48
Participants
Start Date
May 31, 2005
Primary Completion Date
January 31, 2008
Study Completion Date
January 31, 2008
Ocrelizumab
Participants will receive a total of 8 intravenous (IV) infusions of ocrelizumab given at intervals of 3 weeks, until disease progression or unacceptable toxicity.
Geneva
Melbourne
Bern
Woolloongabba
Perth
Lugano
Torino
Huddinge
Malmo
Lund
Bergamo
Rennes
Nantes
Lille
Pierre-Bénite
Umeå
Créteil
Edmonton
Vancouver
Halifax
Ottawa
Toronto
Roma
Hoffmann-La Roche
INDUSTRY