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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00086671

Public ClinicalTrials.gov record NCT00086671. 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 Sep 2, 2026, 5:46 AM EDT

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

Official title

A 24-Week, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Dose Finding, Safety, Tolerability, and Efficacy Study of the Human Anti-IL-12 Antibody ABT-874 in Subjects With Multiple Sclerosis With a 24-Week Double-Blind, Active Extension Phase

Brief summary

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

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 throughout the study.

Study identification

NCT ID
NCT00086671
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
215 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 60 Years
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
Mar 31, 2004
Primary completion
Oct 31, 2006
Completion
Oct 31, 2006
Last update posted
Jan 3, 2013

2004 – 2006

United States locations

U.S. sites
27
U.S. states
20
U.S. cities
26
Facility City State ZIP Site status
Site Reference ID/Investigator# 107 Phoenix Arizona 85013
Site Reference ID/Investigator# 163 Sun City Arizona 85351
Site Reference ID/Investigator# 156 Little Rock Arkansas 72205
Site Reference ID/Investigator# 154 Irvine California 92618
Site Reference ID/Investigator# 161 Laguna Hills California 92653
Site Reference ID/Investigator# 84 Sacramento California 95817
Site Reference ID/Investigator# 119 Boulder Colorado 80304
Site Reference ID/Investigator# 111 Miami Florida 33136
Site Reference ID/Investigator# 151 Tallahassee Florida 32308
Site Reference ID/Investigator# 108 Atlanta Georgia 30309
Site Reference ID/Investigator# 109 Atlanta Georgia 30327
Site Reference ID/Investigator# 105 Northbrook Illinois 60062
Site Reference ID/Investigator# 152 Indianapolis Indiana 46260
Site Reference ID/Investigator# 258 Lenexa Kansas 66214
Site Reference ID/Investigator# 261 Lexington Kentucky 40503
Site Reference ID/Investigator# 116 Detroit Michigan 48201
Site Reference ID/Investigator# 158 Traverse City Michigan 49684
Site Reference ID/Investigator# 124 St Louis Missouri 63110
Site Reference ID/Investigator# 259 Henderson Nevada 89052
Site Reference ID/Investigator# 153 Lebanon New Hampshire 03766
Site Reference ID/Investigator# 110 Albany New York 12205
Site Reference ID/Investigator# 117 Charlotte North Carolina 28207
Site Reference ID/Investigator# 113 Columbus Ohio 43210
Site Reference ID/Investigator# 157 Dayton Ohio 45409
Site Reference ID/Investigator# 114 Allentown Pennsylvania 18103
Site Reference ID/Investigator# 128 Houston Texas 77030
Site Reference ID/Investigator# 155 Bennington Vermont 05201

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00086671, 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 Jan 3, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00086671 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →