ClinicalTrials.gov
skipnavHome|Search|Browse|Resources|Help|What's New|About

Safety and Effectiveness of Two Doses of ABT-874 as Compared to Placebo in Subjects with Multiple Sclerosis (MS)

This study is currently recruiting patients.

Sponsored by: Abbott Laboratories
Information provided by: Abbott Laboratories

Purpose

The objective of the trial is to study the safety and effectiveness of ABT-874 administered weekly or every other week in patients with relapsing remitting and secondary progressive multiple sclerosis as compared to placebo. Effectiveness will be measured based on MRI scans done periodically thoughout the study.

Condition Treatment or Intervention Phase
Multiple Sclerosis
Multiple Sclerosis, Relapsing Remitting
Multiple Sclerosis, Secondary Progressive
 Drug: ABT-874/Human monoclonal antibody against IL-12
Phase II

MedlinePlus related topics:  Multiple Sclerosis

Study Type: Interventional
Study Design: Treatment, Safety/Efficacy Study

Further Study Details: 

Study start: May 2004

Eligibility

Ages Eligible for Study:  18 Years   -   55 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

Exclusion Criteria:

Patients with the following conditions are not eligible to participate in the study:


Location and Contact Information

Dulari Menon, MS      973-394-5479    dulari.menon@abbott.com

Arizona
      St. Joseph's Hospital & Medical Center, Phoenix,  Arizona,  85013,  United States; Recruiting
Lou DiCave  602-406-7711    ldicave@chw.edu 
Timothy Vollmer, MD,  Principal Investigator

California
      UC Davis Medical Center, Sacramento,  California,  95817,  United States; Recruiting
Janelle Butters  916-734-6276    janelle.adams@ucdmc.ucdavis.edu 
Mark Aguis, MD,  Principal Investigator

      USC Keck School of Medicine, Los Angeles,  California,  90033,  United States; Recruiting
Pat Gutierrez  323-224-5333    pgutierrez@usc.edu 
Leslie Weiner, MD,  Principal Investigator

Colorado
      Alpine Clinical Reasearch Center, Boulder,  Colorado,  80304,  United States; Recruiting
Peg Sharp  303-449-7229    peg@alpineresearch.com 
George Garmany, MD,  Principal Investigator

Florida
      University of Miami, Miami,  Florida,  33136,  United States; Recruiting
Marilyn Martinez  305-243-1088    mmartinez13@med.miami.edu 
William Sheramata, MD,  Principal Investigator

Georgia
      The MS Center of Atlanta, Atlanta,  Georgia,  30327,  United States; Recruiting
Donna Court  404-351-0205    d.court@mscatl.com 
William Stuart, MD,  Principal Investigator

      Shepherd Center, Atlanta,  Georgia,  30308,  United States; Recruiting
Ismari Clesson  404-350-7651    ismari_clesson@shepherd.org 
Ben Thrower, MD,  Principal Investigator

Illinois
      University of Chicago Hospitals, Chicago,  Illinois,  60637,  United States; Recruiting
Mildred Valentine  773-834-1811    mvalenti@neurology.bsd.uchicago.edu 
Anthony Reder, MD,  Principal Investigator

      Consultants in Neurology, Ltd, Northbrook,  Illinois,  60062,  United States; Recruiting
Catherine Meyer  847-509-0270    dwynnmd@interaccess.com 
Daniel Wynn, MD,  Principal Investigator

Indiana
      Indiana University Hospital, Indianapolis,  Indiana,  46202,  United States; Recruiting
Lee Hayward  317-274-4030    lhayward@iupui.edu 
David Mattson, MD, PhD,  Principal Investigator

Michigan
      Wayne Steet University, Detroit,  Michigan,  48201,  United States; Recruiting
Melissa Reznar  313-966-5068    mreznar@med.wayne.edu 
Omar Khan, MD,  Principal Investigator

Missouri
      Washington University School of Medicine, St. Louis,  Missouri,  63110,  United States; Recruiting
Joanne Lauber  314-362-3371    laugerj@neuro.wustl.edu 
Becky Parks, MD,  Principal Investigator

New Jersey
      University of Medicine & Dentistry of New Jersey, Newark,  New Jersey,  07103,  United States; Recruiting
Jim Quinless  973-972-7395    quinlessj@umdnj.edu 
Stuart Cook, MD,  Principal Investigator

New York
      University of Rochester Medical Center, Rochester,  New York,  14642,  United States; Recruiting
Eileen Scheid  585-275-6673    Eileen_Scheid@urmc.rochester.edu 
Andrew Goodman, MD,  Principal Investigator

      Upstate Clinical research, Albany,  New York,  12205,  United States; Recruiting
Suzanne Alterman  518-533-1500  Ext. x 546    salterman@upstateneurology.com 
James Storey, MD,  Principal Investigator

North Carolina
      Carolinas Medical Center, Charlotte,  North Carolina,  28203,  United States; Recruiting
Priscilla Russo  704-446-1910    priscilla.russo@carolinashealthcare.org 
Michael Kauffman, MD,  Principal Investigator

Ohio
      Ohio State University, Columbus,  Ohio,  43210,  United States; Recruiting
Megan Nussbaum  614-293-4964    nussbaum-1@medctr.osu.edu 
Kottil Rammohan, MD,  Principal Investigator

Pennsylvania
      Lehigh Valley Hospital, Allentown,  Pennsylvania,  18103,  United States; Recruiting
Joanne Rodgers  610-402-9004    joanne.rodgers@lvh.com 
Alexander Rae-Grant, MD,  Principal Investigator

Texas
      University of TexasHouston Health Science Center, Houston,  Texas,  77030,  United States; Recruiting
Myrna Koh  713-500-7045    myrna.koh@uth.tmc.edu 
Stanley Brod, MD,  Principal Investigator

Washington
      MS Hub Medical Group, Seattle,  Washington,  98101,  United States; Recruiting
Jerrie Sims  206-262-0110    jsims@mshub.org 
Craig Smith, MD,  Principal Investigator

More Information

Study ID Numbers:  M03-654
Record last reviewed:  July 2004
Record first received:  July 7, 2004
ClinicalTrials.gov Identifier:  NCT00086671
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2004-11-10
line
U.S. National Library of Medicine, Contact NLM Customer Service
National Institutes of Health, Department of Health & Human Services
Copyright, Privacy, Accessibility, Freedom of Information Act