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NCT00290641 · ClinicalTrials.gov registry record · NA

Chemotherapy and Total-Body Irradiation Followed by Donor Umbilical Cord Blood Transplant, Cyclosporine, and Mycophenolate Mofetil in Treating Patients With Hematologic Cancer

A NA study, sponsored by Masonic Cancer Center, University of Minnesota.

Completed
Registry status
NA
Development phase
68
Enrollment target

NCT00290641 is a NA study that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 68 participants.

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The verdict

NCT00290641, a NA study, has completed, sponsored by Masonic Cancer Center, University of Minnesota.

COMPLETED
Registry status
NA
Development phase
68 participants
Enrollment target

Study Summary

RATIONALE: Giving low doses of chemotherapy, such as cyclophosphamide and fludarabine, and radiation therapy before a donor umbilical cord blood stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune system and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after the transplant may stop this from happening. PURPOSE: This clinical trial is studying how well giving chemotherapy together with total-body irradiation followed by donor umbilical cord blood transplant, cyclosporine, and mycophenolate mofetil works in treating patients with hematologic cancer.

Interventions

  • DRUG cyclophosphamide
  • DRUG fludarabine phosphate
  • BIOLOGICAL filgrastim
  • DRUG cyclosporine
  • BIOLOGICAL graft-versus-tumor induction therapy

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2001-04
Est. Completion 2006-01
Phase NA

What the Registry Record Tells You About NCT00290641

The ClinicalTrials.gov registry entry for NCT00290641 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.

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

NCT00290641 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00290641 about?

NCT00290641 is a clinical study titled "Chemotherapy and Total-Body Irradiation Followed by Donor Umbilical Cord Blood Transplant, Cyclosporine, and Mycophenolate Mofetil in Treating Patients With Hematologic Cancer". RATIONALE: Giving low doses of chemotherapy, such as cyclophosphamide and fludarabine, and radiation therapy before a donor umbilical cord blood stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated st...

What is the current status of trial NCT00290641?

This trial is currently completed. It is a NA study. The enrollment target is 68 participants. The study started on 2001-04. Estimated completion is 2006-01.

What interventions are being tested in trial NCT00290641?

The interventions under investigation include: cyclophosphamide (DRUG), fludarabine phosphate (DRUG), filgrastim (BIOLOGICAL), cyclosporine (DRUG), graft-versus-tumor induction therapy (BIOLOGICAL).

Who is sponsoring clinical trial NCT00290641?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

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

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