Enzastaurin in Treating Young Patients With Refractory Primary CNS Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

May 31, 2010

Study Completion Date

May 31, 2010

Conditions
Brain and Central Nervous System TumorsNeuroblastoma
Interventions
DRUG

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).

Trial Locations (8)

15213

Children's Hospital of Pittsburgh, Pittsburgh

27710

Duke Comprehensive Cancer Center, Durham

38105

St. Jude Children's Research Hospital, Memphis

60614

Children's Memorial Hospital - Chicago, Chicago

94143-0372

UCSF Medical Center at Parnassus, San Francisco

20010-2970

Children's National Medical Center, Washington D.C.

19104-4318

Children's Hospital of Philadelphia, Philadelphia

77030-2399

Texas Children's Cancer Center and Hematology Service at Texas Children's Hospital, Houston

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

lead

Pediatric Brain Tumor Consortium

NETWORK

NCT00503724 - Enzastaurin in Treating Young Patients With Refractory Primary CNS Tumors | Biotech Hunter | Biotech Hunter