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(Commission File No.)
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(IRS Employer Identification No.)
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
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Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
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Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
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Title of each class
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Trading symbol
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Name of each exchange on which registered
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“
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Item 2.02 |
Results of Operations and Financial Condition.
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Item 9.01. |
Financial Statements and Exhibits.
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Exhibit No.
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Description
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Press Release dated May 4, 2022.
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104 | Cover Page Interactive Data File (embedded within the Inline XBRL document). |
Ionis Pharmaceuticals, Inc.
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Dated: May 4, 2022
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By:
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/s/ Patrick R. O’Neil
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Patrick R. O’Neil
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Executive Vice President, Chief Legal Officer and General Counsel
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•
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$142 million in total revenues
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•
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$173 million of operating expenses on a non-GAAP basis(1) and $199 million on a GAAP basis
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•
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$39 million net loss on a non-GAAP basis(1) and $65 million on a GAAP basis
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•
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$2.1 billion of cash and short-term investments
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•
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$473 million in worldwide SPINRAZA sales in the first quarter
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•
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Biogen provided updates from the ASCEND, RESPOND and NURTURE studies of SPINRAZA at the Muscular Dystrophy Association (MDA) Clinical and Scientific conference and the American Academy of Neurology (AAN)
annual meeting
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•
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Continued to progress into new and existing markets in Europe and Latin America in the first quarter through Swedish Orphan Biovitrum AB (Sobi) and PTC Therapeutics, respectively
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•
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Increased study size and duration in the Phase 3 CARDIO-TTRansform study of eplontersen in patients with ATTR cardiomyopathy with the aim to generate even more robust data and ensure a highly positive
study outcome to successfully compete in this growing and dynamic market. Data from this study are expected in the first half of 2025
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•
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The U.S. FDA granted orphan drug designation to eplontersen for the treatment of patients with ATTR
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•
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Published positive data from the Phase 2 study of olezarsen in patients with hypertriglyceridemia and either at high risk for or with established cardiovascular disease in the European Heart Journal
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•
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Initiated a study of olezarsen in patients with hypertriglyceridemia to support the broad Phase 3 program
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•
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Published positive data from the Phase 2 study of donidalorsen in patients with hereditary angioedema (HAE) in the New England Journal of Medicine
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•
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Presented additional positive data from the Phase 2 study of donidalorsen in patients with HAE at the American Academy of Allergy, Asthma and Immunology (AAAAI) annual meeting
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•
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AstraZeneca presented positive data from the Phase 2b ETESIAN study of ION449 (AZD8233) targeting PCSK9 in statin treated patients with dyslipidemia at the American College of Cardiology (ACC) annual
scientific session
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•
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Achieved full enrollment in the Phase 2b study of IONIS-AGT-LRx in patients with treatment-resistant hypertension, with data expected in the second half of 2022
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•
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Roche plans to initiate a new Phase 2 study of tominersen in patients with Huntington’s disease based on findings from a post-hoc analysis of the GENERATION-HD1 study
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•
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Biogen initiated a Phase 1/2 study of ION260 (BIIB132) targeting ataxin-3 (ATXN3) in patients with spinocerebellar ataxia type 3 (SCA3), resulting in an $8 million milestone payment from Biogen
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•
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Biogen advanced the Phase 1/2 study of ION859 (BIIB094) targeting LRRK2 in patients with Parkinson’s disease, resulting in a $10 million milestone payment from Biogen
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•
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Announced the discontinuation of IONIS-C9Rx (BIIB078) due to lack of patient benefit demonstrated in the Phase 1/2 study in patients with C9orf72-ALS
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Anticipated 2022 Regulatory Updates
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|||||
Program
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Anticipated Indication
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Regulatory Action
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H1
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H2
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Eplontersen
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ATTRv polyneuropathy
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NDA filing
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●
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||
Anticipated Key 2022 Data Readouts
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|||||
Program
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Data Readout
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Anticipated Indication
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H1
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H2
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Tominersen
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Phase 3 post hoc
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Huntington’s disease
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✓
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||
ION449 (PCSK9)
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Phase 2b (ETESIAN)
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Cardiovascular disease
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✓
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||
Donidalorsen
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Phase 2
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HAE
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✓
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||
IONIS-C9Rx (BIIB078)
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Phase 1/2
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C9-ALS
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✓
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||
Tofersen
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Phase 3 OLE
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SOD1-ALS
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●
|
||
Eplontersen
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Phase 3
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ATTRv polyneuropathy
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●
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||
IONIS-AGT-LRx
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Phase 2b
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Treatment-resistant hypertension
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●
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||
Fesomersen (FXI)
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Phase 2b
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Thrombosis
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●
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||
Bepirovirsen (HBV)
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Phase 2b
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Hepatitis B virus infection
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●
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||
Donidalorsen
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Phase 2 OLE
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HAE
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●
|
||
Cimdelirsen (GHR)
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Phase 2 (monotherapy)
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Acromegaly
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●
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||
Anticipated Key 2022 Study Initiations
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|||||
Program
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Phase
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Anticipated Indication
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H1
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H2
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Sapablursen
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2
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Polycythemia vera
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✓
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||
IONIS-MAPTRx (BIIB080)
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2
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Alzheimer’s disease
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●
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ION904 (AGT)
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2
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Uncontrolled hypertension
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●
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ION717 (PRNP)
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1/2
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Prion disease
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●
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||
Anticipated Key 2022 Technology Advancements
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|||||
Program
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Anticipated Advancement
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H1
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H2
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||
SMA
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Advance follow-on program
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✓
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|||
Muscle LICA
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Advance into preclinical development (IND-supporting)
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●
|
|||
MsPA Backbone
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Advance into preclinical development (IND-supporting)
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●
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(1)
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All non-GAAP amounts referred to in this press release exclude non-cash compensation expense related to equity awards. In 2021 all non-GAAP amounts also excluded expenses related to the Akcea Merger and
restructured commercial operations and the related tax effects. Please refer to the detailed reconciliation of non-GAAP and GAAP measures, which is provided later in this press release.
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(2)
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Partnered program milestones are based on partners’ most recent publicly available disclosures.
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Three months ended
March 31, |
||||||||
2022
|
2021
|
|||||||
Revenue:
|
||||||||
Commercial revenue:
|
||||||||
SPINRAZA royalties
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$
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54
|
$
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60
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||||
TEGSEDI and WAYLIVRA revenue, net
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6
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20
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||||||
Licensing and royalty revenue
