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

Primary Purpose

Severe Ulcerative Colitis

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Visilizumab
Sponsored by
Facet Biotech
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Ulcerative Colitis

Eligibility Criteria

16 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Inflammatory Bowel Disease Center
  • University of California, San Francisco
  • Atlanta Gastroenterology Associates
  • Northwestern University
  • University of Chicago Medical Center
  • Mayo Clinic Rochester
  • Weill Medical College of Cornell
  • Mount Sinai School of Medicine
  • UPHS/Presbyterian Medical Center
  • University of Pittsburgh Medical Center
  • University of Texas Medical Branch

Outcomes

Primary Outcome Measures

Evaluate the safety and tolerability of visilizumab in patients with severe ulcerative colitis that is resistant to intravenous steroids

Secondary Outcome Measures

Full Information

First Posted
December 16, 2005
Last Updated
March 8, 2012
Sponsor
Facet Biotech
Collaborators
PDL BioPharma, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00267306
Brief Title
Ulcerative Colitis Study: Study of Visilizumab in Patients With Severe Ulcerative Colitis
Official Title
A Phase 1/2, Partially Randomized, Open-Label Study of Visilizumab in Patients With Severe Ulcerative Colitis Refractory to Intravenous Corticosteroids
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Facet Biotech
Collaborators
PDL BioPharma, Inc.

4. Oversight

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Ulcerative Colitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
144 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Visilizumab
Primary Outcome Measure Information:
Title
Evaluate the safety and tolerability of visilizumab in patients with severe ulcerative colitis that is resistant to intravenous steroids

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Inflammatory Bowel Disease Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
Country
United States
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States
Facility Name
Atlanta Gastroenterology Associates
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30342
Country
United States
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
University of Chicago Medical Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
Facility Name
Mayo Clinic Rochester
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
Weill Medical College of Cornell
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Mount Sinai School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
UPHS/Presbyterian Medical Center
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15261
Country
United States
Facility Name
University of Texas Medical Branch
City
Galveston
State/Province
Texas
ZIP/Postal Code
77555
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19714757
Citation
Baumgart DC, Targan SR, Dignass AU, Mayer L, van Assche G, Hommes DW, Hanauer SB, Mahadevan U, Reinisch W, Plevy SE, Salzberg BA, Buchman AL, Mechkov GM, Krastev ZA, Lowder JN, Frankel MB, Sandborn WJ. Prospective randomized open-label multicenter phase I/II dose escalation trial of visilizumab (HuM291) in severe steroid-refractory ulcerative colitis. Inflamm Bowel Dis. 2010 Apr;16(4):620-9. doi: 10.1002/ibd.21084.
Results Reference
derived
Links:
URL
http://www.pdl.com
Description
Sponsor Information

Learn more about this trial

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

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