341
Participants
Start Date
June 30, 2004
Primary Completion Date
June 30, 2013
Study Completion Date
June 30, 2013
methotrexate
a 10-25 mg stable dose given orally or parenterally throughout study
rituximab [MabThera/Rituxan]
1 g given by intravenous infusion on Days 1 and 15 of each treatment course
Dublin
Brussels
Brussels
Drammen
Ghent
Tromsø
New York
Berlin
Manhasset
Smithtown
Albany
Rochester
Duncansville
Philadelphia
Philadelphia
Philadelphia
Baltimore
Brescia
Greenville
Toulouse
Orlando
Udine
Fort Lauderdale
Jupiter
Delray Beach
Boca Raton
Montpellier
Ratingen
Mayfield
Dayton
Indianapolis
Lansing
Kalamazoo
Madison
Rochester
Pisa
Chicago
Chicago
St Louis
St Louis
Shreverport
Little Rock
Oklahoma City
Oklahoma City
Tulsa
Dallas
Dallas
Paris
Bois-Guillaume
Waco
Houston
Amarillo
Meridian
Boise
Coeur d'Alene
Salt Lake City
Mesa
Paradise Valley
Tucson
Los Angeles
Los Angeles
Pasadena
Rancho Mirage
Fullerton
Santa Maria
Le Kremlin-Bicêtre
Würzburg
Seattle
Seattle
Spokane
Haifa
Haifa
Petah Tikva
Ramat Gan
Tel Aviv
Jerusalem
Danbury
Indianapolis
Boston
Chapel Hill
Cincinnati
Burlington
Calgary
Edmonton
Hamilton
London
Toronto
Dresden
Leipzig
Cork
Amsterdam
Oslo
Cannock
Leeds
London
Manchester
Newcastle upon Tyne
Collaborators (1)
Biogen
INDUSTRY
Hoffmann-La Roche
INDUSTRY