|
|
|
(Commission File No.)
|
(IRS Employer Identification No.)
|
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))
|
Title of each class
|
Trading symbol
|
Name of each exchange on which registered
|
||
|
|
Item 2.02 |
Results of Operations and Financial Condition.
|
Item 9.01. |
Financial Statements and Exhibits.
|
Exhibit No.
|
Description
|
Press Release dated February 24, 2022.
|
|
104
|
Cover Page Interactive Data File (embedded within the Inline XBRL document).
|
Ionis Pharmaceuticals, Inc.
|
|||
Dated: February 24, 2022
|
By:
|
/s/ Patrick R. O’Neil
|
|
Patrick R. O’Neil
|
|||
Chief Legal Officer and General Counsel
|
• |
Exceeded 2021 financial guidance
|
o |
$810 million in total revenues
|
o |
$695 million of operating expenses on a non-GAAP basis(1) and $840 million on a GAAP basis
|
o |
Net income of $116 million on a non-GAAP basis(1) and a net loss of $29 million on a GAAP basis
|
• |
Well capitalized with cash and short-term investments of $2.1 billion at year-end, enabling accelerating investments in 2022 with the goal to drive substantial future growth
|
• |
SPINRAZA®: the global market leader for the treatment of spinal muscular atrophy (SMA) patients of all ages
|
o |
$1.9 billion in worldwide SPINRAZA sales in 2021
|
o |
More than 11,000 patients worldwide on therapy at the end of 2021 across commercial, expanded access and clinical trial settings
|
o |
Biogen continued to expand upon SPINRAZA’s competitive profile through the ongoing ASCEND, RESPOND and DEVOTE studies
|
• |
TEGSEDI® and WAYLIVRA®: important medicines approved for the treatment of patients with hereditary TTR amyloidosis with polyneuropathy and familial chylomicronemia syndrome, respectively
|
o |
TEGSEDI and WAYLIVRA achieved innovative drug pricing in Brazil
|
o |
WAYLIVRA is under review in Brazil for the treatment of familial partial lipodystrophy (FPL). If approved, WAYLIVRA will be the first approved treatment for patients with FPL in Brazil
|
• |
Advancing Ionis’ near-term commercial opportunities toward the market
|
o |
Eplontersen: potential to change the standard-of-care for patients with TTR amyloidosis (ATTR)
|
◾ |
Initiated a collaboration with AstraZeneca to jointly develop and commercialize eplontersen valued at up to $3.6 billion in an upfront and potential milestone payments, plus cost-sharing and royalties
|
◾ |
The U.S. FDA granted orphan drug designation to eplontersen for the treatment of patients with ATTR
|
o |
Olezarsen: potential first-in-class treatment for patients with elevated triglycerides
|
◾ |
Initiated the Phase 3 CORE study of olezarsen in patients with severe hypertriglyceridemia (SHTG) with data expected in 2024
|
◾ |
Reported positive data from the Phase 2 study of olezarsen in patients with moderate hypertriglyceridemia and at high risk for or with established cardiovascular disease in the European Heart Journal
|
o |
Donidalorsen: potential best-in-class prophylactic treatment for patients with hereditary angioedema (HAE)
|
◾ |
Initiated the Phase 3 OASIS-HAE study of donidalorsen in patients with HAE with data expected in 2024
|
◾ |
Presented positive data from the Phase 2 study of donidalorsen in patients with HAE at the ACAAI annual scientific meeting
|
• |
Advancing Ionis’ leading cardiovascular disease franchise
|
o |
AstraZeneca presented new data from the Phase 1 multiple ascending dose study of ION449 (AZD8233) targeting PCSK9 in statin treated subjects with dyslipidemia at the AHA scientific sessions
|
• |
Addressing substantial unmet medical needs with Ionis’ broad neurological disease franchise
|
o |
Biogen licensed ION306 (BIIB115) for the treatment of SMA with the potential for extended dosing intervals, resulting in a $60 million payment from Biogen
|
o |
Biogen reported that while the Phase 3 VALOR study of tofersen in patients with SOD1-ALS did not meet the primary endpoint, signs of reduced disease progression across multiple secondary and exploratory endpoints were observed. Biogen
continues to engage with regulators to discuss a path forward for tofersen
|
o |
Roche announced plans to initiate a new Phase 2 study of tominersen in patients with Huntington’s disease based on new findings from a post-hoc analysis of the Phase 3 GENERATION-HD1 study
|
o |
Initiated the Phase 1/2 HALOS study of ION582 (BIIB121) in patients with Angelman syndrome, resulting in a $10 million payment from Biogen
|
o |
Advanced three neurological disease programs, resulting in $23 million in payments from Biogen
|
o |
Dynacure advanced IONIS-DNM2-2.5Rx, resulting in $7.5 million in payments from Dynacure
|
• |
Advancing additional programs in Ionis’ clinical pipeline for diseases with unmet medical need
|
o |
Initiated a Phase 2 study of sapablursen (formerly known as IONIS-TMPRSS6-LRx) in patients with polycythemia vera, the second indication for sapablursen
|
o |
Reported topline results from the Phase 2 study of cimdelirsen (formerly known as IONIS-GHR-LRx) in patients with uncontrolled acromegaly, achieving proof of mechanism with a strong indication of proof of concept
|
o |
Advanced two metabolic disease programs, resulting in $40 million in payments from AstraZeneca
|
Anticipated 2022 Regulatory Filings
|
||||
Program
|
Anticipated Indication
|
H1
|
H2
|
|
Eplontersen
|
hATTR polyneuropathy
|
•
|
||
Anticipated Key 2022 Data Readouts
|
||||
Program
|
Data Readout
|
Anticipated Indication
|
H1
|
H2
|
Tominersen
|
Phase 3 post hoc
|
Huntington’s disease
|
||
Eplontersen
|
Phase 3
|
hATTR polyneuropathy
|
•
|
|
ION449 (PCSK9)
|
Phase 2b
|
Cardiovascular disease
|
•
|
|
Donidalorsen
|
Phase 2
|
HAE
|
•
|
|
IONIS-C9Rx (BIIB078)
|
Phase 2
|
C9-ALS
|
•
|
|
IONIS-AGT-LRx
|
Phase 2b
|
Treatment-resistant hypertension
|
•
|
|
Fesomersen (FXI)
|
Phase 2b
|
Thrombosis
|
•
|
|
Bepirovirsen (HBV)
|
Phase 2b
|
Hepatitis B virus infection
|
•
|
|
Donidalorsen
|
Phase 2 OLE
|
HAE
|
•
|
|
Cimdelirsen
|
Phase 2
|
Acromegaly (monotherapy)
|
•
|
|
Anticipated Key 2022 Study Initiations
|
||||
Program
|
Phase
|
Anticipated Indication
|
H1
|
H2
|
Sapablursen
|
2
|
Polycythemia vera
|
||
IONIS-MAPTRx (BIIB080)
|
2
|
Alzheimer’s disease
|
•
|
|
ION904 (AGT)
|
2
|
Uncontrolled hypertension
|
•
|
|
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)
|
•
|
Guidance
|
|
Revenue
|
>$575 million
|
Operating Expenses (1)
|
$825 million to $850 million
|
Net Loss (1)
|
<$275 million
|
Cash and Short-Term Investments
|
~$1.7 billion
|
(1) |
All non-GAAP amounts referred to in this press release exclude non-cash compensation expense related to equity awards. In 2021 and 2020 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 section below titled “Financial Impacts of Akcea Merger and Restructured Commercial Operations” for a summary of the costs specific to these transactions. Additionally, please
refer to the detailed reconciliation of non-GAAP and GAAP measures, which is provided later in this press release.
|
(2) |
Partnered program milestones are based on partners’ most recent publicly available disclosures.
