Safety Study of IPI-504 in Patients With Gastrointestinal Stromal Tumors (GIST) or Soft Tissue Sarcomas (STS)

PHASE1CompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

December 31, 2005

Primary Completion Date

November 30, 2010

Study Completion Date

November 30, 2010

Conditions
Gastrointestinal Stromal TumorsSoft Tissue Sarcomas
Interventions
DRUG

IPI-504

"IV administration of IPI-504 for 21-day cycles. Two different schedules of treatment will be tested. On Schedule A, doses occur on Days 1, 4, 8, and 11 followed by 10 days with no study drug administration. On Schedule B, doses occur on Days 1, 4, 8, 11, 15, and 18, or twice weekly for 3 weeks continuously.~For both Schedule A and B doses will be administered ≥ 72 hours apart."

Trial Locations (5)

48109

University of Michigan Hosptials, Ann Arbor

85260

Premiere Oncology, Scottsdale

90404

Premiere Oncology, Santa Monica

02115

Dana-Farber Cancer Institute, Boston

M5G 1X5

Mount Sinai Hospital, Toronto

Sponsors
All Listed Sponsors
lead

Infinity Pharmaceuticals, Inc.

INDUSTRY

NCT00276302 - Safety Study of IPI-504 in Patients With Gastrointestinal Stromal Tumors (GIST) or Soft Tissue Sarcomas (STS) | Biotech Hunter | Biotech Hunter