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Study identifier: NCT03049189 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Active Not Recruiting

Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients

Condition: Neuroendocrine Tumors  ·  Sponsor: ITM Solucin GmbH

PhasePhase 3
Planned participants324
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The purpose of the study is to evaluate efficacy and safety of Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-Edotreotide compared to targeted molecular therapy with Everolimus in patients with inoperable, progressive, somatostatin receptor-positive (SSTR+), neuroendocrine tumours of gastroenteric or pancreatic origin (GEP-NET).

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

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No contact information is available for this study as per the public registry record.

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Locations (52)

Banner Health d.b.a. Banner MD Anderson Cancer CenterGilbert, Arizona, United States
Stanford UniversityStanford, California, United States
Moffitt Cancer Center & Research InstituteTampa, Florida, United States
Northwestern Memorial HospitalChicago, Illinois, United States
University of Michigan Comprehensive Cancer CenterAnn Arbor, Michigan, United States
Excel Diagnostics & Nuclear Oncology CenterHouston, Texas, United States
Royal North Shore HospitalSaint Leonards, New South Wales, Australia
Olivia Newton-John Cancer & Wellness Centre, Austin HospitalHeidelberg, Victoria, Australia
Peter MacCallum Cancer CentreMelbourne, Victoria, Australia
Fiona Stanley HospitalMurdoch, Western Australia, Australia
Allgemeines Krankenhaus WienVienna, Austria
Institut Jules BordetBrussels, Belgium

+ 40 more locations — full list on the registry record.

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