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Clinical Trials/EUCTR2005-004105-28-DE
EUCTR2005-004105-28-DE
Active, not recruiting
Not Applicable

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

PDL BioPharma, Inc.0 sites300 target enrollmentApril 10, 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
PDL BioPharma, Inc.
Enrollment
300
Status
Active, not recruiting
Last Updated
14 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 10, 2006
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Eligible subjects will be considered for inclusion in this study if they meet all of the following criteria:
  • 1\) Previous participation in an IVSR\-UC visilizumab study.
  • 2\) Disease progression while enrolled in a previous visilizumab study, and subsequent treatment with salvage therapy
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • 1\) Unable to understand the purpose and risks of the study, or unwilling or unable to provide signed and dated informed consent.

Outcomes

Primary Outcomes

Not specified

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