8-K
Ionis Pharmaceuticals Inc (IONS)
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of report (Date of earliest event reported): February 21, 2024
IONIS PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Charter)
Delaware
(State or Other Jurisdiction of Incorporation)
| 000-19125 | 33-0336973 |
|---|---|
| (Commission File No.) | (IRS Employer Identification No.) |
2855 Gazelle Court
Carlsbad, CA 92010
(Address of Principal Executive Offices and Zip Code)
Registrant’s telephone number, including area code: (760) 931-9200
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ☐ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|---|---|
| ☐ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| --- | --- |
| ☐ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| --- | --- |
| ☐ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
| --- | --- |
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Trading symbol | Name of each exchange on which registered |
|---|---|---|
| Common Stock, $.001 Par Value | “IONS” | The Nasdaq Stock Market, LLC |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (Section 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (Section 240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
| Item 2.02 | Results of Operations and Financial Condition. |
|---|
On February 21, 2024, Ionis Pharmaceuticals, Inc. (the “Company”) issued a press release announcing the
Company’s financial results for the quarter and fiscal year ended December 31, 2023. In addition to disclosing results that are determined in accordance with Generally Accepted Accounting Principles \(“GAAP”\), the Company also discloses pro forma or non-GAAP results of operations, which are adjusted from GAAP to exclude non-cash compensation expense related to equity awards and the related tax effects. In addition, in 2022, the
Company’s non-GAAP net loss excluded the gain on real estate assets related to the Company’s sale and leaseback transaction and the related tax effects. The Company is presenting pro forma information with such exclusions because the Company
believes it is useful for investors in assessing the Company’s operating results compared to the prior year. A copy of the release is furnished with this report as an exhibit pursuant to “Item 2.02. Results of Operations and Financial Condition”
of Form 8-K in accordance with SEC Release Nos. 33-8216 and 34-47583.
The information in this Current Report on Form 8-K and the Exhibit attached hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange
Act of 1934 \(the “Exchange Act”\) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or
the Exchange Act, regardless of any general incorporation language in such filing.
| Item 9.01. | Financial Statements and Exhibits. |
|---|
(d) Exhibits.
| Exhibit No. | Description |
|---|---|
| 99.1 | Press Release dated February 21, 2024. |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document). |
SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
| Ionis Pharmaceuticals, Inc. | ||
|---|---|---|
| Dated: February 21, 2024 | By: | /s/ Patrick R. O’Neil |
| Patrick R. O’Neil | ||
| Executive Vice President, Chief Legal Officer and General Counsel |
Exhibit 99.1
Ionis reports fourth quarter and full year 2023 financial results
WAINUA^TM^ approved with launch underway; on track for EU and Canada approval decisions this year
Positive Phase 3 olezarsen and donidalorsen data, preparing regulatory submissions for FCS and HAE, respectively
Olezarsen granted Breakthrough Therapy designation by the FDA for FCS
Ionis provides full year 2024 financial guidance
CARLSBAD, Calif., February 21, 2024 – Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) (the “Company”), today reported financial results for the fourth quarter and full year ended December 31, 2023.
“This past year included many remarkable achievements as we continued to advance our vision to bring better futures to people with serious diseases. Ionis achieved two FDA approvals, delivered three positive Phase 3 data readouts, expanded our rich Phase 3 pipeline to nine medicines and advanced our next wave of wholly owned medicines as well as our technology,” said Brett P. Monia, Ph.D., chief executive officer of Ionis. “In 2024, we anticipate building on our success with important catalysts and continued value creation. The WAINUA U.S. launch is underway for patients with hereditary ATTR polyneuropathy, and we expect additional approvals in other countries this year. We plan to present positive Phase 3 data for olezarsen in familial chylomicronemia syndrome and donidalorsen in hereditary angioedema, positioning Ionis to independently launch these two medicines. We also anticipate additional readouts from multiple mid-stage programs that, if positive, would advance into Phase 3 development, further strengthening our ability to deliver a steady cadence of potentially transformational medicines for years to come.”
