Ionis Pharmaceuticals IncFDA expanded Tryngolza label to treat severe hypertriglyceridemia, expanding addressable patient population to nearly 3 million in the US.

The FDA has approved Ionis Pharmaceuticals' drug Tryngolza as an adjunct to diet to reduce triglycerides and the risk of acute pancreatitis in adults with severe hypertriglyceridemia, making it the first approved treatment for the condition in the United States. The approval is supported by data from two phase III studies, CORE and CORE2, which showed statistically significant reductions in triglyceride levels and acute pancreatitis events. Ionis plans to commercially launch the drug for this new indication next month, significantly expanding its commercial opportunity to nearly 3 million people in the United States living with severe hypertriglyceridemia. Tryngolza was previously approved in 2024 for familial chylomicronemia syndrome, a rare form of severe hypertriglyceridemia, and generated $108 million in product sales in 2025 followed by $27 million in the first quarter of 2026. Ionis also has partnerships with AstraZeneca, Biogen, GSK, and Novartis, providing a diverse revenue stream from drugs such as Spinraza, Qalsody, Wainua, pelacarsen, and bepirovirsen.
Ionis Pharmaceuticals IncFDA expanded Tryngolza label to treat severe hypertriglyceridemia, expanding addressable patient population to nearly 3 million in the US.
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