The purpose of this study is to investigate the safety and potential effectiveness of the imaging compound 18F MEL050 for finding sites of melanoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
12
Diagnostic intervention to establish the safety and biodistribution of MEL050 in participants with melanoma.
Peter MacCallum Cancer Centre
East Melbourne, Victoria, Australia
Safety of 18F MEL050 administration as measured by occurrence of adverse clinical, biochemical or haematological events following 18F MEL050 administration.
Time frame: Up to 28 days following 18F MEL050 administration (+/- 7 days)
Percentage of injected 18F MEL050 dose in organs of interest.
Time frame: 10, 30, 60 and 120 minutes post 18F MEL050 administration
Percentage of unmetabolized 18F MEL050 in plasma and urine after radiotracer administration.
Time frame: 60, 120 and 180 minutes post 18F MEL050 administration.
Absorbed organ doses and whole body dose expressed as milliSv/200MBq administered dose.
Time frame: 10, 30, 60 and 120 minutes post 18F MEL050 administration
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