42
Participants
Start Date
February 28, 2005
Primary Completion Date
October 31, 2006
Study Completion Date
February 29, 2008
laromustine
This is a dose escalation study. Participants receive 20, 30, 45, 60, 78, 103, 137, 182, or 242 mg/m2/day intravenously over 30 minutes for 5 consecutive days every 6 weeks up to 48 weeks.
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 Comprehensive Cancer Center, San Francisco
Children's Hospital and Regional Medical Center - Seattle, Seattle
Children's National Medical Center, Washington D.C.
Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute, Boston
Children's Hospital of Philadelphia, Philadelphia
Texas Children's Cancer Center and Hematology Service at Texas Children's Hospital, Houston
National Cancer Institute (NCI)
NIH
Pediatric Brain Tumor Consortium
NETWORK