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NCT00434629 · ClinicalTrials.gov registry record · Phase 1

Safety and Efficacy of Bexxar Therapy in the Treatment of Relapsed/Residual B-Cell Lymphoma After Autologous Transplant

A Phase 1 study, sponsored by University of Pennsylvania.

Completed
Registry status
Phase 1
Development phase
16
Enrollment target

NCT00434629: Completed Phase 1 study, sponsored by University of Pennsylvania.

NCT00434629 is a Phase 1 study that has completed, run by University of Pennsylvania. The registered enrollment target is 16 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00434629, a Phase 1 study, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

Patients with B-cell lymphoma who relapse after autologous transplant tend to have a poor prognosis. Currently, there is no standard treatment for such patients. Bexxar is a radioactive antibody therapy that has shown a 60-80% response rate in non-transplanted patients with relapsed B-cell lymphoma. This study will test the safety and efficacy of Bexxar in the treatment of patients whose B-cell lymphoma has relapsed after an autologous transplant.

Interventions

  • DRUG Bexxar

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2007-02
Est. Completion 2015-05
Phase Phase 1

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT00434629

The ClinicalTrials.gov registry entry for NCT00434629 describes a study currently listed as completed, categorized as Phase 1. 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 University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bexxar is the first listed.

NCT00434629 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00434629 about?

NCT00434629 is a clinical study titled "Safety and Efficacy of Bexxar Therapy in the Treatment of Relapsed/Residual B-Cell Lymphoma After Autologous Transplant". Patients with B-cell lymphoma who relapse after autologous transplant tend to have a poor prognosis. Currently, there is no standard treatment for such patients. Bexxar is a radioactive antibody therapy that has shown a 60-80% response rate in non-transplanted patients with relapsed B-cell lymphoma....

What is the current status of trial NCT00434629?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2007-02. Estimated completion is 2015-05.

What interventions are being tested in trial NCT00434629?

The interventions under investigation include: Bexxar (DRUG).

Who is sponsoring clinical trial NCT00434629?

This trial is sponsored by University of Pennsylvania, which has 1,423 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.