Novartis casts a broader Netter for Lutathera
Novartis’s SSTR2-targeting radioconjugate Lutathera already has a broad US label for SSTR-positive gastroenteropancreatic neuroendocrine tumours, but this isn’t stopping the company from starting another phase 3 in early-line disease. Netter-3, recently listed on clinicaltrials.gov, will test Lutathera plus Sandostatin, versus Sandostatin alone, in around 240 patients with first-line grade 1 and 2 GEP-NETs and a high disease burden. Grade 1 GEP-NETs are the least advanced type, and are said to be slow growing. The new trial could take Lutathera into even earlier territory than Netter-2, which tested the same combo in first-line patients with grade 2 and 3 disease. Positive Netter-2 data were presented at last year’s ASCO-GI meeting; the trial formed the basis of a 2024 EU filing in first-line disease, and Novartis previously said it would also be important to convince US doctors of the merits of earlier use. The group seems likely to be following a similar strategy with Netter-3. Still, Novartis hopes that Lutathera, which made $600m in 2023, might have utility beyond GEP-NETs: a phase 3 in small-cell lung cancer is slated for 2027, the Swiss company said at the recent JP Morgan healthcare conference.
Expanding the Netter: selected studies of Novartis’s Lutathera
Trial | Setting | Note |
---|---|---|
Netter-1 | 2nd-line GEP-NETs | PFS NR with Lutathera + Sandostatin, vs 8.5mth with Sandostatin; approved with broad label in Jan 2018 |
Netter-2 | 1st-line GEP-NETs, grade 2 & 3 | PFS 22.8mth with Lutathera + Sandostatin, vs 8.5mth for Sandostatin; awaiting EU approval decision |
Netter-3 | 1st-line GEP-NETs, grade 1 & 2 | To begin May 2025 |
Source: OncologyPipeline & clinicaltrials.gov.
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