CCI-779 in Treating Patients With Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

January 31, 2001

Primary Completion Date

June 30, 2002

Study Completion Date

June 30, 2002

Conditions
Brain and Central Nervous System TumorsMetastatic CancerUnspecified Adult Solid Tumor, Protocol Specific
Interventions
DRUG

temsirolimus

"•Part I: Patients receive CCI-779 IV over 30 minutes on days 1-5, followed by a 9 day rest period. Treatment courses repeat every 2 weeks in the absence of disease progression or unacceptable toxicity.~The maximum tolerated dose for part I is defined as the dose level at which 33% of patients experience dose limiting toxicity.~•Part II: Patients receive the same treatment schedule as part I. Three patients with CNS tumors are entered at the dose of CCI-779 determined to be the MTD in Part I. At least 3 patients are entered at each dose level in part II."

Trial Locations (2)

55905

Mayo Clinic Cancer Center, Rochester

78229-3264

San Antonio Cancer Institute, San Antonio

All Listed Sponsors
collaborator

National Cancer Institute (NCI)

NIH

collaborator

University of Texas

OTHER

collaborator

Wyeth is now a wholly owned subsidiary of Pfizer

INDUSTRY

lead

The University of Texas Health Science Center at San Antonio

OTHER

NCT00003712 - CCI-779 in Treating Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter