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NCT00144677 · ClinicalTrials.gov registry record · Phase 2

Sirolimus With Tacrolimus for Graft-vs-Host Disease Prophylaxis After Un-Related Stem Cell Transplantation

A Phase 2 study of Myelodysplastic Syndromes and Acute Lymphoblastic Leukemia, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
Phase 2
Development phase
30
Enrollment target
1
Study location

NCT00144677 is a Phase 2 study of Myelodysplastic Syndromes and Acute Lymphoblastic Leukemia that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 30 participants, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00144677, a Phase 2 study of Myelodysplastic Syndromes and Acute Lymphoblastic Leukemia, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
Phase 2
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the ability of sirolimus to prevent graft versus host disease (GVHD) in patients following stem cell transplant from an unrelated donor. This trial is designed to test the hypothesis that elimination of methotrexate in the unrelated donor group would lead to less transplant-related toxicity while still preserving the effective control of GVHD.

Interventions

  • DRUG tacrolimus
  • DRUG sirolimus

Study Locations (1)

Massachusetts

  • Dana-Farber Cancer Center - Boston

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2003-11
Est. Completion 2006-06
Phase Phase 2

Sponsor

Dana-Farber Cancer Institute

781 total trials

What the Registry Record Tells You About NCT00144677

The ClinicalTrials.gov registry entry for NCT00144677 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (89% lower). The listed sponsor is Dana-Farber Cancer Institute, which has 781 total studies on file at ClinicalTrials.gov.

The record links to 7 conditions, with Myelodysplastic Syndromes appearing as the primary indexed condition, and to 2 interventions - of which tacrolimus is the first listed.

NCT00144677 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00144677 about?

NCT00144677 is a clinical study titled "Sirolimus With Tacrolimus for Graft-vs-Host Disease Prophylaxis After Un-Related Stem Cell Transplantation". The purpose of this study is to evaluate the ability of sirolimus to prevent graft versus host disease (GVHD) in patients following stem cell transplant from an unrelated donor. This trial is designed to test the hypothesis that elimination of methotrexate in the unrelated donor group would lead to ...

What is the current status of trial NCT00144677?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2003-11. Estimated completion is 2006-06.

What conditions does trial NCT00144677 study?

This clinical trial studies the following conditions: Myelodysplastic Syndromes, Acute Lymphoblastic Leukemia, Non-Hodgkin's Lymphoma, Graft-Versus-Host Disease, Acute Myelogenous Leukemia.

What interventions are being tested in trial NCT00144677?

The interventions under investigation include: tacrolimus (DRUG), sirolimus (DRUG).

Who is sponsoring clinical trial NCT00144677?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00144677 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.