Ulcerative Colitis Study: Study of Visilizumab in Patients With Severe Ulcerative Colitis

Last updated: March 8, 2012
Sponsor: Facet Biotech
Overall Status: Completed

Phase

1/2

Condition

Crohn's Disease

Inflammatory Bowel Disease

Treatment

N/A

Clinical Study ID

NCT00267306
291-408
  • Ages 16-70
  • All Genders

Study Summary

The purpose of this study is to evaluate the safety and tolerability of visilizumab in patients with severe ulcerative colitis that has failed to respond to steroid therapy.

What is visilizumab?

Visilizumab is an antibody designed to reduce inflammation. Antibodies are proteins that are normally made by the immune system to help defend the body from infections and other foreign substances. Visilizumab is thought to selectively affect the immune system to decrease inflammation and, in doing so, it may prevent damage to the intestine caused by ulcerative colitis.

Who can participate in this study?

The target population for this study is adults with severe ulcerative colitis that has resisted intravenous (IV) steroids. This study is open to patients with the following characteristics:

  • 16-70 year olds

  • A diagnosis of ulcerative colitis verified by colonoscopy or barium enema performed within 36 months prior to study entry

  • Active disease despite ongoing treatment with steroids

How is this study conducted?

Eligible participants will be administered visilizumab as one daily injection on two consecutive days. All medication and study-related care, except for the costs of in-patient hospitalization, are provided to qualified participants at no cost. This includes all visits, examinations and laboratory work.

How does one get more information?

This study is currently enrolling patients at hospitals and clinics in North America and Europe. For more information on the study or how to participate in it, please call 1-800-772-0482, email InfoCenter@pdl.com or visit www.IBDtrials.com.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 16 -70 year olds

  • A diagnosis of ulcerative colitis verified by colonoscopy or barium enema performed within 36 months prior to study entry

  • Active disease despite ongoing treatment with IV steroids

Study Design

Total Participants: 144
Study Start date:
January 01, 2004
Estimated Completion Date:
December 31, 2006

Study Description

PDL BioPharma, Inc. was formerly known as Protein Design Labs, Inc.

Connect with a study center

  • Inflammatory Bowel Disease Center

    Los Angeles, California 90048
    United States

    Site Not Available

  • University of California, San Francisco

    San Francisco, California 94115
    United States

    Site Not Available

  • Atlanta Gastroenterology Associates

    Atlanta, Georgia 30342
    United States

    Site Not Available

  • Northwestern University

    Chicago, Illinois 60611
    United States

    Site Not Available

  • University of Chicago Medical Center

    Chicago, Illinois 60637
    United States

    Site Not Available

  • Mayo Clinic Rochester

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Mount Sinai School of Medicine

    New York, New York 10029
    United States

    Site Not Available

  • Weill Medical College of Cornell

    New York, New York 10021
    United States

    Site Not Available

  • UPHS/Presbyterian Medical Center

    Philadelphia, Pennsylvania 19104
    United States

    Site Not Available

  • University of Pittsburgh Medical Center

    Pittsburgh, Pennsylvania 15261
    United States

    Site Not Available

  • University of Texas Medical Branch

    Galveston, Texas 77555
    United States

    Site Not Available

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