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NCT00121186 · ClinicalTrials.gov registry record · Phase 2

S0501 Fludarabine, Melphalan, and Donor Stem Cell Transplant Followed By Tacrolimus and Methotrexate in Treating Patients for Relapsed Lymphoma

A Phase 2 study, sponsored by SWOG Cancer Research Network.

Terminated
Registry status
Phase 2
Development phase
1
Enrollment target

NCT00121186 is a Phase 2 study that was terminated before completion, run by SWOG Cancer Research Network. The registered enrollment target is 1 participants.

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The verdict

NCT00121186, a Phase 2 study, was terminated before completion, sponsored by SWOG Cancer Research Network.

TERMINATED
Registry status
Phase 2
Development phase
1 participants
Enrollment target

Study Summary

RATIONALE: Giving low doses of chemotherapy, such as fludarabine and melphalan, before a donor bone marrow or peripheral 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 tacrolimus and methotrexate after transplant may stop this from happening. PURPOSE: This phase II trial is studying how well giving fludarabine together with melphalan followed by tacrolimus and methotrexate works in treating patients who are undergoing a donor stem cell transplant for relapsed lymphoma.

Interventions

  • DRUG fludarabine phosphate
  • DRUG tacrolimus
  • DRUG melphalan
  • DRUG methotrexate
  • PROCEDURE allogeneic bone marrow transplantation

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2005-07
Est. Completion 2011-12
Phase Phase 2

Sponsor

SWOG Cancer Research Network

270 total trials

What the Registry Record Tells You About NCT00121186

The ClinicalTrials.gov registry entry for NCT00121186 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SWOG Cancer Research Network, which has 270 total studies on file at ClinicalTrials.gov.

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

NCT00121186 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00121186 about?

NCT00121186 is a clinical study titled "S0501 Fludarabine, Melphalan, and Donor Stem Cell Transplant Followed By Tacrolimus and Methotrexate in Treating Patients for Relapsed Lymphoma". RATIONALE: Giving low doses of chemotherapy, such as fludarabine and melphalan, before a donor bone marrow or peripheral 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 repla...

What is the current status of trial NCT00121186?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 1 participants. The study started on 2005-07. Estimated completion is 2011-12.

What interventions are being tested in trial NCT00121186?

The interventions under investigation include: fludarabine phosphate (DRUG), tacrolimus (DRUG), melphalan (DRUG), methotrexate (DRUG), allogeneic bone marrow transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT00121186?

This trial is sponsored by SWOG Cancer Research Network, which has 270 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.