32
Participants
Start Date
June 30, 2007
Primary Completion Date
May 31, 2010
Study Completion Date
May 31, 2010
enzastaurin hydrochloride
Participants receive 200, 260, 340, or 440 mg/m2/day of enzastaurin orally once daily for 28 days (one course) during the dose escalation phase of the study. To study the toxicity profile of the MTD or phase II recommended dose established during the dose escalation phase, participants receive twice daily doses of enzastaurin orally at the phase II recommended dose for 28 days (one course). In the absence of unacceptable toxicity or disease progression, treatment may continue for 13 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 Medical Center at Parnassus, 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
National Cancer Institute (NCI)
NIH
Pediatric Brain Tumor Consortium
NETWORK