Stage IV Melanoma Clinical Trial
Official title:
A Phase 1 Dose-Escalation Trial To Evaluate Safety, Tolerability And Immune Pharmacodynamics Of Combined Administration Of Tremelimumab (Blocking Anti-CTLA-4 Antibody) And CP-870,893 (Agonist Anti-CD40 Antibody) In Patients With Metastatic Melanoma
RATIONALE: Monoclonal antibodies, such as tremelimumab and CD40 agonist monoclonal antibody
CP-870,893, can block tumor growth in different ways. Some block the ability of tumor cells
to grow and spread. Others find tumor cells and help kill them or carry cancer-killing
substances to them. Giving tremelimumab together with CD 40 agonist monoclonal antibody
CP-870, 893 may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of giving tremelimumab
together with CD40 agonist monoclonal antibody CP-870,893 in treating patients with
metastatic melanoma.
PRIMARY OBJECTIVES:
I. To assess the safety, dose-limiting toxicities and maximum tolerated doses of tremelimumab
(administered intravenously every 12 weeks) and CP- 870,893 (administered intravenously every
3 weeks).
SECONDARY OBJECTIVES:
I To seek preliminary evidence of anti-tumor efficacy of the combination of tremelimumab and
CP-870,893, including objective response rate at MTD.
II. To determine the immune pharmacodynamic changes associated with the administration of the
combination of tremelimumab and CP-870,893.
OUTLINE: Patients receive tremelimumab IV over 1 hour on day 1 and CD40 agonist monoclonal
antibody CP-870,893 IV over 30 minutes on days 2, 22, 43, and 64. Treatment repeats every 12
weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed for 4 weeks.
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