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Ionis Pharmaceuticals — Apr 29, 2026 release

Fiscal 2026 first-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001140361-26-017637
Open on SEC.gov ↗
Showing in the filing
Operating loss on a non-GAAP basis
“$425-475 million”
Period
FY2026
Measure
Company-defined measure
Source
Prose
All guidance in this release · 7
Annual olezarsen peak net sales for FY2026
“>$3 billion”
Goal of reaching cash-flow breakeven for FY2028
“cash-flow breakeven in 2028”
Total Revenue for FY2026
“$875-900 million”
TRYNGOLZA product sales, net for FY2026
“$100-110 million”
DAWNZERA product sales, net for FY2026
“$110-120 million”
Operating loss on a non-GAAP basis for FY2026
“$425-475 million”
Cash, cash equivalents and short-term invest… for FY2026
“>$1.6 billion”
Exhibit 99.1 · the passage around this item
… earlier in the release
    Full Year 2026 Guidance Previous Guidance New Guidance Total Revenue $800-825 million $875-900 million TRYNGOLZA   product sales, net NA $100-110 million DAWNZERA   product sales, net NA $110-120 million Operating loss on a non-GAAP basis $500-550 million $425-475 million Cash, cash equivalents and short-term investments >$1.6 billion >$1.6 billion Webcast and Other Updates Management will host a conference call and webcast to discuss Ionis’ first quarter 2026 results at 8:30 a.m. Eastern time on Wednesday, April 29, 2026. Interested parties may access the webcast here . A webcast replay will be available for a limited time at the same address. To access the Company’s first quarter 2026 earnings slides click here . Ionis’ Marketed Medicines   INDICATION for TRYNGOLZA ®   (olezarsen)   TRYNGOLZA ®   (olezarsen) was approved by the U.S. Food and Drug Administration as an adjunct to diet to reduce triglycerides in adults with familial chylomicronemia syndrome (FCS).   IMPORTANT SAFETY INFORMATION   CONTRAINDICATIONS TRYNGOLZA is contraindicated in patients with a history of serious hypersensitivity to TRYNGOLZA or any of the excipients in TRYNGOLZA. Hypersensitivity reactions requiring medical treatment have occurred.   WARNINGS AND PRECAUTIONS Hypersensitivity Reactions Hypersensitivity reactions (including symptoms of bronchospasm, diffuse erythema, facial swelling, urticari
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.