28
Participants
Start Date
November 30, 2010
Primary Completion Date
January 31, 2015
Study Completion Date
January 31, 2015
VEGF inhibitor PTC299
This is a dose escalation study. Study participants will receive .6 or 1.2 mg/kg orally twice daily or 1.2, 1.5, or 2.0 mg/kg orally three times daily for four consecutive weeks (a course). In the absence of unacceptable toxicity or disease progression, treatment may continue for up to 12 courses (approximately one year)
Children's Hospital of Pittsburgh, Pittsburgh
Duke Comprehensive Cancer Center, Durham
St. Jude Children's Research Hospital, Memphis
Children's Memorial Hospital - Chicago, Chicago
UCSF Cancer Center and Cancer Research Institute, San Francisco
Children's National Medical Center, Washington D.C.
Children's Hospital of Philadelphia, Philadelphia
Texas Children's Cancer Center and Hematology Service at Texas Children's Hospital, Houston
Collaborators (1)
National Cancer Institute (NCI)
NIH
PTC Therapeutics
INDUSTRY
Pediatric Brain Tumor Consortium
NETWORK