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NCT00354172 · ClinicalTrials.gov registry record · Phase 2

Donor Umbilical Cord Blood Natural Killer Cells, Aldesleukin and Umbilical Cord Blood Transplant in Patients With Refractory Hematologic Cancers.

A Phase 2 study, sponsored by Masonic Cancer Center, University of Minnesota.

Terminated
Registry status
Phase 2
Development phase
16
Enrollment target

NCT00354172 is a Phase 2 study that was terminated before completion, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 16 participants.

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The verdict

NCT00354172, a Phase 2 study, was terminated before completion, sponsored by Masonic Cancer Center, University of Minnesota.

TERMINATED
Registry status
Phase 2
Development phase
16 participants
Enrollment target

Study Summary

RATIONALE: Giving chemotherapy, natural killer cells, aldesleukin, and total-body irradiation before a donor umbilical cord blood stem cell transplant helps stop the growth of abnormal cells and cancer cells. It also 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 cyclosporine, mycophenolate mofetil, and methylprednisolone before and after transplant may stop this from happening. PURPOSE: This clinical trial is studying how well giving fludarabine and cyclophosphamide together with total-body irradiation followed by donor umbilical cord blood natural killer cells, aldesleukin, and umbilical cord blood transplant works in treating patients with refractory hematologic cancer or other diseases.

Interventions

  • DRUG cyclophosphamide
  • BIOLOGICAL aldesleukin
  • BIOLOGICAL filgrastim
  • DRUG cyclosporine
  • BIOLOGICAL natural killer cell (NK) therapy

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2006-02
Est. Completion 2008-08
Phase Phase 2

What the Registry Record Tells You About NCT00354172

The ClinicalTrials.gov registry entry for NCT00354172 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 16 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.

NCT00354172 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00354172 about?

NCT00354172 is a clinical study titled "Donor Umbilical Cord Blood Natural Killer Cells, Aldesleukin and Umbilical Cord Blood Transplant in Patients With Refractory Hematologic Cancers.". RATIONALE: Giving chemotherapy, natural killer cells, aldesleukin, and total-body irradiation before a donor umbilical cord blood stem cell transplant helps stop the growth of abnormal cells and cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. When ...

What is the current status of trial NCT00354172?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 16 participants. The study started on 2006-02. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00354172?

The interventions under investigation include: cyclophosphamide (DRUG), aldesleukin (BIOLOGICAL), filgrastim (BIOLOGICAL), cyclosporine (DRUG), natural killer cell (NK) therapy (BIOLOGICAL).

Who is sponsoring clinical trial NCT00354172?

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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