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NCT00473551 · ClinicalTrials.gov registry record · Phase 1

Anti-Third Party T Lymphocytes With Nonmyeloablative Stem Cell Transplantation for Indolent Lymphoid Malignancies

A Phase 1 study, sponsored by M.D. Anderson Cancer Center.

Terminated
Registry status
Phase 1
Development phase
4
Enrollment target

NCT00473551: Clinical Trial Phase 1 study, sponsored by M.D. Anderson Cancer Center.

NCT00473551 is a Phase 1 study that was terminated before completion, run by M.D. Anderson Cancer Center. The registered enrollment target is 4 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00473551, a Phase 1 study, was terminated before completion, sponsored by M.D. Anderson Cancer Center.

TERMINATED
Registry status
Phase 1
Development phase
4 participants
Enrollment target

Study Summary

Primary Objective: 1\. To determine the maximally tolerated dose of anti-third party cytolytic T-lymphocytes, defined as the dose which achieve engraftment without severe GVHD (graft-vs-host disease) at 90 days after allogeneic transplantation of CD34+ hematopoietic progenitor cells. Secondary Objective: 1\. Toxicity, response rate, time to progression and overall survival.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG Mesna
  • DRUG Rituximab
  • RADIATION Radiation Treatment

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2007-05
Est. Completion 2009-11
Phase Phase 1

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT00473551

The ClinicalTrials.gov registry entry for NCT00473551 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

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

NCT00473551 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00473551 about?

NCT00473551 is a clinical study titled "Anti-Third Party T Lymphocytes With Nonmyeloablative Stem Cell Transplantation for Indolent Lymphoid Malignancies". Primary Objective: 1\. To determine the maximally tolerated dose of anti-third party cytolytic T-lymphocytes, defined as the dose which achieve engraftment without severe GVHD (graft-vs-host disease) at 90 days after allogeneic transplantation of CD34+ hematopoietic progenitor cells. Secondary Obj...

What is the current status of trial NCT00473551?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2007-05. Estimated completion is 2009-11.

What interventions are being tested in trial NCT00473551?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Mesna (DRUG), Rituximab (DRUG), Radiation Treatment (RADIATION).

Who is sponsoring clinical trial NCT00473551?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

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

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, the data changelog, or report a data error.