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12
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5
|
||||||
Total commercial revenue
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72
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85
|
||||||
Research and development revenue:
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||||||||
Amortization from upfront payments
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17
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20
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||||||
Milestone payments
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27
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5
|
||||||
License fees
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2
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-
|
||||||
Other services
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4
|
2
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||||||
Collaborative agreement revenue
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50
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27
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||||||
Eplontersen joint development revenue
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20
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-
|
||||||
Total research and development revenue
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70
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27
|
||||||
Total revenue
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$
|
142
|
$
|
112
|
Three months ended
March 31, |
||||||||
2022
|
2021
|
|||||||
(unaudited)
|
||||||||
Revenue:
|
||||||||
Commercial revenue:
|
||||||||
SPINRAZA royalties
|
$
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54
|
$
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60
|
||||
TEGSEDI and WAYLIVRA revenue, net
|
6
|
20
|
||||||
Licensing and royalty revenue
|
12
|
5
|
||||||
Total commercial revenue
|
72
|
85
|
||||||
Research and development revenue:
|
||||||||
Collaborative agreement revenue
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50
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27
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||||||
Eplontersen joint development revenue
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20
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-
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||||||
Total research and development revenue
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70
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27
|
||||||
Total revenue
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142
|
112
|
||||||
Expenses:
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||||||||
Cost of sales
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4
|
3
|
||||||
Research, development and patent
|
161
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140
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||||||
Selling, general and administrative
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34
|
61
|
||||||
Total operating expenses
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199
|
204
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||||||
Loss from operations
|
(57
|
)
|
(92
|
)
|
||||
Other income (expense):
|
||||||||
Other income (expense), net
|
(7
|
)
|
2
|
|||||
Loss before income tax expense
|
(64
|
)
|
(90
|
)
|
||||
Income tax expense
|
(1
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)
|
-
|
|||||
Net loss
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$
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(65
|
)
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$
|
(90
|
)
|
||
Basic and diluted net loss per share
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$
|
(0.46
|
)
|
$
|
(0.64
|
)
|
||
Shares used in computing basic and diluted net loss per share
|
142
|
141
|
Three months ended
March 31,
|
||||||||
2022
|
2021
|
|||||||
(unaudited)
|
||||||||
As reported research, development and patent expenses according to GAAP
|
$
|
161
|
$
|
140
|
||||
Excluding compensation expense related to equity awards
|
(19
|
)
|
(26
|
)
|
||||
Excluding Akcea merger and restructured commercial operation costs*
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-
|
(3
|
)
|
|||||
Non-GAAP research, development and patent expenses
|
$
|
142
|
$
|
111
|
||||
As reported selling, general and administrative expenses according to GAAP
|
$
|
34
|
$
|
61
|
||||
Excluding compensation expense related to equity awards
|
(7
|
)
|
(12
|
)
|
||||
Excluding Akcea merger and restructured commercial operation costs*
|
-
|
(4
|
)
|
|||||
Non-GAAP selling, general and administrative expenses
|
$
|
27
|
$
|
45
|
||||
As reported operating expenses according to GAAP
|
$
|
199
|
$
|
204
|
||||
Excluding compensation expense related to equity awards
|
(26
|
)
|
(38
|
)
|
||||
Excluding Akcea merger and restructured commercial operation costs*
|
-
|
(7
|
)
|
|||||
Non-GAAP operating expenses
|
$
|
173
|
$
|
159
|
||||
As reported loss from operations according to GAAP
|
$
|
(57
|
)
|
$
|
(92
|
)
|
||
Excluding compensation expense related to equity awards
|
(26
|
)
|
(38
|
)
|
||||
Excluding Akcea merger and restructured commercial operation costs*
|
-
|
(7
|
)
|
|||||
Non-GAAP loss from operations
|
$
|
(31
|
)
|
$
|
(47
|
)
|
||
As reported net loss according to GAAP
|
$
|
(65
|
)
|
$
|
(90
|
)
|
||
Excluding compensation expense related to equity awards
|
(26
|
)
|
(38
|
)
|
||||
Excluding Akcea merger and restructured commercial operation costs*
|
-
|
(7
|
)
|
|||||
Income tax effect related to compensation expense related to equity awards
|
-
|
-
|
||||||
Non-GAAP net loss according to GAAP
|
$
|
(39
|
)
|
$
|
(45
|
)
|
* |
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 these costs from its
non-GAAP amounts for the applicable periods.
|
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)
|
$20M
|
55% of Ionis’ Phase 3 development expenses, including internal+external costs & CMC costs
|
|||
Development Expenses
(R&D Expenses)
|
$36M
|
100% of Ionis’ Phase 3 development expenses
|
March 31,
2022 |
December 31,
2021 |
|||||||
(unaudited)
|
||||||||
Assets:
|
||||||||
Cash, cash equivalents and short-term investments
|
$
|
2,052
|
$
|
2,115
|
||||
Contracts receivable
|
26
|
62
|
||||||
Other current assets
|
175
|
168
|
||||||
Property, plant and equipment, net
|
178
|
178
|
||||||
Other assets
|
88
|
89
|
||||||
Total assets
|
$
|
2,519
|
$
|
2,612
|
||||
Liabilities and stockholders’ equity:
|
||||||||
Other current liabilities
|
$
|
137
|
$
|
143
|
||||
Current portion of deferred contract revenue
|
91
|
98
|
||||||
0% convertible senior notes, net
|
620
|
619
|
||||||
0.125% convertible senior notes, net
|
543
|
542
|
||||||
Long-term obligations, less current portion
|
85
|
86
|
||||||
Long-term deferred contract revenue
|
333
|
352
|
||||||
Total stockholders’ equity
|
710
|
772
|
||||||
Total liabilities and stockholders’ equity
|
$
|
2,519
|
$
|
2,612
|