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Terminated No phase listed Observational

An Observational Follow-up Study for Subjects Receiving Salvage Therapy After Previous Treatment in a Visilizumab Study for Intravenous Steroid-Refractory Ulcerative Colitis

ClinicalTrials.gov ID: NCT00355901

Public ClinicalTrials.gov record NCT00355901. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To assess the effects of visilizumab on the safety of subsequent salvage therapies in subjects who experienced disease progression in a previous visilizumab study and subsequently received salvage therapy.

Study identification

NCT ID
NCT00355901
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
PDL BioPharma, Inc.
Industry
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2006 (Type not available)
Primary completion
Not listed
Completion
Nov 2012 (Type not available)
Last update posted
Aug 5, 2008

2006 – 2012

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Not listed San Francisco California 94115 —
Not listed Gainesville Florida 32610 —
Not listed Atlanta Georgia 30342 —
Not listed Louisville Kentucky 40202 —
Not listed Worcester Massachusetts 01655 —
Not listed Rochester Minnesota 55905 —
Not listed St Louis Missouri 63110 —
Not listed Manhasset New York 11030 —
Not listed Mineola New York 11501 —
Not listed New York New York 10021 —
Not listed New York New York 10029 —
Not listed Cleveland Ohio 44106 —
Not listed Hershey Pennsylvania 17033 —
Not listed Charleston South Carolina 29425 —
Not listed Salt Lake City Utah 84107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00355901, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2008 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00355901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →