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Clinical Trial Active — Not Recruiting Phase III NCT03049189

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

Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients — Active Not Recruiting • Phase III • Oncology • NCT03049189.

📅 06 Apr 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase III
NCT ID
NCT03049189
Start
2017-02-02
Completion
2024-11-27
ClinicaliQ Trial Snapshot
  • Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients — Active Not Recruiting • Phase III • Oncology • NCT03049189.
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What This Trial Is Studying

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). Conditions: Neuroendocrine Tumors Interventions: 177Lu-edotreotide PRRT, Everolimus, Amino-Acid Solution Lead Sponsor: ITM Solucin GmbH Planned Enrollment: 324 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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