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

F

Facet Biotech

Status and phase

Completed
Phase 2
Phase 1

Conditions

Severe Ulcerative Colitis

Treatments

Drug: Visilizumab

Study type

Interventional

Funder types

Industry

Identifiers

NCT00267306
291-408

Details and patient eligibility

About

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.

Full description

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

Sex

All

Ages

16 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

11

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Data sourced from clinicaltrials.gov

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