Study Title
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
Study Details
Description:
A Phase III Multi-center, Randomized, Open-label Study to Evaluate the Efficacy and Safety of [177Lu]Lu-DOTA-TATE in Patients Newly Diagnosed With Grade 1 and Grade 2 (Ki-67 <10%) Advanced GEP-NET With High Disease Burden (NETTER-3)
Sponsor:
NovartisContacts:
Novartis Pharmaceuticalsnovartis.email@novartis.com
+41613241111
Government Study Link:
NCT06784752 - Click here to see study onClinicalTrials.gov
Drug Details
Patient Education
Patient Education Not Yet Provided
Publications
Publications Not Yet Provided
Locations
Switzerland