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Terminated Phase 2 Interventional

Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323

ClinicalTrials.gov ID: NCT00484536

Public ClinicalTrials.gov record NCT00484536. 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 30, 2026, 12:50 PM EDT

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

Official title

Double-blind, Placebo-controlled, Randomized, Parallel-group Phase II Study in Subjects With Relapsing Forms of Multiple Sclerosis (MS) to Evaluate the Safety, Tolerability, and Effects of CDP323.

Brief summary

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

The objective of the study is to evaluate the effect, safety and tolerability of CDP323 in patients with relapsing forms of multiple sclerosis

Study identification

NCT ID
NCT00484536
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Pharma
Industry
Enrollment
232 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 55 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
May 2007 (Type not available)
Primary completion
Nov 2009 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Sep 12, 2011

2007 – 2010

United States locations

U.S. sites
22
U.S. states
19
U.S. cities
22
Facility City State ZIP Site status
Not listed Cullman Alabama — —
Not listed Phoenix Arizona — —
Not listed Tucson Arizona — —
Not listed Springs Colorado — —
Not listed Washington D.C. District of Columbia — —
Not listed Maitland Florida — —
Not listed Atlanta Georgia — —
Not listed Northbrook Illinois — —
Not listed Fort Wayne Indiana — —
Not listed Kansas City Kansas — —
Not listed Lenexa Kansas — —
Not listed Lexington Kentucky — —
Not listed Louisville Kentucky — —
Not listed Farmington Hills Michigan — —
Not listed Charlotte North Carolina — —
Not listed Columbus Ohio — —
Not listed Providence Rhode Island — —
Not listed Nashville Tennessee — —
Not listed Dallas Texas — —
Not listed Kirkland Washington — —
Not listed Charleston West Virginia — —
Not listed Milwaukee Wisconsin — —

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 49 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00484536, 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 Sep 12, 2011 · Synced Oct 30, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00484536 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →