The purpose of this study is to determine whether Lipovaxin-MM, a new anti-cancer vaccine, is safe and effective in improving the body's ability to destroy cancer cells in patients with metastatic melanoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
12
Patients will receive three doses of Lipovaxin-MM by intravenous infusion at intervals of four weeks OR patients will receive 4 doses of Lipovaxin-MM by intravenous infusion at weekly intervals
Pain & Anaesthesia Research Clinic
Adelaide, South Australia, Australia
Adverse events
Time frame: Within 84 days after first dose
Immunogenicity
antigen specific immune responses will be monitored
Time frame: Within 42 days of first dose
Anti-cancer activity (RECIST criteria)
assessed every 6 weeks of study
Time frame: Within 84 days of first dose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.