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NCT00725062 · ClinicalTrials.gov registry record · Phase 1

Donor T Cells in Treating Patients With High-Risk Hematologic Cancer Undergoing Donor Peripheral Blood Stem Cell Transplant

A Phase 1 study, sponsored by Masonic Cancer Center, University of Minnesota.

Terminated
Registry status
Phase 1
Development phase
3
Enrollment target

NCT00725062 is a Phase 1 study that was terminated before completion, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 3 participants.

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The verdict

NCT00725062, a Phase 1 study, was terminated before completion, sponsored by Masonic Cancer Center, University of Minnesota.

TERMINATED
Registry status
Phase 1
Development phase
3 participants
Enrollment target

Study Summary

RATIONALE: A donor peripheral stem cell transplant helps stop the growth of cancer 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. Once the donated stem cells begin working, the patient's immune system may see the remaining cancer cells as not belonging in the patient's body and destroy them. Giving an infusion of donor T cells may helps stop the patient's immune system from rejecting the donor's stem cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of donor T cells in treating patients with high-risk hematologic cancer who are undergoing donor peripheral blood stem cell transplant. Note: Only Phase I portion of study was performed. Due to slow accrual, study was closed before Phase II portion of study.

Interventions

  • PROCEDURE allogeneic hematopoietic stem cell transplantation
  • BIOLOGICAL CD4+CD25+ regulatory T cells

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2008-06
Est. Completion 2010-04
Phase Phase 1

What the Registry Record Tells You About NCT00725062

The ClinicalTrials.gov registry entry for NCT00725062 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 3 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 2 interventions - of which allogeneic hematopoietic stem cell transplantation is the first listed.

NCT00725062 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00725062 about?

NCT00725062 is a clinical study titled "Donor T Cells in Treating Patients With High-Risk Hematologic Cancer Undergoing Donor Peripheral Blood Stem Cell Transplant". RATIONALE: A donor peripheral stem cell transplant helps stop the growth of cancer 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. Once the donated stem cells begi...

What is the current status of trial NCT00725062?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 3 participants. The study started on 2008-06. Estimated completion is 2010-04.

What interventions are being tested in trial NCT00725062?

The interventions under investigation include: allogeneic hematopoietic stem cell transplantation (PROCEDURE), CD4+CD25+ regulatory T cells (BIOLOGICAL).

Who is sponsoring clinical trial NCT00725062?

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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