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NCT00109161 · ClinicalTrials.gov registry record · Phase 2

Study of Subcutaneous Daclizumab in Patients With Active, Relapsing Forms of Multiple Sclerosis

A Phase 2 study of Multiple Sclerosis, sponsored by PDL BioPharma.

Completed
Registry status
Phase 2
Development phase
270
Enrollment target
20
Study locations

NCT00109161 is a Phase 2 study of Multiple Sclerosis that has completed, run by PDL BioPharma. The registered enrollment target is 270 participants, below the 584-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (54% lower). The trial reports 20 study locations across 13 states.

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The verdict

NCT00109161, a Phase 2 study of Multiple Sclerosis, has completed, sponsored by PDL BioPharma.

COMPLETED
Registry status
Phase 2
Development phase
270 participants
Enrollment target
20
Study locations

Study Summary

This research study is being conducted in the U.S. and Europe to evaluate the safety and efficacy of daclizumab for the treatment of multiple sclerosis (MS).

Conditions Studied

Interventions

  • DRUG Daclizumab (Anti-CD25 Humanized Monoclonal Antibody)

Study Locations (20)

New York

  • Upstate Clinical Research - Albany
  • Albany Medical Center - Albany
  • Winthrop University Hospital - Mineola
  • Hospital for Joint Diseases, MS Care Center - New York
  • University of Rochester Medical Center - Rochester

Michigan

  • Wayne State University MS Center - Detroit
  • Michigan State University - East Lansing
  • Michigan Medical P.C. Neurology - Grand Rapids

Arizona

  • St. Joseph's Hospital and Medical Center - Phoenix
  • Mayo Clinic - Scottsdale

California

  • Sutter East Bay Medical Foundation - Berkeley

Florida

  • Neurology Associates, P.A. - Maitland

Georgia

  • The Multiple Sclerosis Center of Atlanta - Atlanta

Illinois

  • Consultants in Neurology - Northbrook

Kansas

  • KUMC Neurology - Kansas City

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2005-04
Est. Completion 2006-10
Phase Phase 2

Sponsor

PDL BioPharma

4 total trials

What the Registry Record Tells You About NCT00109161

The ClinicalTrials.gov registry entry for NCT00109161 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 584-participant average among 315 other Multiple Sclerosis trials with a reported enrollment target (54% lower). The listed sponsor is PDL BioPharma, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Sclerosis appearing as the primary indexed condition, and to 1 intervention - of which Daclizumab (Anti-CD25 Humanized Monoclonal Antibody) is the first listed.

NCT00109161 reports 20 study locations spanning 13 distinct geographic areas - top geographies include New York, Michigan, Arizona.

Frequently Asked Questions

What is clinical trial NCT00109161 about?

NCT00109161 is a clinical study titled "Study of Subcutaneous Daclizumab in Patients With Active, Relapsing Forms of Multiple Sclerosis". This research study is being conducted in the U.S. and Europe to evaluate the safety and efficacy of daclizumab for the treatment of multiple sclerosis (MS).

What is the current status of trial NCT00109161?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 270 participants. The study started on 2005-04. Estimated completion is 2006-10.

What conditions does trial NCT00109161 study?

This clinical trial studies the following conditions: Multiple Sclerosis.

What interventions are being tested in trial NCT00109161?

The interventions under investigation include: Daclizumab (Anti-CD25 Humanized Monoclonal Antibody) (DRUG).

Who is sponsoring clinical trial NCT00109161?

This trial is sponsored by PDL BioPharma, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00109161 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.