SUTENT (SUNITINIB, SU11248)in Patients With Recurrent or Progressive Glioblastoma Multiforme

PHASE2UnknownINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

December 31, 2010

Study Completion Date

January 31, 2011

Conditions
Glioblastoma Multiforme
Interventions
DRUG

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.

Trial Locations (10)

5020

Paracelsus Medical University, Salzburg

6020

Medical University Innsbruck, Innsbruck

13353

University Hospital of Berlin, Berlin

53105

University Hospital of Bonn, Bonn

68167

University Hospital of Mannheim, Mannheim

69120

University Hospital of Heidelberg, Heidelberg

Unknown

LKH Feldkirch, Feldkirch

LNK Wagner-Jauregg, Linz

Kaiser-Franz-Josef Spital Wien, Vienna

Medical University Vienna, Vienna

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

Medical University Innsbruck

OTHER

NCT00535379 - SUTENT (SUNITINIB, SU11248)in Patients With Recurrent or Progressive Glioblastoma Multiforme | Biotech Hunter | Biotech Hunter