Study of MDX-010 in Subjects With Unresectable Stage III or Stage IV Malignant Melanoma

PHASE1CompletedINTERVENTIONAL
Enrollment

92

Participants

Timeline

Start Date

July 31, 2003

Primary Completion Date

October 31, 2005

Study Completion Date

June 30, 2007

Conditions
Malignant Melanoma
Interventions
BIOLOGICAL

MDX-010

Subjects will be treated with transfectoma-derived MDX-010 at 2.8 or 5 mg/kg/dose, or with hybridoma-derived MDX-010 at 3 mg/kg/dose administered on Days 1, 57, and 85. The 2.8, 3, and 5 mg/kg dosage cohorts may be initiated concurrently. Additionally, 6 subjects per cohort will receive single doses of transfectoma-derived MDX-010 at 7.5, 10, 15, and 20 mg/kg.

Trial Locations (4)

28207

Piedmont Oncology Specialists, Charlotte

90033

USC/Norris Comprehensive Cancer Center, Los Angeles

97213

Providence Portland Medical Center, Portland

85724-5024

Arizona Cancer Center, Tucson

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY