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    Ionis reports third quarter financial results

    11/9/22 7:00:00 AM ET
    $IONS
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $IONS alert in real time by email

    Advanced key priorities: initiated manufacturing infrastructure project to support growth

    Increased 2022 cash and investments guidance

    CARLSBAD, Calif., Nov. 9, 2022 /PRNewswire/ -- Ionis Pharmaceuticals, Inc. (NASDAQ:IONS) (the "Company") today reported financial results for the third quarter of 2022. Financial results are summarized below:

    (PRNewsfoto/Ionis Pharmaceuticals, Inc.)





    Three months ended

    September 30,



    Nine months ended

    September 30,





    2022



    2021



    2022



    2021





    (amounts in millions)

    Total revenue



    $160



    $133



    $435



    $370

    Operating expenses



    $219



    $219



    $637



    $621

    Operating expenses on a non-GAAP basis



    $195



    $185



    $562



    $499

    Net loss



    ($47)



    ($82)



    ($217)



    ($253)

    Net loss on a non-GAAP basis



    ($23)



    ($48)



    ($142)



    ($131)

    Financial Highlights

    • Revenue increased 20% for the third quarter of 2022 and 18% on a year-to-date basis compared to the same periods last year driven by significant partner payments earned across multiple programs
    • Non-GAAP operating expenses increased 5% for the third quarter of 2022 and 13% on a year-to-date basis compared to the same periods last year driven by advancing Phase 3 pipeline
    • Entered into a long-term lease in October 2022 to construct a new manufacturing facility supporting continued growth
    • Entered into a sale-leaseback transaction in October 2022 for several real estate assets, generating net proceeds of $240 million plus full funding to expand R&D campus
    • Reaffirmed 2022 P&L guidance; increased cash and investments guidance to approximately $2.0 billion

    Late-Stage Pipeline Highlights

    • Presented positive data from the Phase 3 NEURO-TTRansform study of eplontersen in patients with polyneuropathy caused by hereditary TTR amyloidosis; on track to file U.S. New Drug Application this year
    • Expanded enrollment in the Phase 3 CARDIO-TTRansform study of eplontersen in patients with ATTR cardiomyopathy; data still expected first half of 2025
    • NDA for tofersen was accepted and granted priority review by the FDA; Prescription Drug User Fee Act date of April 25, 2023
    • Initiated CORE2, a confirmatory Phase 3 study of olezarsen in patients with severe hypertriglyceridemia (SHTG)
    • Initiated ESSENCE, a supporting Phase 3 study of olezarsen in patients with SHTG or hypertriglyceridemia and cardiovascular disease

    Mid-Stage Pipeline Highlights

    • GSK presented positive end of study data from the Phase 2b B-Clear study of bepirovirsen demonstrating potential for functional cures in patients with chronic hepatitis B; GSK plans to advance bepirovirsen into Phase 3 development in the first half of 2023
    • Presented positive data from the Phase 2 study of IONIS-FB-LRx in patients with immunoglobulin A nephropathy; Roche plans to advance IONIS-FB-LRx into Phase 3 development in the first half of 2023
    • Bayer presented positive data from the Phase 2b study of fesomersen in patients with end-stage renal disease; Ionis regained rights to fesomersen from Bayer and is assessing next steps
    • Roche presented the Phase 2 GENERATION HD2 study design of tominersen in Huntington's disease patients; Roche plans to begin enrollment in early 2023
    • Reported ION449 (AZD8233) targeting PCSK9 met the primary endpoint in Phase 2b SOLANO study in patients with hypercholesterolemia; based on pre-specified efficacy criteria, AstraZeneca is not advancing ION449

    "We have made significant progress on our key priorities this year, building our commercial pipeline, delivering an abundance of new medicines to the market and expanding and diversifying our technology. We delivered positive data from eight key programs, positioning us to potentially add two new marketed medicines to our portfolio and expand our rich Phase 3 pipeline to eight medicines next year. Additionally, we have recently begun work on a manufacturing facility to support our pipeline growth," said Brett P. Monia, Ph.D., chief executive officer of Ionis. "As we advance our near-term opportunities, including filing the NDA this year for eplontersen, and expanding our rich late-stage pipeline, we are well positioned to drive increasing value for all stakeholders."

    Third Quarter 2022 Financial Results

    Revenue

    Ionis' revenue was comprised of the following:





    Three months ended



    Nine months ended







    September 30,



    September 30,







    2022



    2021



    2022



    2021



    Revenue:



    (amounts in millions)



         Commercial revenue:



















    SPINRAZA royalties



    $62



    $67



    $175



    $199



    TEGSEDI and WAYLIVRA revenue, net



    6



    15



    23



    47



    Licensing and royalty revenue



    5



    3



    25



    9



    Total commercial revenue



    73



    85



    223



    255



    Research and development revenue:



















    Amortization from upfront payments



    18



    17



    54



    57



    Milestone payments



    15



    28



    60



    48



    License fees



    35



    -



    37



    -



    Other services



    1



    3



    6



    10



    Collaborative agreement revenue



    69



    48



    157



    115



    Eplontersen joint development revenue



    18



    -



    55



    -



    Total research and

    development revenue



    87



    48



    212



    115



    Total revenue



    $160



    $133



    $435



    $370













































    Total revenue for the three and nine months ended September 30, 2022 increased 20 percent and 18 percent compared to the same periods last year, respectively. The increase was driven by significant payments Ionis earned across multiple partnered programs. R&D revenue for the nine months ended September 30, 2022 included $85 million from Biogen for advancing several neurology disease programs, $63 million from Roche for licensing and advancing IONIS-FB-LRx and $55 million from AstraZeneca for its share of the global Phase 3 development costs for eplontersen.

    Commercial revenue for the three and nine months ended September 30, 2022 decreased 15 percent and 13 percent compared to the same periods last year, respectively. SPINRAZA royalties for the three and nine months ended September 30, 2022 decreased 7 percent and 12 percent compared to the same periods last year, respectively. In the U.S., SPINRAZA sales were flat in the first nine months of 2022 compared to the same period last year. Outside of the U.S. SPINRAZA royalties were lower due to lower SPINRAZA product sales primarily due to decreased pricing, foreign currency exchange and competition. TEGSEDI and WAYLIVRA revenue was also lower due to the shift to distribution fees in 2021.

    Operating Expenses

    Ionis' non-GAAP operating expenses increased for the three and nine months ended September 30, 2022 compared to the same periods in 2021, in line with expectations. For both periods, higher R&D expenses were driven by the expanded number of Phase 3 studies the Company is conducting, which doubled from three to six studies in 2021. SG&A expenses increased for the three months ended September 30, 2022 compared to the same period last year driven by Ionis' go-to-market activities for eplontersen, donidalorsen and olezarsen. SG&A expenses were lower for the nine months ended September 30, 2022 compared to the same period last year largely due to the substantial savings the Company achieved from integrating Akcea and restructuring its commercial operations in 2021.

    Balance Sheet

    As of September 30, 2022, Ionis had cash, cash equivalents and short-term investments of $2.0 billion, compared with $2.1 billion at December 31, 2021. Ionis' debt obligations and working capital did not change significantly from December 31, 2021 to September 30, 2022.

    In October 2022, Ionis entered into a sale and leaseback transaction for several of its real estate assets. Under the agreement, Ionis will receive net proceeds of approximately $240 million plus full funding to expand the Company's R&D campus. The net proceeds reflect the Company's extinguishment of its mortgage debt for the related properties. Ionis' fourth quarter financial results will reflect the impact this transaction.

    2022 Financial Guidance

    The Company reaffirmed its full year 2022 guidance for total revenue, operating expenses and net loss, on a non-GAAP basis. The Company's 2022 operating expense guidance, compared to the prior year, includes increasing R&D expenses between 25% and 30% and consistent SG&A expenses. Ionis expects to recognize a substantial gain on the sale of its real estate assets in the fourth quarter. The gain will not impact the Company's non-GAAP results since the sale was non-recurring and not part of the Company's normal business operations.

    The Company increased its full year 2022 cash and investments guidance to approximately $2.0 billion from the previous guidance of $1.7 billion.

    Full Year 2022 Guidance



    Current

    As of 3Q22



    Previous

    As of 2Q22



    Revenue



    >$575 million



    >$575 million



    Operating expenses on a non-GAAP basis



    $825-$850 million



    $825-$850 million



    Net loss on a non-GAAP basis



    <$275 million



    <$275 million



    Cash, cash equivalents and short-term investments



    ~$2.0 billion



    ~$1.7 billion



    "Our strong year-to-date results, including year-over-year revenue growth of nearly 20 percent, keep us on track to meet our 2022 P&L guidance," said Elizabeth L. Hougen, chief financial officer of Ionis. "Additionally, we recently bolstered our balance sheet when we unlocked net proceeds of approximately $240 million plus full funding to expand our R&D campus by capitalizing on the favorable life sciences real estate market and monetizing several of our facilities through a sale and leaseback transaction. As a result, we are increasing our 2022 cash and short-term investment guidance to approximately $2 billion."

    Webcast

    Management will host a conference call and webcast to discuss Ionis' third quarter 2022 results at 11:30 a.m. Eastern time on Wednesday, November 9, 2022. 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 third quarter 2022 earnings slides click here.

    About Ionis Pharmaceuticals, Inc.

    For more than 30 years, Ionis has been the leader in RNA-targeted therapy, pioneering new markets and changing the standards of care with its novel antisense technology. Ionis currently has three marketed medicines and a premier late-stage pipeline highlighted by industry leading cardiovascular and neurological franchises. Our scientific innovation began and continues with the knowledge that sick people depend on us, which fuels our vision of becoming a leading, fully integrated biotechnology company.



    To learn more about Ionis visit www.ionispharma.com or follow us on Twitter @ionispharma.

    Ionis' Forward-looking Statement

    This press release includes forward-looking statements regarding Ionis' business, financial guidance and the therapeutic and commercial potential of SPINRAZA (nusinersen), TEGSEDI (inotersen), WAYLIVRA (volanesorsen), eplontersen, olezarsen, donidalorsen, ION363, pelacarsen, tofersen, Ionis' technologies and Ionis' other products in development. 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 related to the impact COVID-19 could have on our business, and 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. 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, 2021, 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. SPINRAZA® is a registered trademark of Biogen.

    IONIS PHARMACEUTICALS, INC.

    SELECTED FINANCIAL INFORMATION

    Condensed Consolidated Statements of Operations

    (In Millions, Except Per Share Data)







    Three months ended,



    Nine months ended





    September 30,



    September 30,





    2022



    2021



    2022



    2021





    (unaudited)

    Revenue:

















         Commercial revenue:

















    SPINRAZA royalties



    $62



    $67



    $175



    $199

    TEGSEDI and WAYLIVRA revenue, net



    6



    15



    23



    47

    Licensing and royalty revenue



    5



    3



    25



    9

    Total commercial revenue



    73



    85



    223



    255

    Research and development revenue:

















    Collaborative agreement revenue



    69



    48



    157



    115

    Eplontersen joint development revenue



    18



    -



    55



    -

    Total research and development revenue



    87



    48



    212



    115

    Total revenue



    160



    133



    435



    370

    Expenses:

















           Cost of sales



    2



    3



    10



    9

        Research, development and patent



    183



    185



    525



    464

        Selling, general and administrative



    34



    31



    102



    148

    Total operating expenses



    219



    219



    637



    621

    Loss from operations



    (59)



    (86)



    (202)



    (251)



















    Other expense (income)



    12



    2



    (12)



    (3)

    Loss before income tax benefit (expense)



    (47)



    (84)



    (214)



    (254)



















    Income tax benefit (expense)



    -



    2



    (3)



    1



















    Net loss



    ($47)



    ($82)



    ($217)



    ($253)



















    Basic and diluted net loss per share



    ($0.33)



    ($0.58)



    ($1.53)



    ($1.80)

    Shares used in computing basic and diluted net loss per share



    142



    141



    142



    141

     

    IONIS PHARMACEUTICALS, INC.

    Reconciliation of GAAP to Non-GAAP Basis:

    Condensed Consolidated Operating Expenses, Loss From Operations, and Net Loss

    (In Millions)







    Three months ended

    September 30,



    Nine months ended

    September 30,





    2022



    2021



    2022



    2021





    (unaudited)

    As reported research, development and patent expenses according to GAAP



    $183



    $185



    $525



    $464

        Excluding compensation expense related to equity awards      



    (18)



    (23)



    (55)



    (72)

        Excluding Akcea merger and restructured commercial operation costs*      



    -



    (2)



    -



    (8)

    Non-GAAP research, development and patent expenses



    $165



    $160



    $470



    $384



















    As reported selling, general and administrative expenses according to GAAP



    $34



    $31



    $102



    $148

        Excluding compensation expense related to equity awards      



    (6)



    (7)



    (19)



    (26)

        Excluding Akcea merger and restructured commercial operation costs*      



    -



    (1)



    -



    (16)

    Non-GAAP selling, general and administrative expenses



    $28



    $23



    $83



    $106



















    As reported operating expenses according to GAAP



    $219



    $219



    $637



    $621

    Excluding compensation expense related to equity awards      



    (24)



    (31)



    (75)



    (98)

        Excluding Akcea merger and restructured commercial operation costs*      



    -



    (3)



    -



    (24)

    Non-GAAP operating expenses



    $195



    $185



    $562



    $499



















    As reported loss from operations according to GAAP



    ($59)



    ($86)



    ($202)



    ($251)

        Excluding compensation expense related to equity awards      



    (24)



    (31)



    (75)



    (98)

        Excluding Akcea merger and restructured commercial operation costs*      



    -



    (3)



    -



    (24)

    Non-GAAP loss from operations



    ($35)



    ($52)



    ($127)



    ($129)



















    As reported net loss according to GAAP



    ($47)



    ($82)



    ($217)



    ($253)

        Excluding compensation expense related to equity awards      



    (24)



    (31)



    (75)



    (98)

        Excluding Akcea merger and restructured commercial operation costs*      



    -



    (3)



    -



    (24)

    Non-GAAP net loss



    ($23)



    ($48)



    ($142)



    ($131)



    *In October 2020, Ionis completed a merger transaction with Akcea such that following the completion of the merger Akcea became a wholly owned subsidiary of Ionis. Additionally, in December 2020 and April 2021, Ionis restructured its European operations and its North American TEGSEDI operations, respectively, as a result of entering into distribution agreements with Sobi. The Company excluded the Akcea merger and restructured commercial operation costs from its non-GAAP amounts for the applicable periods.

    Reconciliation of GAAP to Non-GAAP Basis

    As illustrated in the Selected Financial Information in this press release, non-GAAP operating expenses, non-GAAP loss from operations, and non-GAAP net 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 2021 all non-GAAP amounts also excluded expenses related to the Akcea merger and restructured commercial operations. Expenses related to the Akcea merger and restructured commercial operations included: severance costs, retention costs and other costs related to commercial operations. Ionis has regularly reported non-GAAP measures for operating results as non-GAAP results. 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.

    IONIS PHARMACEUTICALS, INC. 

    Summary of the Financial Impacts of the Eplontersen Collaboration with AstraZeneca 

    For the Nine Months Ended, September 30, 2022 

    (Unaudited) 



    Collaboration

    Activities



    Financial

    Statement Line



    Impact of Cost-Sharing Provisions

    on Ionis' Statement of Operations















    Phase 3 Development:

    Ionis leads and conducts



    Eplontersen Joint

    Development

    Revenue

    (R&D Revenue)



    $55M



    55% of Total Phase 3

    development expenses,

    including

    internal+external costs &

    CMC costs, net of Ionis'

    share of AstraZeneca's

    Phase 3 development

    expenses















    Development

    Expenses

    (R&D Expenses)



    $107M



    100% of Ionis' Phase 3

    development expenses



    Ionis' financial results for the nine months ended September 30, 2022 reflected the cost-sharing provisions related to its collaboration with AstraZeneca to develop and commercialize eplontersen for the treatment of ATTR. Under the terms of the collaboration agreement, AstraZeneca is paying 55 percent of the costs associated with the ongoing global Phase 3 development program. Because Ionis is leading and conducting the Phase 3 development program, Ionis is recognizing the 55 percent of cost-share funding AstraZeneca is responsible for, net of Ionis' share of AstraZeneca's development expenses, as R&D revenue in the same period Ionis incurs the related development expenses. For the nine months ended September 30, 2022 Ionis earned $55 million in joint development revenue under this collaboration.

    Because AstraZeneca is responsible for the majority of the medical affairs and commercial costs in the U.S. and all costs associated with bringing eplontersen to market outside the U.S., Ionis is recognizing cost-share funding it receives from AstraZeneca related to these activities as a reduction of its medical affairs (R&D expenses) and commercialization expenses (SG&A expenses). For the nine months ended September 30, 2022 Ionis recognized $1.4 million and $1.5 million of medical affairs expenses and commercialization expenses for eplontersen, respectively, net of cost-share funding from AstraZeneca. Ionis expects its medical affairs and commercialization expenses to increase as this collaboration progresses.

    IONIS PHARMACEUTICALS, INC.

    Condensed Consolidated Balance Sheets

    (In Millions)



















    September 30,



    December 31,







    2022



    2021







    (unaudited)







    Assets:











      Cash, cash equivalents and short-term investments



    $1,982



    $2,115



      Contracts receivable



    7



    62



      Other current assets



    164



    168



      Property, plant and equipment, net



    181



    178



      Other assets



    88



    89



         Total assets



    $2,422



    $2,612















    Liabilities and stockholders' equity:











      Other current liabilities



    $184



    $143



      Current portion of deferred contract revenue



    100



    98



      0% convertible senior notes, net



    621



    619

      0.125% convertible senior notes, net



    544



    542



      Long-term obligations, less current portion



    84



    86



      Long-term deferred contract revenue



    295



    352



      Total stockholders' equity



    594



    772



        Total liabilities and stockholders' equity



    $2,422



    $2,612

















    2022 Pipeline Milestones(1) 

    Anticipated 2022 Regulatory Updates

    Program

    Regulatory Action

    Anticipated Indication

    H1

    H2

    Tofersen

    NDA acceptance

    SOD1-ALS



    ✓

    Eplontersen (TTR)

    NDA filing

    ATTRv polyneuropathy



    •



    Anticipated Key 2022 Data Readouts

    Program

    Data Readout

    Anticipated Indication

    H1

    H2

    Eplontersen (TTR)

    Phase 3

    ATTRv polyneuropathy

    ✓



    Tofersen

    Phase 3 OLE

    SOD1-ALS

    ✓



    Tominersen (HTT)

    Phase 3 post hoc

    Huntington's disease

    ✓



    ION449 (PCSK9)

    Phase 2b

    (ETESIAN)

    Cardiovascular disease

    ✓



    Bepirovirsen (HBV)

    Phase 2b

    Hepatitis B virus infection

    ✓



    Donidalorsen (PKK)

    Phase 2

    HAE

    ✓



    IONIS-C9Rx (BIIB078)

    Phase 1/2

    C9-ALS

    ✓



    Fesomersen (FXI)

    Phase 2b

    Thrombosis



    ✓

    IONIS-FB-LRx

    Phase 2

    Immunoglobulin A nephropathy



    ✓

    ION449 (PCSK9)

    Phase 2b

    (SOLANO)

    Cardiovascular disease



    ✓

    Donidalorsen (PKK)

    Phase 2 OLE

    HAE



    •

    IONIS-AGT-LRx

    Phase 2b

    Treatment-resistant hypertension



    ­•

    Cimdelirsen (GHR)

    Phase 2 (monotherapy)

    Acromegaly



    •



    Anticipated Key 2022 Study Initiations

    Program

    Phase

    Anticipated Indication

    H1

    H2

    Sapablursen (TMPRSS6)

    2

    Polycythemia vera

    ✓



    ION904 (AGT)

    2

    Uncontrolled hypertension

    ✓



    IONIS-MAPTRx (BIIB080)

    2

    Alzheimer's disease



    •

    ION717 (PRNP)

    1/2

    Prion disease



    •



    Anticipated Key 2022 Technology Advancements

    Program

    Anticipated Advancement

    H1

    H2

    SMA

    Advance follow-on program

    ✓



    Muscle LICA

    Advance into preclinical development (IND-

    supporting)



    ✓

    MsPA Backbone

    Advance into preclinical development (IND-

    supporting)



    ✓



    ✓ = achieved      • = planned 



    (1)    Timing expectations based on current assumptions and subject to change.

     

    Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/ionis-reports-third-quarter-financial-results-301672361.html

    SOURCE Ionis Pharmaceuticals, Inc.

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    Biogen Receives European Commission Approval for High Dose Regimen of SPINRAZA® (nusinersen) for Spinal Muscular Atrophy

    Approval is supported by data from the DEVOTE study which showed the benefit of the SPINRAZA 50 mg and 28 mg regimen in both treatment-naïve and previously-treated nusinersen patients with SMA1Biogen is dedicated to partnering with the SMA community to advance care through scientific innovation and a commitment to enhancing outcomes for people living with SMA CAMBRIDGE, Mass., Jan. 12, 2026 (GLOBE NEWSWIRE) -- Biogen Inc. (NASDAQ:BIIB) today announced the European Commission (EC) has granted marketing authorization for a high dose regimen of SPINRAZA® (nusinersen) which is comprised of 50 mg/5 mL and 28 mg/5 mL doses for the treatment of 5q spinal muscular atrophy (SMA). 5q SMA is the mos

    1/12/26 11:05:00 AM ET
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    SEC Form 144 filed by Ionis Pharmaceuticals Inc.

    144 - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    2/2/26 4:22:41 PM ET
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    SEC Form 144 filed by Ionis Pharmaceuticals Inc.

    144 - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    1/30/26 8:19:20 PM ET
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    SEC Form 144 filed by Ionis Pharmaceuticals Inc.

    144 - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    1/16/26 6:37:38 PM ET
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    Insider Trading

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    EVP, Chief Scientific Officer Bennett C Frank sold $7,056,216 worth of shares (85,089 units at $82.93) and exercised 65,089 shares at a strike of $53.73, decreasing direct ownership by 20% to 80,293 units (SEC Form 4)

    4 - IONIS PHARMACEUTICALS INC (0000874015) (Issuer)

    2/4/26 4:06:04 PM ET
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    EVP Research Swayze Eric was granted 11,991 shares and sold $512,446 worth of shares (6,179 units at $82.93), increasing direct ownership by 14% to 47,747 units (SEC Form 4)

    4 - IONIS PHARMACEUTICALS INC (0000874015) (Issuer)

    2/2/26 8:52:12 PM ET
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    EVP CLO & General Counsel O'Neil Patrick R. was granted 11,991 shares and sold $516,153 worth of shares (6,179 units at $83.53), increasing direct ownership by 9% to 71,983 units (SEC Form 4)

    4 - IONIS PHARMACEUTICALS INC (0000874015) (Issuer)

    2/2/26 8:51:59 PM ET
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    Director Hayden Michael R bought $477,900 worth of shares (15,000 units at $31.86), increasing direct ownership by 43% to 50,219 units (SEC Form 4)

    4 - IONIS PHARMACEUTICALS INC (0000874015) (Issuer)

    5/2/25 4:38:26 PM ET
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    Director Hayden Michael R bought $181,079 worth of shares (5,000 units at $36.22), increasing direct ownership by 17% to 35,219 units (SEC Form 4)

    4 - IONIS PHARMACEUTICALS INC (0000874015) (Issuer)

    12/26/24 4:57:52 PM ET
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    Barclays resumed coverage on Ionis Pharma with a new price target

    Barclays resumed coverage of Ionis Pharma with a rating of Overweight and set a new price target of $95.00

    1/28/26 7:17:25 AM ET
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    Ionis Pharma upgraded by Analyst with a new price target

    Analyst upgraded Ionis Pharma from Neutral to Overweight and set a new price target of $80.00

    10/8/25 8:16:23 AM ET
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    Ionis Pharma upgraded by Goldman with a new price target

    Goldman upgraded Ionis Pharma from Sell to Neutral and set a new price target of $65.00

    9/26/25 8:00:14 AM ET
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    Alltrna Announces Updates to Its Board of Directors

    Chris Schade appointed as Board ChairpersonLynne Parshall, Robert Plenge, M.D., Ph.D., and Nancy Simonian, M.D., appointed to Board of DirectorsCAMBRIDGE, Mass., July 17, 2024 /PRNewswire/ -- Alltrna, a Flagship Pioneering company unlocking transfer RNA (tRNA) biology and pioneering tRNA therapeutics to regulate the protein universe and resolve disease, today announced the appointment of Chris Schade, Growth Partner at Flagship Pioneering, as Chairperson of the Board, succeeding Noubar Afeyan, Ph.D., Co-Founder of Alltrna and Founder and CEO of Flagship Pioneering. In addition, Alltrna also announced the appointments to the company's Board of Directors of Lynne Parshall, founding Chief Opera

    7/17/24 8:00:00 AM ET
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    Contineum Therapeutics Announces Appointment of Sarah Boyce to Board of Directors

