SU5416 in Treating Patients With Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

May 31, 2000

Primary Completion Date

December 31, 2002

Study Completion Date

November 30, 2005

Conditions
Unspecified Adult Solid Tumor, Protocol Specific
Interventions
DRUG

semaxanib

This is a dose-deescalation study. Patients receive SU5416 IV over 1 hour twice weekly for 4 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Cohorts of 6-12 patients receive deescalating doses of SU5416 until the maximum target-inhibiting dose (MTID) is determined.

Trial Locations (1)

44106-5065

Ireland Cancer Center at University Hospitals Case Medical Center, Case Comprehensive Cancer Center, Cleveland

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

lead

Case Comprehensive Cancer Center

OTHER

NCT00005642 - SU5416 in Treating Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter