about?

NCT00782379 is a clinical study titled "Combination Chemotherapy, Donor Stem Cell Transplant, Tacrolimus, Mycophenolate Mofetil, and Cyclophosphamide in Treating Patients With Hematologic Cancer". RATIONALE: Giving chemotherapy, such as fludarabine, busulfan, and cyclophosphamide, before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells and helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor a...

What is the current status of trial NCT00782379?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2008-10. Estimated completion is 2012-04.

What interventions are being tested in trial NCT00782379?

The interventions under investigation include: cyclophosphamide (DRUG), fludarabine phosphate (DRUG), tacrolimus (DRUG), busulfan (DRUG), mycophenolate mofetil (DRUG).

Who is sponsoring clinical trial NCT00782379?

This trial is sponsored by Northside Hospital, which has 26 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.