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Clinical Trial Enrolling PHASE3

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

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 […]

📅 06 Apr 2026 ⏱ 1 min read
Enrolling
Check the registry for current status and eligibility criteria.
Status
Enrolling
Phase
PHASE3
Start
2017-02-02
Completion
2024-11-27

Key Clinical Points

• Radioactive peptide therapy with 177Lu-edotreotide proved more effective than everolimus for advanced somatostatin receptor-positive neuroendocrine tumours.

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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