A Study Evaluating the Safety and Antitumor Activity of IPI-504, in Patients With Metastatic Melanoma

PHASE2TerminatedINTERVENTIONAL
Enrollment

1

Participants

Timeline

Start Date

February 29, 2008

Primary Completion Date

October 31, 2009

Study Completion Date

October 31, 2009

Conditions
Metastatic Melanoma
Interventions
DRUG

IPI-504

Dose as a 30 to 60 minute IV infusion as part of a 21-day treatment cycle until unacceptable toxicity, disease progression, initiation of alternative anticancer therapy, or other reasons for patient withdrawal. IPI-504 will be administered twice weekly on Study Days 1, 4, 8, and 11 of each 21-day cycle.

Trial Locations (17)

10032

Columbia University, New York

15213

Univ. of Pittsburgh Cancer Institute, Pittsburgh

30322

Winship Cancer Institute of Emory University, Atlanta

33136

University of Miami - Sylvester Comprehensive Cancer Center, Miami

37232

Vanderbilt Ingram Cancer Center, Nashville

44718

Gabrail Cancer Center, Canton

46202

Indiana Univ. Melvin and Bren Simon Cancer Center, Indianapolis

55905

Mayo Comprehensive Cancer Center, Rochester

63110

Washington School of Medicine, St Louis

66160

University of Kansas Cancer Center, Kansas City

77030

Univ. of TX, MD Anderson Cancer Center, Houston

80010

University of Colorado Health Sciences Center, Aurora

85724

Arizona Cancer Center, Tuscon

90025

The Angeles Clinic and Research Institute, Los Angeles

92123

Sharp Memorial Hospital, San Diego

02021

Dana-Farber Cancer Institute, Boston

03756

Dartmouth-Hitchcock Medical Center, Lebanon

Sponsors
All Listed Sponsors
lead

Infinity Pharmaceuticals, Inc.

INDUSTRY

NCT00627419 - A Study Evaluating the Safety and Antitumor Activity of IPI-504, in Patients With Metastatic Melanoma | Biotech Hunter | Biotech Hunter