|
Three months ended
December 31,
|
Year ended
December 31,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
69
|
$
|
75
|
$
|
268
|
$
|
287
|
||||||||
TEGSEDI and WAYLIVRA revenue, net
|
9
|
19
|
56
|
70
|
||||||||||||
Licensing and royalty revenue
|
9
|
2
|
18
|
8
|
||||||||||||
Total commercial revenue
|
87
|
96
|
342
|
365
|
||||||||||||
R&D revenue:
|
||||||||||||||||
Amortization from upfront payments
|
21
|
12
|
78
|
80
|
||||||||||||
Milestone payments
|
40
|
110
|
88
|
183
|
||||||||||||
License fees
|
290
|
71
|
291
|
86
|
||||||||||||
Other services
|
2
|
1
|
11
|
15
|
||||||||||||
Total R&D revenue
|
353
|
194
|
468
|
364
|
||||||||||||
Total revenue
|
$
|
440
|
$
|
290
|
$
|
810
|
$
|
729
|
Three months ended,
December 31,
|
Year ended
December 31,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
(as revised*)
|
(as revised*)
|
|||||||||||||||
(unaudited)
|
||||||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
69
|
$
|
75
|
$
|
268
|
$
|
287
|
||||||||
TEGSEDI and WAYLIVRA revenue, net
|
9
|
19
|
56
|
70
|
||||||||||||
Licensing and royalty revenue
|
9
|
2
|
18
|
8
|
||||||||||||
Total commercial revenue
|
87
|
96
|
342
|
365
|
||||||||||||
Research and development revenue under collaborative agreements
|
353
|
194
|
468
|
364
|
||||||||||||
Total revenue
|
440
|
290
|
810
|
729
|
||||||||||||
Expenses:
|
||||||||||||||||
Cost of sales
|
2
|
3
|
11
|
12
|
||||||||||||
Research, development and patent
|
179
|
171
|
643
|
535
|
||||||||||||
Selling, general and administrative
|
38
|
139
|
186
|
354
|
||||||||||||
Total operating expenses
|
219
|
313
|
840
|
901
|
||||||||||||
Income (loss) from operations
|
221
|
(23
|
)
|
(30
|
)
|
(172
|
)
|
|||||||||
Other income (expense):
|
||||||||||||||||
Loss on early retirement of debt
|
-
|
-
|
(9
|
)
|
-
|
|||||||||||
Other income, net
|
4
|
8
|
9
|
37
|
||||||||||||
Income (loss) before income tax benefit (expense)
|
225
|
(15
|
)
|
(30
|
)
|
(135
|
)
|
|||||||||
Income tax benefit (expense)
|
-
|
(341
|
)
|
1
|
(345
|
)
|
||||||||||
Net income (loss)
|
$
|
225
|
$
|
(356
|
)
|
$
|
(29
|
)
|
$
|
(480
|
)
|
|||||
Net loss attributable to noncontrolling interest in Akcea Therapeutics, Inc.
