Multiple Sclerosis Clinical Trial

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

Summary

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

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

relapsing form of MS
screening EDSS score 0 - 5.5, inclusive
at least one clinical relapse in the 12 months before screening
active disease, defined by set of MRI activity criteria
failed prior treatment with beta-interferons or glatiramer acetate

Exclusion Criteria:

signs of silent infections, including positive tests for HIV1, HIV2 or Hepatitis B or Hepatitis C or tuberculosis
known allergy to gadolinium-DTPA, and/or ingredients of the study drug formulation
pre-treatment with immunosuppressive or immunomodulatory drugs prior to screening within certain time frames

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

232

Study ID:

NCT00484536

Recruitment Status:

Terminated

Sponsor:

UCB Pharma

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There is 1 Location for this study

See Locations Near You


Cullman Alabama, , United States

Phoenix Arizona, , United States

Tucson Arizona, , United States

Springs Colorado, , United States

Washington District of Columbia, , United States

Maitland Florida, , United States

Atlanta Georgia, , United States

Northbrook Illinois, , United States

Fort Wayne Indiana, , United States

Kansas City Kansas, , United States

Lenexa Kansas, , United States

Lexington Kentucky, , United States

Louisville Kentucky, , United States

Farmington Hills Michigan, , United States

Charlotte North Carolina, , United States

Columbus Ohio, , United States

Providence Rhode Island, , United States

Nashville Tennessee, , United States

Dallas Texas, , United States

Kirkland Washington, , United States

Charleston West Virginia, , United States

Milwaukee Wisconsin, , United States

Diepenbeek , , Belgium

Gent , , Belgium

Melsbroek , , Belgium

Overpelt , , Belgium

Sijsele , , Belgium

Sint-Truiden , , Belgium

London Ontario, , Canada

Ottawa Ontario, , Canada

Gatineau Quebec, , Canada

Greenfield Park Quebec, , Canada

Sherbrooke Quebec, , Canada

Oulu , , Finland

Tampere , , Finland

Turku , , Finland

Besancon , , France

Clermont-Ferrand , , France

Lyon Cedex 03 , , France

Rennes , , France

Strasbourg , , France

Bayreuth , , Germany

Berlin , , Germany

Giessen , , Germany

Hamburg , , Germany

Marburg , , Germany

Rostock , , Germany

Ulm , , Germany

Wiesbaden , , Germany

Budapest , , Hungary

Gyor , , Hungary

Nyiregyhaza , , Hungary

Pecs , , Hungary

Amsterdam , , Netherlands

Breda , , Netherlands

Nieuwegein , , Netherlands

Nijmegen , , Netherlands

Barcelona , , Spain

Bilbao , , Spain

Girona , , Spain

Madrid , , Spain

Malaga , , Spain

Oviedo , , Spain

Santa Cruz de Tenerife , , Spain

Sevilla , , Spain

Goteborg , , Sweden

Umea , , Sweden

Hartshill , , United Kingdom

Newcastle , , United Kingdom

Nottingham , , United Kingdom

Sheffield , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 2

Estimated Enrollment:

232

Study ID:

NCT00484536

Recruitment Status:

Terminated

Sponsor:


UCB Pharma

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