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Clinical Trial · NCT07370597
Overview
If dosimetry calculations could predict which patients would ultimately respond or not respond to treatment, administered dose and number of 177Lu-PSMA-RLT cycles could be adapted early during the treatment course. In this context, our study aims to analyze if absorbed tumour dose obtained by dosimetry calculations could be used as a biomarker to predict non-response to treatment early after one cycle, as the first step towards treatment dose adaptation of a personalized radionuclide treatment approach.
Sponsor
Jules Bordet Institute
Phase
N/A
Contacts
Carlos Artigas, MD
carlos.artigas@hubruxelles.be
02.54137.81
ClinicalTrials.gov
NCT07370597Drug / Compound
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