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Study identifier: NCT06784752 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Evaluate the Efficacy and Safety of [177Lu]Lu-DOTA-TATE in Patients With Grade 1 and Grade 2 Advanced GEP-NET

Condition: Somatostatin Receptor Positive (SSTR+) · Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET)  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 3
Planned participants240
Who can joinAll sexes, 12 Years to 100 Years
Healthy volunteersNo

About this study

The purpose of the current study is to evaluate the efficacy and safety of \[177Lu\]Lu-DOTA-TATE plus octreotide long-acting release (LAR) versus octreotide LAR alone in newly diagnosed patients with somatostatin receptor positive (SSTR+), well differentiated Grade1 and Grade 2 (G1 and G2) (Ki-67 \<10%) advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs) with high disease burden

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

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Novartis Pharmaceuticals  ·  +41613241111

Always discuss trial participation with your own doctor first.

Locations (65)

Mayo Clinic ArizonaScottsdale, Arizona, United StatesRecruiting
Highlands Oncology GroupFayetteville, Arkansas, United StatesRecruiting
Rocky Mountain Cancer CentersDenver, Colorado, United StatesRecruiting
Hartford HospitalHartford, Connecticut, United StatesRecruiting
Yale New Haven HospitalNew Haven, Connecticut, United StatesRecruiting
Mayo Clinic JacksonvilleJacksonville, Florida, United StatesRecruiting
Winship Cancer InstituteAtlanta, Georgia, United StatesRecruiting
St Elizabeth HealthcareEdgewood, Kentucky, United StatesRecruiting
LSU Medical CenterNew Orleans, Louisiana, United StatesRecruiting
Henry Ford HospitalDetroit, Michigan, United StatesRecruiting
Mount Sinai Medical CenterNew York, New York, United StatesRecruiting
Piedmont HealthcareWinston-Salem, North Carolina, United StatesRecruiting

+ 53 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06784752