|
-
|
1
|
-
|
36
|
||||||||||||
Net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
$
|
225
|
$
|
(355
|
)
|
$
|
(29
|
)
|
$
|
(444
|
)
|
|||||
Basic net income (loss) per share
|
$
|
1.59
|
$
|
(2.54
|
)
|
$
|
(0.20
|
)
|
$
|
(3.18
|
)
|
|||||
Diluted net income (loss) per share
|
$
|
1.41
|
$
|
(2.54
|
)
|
$
|
(0.20
|
)
|
$
|
(3.18
|
)
|
|||||
Shares used in computing basic net income (loss) per share
|
141
|
140
|
141
|
140
|
||||||||||||
Shares used in computing diluted net income (loss) per share
|
160
|
140
|
141
|
140
|
Three months ended
December 31,
|
Year ended
December 31,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
(as revised*)
|
(as revised*)
|
|||||||||||||||
(unaudited)
|
||||||||||||||||
As reported research, development and patent expenses according to GAAP
|
$
|
179
|
$
|
171
|
$
|
643
|
$
|
535
|
||||||||
Excluding compensation expense related to equity awards
|
(16
|
)
|
(22
|
)
|
(88
|
)
|
(99
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(1
|
)
|
(26
|
)
|
(9
|
)
|
(26
|
)
|
||||||||
Non-GAAP research, development and patent expenses
|
$
|
162
|
$
|
123
|
$
|
546
|
$
|
410
|
||||||||
As reported selling, general and administrative expenses according to GAAP
|
$
|
38
|
$
|
139
|
$
|
186
|
$
|
354
|
||||||||
Excluding compensation expense related to equity awards
|
(7
|
)
|
(15
|
)
|
(33
|
)
|
(72
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
1
|
(64
|
)
|
(15
|
)
|
(64
|
)
|
|||||||||
Non-GAAP selling, general and administrative expenses
|
$
|
32
|
$
|
60
|
$
|
138
|
$
|
218
|
||||||||
As reported operating expenses according to GAAP
|
$
|
219
|
$
|
313
|
$
|
840
|
$
|
901
|
||||||||
Excluding compensation expense related to equity awards
|
(23
|
)
|
(36
|
)
|
(121
|
)
|
(171
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
-
|
(90
|
)
|
(24
|
)
|
(90
|
)
|
|||||||||
Non-GAAP operating expenses
|
$
|
196
|
$
|
187
|
$
|
695
|
$
|
640
|
||||||||
As reported income (loss) from operations according to GAAP
|
$
|
221
|
$
|
(23
|
)
|
$
|
(30
|
)
|
$
|
(172
|
)
|
|||||
Excluding compensation expense related to equity awards
|
(23
|
)
|
(36
|
)
|
(121
|
)
|
(171
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
-
|
(90
|
)
|
(24
|
)
|
(90
|
)
|
|||||||||
Non-GAAP income from operations
|
$
|
244
|
$
|
103
|
$
|
115
|
$
|
89
|
||||||||
As reported net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders
according to GAAP
|
$
|
225
|
$
|
(355
|
)
|
$
|
(29
|
)
|
$
|
(444
|
)
|
|||||
Excluding compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
(23
|
)
|
(36
|
)
|
(121
|
)
|
(162
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
-
|
(90
|
)
|
(24
|
)
|
(90
|
)
|
|||||||||
Income tax effect related to compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
-
|
(16
|
)
|
-
|
2
|
|||||||||||
Income tax effect related to the Akcea merger and restructured commercial operation costs**
|
-
|
(340
|
)
|
-
|
(340
|
)
|
||||||||||
Non-GAAP net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders according
to GAAP
|
$
|
248
|
$
|
127
|
$
|
116
|
$
|
146
|
December 31,
2021
|
December 31,
2020
|
|||||||
(as revised*)
|
||||||||
Assets:
|
||||||||
Cash, cash equivalents and short-term investments
|
$
|
2,115
|
$
|
1,892
|
||||
Contracts receivable
|
62
|
76
|
||||||
Other current assets
|
168
|
162
|
||||||
Property, plant and equipment, net
|
178
|
181
|
||||||
Other assets
|
89
|
79
|
||||||
Total assets
|
$
|
2,612
|
$
|
2,390
|
||||
Liabilities and stockholders’ equity:
|
||||||||
Other current liabilities
|
$
|
143
|
$
|
183
|
||||
Current portion of 1% convertible senior notes, net
|
-
|
309
|
||||||
Current portion of deferred contract revenue
|
98
|
108
|
||||||
0% convertible senior notes, net
|
619
|
-
|
||||||
0.125% convertible senior notes, net
|
542
|
540
|
||||||
Long-term obligations, less current portion
|
86
|
83
|
||||||
Long-term deferred contract revenue
|
352
|
424
|
||||||
Total stockholders’ equity
|
772
|
743
|
||||||
Total liabilities and stockholders’ equity
|
$
|
2,612
|
$
|
2,390
|