Successful Launch of Tryngolza
Tryngolza, the first FDA-approved treatment for familial chyloymicronemia syndrome, exceeded revenue expectations with $19 million in net product sales for the second quarter, reflecting a threefold increase quarter-over-quarter.
Record Revenue and Increased Financial Guidance
Ionis reported $452 million in revenue for Q2, a twofold increase year-over-year, and raised the 2025 revenue guidance by $100 million to $850 million.
Strong Pipeline Progress
Anticipated FDA approval for Donidalorsen for HAE next month, with potential launches for Olezarsen and Zilganersen in the pipeline, representing significant revenue potential.
Early Commercial Success and Strategic Execution
The commercial team reached over 3,000 physicians, with favorable payer dynamics leading to over 90% of patients paying $0 out-of-pocket for Tryngolza.