Overview of the Neuroendocrine Tumor Treatment Industry
The scope of the neuroendocrine tumor treatment industry is immense. To capitalize on emerging opportunities, leading companies are employing different strategies. From advancements in treatment modalities to increasing investments in oncology research, the target industry is witnessing a rapid transformation.
Key Developments in Neuroendocrine Tumor Treatments
In April 2024, Novartis received the U.S. Food and Drug Administration (FDA) approval for Lutathera for the treatment of gastroenteropancreatic neuroendocrine tumors in pediatric patients. This marks the beginning of a new era for pediatric NET treatment, highlighting the growing role of precision medicine in oncology.
Radioligand therapies have great potential to shape the future of cancer care. With this approval, Lutathera became the very first therapy for children with GEP-NETs. It will offer new hope for young patients living with GEP-NETs.
In November 2024, the U.S. FDA notified Exelixis, Inc. that the supplemental new drug application for cabozantinib (CABOMETYX) for the treatment of adults with advanced pNET and epNET will be discussed at the Oncology Drugs Advisory Committee in March 2025. Previously, the FDA granted orphan drug designation to cabozantinib for the treatment of pNET in August 2024.
In July 2024, Ispen expanded its collaboration and license agreement with Exelixis, Inc. for the development of Cabometyx in advanced NETs. The agreement is based on positive CABINET Phase 3 trial outcomes.