    Contineum Therapeutics, Inc. (NASDAQ:CTNM), a clinical stage biopharmaceutical company focused on discovering and developing novel, oral small molecule therapies that target biological pathways associated with specific clinical impairments for the treatment of neuroscience, inflammation and immunology (NI&I) indications, today announced the appointment of Sarah Boyce, President and Chief Executive Officer of Avidity Biosciences, Inc. (NASDAQ:RNA), as an independent member of its Board of Directors. Ms. Boyce brings over 25 years of global commercial and clinical development expertise in the life sciences industry to Contineum's board. Ms. Boyce has extensive expertise in global pharmaceut

    6/24/24 4:05:00 PM ET
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    Ionis announces the appointment of Michael Yang to Board of Directors

    CARLSBAD, Calif., Dec. 14, 2023 /PRNewswire/ -- Ionis Pharmaceuticals, Inc. (NASDAQ:IONS) today announced the appointment of Michael Yang, an experienced biopharmaceutical executive, to the Ionis Board of Directors. Mr. Yang's appointment expands the total number of Ionis Board members to 10. Mr. Yang has more than 20 years of broad senior level leadership experience in biotech, pharmaceutical and medical device companies, where he launched new platforms, expanded global revenues and diversified product lines. He most recently served as President, Chief Executive Officer and B

    12/14/23 4:05:00 PM ET
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    Biogen Completes Acquisition of Alcyone Therapeutics

    CAMBRIDGE, Mass., Nov. 14, 2025 (GLOBE NEWSWIRE) -- Biogen Inc. (NASDAQ:BIIB) has completed the acquisition of Alcyone Therapeutics, a clinical-stage biotechnology company known for its innovative CNS therapy delivery solutions, such as the ThecaFlex DRx™ drug delivery system. ThecaFlex DRx™ is an investigational implantable device designed to provide an alternative to repeat lumbar punctures in chronic intrathecal administration of medicines, which could ease both patient experience and accessibility for a broader population of people living with neurologic disorders. ThecaFlex DRx™ has been in development since 2019, with the PIERRE and PIERRE-PK clinical studies for nusinersen curren

    11/14/25 4:05:00 PM ET
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    Ionis reports third quarter 2025 financial results and highlights progress on key programs

    - TRYNGOLZA® generated $32 million in net product sales in the third quarter 2025 - - DAWNZERA™ (donidalorsen) launch off to encouraging start - - Olezarsen significantly reduced triglycerides and acute pancreatitis events in severe hypertriglyceridemia (sHTG) in landmark Phase 3 studies; sNDA submission on track by year-end – - Positive pivotal zilganersen results in Alexander disease position Ionis for first independent neurology launch in 2026 - - Increasing 2025 financial guidance driven by continued strength across the business – Ionis Pharmaceuticals, Inc. (NASDAQ:IONS) (the "Company") today reported financial results and provided key updates for the third quarter ended Sept

    10/29/25 7:00:00 AM ET
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    Ionis reports second quarter 2025 financial results and highlights progress on key programs

    - TRYNGOLZATM delivers $19 million in net product sales in the second quarter 2025 - - Donidalorsen approval in hereditary angioedema (HAE) anticipated next month; Ionis' second independent launch - - Phase 3 data from the pivotal CORE and CORE2 studies in severe hypertriglyceridemia (sHTG) expected in September 2025 - - Increasing 2025 financial guidance based on strong performance and improved outlook - Ionis Pharmaceuticals, Inc. (NASDAQ:IONS) (the "Company") today reported financial results and provided key updates for the second quarter ended June 30, 2025. "During the second quarter, we continued to build momentum across our business," said Brett P. Monia, Ph.D., chief execu

    7/30/25 7:00:00 AM ET
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    Amendment: SEC Form SC 13G/A filed by Ionis Pharmaceuticals Inc.

    SC 13G/A - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    11/14/24 8:34:57 PM ET
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    Amendment: SEC Form SC 13G/A filed by Ionis Pharmaceuticals Inc.

    SC 13G/A - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    11/14/24 1:28:29 PM ET
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    SEC Form SC 13G filed by Ionis Pharmaceuticals Inc.

    SC 13G - IONIS PHARMACEUTICALS INC (0000874015) (Subject)

    11/8/24 10:52:38 AM ET
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