Ticilimumab (CP-675,206) in Treating Patients With Stage IIIC or Stage IV Melanoma

PHASE2CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

January 31, 2007

Primary Completion Date

July 31, 2011

Study Completion Date

March 31, 2015

Conditions
Melanoma (Skin)
Interventions
BIOLOGICAL

CP-675,206

Patients will receive intravenous administration of CP-675,206 at a dose of 15mg/kg on Day 1 of an every 90 day cycles. For purposes of treatment visits and scheduling, each cycle is defined as a 90 day period. Patients may receive up to 8 dose (8 cycles) in a 24-month period until progression of disease or intolerable toxicity.

Trial Locations (1)

90095-1781

Jonsson Comprehensive Cancer Center at UCLA, Los Angeles

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

Jonsson Comprehensive Cancer Center

OTHER