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Clinical Trial · NCT04837885
Overview
The management of liver metastases in neuroendocrine neoplasms is challenging. Peptide receptor radionuclide therapy with radiolabeled somatostatin analogs (SSA) is one of the most promising therapeutic options. As liver is the most frequent site of metastatic disease, our project proposes to compare administration of radiolabeled SSA by arterial intrahepatic infusion (experimental approach) vs intravenous administration (conventional). Evaluation will be made by (i) comparing 68Ga-DOTA-peptides uptake after intra-hepatic versus intravenous route (imaging), (ii) by evaluating the safety of an additional intra-hepatic administration of therapeutic radiolabeled SSA (therapy).
Sponsor
University Hospital, Bordeaux
Phase
Phase 2
Contacts
Ghoufrane TLILI, Dr
ghoufrane.tlili@chu-bordeaux.fr
05 57 65 64 08
Macary Guillaume
guillaume.macary@chu-bordeaux.fr
05 57 62 32 52
ClinicalTrials.gov
NCT04837885Drug / Compound
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