This is an explorative phase II study to investigate the suitability of PD L 506 in the specific intra-operative detection of breast tumour tissue.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
TRIPLE
Enrollment
8
Two different doses will be compared
Unnamed facility
Munich, Germany
Fluorescence intensity in breast cancer tissue
Time frame: 3 h after intake of study medication
Laboratory data and adverse events
Time frame: 14 days
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