Study of BMS-663513 in Patients With Advanced Cancer

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

115

Participants

Timeline

Start Date

December 31, 2005

Primary Completion Date

December 31, 2008

Study Completion Date

September 30, 2009

Conditions
Tumors
Interventions
DRUG

BMS-663513

mg/kg, intravenous (IV), 0.3, 1, 3, 6, 10 or 15 mg/kg, once every 3 weeks (q 3 wks), 12 weeks depending on response

Trial Locations (12)

15213

Hillman Cancer Center, Pittsburgh

33076

Local Institution, Bordeaux

44805

Local Institution, Saint-Herblain

46202

Indiana University Cancer Center, Indianapolis

75004

Local Institution, Paris

75908

Local Institution, Paris

91010

City Of Hope National Medical Center, Duarte

94800

Local Institution, Villejuif

06520

Yale University School Of Medicine, New Haven

02215

Beth Israel Deaconess Medical Center, Boston

03756

Dartmouth-Hitchcock Medical Center, Lebanon

M5G 2M9

Local Institution, Toronto

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY