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Study identifier: NCT04837885 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intra-arterial Hepatic (IAH) Infusion of Radiolabelled Somatostatin Analogs in GEP-NET Patients With Dominant Liver Metastases

Condition: Neuroendocrine Tumor · Liver Metastases · Neuroendocrine Gastroenteropancreatic Tumour  ·  Sponsor: University Hospital, Bordeaux

PhasePhase 2
Planned participants23
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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).

This description comes directly from the study's public registry record.

Talk to the study team

Ghoufrane TLILI, Dr  ·  05 57 65 64 08  ·  ghoufrane.tlili@chu-bordeaux.fr

Macary Guillaume  ·  05 57 62 32 52  ·  guillaume.macary@chu-bordeaux.fr

Always discuss trial participation with your own doctor first.

Locations (4)

Institut BergoniéBordeaux, FranceNot Yet Recruiting
Institut de cancérologie du Gard (ICG) - CHU de NîmesNîmes, FranceNot Yet Recruiting
CHU Bordeaux - Hôpital Haut LévêquePessac, FranceRecruiting
Institut universitaire du cancer de Toulouse (IUCT) OncopoleToulouse, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT04837885