280
Participants
Start Date
July 31, 2007
Primary Completion Date
March 31, 2013
Study Completion Date
March 31, 2013
Bevacizumab
Treatment continued until unacceptable toxicity, withdrawal of consent, disease progression, or a decision to terminate at the discretion of the Investigator if medically indicated. Bevacizumab was supplied in single-use vials.
Capecitabine
Treatment continued until unacceptable toxicity, withdrawal of consent, disease progression, or a decision to terminate at the discretion of the Investigator if medically indicated. Capecitabine was supplied as tablets.
Ljubljana
Budapest
Budapest
Vienna
Vienna
Linz
Salzburg
Innsbruck
Zalaegerszeg-Pozva
Győr
Mexico City
Mexico City
Mexico City
Piraeus
Jaén
Madrid
Leganés
Murcia
Las Palmas de Gran Canaria
León
Reggio Emilia
Zaragoza
Florence
Puebla City
Lecce
Calgary
Vancouver
Halifax
London
Ottawa
Toronto
Toronto
Montreal
Larissa
Rome
Apeldoorn
Eindhoven
Utrecht
Krakow
Krakow
Warsaw
Gyeonggi-do
Incheon
Seoul
Seoul
Barcelona
Bristol
Colchester
Glasgow
Leicester
London
Manchester
Nottingham
Rhyl
Sutton
Hoffmann-La Roche
INDUSTRY