210
Participants
Start Date
January 13, 2006
Primary Completion Date
September 29, 2010
Study Completion Date
October 18, 2010
Pegylated liposomal doxorubicin (SCH 200746)
pegylated liposomal doxorubicin (50 mg/m\^2 q 28 days) was administered intravenously until disease progression or unacceptable toxicity
Capecitabine
capecitabine (1250 mg/m\^2 BID x 14 days q 21 days) in tablets of 150 mg and 500 mg was administered orally, until disease progression or unacceptable toxicity
Essex Pharma GmbH
INDUSTRY
Merck Sharp & Dohme LLC
INDUSTRY