A Phase III Multi-Center, Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Lutathera in Patients with Grade 2 and Grade 3 Advanced GEP-NET
Primary Objective: To demonstrate that Lutathera is superior to active comparator in delaying the time-to-first occurrence of progression or death (PFS) as first line treatment Key Secondary Objectives: To demonstrate the superiority of Lutathera, compared to active comparator, in terms of objective response. To demonstrate the superiority of Lutathera, compared to active comparator, in terms of time to deterioration in selected QoL items/scales
Radiotherapy; Therapy (NOS)
177Lu-DOTA0-Ty3-Octreotate (Lutathera); Lutathera (); octreotide LAR ()
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