Fourth Quarter and Full Year 2023 Summary Financial Results^(1)^:
| Three months ended<br><br> <br>December 31, | Year ended<br><br> <br>December 31, | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2023 | 2022 | 2023 | 2022 | |||||||||
| (amounts in millions) | ||||||||||||
| Total revenue | $ | 325 | $ | 152 | $ | 788 | $ | 587 | ||||
| Operating expenses | $ | 331 | $ | 360 | $ | 1,141 | $ | 998 | ||||
| Operating expenses on a non-GAAP basis | $ | 305 | $ | 335 | $ | 1,035 | $ | 898 | ||||
| Loss from operations | $ | (6 | ) | $ | (208 | ) | $ | (353 | ) | $ | (411 | ) |
| Income (Loss) from operations on a non-GAAP basis | $ | 20 | $ | (183 | ) | $ | (247 | ) | $ | (311 | ) | |
| (1) | Reconciliation of GAAP to non-GAAP basis contained later in this release. | |||||||||||
| --- | --- |
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Financial Highlights
| • | Revenue more than doubled for the fourth quarter of 2023 compared to the same period in the prior year and increased 34% for the full year, driven by the successful progression of Ionis’ pipeline<br> and technology platform |
|---|---|
| • | Operating expenses increased compared to the prior year, primarily due to strategic investments to bring eplontersen, olezarsen and donidalorsen to patients |
| --- | --- |
| • | 2023 operating loss significantly improved over prior year due to substantial revenue earned during the year |
| --- | --- |
| • | Cash and short-term investments of $2.3 billion as of December 31, 2023 enables continued investments to drive increasing value, including supporting our potential upcoming launches |
| --- | --- |
Recent Marketed Medicines Highlights
| • | WAINUA approved in the U.S., resulting in a $50 million milestone payment from AstraZeneca;<br> launch underway for treatment of adults with polyneuropathy of hereditary transthyretin-mediated amyloidosis (ATTRv-PN) |
|---|---|
| • | SPINRAZA continued to be the global market leader for the treatment of spinal muscular atrophy (SMA) with global sales of $1.7 billion in 2023 |
| --- | --- |
Recent Late-Stage Pipeline Highlights
| • | Eplontersen granted Fast Track designation by the FDA for the treatment of patients with ATTR cardiomyopathy (ATTR-CM) |
|---|---|
| • | Olezarzen granted Breakthrough Therapy designation by the FDA for the treatment of patients with familial chylomicronemia syndrome (FCS) |
| --- | --- |
| • | Olezarsen granted orphan drug designation by the FDA for the treatment of patients with FCS |
| --- | --- |
| • | Achieved multiple milestones with donidalorsen for the treatment of patients with hereditary angioedema (HAE): |
| --- | --- |
| o | Reported positive topline data from the Phase 3 OASIS-HAE study in patients treated every four weeks or every eight weeks; preparing to submit NDA |
| --- | --- |
| o | Licensed European donidalorsen commercialization rights to Otsuka; Otsuka preparing to submit MAA |
| --- | --- |
| o | Donidalorsen granted orphan drug designation by EMA |
| --- | --- |
| o | Reported positive Phase 2 data from the open label extension study in patients with HAE treated for two years |
| --- | --- |
| • | Bepirovirsen granted fast track designation by the FDA for the treatment of patients with chronic hepatitis B (CHB) |
| --- | --- |
Recent Other Pipeline Highlights
| • | Achieved multiple milestones with ION582 (BIIB121) for the treatment of patients with Angelman syndrome: |
|---|---|
| o | Completed enrollment in the Phase 1/2 HALOS study in patients with Angelman syndrome; on track for data readout in mid-2024 |
| --- | --- |
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| o | Presented positive clinical update from ongoing HALOS study at the FAST (Foundation for Angelman Syndrome Therapeutics) Summit |
|---|---|
| o | Extended the long-term extension portion of HALOS study |
| --- | --- |
| • | Sapablursen and ION356 granted fast track designation by the FDA for the treatment of patients with polycythemia vera (PV) and Pelizaeus-Merzbacher disease (PMD), respectively |
| --- | --- |
| • | Initiated the Phase 1/2 PrProfile study of ION717 in patients with Prion disease |
| --- | --- |
| • | AstraZeneca licensed ION826 for the treatment of heart failure, resulting in a $36 million payment from AstraZeneca |
| --- | --- |
Recent Technology Advancement Highlights
| • | Licensed Vect-Horus’ blood-brain barrier crossing technology for the development of RNA-targeted neurological disease medicines |
|---|
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Fourth Quarter, Full Year 2023 Financial Results and 2024 Financial Guidance
“In 2023, we earned substantial revenues due to continued success with our pipeline and technology. As a result, we exceeded our 2023 revenue guidance, which drove a smaller than anticipated operating loss,” said Elizabeth L. Hougen, chief financial officer of Ionis. “In 2024, with WAINUA’s launch for ATTRv-PN underway, we are adding a new stream of royalty revenue to our substantial and sustained revenues. We will continue to deploy our capital resources toward growth opportunities that can enable Ionis to unlock next-level value. This includes continuing to make significant investments in near-term commercial opportunities, the expansion of our wholly owned pipeline, and advancing our technology, all of which should empower future growth.”
Revenue
Ionis’ revenue was comprised of the following:
| Three months ended | Year ended | |||||||
|---|---|---|---|---|---|---|---|---|
| December 31, | December 31, | |||||||
| 2023 | 2022 | 2023 | 2022 | |||||
| Revenue: | (amounts in millions) | |||||||
| Commercial revenue: | ||||||||
| SPINRAZA royalties | $ | 62 | $ | 67 | $ | 240 | $ | 242 |
| Other commercial revenue: | ||||||||
| TEGSEDI and WAYLIVRA revenue, net | 9 | 7 | 35 | 30 | ||||
| Licensing and royalty revenue | 8 | 6 | 34 | 31 | ||||
| Total commercial revenue | 79 | 80 | 309 | 303 | ||||
| Research and development revenue: | ||||||||
| Amortization from upfront payments | 76 | 15 | 125 | 69 | ||||
| Milestone payments | 11 | 14 | 101 | 74 | ||||
| License fees | 92 | - | 117 | 37 | ||||
| Other services | - | 22 | 10 | 27 | ||||
| Collaborative agreement revenue | 179 | 51 | 353 | 207 | ||||
| WAINUA joint development revenue | 67 | 21 | 126 | 77 | ||||
| Total research and development revenue | 246 | 72 | 479 | 284 | ||||
| Total revenue | $ | 325 | $ | 152 | $ | 788 | $ | 587 |
Commercial revenues in 2023 were comparable to 2022. Commercial revenue for 2023 included $240 million from SPINRAZA royalties, which was comparable to 2022. Ionis’ commercial revenue in 2023 also included royalties from QALSODY U.S. product sales.
R&D revenue significantly increased in 2023 compared to 2022 primarily due to continued success with Ionis’ pipeline and technology. As a result, Ionis earned significant partner payments, including $50 million from AstraZeneca for the FDA approval of WAINUA for ATTRv-PN in the U.S., $36 million from AstraZeneca for licensing ION826 and payments from Ionis’ new collaborations with Otsuka, Roche and Novartis.
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Operating Expenses
Ionis’ operating expenses increased for the year ended December 31, 2023 compared to 2022 primarily due to certain one-time costs, including a non-cash charge associated with a lease exit and the license fee Ionis paid to Vect-Horus. As Ionis advanced its robust pipeline, study costs increased compared to the same periods in 2022 as many of the Company’s Phase 3 studies are either fully enrolled or approaching full enrollment, resulting in higher R&D expenses year over year. R&D expenses for the fourth quarter of 2023 were lower compared to the fourth quarter of 2022, primarily due to the $80 million upfront payment Ionis paid to Metagenomi in 2022. Ionis’ SG&A expenses increased year over year primarily due to launch preparation activities for WAINUA, olezarsen and donidalorsen.
Balance Sheet
As of December 31, 2023, Ionis’ cash, cash equivalents and short-term investments increased to $2.3 billion compared to $2.0 billion at December 31, 2022 primarily due to the $500 million Ionis received from Royalty Pharma in January 2023 and significant partner payments throughout 2023. Ionis’ working capital also increased over the same period primarily due to the Company’s higher cash and short-term investments balance. In 2023, the Company recorded a long-term liability for future royalties due to Royalty Pharma. In June 2023, Ionis issued $575 million of senior convertible notes due in June 2028 with an interest rate of 1.75%. The Company used the majority of the proceeds to repurchase $504 million of its 0.125% convertible notes.
2024 Financial Guidance
The Company’s 2024 guidance reflects its plan to deploy its capital resources toward growth opportunities, including continued investments in its near-term commercial opportunities, expanding its wholly owned pipeline and advancing its technology platform. Additionally, the Company expects to continue earning substantial revenue from its commercial portfolio and partnered programs.
| Full Year 2024 Guidance | |
|---|---|
| Revenue | >$575 million |
| Operating loss on a non-GAAP basis | <$475 million |
| Cash, cash equivalents and short-term investments | ~$1.7 billion |
Webcast
Management will host a conference call and webcast to discuss Ionis’ fourth quarter and full year 2023 results at 11:30 a.m. Eastern time on Wednesday, February 21, 2024. 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 fourth quarter and full year 2023 earnings slides click here.
For more information about SPINRAZA and QALSODY, visit https://www.spinraza.com/ and https://www.qalsody.com/, respectively. QALSODY is approved under accelerated approval based on reduction in plasma neurofilament light chain (NfL) observed in patients treated with QALSODY. Continued approval may be contingent upon verification of clinical benefit in confirmatory trial(s).
INDICATION for WAINUA™ (eplontersen)
WAINUA injection, for subcutaneous use, 45 mg is indicated for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults.
IMPORTANT SAFETY INFORMATION for WAINUA™ (eplontersen)
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WARNINGS AND PRECAUTIONS
Reduced Serum Vitamin A Levels and Recommended Supplementation WAINUA leads to a decrease in serum vitamin A levels. Supplement with recommended daily allowance of vitamin A. Refer patient to an ophthalmologist if ocular symptoms suggestive of vitamin A deficiency occur.
ADVERSE REACTIONS
Most common adverse reactions (≥9% in WAINUA-treated patients) were vitamin A decreased (15%) and vomiting (9%).
Please see link to U.S. Full Prescribing Information for WAINUA.
About Ionis Pharmaceuticals, Inc.
For three decades, Ionis has invented medicines that bring better futures to people with serious diseases. Ionis currently has five marketed medicines and a leading pipeline in neurology, cardiology, and other areas of high patient need. As the pioneer in RNA-targeted medicines, Ionis continues to drive innovation in RNA therapies in addition to advancing new approaches in gene editing. A deep understanding of disease biology and industry-leading technology propels our work, coupled with a passion and urgency to deliver life-changing advances for patients. To learn more about Ionis, visit Ionispharma.com and follow us on X (Twitter) and LinkedIn.
Ionis’ Forward-looking Statement
This press release includes forward-looking statements regarding Ionis’ business, financial guidance and the therapeutic and commercial potential of our commercial medicines, additional medicines in development and technologies. Any statement describing Ionis’ goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties including those inherent in the process of discovering, developing and commercializing medicines that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such medicines. Ionis’ forward-looking statements also involve assumptions that, if they never materialize or prove correct, could cause its results to differ materially from those expressed or implied by such forward-looking statements. Although Ionis’ forward-looking statements reflect the good faith judgment of its management, these statements are based only on facts and factors currently known by Ionis. Except as required by law, we undertake no obligation to update any forward-looking statements for any reason. As a result, you are cautioned not to rely on these forward-looking statements. These and other risks concerning Ionis' programs are described in additional detail in Ionis' annual report on Form 10-K for the year ended December 31, 2022, and most recent Form 10-Q, which are on file with the Securities and Exchange Commission. Copies of these and other documents are available from the Company.
In this press release, unless the context requires otherwise, “Ionis,” “Company,” “we,” “our” and “us” all refer to Ionis Pharmaceuticals and its subsidiaries.
Ionis Pharmaceuticals^®^ is a registered trademark of Ionis Pharmaceuticals, Inc. Akcea Therapeutics^®^ is a registered trademark of Akcea Therapeutics, Inc. TEGSEDI^®^ is a registered trademark of Akcea Therapeutics, Inc. WAYLIVRA^®^ is a registered trademark of Akcea Therapeutics, Inc. QALSODY^TM^ is a trademark of Biogen. SPINRAZA^®^ is a registered trademark of Biogen. WAINUA^TM^is a registered trademark of the AstraZeneca group of companies.
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Ionis Investor Contact:
D. Wade Walke, Ph.D.
info@ionisph.com 760-603-2331
Ionis Media Contact:
Hayley Soffer
CorporateCommunications@ionisph.com 760-603-4679
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IONIS PHARMACEUTICALS, INC.
SELECTED FINANCIAL INFORMATION
| Condensed Consolidated Statements of Operations<br><br> <br>(In Millions, Except Per Share Data) | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Three months ended, | Year ended | |||||||||||
| December 31, | December 31, | |||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||
| (unaudited) | ||||||||||||
| Revenue: | ||||||||||||
| Commercial revenue: | ||||||||||||
| SPINRAZA royalties | $ | 62 | $ | 67 | $ | 240 | $ | 242 | ||||
| Other commercial revenue | 17 | 13 | 69 | 61 | ||||||||
| Total commercial revenue | 79 | 80 | 309 | 303 | ||||||||
| Research and development revenue: | ||||||||||||
| Collaborative agreement revenue | 179 | 51 | 353 | 207 | ||||||||
| WAINUA joint development revenue | 67 | 21 | 126 | 77 | ||||||||
| Total research and development revenue | 246 | 72 | 479 | 284 | ||||||||
| Total revenue | 325 | 152 | 788 | 587 | ||||||||
| Expenses: | ||||||||||||
| Cost of sales | 3 | 4 | 9 | 14 | ||||||||
| Research, development and patent | 257 | 308 | 900 | 833 | ||||||||
| Selling, general and administrative | 71 | 48 | 232 | 151 | ||||||||
| Total operating expenses | 331 | 360 | 1,141 | 998 | ||||||||
| Loss from operations | (6 | ) | (208 | ) | (353 | ) | (411 | ) | ||||
| Other income (expense): | ||||||||||||
| Interest expense related to the sale of future royalties | (18 | ) | - | (69 | ) | - | ||||||
| Gain on sale of real estate assets | - | 150 | - | 150 | ||||||||
| Other income (expense), net | 21 | 14 | 88 | 3 | ||||||||
| Loss before income tax expense | (3 | ) | (44 | ) | (334 | ) | (258 | ) | ||||
| Income tax expense | (6 | ) | (8 | ) | (32 | ) | (12 | ) | ||||
| Net loss | $ | (9 | ) | $ | (52 | ) | $ | (366 | ) | $ | (270 | ) |
| Basic and diluted net loss per share | $ | (0.06 | ) | $ | (0.37 | ) | $ | (2.56 | ) | $ | (1.90 | ) |
| Shares used in computing basic and diluted net loss per share | 144 | 142 | 143 | 142 |
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IONIS PHARMACEUTICALS, INC.
Reconciliation of GAAP to Non-GAAP Basis:
| Condensed Consolidated Operating Expenses, Income (Loss) From Operations, and Net Income (Loss)<br><br> <br>(In Millions) | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Three months<br><br> <br>ended<br><br> <br>December 31, | Year ended<br><br> <br>December 31, | |||||||||||
| 2023 | 2022 | 2023 | 2022 | |||||||||
| (unaudited) | ||||||||||||
| As reported research, development and patent expenses according to GAAP | $ | 257 | $ | 308 | $ | 900 | $ | 833 | ||||
| Excluding compensation expense related to equity awards | (20 | ) | (19 | ) | (78 | ) | (74 | ) | ||||
| Non-GAAP research, development and patent expenses | $ | 237 | $ | 289 | $ | 822 | $ | 759 | ||||
| As reported selling, general and administrative expenses according to GAAP | $ | 71 | $ | 48 | $ | 232 | $ | 151 | ||||
| Excluding compensation expense related to equity awards | (6 | ) | (7 | ) | (27 | ) | (26 | ) | ||||
| Non-GAAP selling, general and administrative expenses | $ | 65 | $ | 41 | $ | 205 | $ | 125 | ||||
| As reported operating expenses according to GAAP | $ | 331 | $ | 360 | $ | 1,141 | $ | 998 | ||||
| Excluding compensation expense related to equity awards | (26 | ) | (25 | ) | (106 | ) | (100 | ) | ||||
| Non-GAAP operating expenses | $ | 305 | $ | 335 | $ | 1,035 | $ | 898 | ||||
| As reported loss from operations according to GAAP | $ | (6 | ) | $ | (208 | ) | $ | (353 | ) | $ | (411 | ) |
| Excluding compensation expense related to equity awards | (26 | ) | (25 | ) | (106 | ) | (100 | ) | ||||
| Non-GAAP income (loss) from operations | $ | 20 | $ | (183 | ) | $ | (247 | ) | $ | (311 | ) | |
| As reported net loss according to GAAP | $ | (9 | ) | $ | (52 | ) | $ | (366 | ) | $ | (270 | ) |
| Excluding compensation expense related to equity awards and related tax effects | (26 | ) | (25 | ) | (106 | ) | (100 | ) | ||||
| Excluding gain on sale of real estate assets* | - | 150 | - | 150 | ||||||||
| Excluding income tax effect related to gain on sale of real estate assets | - | (9 | ) | - | (9 | ) | ||||||
| Non-GAAP net income (loss) | $ | 17 | $ | (168 | ) | $ | (260 | ) | $ | (311 | ) |
*In October 2022, Ionis entered into a sale and leaseback transaction for several of its real estate assets. As a result, the Company recognized a $150 million gain on sale of real estate assets in the fourth quarter of 2022. The Company excluded the gain on sale of real estate assets and the related tax effect from its non-GAAP amounts for the applicable periods.
