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|
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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
|
Name of each exchange on which registered
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||
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Item 2.02 |
Results of Operations and Financial Condition.
|
Item 9.01.
|
Financial Statements and Exhibits.
|
Exhibit No.
|
Description
|
Press Release dated February 24, 2021.
|
|
104
|
Cover Page Interactive Data File (embedded within the Inline XBRL document).
|
Ionis Pharmaceuticals, Inc.
|
||
Dated: February 24, 2021
|
By:
|
/s/ Patrick R. O’Neil
|
Patrick R. O’Neil
|
||
Executive Vice President, Legal, General Counsel and Chief Compliance Officer
|
• |
Achieved 2020 financial guidance
|
o |
$729 million in total revenues, with half from marketed products
|
o |
$640 million of operating expenses on a non-GAAP basis(1) and $901 million on a GAAP basis, reflecting investments in Ionis’ wholly owned pipeline
|
o |
Net income of $111 million on a non-GAAP basis(1) and a net loss of $451 million on a GAAP basis
|
• |
• |
SPINRAZA: a global foundation-of-care for the treatment of spinal muscular atrophy (SMA) patients of all ages
|
o |
$2 billion in worldwide sales in 2020
|
o |
More than 11,000 patients worldwide were on therapy at the end of the fourth quarter across post-marketing, expanded access and clinical trial settings
|
o |
Enrollment began in the RESPOND study evaluating potential SPINRAZA benefit in SMA patients with a suboptimal clinical response to gene therapy
|
o |
Enrollment began in the pivotal randomized treatment cohort of the DEVOTE study evaluating higher doses of SPINRAZA
|
• |
o |
Product sales increased more than 65 percent in 2020, compared to 2019
|
o |
Generated growing revenues as major markets launched in 2020
|
o |
Restructured European operations through a distribution agreement with Swedish Orphan Biovitrum AB (Sobi)
|
• |
Phase 3 Pipeline: growing pipeline positioned for 12 or more products on the market in 2026
|
o |
Advanced IONIS-APOCIII-LRx into the Phase 3 BALANCE study in patients with FCS
|
o |
Completed enrollment in the tofersen Phase 3 VALOR study in patients with SOD1-ALS
|
• |
Mid-stage Pipeline: broad and advancing pipeline of potential first-in-class and/or best-in-class medicines
|
o |
Advanced and expanded the IONIS-AGT-LRx development program
|
◾ |
Reported IONIS-AGT-LRx positive topline Phase 2 results in patients with hypertension uncontrolled with two or three antihypertensive medications
|
◾ |
Advanced ION904, the follow-on medicine targeting AGT, into Phase 1 development in healthy volunteers
|
o |
Advanced vupanorsen into Phase 2b development with the initiation of the TRANSLATE-TIMI 70 dose-ranging study in statin-treated patients with dyslipidemia, resulting in a $75 million
payment from Pfizer
|
o |
Advanced ION449 (AZD8233), targeting PCSK9, into Phase 2b development in patients with dyslipidemia and AstraZeneca licensed ION455, a new investigational medicine for the treatment
of nonalcoholic steatohepatitis (NASH), resulting in $50 million from AstraZeneca
|
o |
Unlocked potential new pulmonary disease franchise with positive IONIS-ENAC-2.5Rx data
|
◾ |
Reported positive healthy volunteer results supporting aerosol antisense medicine delivery to the lung
|
◾ |
Completed dosing in the Phase 2 study in patients with cystic fibrosis
|
◾ |
Advanced IONIS-ENAC-2.5Rx into Phase 2 development in patients with chronic obstructive pulmonary disease (COPD)
|
o |
Highlighted IONIS-MAPTRx (BIIB080) Phase 1/2 study in patients with Alzheimer’s disease in which IONIS-MAPTRx was generally well tolerated and demonstrated
durable, time and dose-dependent reductions in CSF tau protein
|
Anticipated 2021 Data Readouts(2)
|
|||||||
Program
|
Phase
|
Anticipated Indication
|
H1
|
H2
|
|||
IONIS-ENAC-2.5Rx
|
2
|
Cystic fibrosis
|
•
|
||||
IONIS-PKK-LRx
|
2
|
Hereditary angioedema (top-line)
|
•
|
||||
IONIS-GHR-LRx
|
2
|
Acromegaly (top-line)
|
•
|
||||
IONIS-AGT-LRx
|
2
|
Hypertension
|
•
|
||||
Tominersen
|
OLE/NHS
|
Huntington’s disease
|
•
|
||||
IONIS-MAPTRx
|
1/2
|
Alzheimer’s disease
|
•
|
||||
Vupanorsen
|
2b
|
sHTG/CVD risk reduction
|
•
|
||||
IONIS-C9Rx
|
1/2
|
C9-ALS
|
•
|
||||
Tofersen
|
3 (VALOR study)
|
SOD1-ALS
|
•
|
Anticipated 2021 Study Initiations(2)
|
|||||||
Program
|
Phase
|
Anticipated Indication
|
H1
|
H2
|
|||
ION363
|
3
|
FUS-ALS
|
•
|
||||
ION373
|
2
|
Alexander disease
|
•
|
||||
IONIS-AGT-LRx
|
2b
|
Resistant hypertension
|
•
|
||||
IONIS-AGT-LRx
|
2
|
Heart failure with reduced ejection fraction
|
•
|
||||
ION224
|
2b
|
NASH
|
•
|
||||
Tofersen
|
3 (ATLAS study)
|
Presymptomatic SOD1-ALS
|
•
|
||||
IONIS-APOCIII-LRx
|
3
|
Second CV indication
|
•
|
||||
IONIS-ENAC-2.5Rx
|
2
|
Cystic fibrosis not amenable to CFTR modulators
|
•
|
Guidance
|
|
Revenue
|
>$600 million
|
Operating Expenses (1)
|
$675 million to $725 million
|
Net Loss (1)
|
<$75 million
|
(1) |
All non-GAAP amounts referred to in this press release exclude non-cash compensation expense related to equity awards and expenses related to the Akcea acquisition and restructured
European operations and the related tax effects. Please refer to the section below titled “Financial Impacts of Akcea Acquisition and Restructured European Operations” for a breakdown 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 release.
|
Three months ended,
|
Year ended,
|
|||||||||||||||
December 31,
|
December 31,
|
|||||||||||||||
2020
|
2019
|
2020
|
2019
|
|||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
75
|
$
|
81
|
$
|
287
|
$
|
293
|
||||||||
Product sales, net
|
19
|
13
|
70
|
42
|
||||||||||||
Licensing and royalty revenue
|
2
|
6
|
8
|
17
|
||||||||||||
Total commercial revenue
|
96
|
100
|
365
|
352
|
||||||||||||
R&D Revenue:
|
||||||||||||||||
Amortization from upfront payments
|
12
|
46
|
80
|
146
|
||||||||||||
Milestone payments
|
110
|
51
|
183
|
115
|
||||||||||||
License fees
|
71
|
292
|
86
|
490
|
||||||||||||
Other services
|
1
|
5
|
15
|
20
|
||||||||||||
Total R&D revenue
|
194
|
394
|
364
|
771
|
||||||||||||
Total revenue
|
$
|
290
|
$
|
494
|
$
|
729
|
$
|
1,123
|
Three months ended
December 31, 2020
|
||||
Severance, retention and other expenses
|
$
|
31
|
||
Non-cash stock-based compensation expense for the acceleration of Akcea equity awards
|
59
|
|||
Total expenses included in GAAP operating expenses
|
$
|
90
|
||
Non-cash adjustment of the valuation allowance for Ionis’ federal net deferred tax assets and other tax adjustments related to
the Akcea acquisition
|
312
|
|||
Total expenses included in GAAP net loss
|
$
|
402
|
Three months ended,
December 31,
|
Year ended,
December 31,
|
|||||||||||||||
2020
|
2019
|
2020
|
2019
|
|||||||||||||
(unaudited)
|
||||||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
75
|
$
|
81
|
$
|
287
|
$
|
293
|
||||||||
Product sales, net
|
19
|
13
|
70
|
42
|
||||||||||||
Licensing and royalty revenue
|
2
|
6
|
8
|
17
|
||||||||||||
Total commercial revenue
|
96
|
100
|
365
|
352
|
||||||||||||
Research and development revenue under collaborative agreements
|
194
|
394
|
364
|
771
|
||||||||||||
Total revenue
|
290
|
494
|
729
|
1,123
|
||||||||||||
Expenses:
|
||||||||||||||||
Cost of products sold
|
3
|
1
|
12
|
4
|
||||||||||||
Research, development and patent
|
171
|
149
|
535
|
466
|
||||||||||||
Selling, general and administrative
|
139
|
83
|
354
|
287
|
||||||||||||
Total operating expenses
|
313
|
233
|
901
|
757
|
||||||||||||
Income (loss) from operations
|
(23
|
)
|
261
|
(172
|
)
|
366
|
||||||||||
Other income (loss), net
|
(1
|
)
|
(23
|
)
|
2
|
(19
|
)
|
|||||||||
Income (loss) before income tax benefit (expense)
|
(24
|
)
|
238
|
(170
|
)
|
347
|
||||||||||
Income tax benefit (expense)
|
(318
|
)
|
(34
|
)
|
(317
|
)
|
(44
|
)
|
||||||||
Net income (loss)
|
$
|
(342
|
)
|
$
|
204
|
$
|
(487
|
)
|
$
|
303
|
||||||
Net loss (income) attributable to noncontrolling interest in Akcea Therapeutics, Inc.
|
2
|
(20
|
)
|
36
|
(9
|
)
|
||||||||||
Net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
$
|
(340
|
)
|
$
|
184
|
$
|
(451
|
)
|
$
|
294
|
||||||
Basic net income (loss) per share
|
$
|
(2.44
|
)
|
$
|
1.31
|
$
|
(3.23
|
)
|
$
|
2.12
|
||||||
Diluted net income (loss) per share
|
$
|
(2.44
|
)
|
$
|
1.28
|
$
|
(3.23
|
)
|
$
|
2.08
|
||||||
Shares used in computing basic net income (loss) per share
|
140
|
141
|
140
|
140
|
||||||||||||
Shares used in computing diluted net income (loss) per share
|
140
|
153
|
140
|
143
|
Three months ended,
December 31,
|
Year ended,
December 31,
|
|||||||||||||||
2020
|
2019
|
2020
|
2019
|
|||||||||||||
(unaudited)
|
||||||||||||||||
As reported operating expenses according to GAAP
|
$
|
313
|
$
|
233
|
$
|
901
|
$
|
757
|
||||||||
Excluding compensation expense related to equity awards
|
(36
|
)
|
(35
|
)
|
(171
|
)
|
(147
|
)
|
||||||||
Excluding Akcea acquisition and restructured European operations costs
|
(90
|
)
|
-
|
(90
|
)
|
-
|
||||||||||
Non-GAAP operating expenses
|
$
|
187
|
$
|
198
|
$
|
640
|
$
|
610
|
||||||||
As reported income (loss) from operations according to GAAP
|
$
|
(23
|
)
|
$
|
261
|
$
|
(172
|
)
|
$
|
366
|
||||||
Excluding compensation expense related to equity awards
|
(36
|
)
|
(35
|
)
|
(171
|
)
|
(147
|
)
|
||||||||
Excluding Akcea acquisition and restructured European operations costs
|
(90
|
)
|
-
|
(90
|
)
|
-
|
||||||||||
Non-GAAP income (loss) from operations
|
$
|
103
|
$
|
296
|
$
|
89
|
$
|
513
|
||||||||
As reported net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders according to
GAAP
|
$
|
(340
|
)
|
$
|
184
|
$
|
(451
|
)
|
$
|
294
|
||||||
Excluding compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
(36
|
)
|
(33
|
)
|
(162
|
)
|
(139
|
)
|
||||||||
Income tax effect related to compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common
stockholders
|
(16
|
)
|
5
|
2
|
31
|
|||||||||||
Excluding Akcea acquisition and restructured European operations costs
|
(90
|
)
|
-
|
(90
|
)
|
-
|
||||||||||
Income tax effect related to the Akcea acquisition and restructured European operations costs
|
(312
|
)
|
-
|
(312
|
)
|
-
|
||||||||||
Non-GAAP net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
$
|
114
|
$
|
212
|
$
|
111
|
$
|
402
|
December 31,
|
December 31,
|
|||||||
2020
|
2019
|
|||||||
Assets:
|
||||||||
Cash, cash equivalents and short-term investments
|
$
|
1,892
|
$
|
2,500
|
||||
Contracts receivable
|
76
|
63
|
||||||
Other current assets
|
162
|
158
|
||||||
Property, plant and equipment, net
|
181
|
154
|
||||||
Other assets
|
79
|
358
|
||||||
Total assets
|
$
|
2,390
|
$
|
3,233
|
||||
Liabilities and stockholders’ equity:
|
||||||||
Other current liabilities
|
$
|
182
|
$
|
155
|
||||
Current portion of deferred contract revenue
|
108
|
118
|
||||||
1% convertible senior notes (current in 2020)
|
293
|
275
|
||||||
0.125% convertible senior notes
|
456
|
435
|
||||||
Long-term obligations, less current portion
|
84
|
75
|
||||||
Long-term deferred contract revenue
|
424
|
490
|
||||||
Total Ionis stockholders’ equity
|
843
|
1,471
|
||||||
Noncontrolling interest in Akcea Therapeutics, Inc.
|
-
|
214
|
||||||
Total stockholders’ equity
|
$
|
843
|
$
|
1,685
|
||||
Total liabilities and stockholders’ equity
|
$
|
2,390
|
$
|
3,233
|