Melanoma (Skin) Clinical Trial
Official title:
An Open-label Study Of MDX-010 In Combination With gp100 Peptides Emulsified With Montanide ISA 51 In The Treatment Of Patients With Stage IV Melanoma
RATIONALE: Vaccines made from peptides may make the body build an immune response to kill
tumor cells. Monoclonal antibodies can locate tumor cells and either kill them or deliver
tumor-killing substances to them without harming normal cells. Combining vaccine therapy
with a monoclonal antibody may cause a stronger immune response and kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of combining vaccine therapy with
monoclonal antibody therapy in treating patients who have stage IV melanoma.
OBJECTIVES:
- Determine the clinical response in patients with stage IV melanoma when treated with
anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody combined with
gp100:209-217 and gp100:280-288 peptides emulsified in Montanide ISA-51.
- Determine a safety and adverse event profile of this regimen in these patients.
- Determine improved immunologic response in patients treated with this regimen.
OUTLINE: This is an open-label study.
Patients receive anti-cytotoxic T-lymphocyte-associated antigen-4 monoclonal antibody IV
over 90 minutes immediately followed by gp100:209-217 and gp100:280-288 peptides emulsified
in Montanide ISA-51 subcutaneously on days 1, 22, 43, and 64. Treatment repeats every 12
weeks in the absence of disease progression or unacceptable toxicity.
Patients are followed at 3 weeks, every 3 months for 1 year, every 6 months for 2 years, and
then annually thereafter.
PROJECTED ACCRUAL: A total of 68 patients will be accrued for this study within 2 years.
;
Masking: Open Label, Primary Purpose: Treatment
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