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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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“
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Emerging growth company
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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 November 9, 2022.
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|
104
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Cover Page Interactive Data File (embedded within the Inline XBRL document).
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Ionis Pharmaceuticals, Inc.
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||
Dated: November 9, 2022
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By:
|
/s/ Patrick R. O’Neil
|
Patrick R. O’Neil
|
||
Executive Vice President, Chief Legal Officer and General Counsel
|
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
|
)
|
• |
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
|
• |
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
|
• |
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
|
Three months ended
September 30,
|
Nine months ended
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
|
||||||||
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
|
Three months ended,
September 30,
|
Nine months ended
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
|
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
|
)
|
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
|
September 30,
2022
|
December 31,
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
|
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)
|
(1) |
Timing expectations based on current assumptions and subject to change.
|