University Medical Center Groningen
Groningen, Provincie Groningen, 9713 GZ, Netherlands
NCT Number: NCT02583568
A need for further investigation for fluorescence image-guided surgery in breast conserving surgery (BCS) has arisen following the results obtained from a phase I feasibility breast cancer trial (BIRDYE study: ABR NL 37479.042011). The aim of this study is to define the optimal dose of the fluorescent tracer Bevacizumab-IRDye800CW for intraoperative delineation of breast cancer tissue using the improved and optimized fluorescent tracer and camera system.
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Notify Me18 year and older
Female
Interventional
Phase 1 / Phase 2
Groningen, Provincie Groningen, 9713 GZ, Netherlands
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
For female subjects who are of childbearing potential, are premenopausal with intact reproductive organs or are less than 2 years post-menopausal:
Main Exclusion Criteria:
three days prior to surgery bevacizumab-800CW will be administered
Other names: Bevacizumab-IRDye800CW
Time frame: day 3
Time frame: up to two weeks
University Medical Center Groningen
Other
Phase II, Open-Label Study to Evaluate Safety and Explore Efficacy of Escalating Doses of Bevacizumab-IRDye800CW as an Optical Imaging Agent to Detect Cancer Tissue Delineation During Tumor Resection Surgery in Patients With Breast Cancer
Acronym: MARGIN
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