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Reconciliation of GAAP to Non-GAAP Basis
As illustrated in the Selected Financial Information in this press release, non-GAAP operating expenses, non-GAAP income (loss) from operations, and non-GAAP net income (loss) were adjusted from GAAP to exclude compensation expense related to equity awards and the related tax effects. Compensation expense related to equity awards are non-cash. In 2022, Ionis’ non-GAAP net loss excluded the gain on real estate assets related to the sale and leaseback transaction and the related tax effects. These measures are provided as supplementary information and are not a substitute for financial measures calculated in accordance with GAAP. Ionis reports these non-GAAP results to better enable financial statement users to assess and compare its historical performance and project its future operating results and cash flows. Further, the presentation of Ionis' non-GAAP results is consistent with how Ionis' management internally evaluates the performance of its operations.
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| IONIS PHARMACEUTICALS, INC.<br><br> <br>Condensed Consolidated Balance Sheets | ||||
|---|---|---|---|---|
| (In Millions) | ||||
| December 31, | December 31, | |||
| --- | --- | --- | --- | --- |
| 2023 | 2022 | |||
| (unaudited) | ||||
| Assets: | ||||
| Cash, cash equivalents and short-term investments | $ | 2,331 | $ | 1,987 |
| Contracts receivable | 98 | 26 | ||
| Other current assets | 213 | 190 | ||
| Property, plant and equipment, net | 71 | 74 | ||
| Right-of-use assets | 172 | 182 | ||
| Other assets | 105 | 75 | ||
| Total assets | $ | 2,990 | $ | 2,534 |
| Liabilities and stockholders’ equity: | ||||
| Current portion of deferred contract revenue | $ | 151 | $ | 91 |
| 0.125% convertible senior notes, net – short-term | 44 | - | ||
| Other current liabilities | 253 | 221 | ||
| 1.75% convertible senior notes, net | 562 | - | ||
| 0% convertible senior notes, net | 625 | 622 | ||
| 0.125% convertible senior notes, net – long-term | - | 545 | ||
| Liability related to sale of future royalties, net | 514 | - | ||
| Long-term lease liabilities | 171 | 178 | ||
| Long-term obligations, less current portion | 42 | 16 | ||
| Long-term deferred contract revenue | 241 | 288 | ||
| Total stockholders’ equity | 387 | 573 | ||
| Total liabilities and stockholders’ equity | $ | 2,990 | $ | 2,534 |
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Key 2024 Value Driving Events^(1)^
| New Product Launches | |||
|---|---|---|---|
| Program | Indication | Achieved | |
| WAINUA | ATTRv-PN |  |
|
| Olezarsen | FCS | ||
| QALSODY (EU) | SOD1-ALS | ||
| Regulatory Actions | |||
| --- | --- | --- | --- |
| Program | Indication | Regulatory Action | Achieved |
| Eplontersen | ATTRv-PN | Additional OUS filings | |
| EMA approval decision | |||
| Additional OUS approval decision(s) | |||
| Olezarsen | FCS | NDA filing | |
| FDA approval decision | |||
| EU filing | |||
| Canada filing | |||
| Donidalorsen | HAE | NDA filing | |
| QALSODY | SOD1-ALS | EMA approval decision | |
| Key Phase 3 Clinical Data Events | |||
| --- | --- | --- | --- |
| Program | Indication | Event | Achieved |
| Donidalorsen | HAE | OASIS-HAE topline data | |
| Donidalorsen | HAE | OASIS-HAE full data | |
| Donidalorsen | HAE | OASIS-Plus: OLE + Switch data | |
| Olezarsen | FCS | Balance study full data | |
| Key Phase 2 Clinical Data Events | |||
| --- | --- | --- | --- |
| Program | Indication | Event | Achieved |
| Donidalorsen | HAE | 3-year OLE data | |
| IONIS-FB-LRx | IgAN | Phase 2 data | |
| IONIS-FB-LRx | GA | GOLDEN study data | |
| ION224 (DGAT2) | NASH | Phase 2 data | |
| ION582 (UBE3A) | Angelman syndrome | HALOS study data | |
| ION541 (ATXN2) | ALS | ALSpire study data | |
| (1) | Timing expectations based on current assumptions and subject to change. | ||
| --- | --- |
# # #
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