70
Participants
Start Date
October 31, 2007
Primary Completion Date
December 31, 2010
Study Completion Date
January 31, 2011
Sunitinib
Patients will receive SUTENT 37.5mg (3 x 12.5mg capsules) PO daily in the morning after breakfast. After 2 weeks without treatment-related adverse events grade ≥ 2 (ECOG common toxicity criteria: refer to Protocol Attachment A.4) a SUTENT dose escalation to 50mg (4 x 12.5mg capsules) PO daily has to be performed. Treatment will continue until patients develop progression of disease or until unacceptable adverse events occur.
Paracelsus Medical University, Salzburg
Medical University Innsbruck, Innsbruck
University Hospital of Berlin, Berlin
University Hospital of Bonn, Bonn
University Hospital of Mannheim, Mannheim
University Hospital of Heidelberg, Heidelberg
LKH Feldkirch, Feldkirch
LNK Wagner-Jauregg, Linz
Kaiser-Franz-Josef Spital Wien, Vienna
Medical University Vienna, Vienna
Collaborators (1)
Pfizer
INDUSTRY
Medical University Innsbruck
OTHER