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NCT00032292 · ClinicalTrials.gov registry record · Phase 1

Research Study of Visilizumab for Treatment of Acute Graft Versus Host Disease

A Phase 1 study of Graft Vs Host Disease, sponsored by Facet Biotech.

Completed
Registry status
Phase 1
Development phase
34
Enrollment target
7
Study locations

NCT00032292 is a Phase 1 study of Graft Vs Host Disease that has completed, run by Facet Biotech. The registered enrollment target is 34 participants, below the 137-participant average among 36 other Graft Vs Host Disease trials with a reported enrollment target (75% lower). The trial reports 7 study locations across 6 states.

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The verdict

NCT00032292, a Phase 1 study of Graft Vs Host Disease, has completed, sponsored by Facet Biotech.

COMPLETED
Registry status
Phase 1
Development phase
34 participants
Enrollment target
7
Study locations

Study Summary

The purpose of this Phase I/II, open-label, dose-escalation study is to evaluate an investigational monoclonal antibody administered as a first-line therapy to patients with acute, Grade II, III, or IV graft-versus-host disease (GVHD). Patients will be eligible for enrollment within 24 hours of beginning standard steroid treatment. The research is being conducted at up to 10 clinical research sites in the US.

Conditions Studied

Interventions

  • DRUG Visilizumab

Study Locations (7)

California

  • City of Hope National Medical Center - Duarte
  • Stanford University Medical Center - Stanford

Missouri

  • Washington University School of Medicine - St Louis

North Carolina

  • Duke University - Durham

Tennessee

  • Vanderbilt University Medical Center - Nashville

Texas

  • MD Anderson Cancer Center - Houston

Washington

  • Fred Hutchinson Cancer Research Center - Seattle

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2002-03
Est. Completion 2006-08
Phase Phase 1

Sponsor

Facet Biotech

13 total trials

What the Registry Record Tells You About NCT00032292

The ClinicalTrials.gov registry entry for NCT00032292 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 137-participant average among 36 other Graft Vs Host Disease trials with a reported enrollment target (75% lower). The listed sponsor is Facet Biotech, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Graft Vs Host Disease appearing as the primary indexed condition, and to 1 intervention - of which Visilizumab is the first listed.

NCT00032292 reports 7 study locations spanning 6 distinct geographic areas - top geographies include California, Missouri, North Carolina.

Frequently Asked Questions

What is clinical trial NCT00032292 about?

NCT00032292 is a clinical study titled "Research Study of Visilizumab for Treatment of Acute Graft Versus Host Disease". The purpose of this Phase I/II, open-label, dose-escalation study is to evaluate an investigational monoclonal antibody administered as a first-line therapy to patients with acute, Grade II, III, or IV graft-versus-host disease (GVHD). Patients will be eligible for enrollment within 24 hours of begi...

What is the current status of trial NCT00032292?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2002-03. Estimated completion is 2006-08.

What conditions does trial NCT00032292 study?

This clinical trial studies the following conditions: Graft Vs Host Disease.

What interventions are being tested in trial NCT00032292?

The interventions under investigation include: Visilizumab (DRUG).

Who is sponsoring clinical trial NCT00032292?

This trial is sponsored by Facet Biotech, which has 13 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00032292 being conducted?

This trial has 7 study locations across California, Missouri, North Carolina, Tennessee, Texas. 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.