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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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Emerging growth company |
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 3, 2021.
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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.
|
||
Dated: November 3, 2021
|
By: |
/s/ Patrick R. O’Neil
|
Patrick R. O’Neil
|
||
Executive Vice President, Chief Legal Officer and General Counsel
|
• |
Third quarter results reflect Ionis’ focus on its strategic objectives
|
o |
$133 million in total revenues
|
o |
$185 million of operating expenses on a non-GAAP basis(1) and $219 million on a GAAP basis
|
o |
Net loss of $48 million on a non-GAAP basis(1) and $82 million on a GAAP basis
|
• |
Well capitalized with cash and investments of $2 billion as of September 30, 2021
|
(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 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.
|
• |
SPINRAZA®: the global market leader for the treatment of spinal muscular atrophy (SMA) patients of all ages
|
o |
$444 million in worldwide sales in the third quarter
|
o |
More than 11,000 patients worldwide on therapy at the end of the third quarter across commercial, expanded access and clinical trial settings
|
o |
Biogen plans to initiate the Phase 3b ASCEND study evaluating the potential benefit of an investigational higher dose of nusinersen in children, teens and adults
with later-onset SMA previously treated with Evrysdi® (risdiplam)
|
• |
TEGSEDI® and WAYLIVRA®: important medicines approved for the treatment of patients with severe rare diseases
|
o |
TEGSEDI achieved innovative drug pricing in Brazil reflecting the significant unmet medical need and prevalence of TTR polyneuropathy in Brazil
|
o |
WAYLIVRA was approved in Brazil as the first and only treatment for patients with familial chylomicronemia syndrome
|
• |
Advancing Ionis’ leading cardiovascular and metabolic disease pipeline
|
o |
Initiated the Phase 3 CORE study of olezarsen (IONIS-APOCIII-LRx) in patients with severe hypertriglyceridemia (sHTG)
|
o |
Reached 50 percent enrollment in the Phase 3 Lp(a) HORIZON outcome study of pelacarsen for patients with established cardiovascular disease and elevated Lp(a),
resulting in a $25 million payment from Novartis
|
o |
Achieved full enrollment in the Bayer Phase 2b RE-THINc ESRD study of fesomersen (IONIS-FXI-LRx), with data expected in the first half of 2022
|
o |
Achieved proof-of-mechanism, a strong indication of proof-of-concept and good safety and tolerability in a Phase 2 study and a preliminary assessment from an
open-label extension study of cimdelirsen (IONIS-GHR-LRx) in acromegaly patients uncontrolled on standard of care therapy, supporting continued development. Data from the ongoing open-label extension study and monotherapy study are
expected in 2022. The results from the Phase 2 study of cimdelirsen are posted to Ionis’ website and may be accessed here
|
• |
Addressing substantial unmet medical need with Ionis’ broad neurological disease pipeline
|
o |
The Biogen Phase 3 VALOR study of tofersen in patients with SOD1-ALS did not meet the primary endpoint of change from baseline to week 28 in the ALS Functional
Rating Scale-Revised (ALSFRS-R); however, signs of reduced disease progression across multiple secondary and exploratory endpoints were observed
|
o |
Achieved full enrollment in the Phase 3 NEURO-TTRansform study of eplontersen in patients with TTR polyneuropathy, with data expected in mid-2022
|
o |
Reported data from the Biogen Phase 1/2 study of IONIS-MAPTRx in patients with Alzheimer’s disease, demonstrating durable, time and dose-dependent
reductions in CSF tau protein; IONIS-MAPTRx was generally well tolerated
|
• |
Investing in expanding the reach of Ionis’ technology
|
o |
Entered a license agreement with Bicycle Therapeutics for exclusive rights to Bicycle’s peptide technology targeting transferrin receptor 1 to expand the
capabilities of Ionis’ LICA technology
|
o |
Entered a license agreement with Flamingo Therapeutics for the development and commercialization of programs from Ionis’ oncology pipeline
|
Program
|
Phase
|
Anticipated Indication
|
H1
|
H2
|
|||
Donidalorsen
|
2
|
Hereditary angioedema (top-line data)
|
|||||
IONIS-AGT-LRx
|
2
|
Hypertension
|
|||||
Tominersen
|
3
|
Huntington’s disease
|
|||||
IONIS-ENAC-2.5Rx
|
2
|
Cystic fibrosis
|
|||||
IONIS-MAPTRx
|
1/2
|
Alzheimer’s disease
|
|||||
Tofersen
|
3 (VALOR)
|
SOD1-ALS
|
|||||
Cimdelirsen
|
2 + OLE
|
Acromegaly
|
|||||
Donidalorsen
|
2
|
Hereditary angioedema (full data)
|
•
|
||||
ION449 (PCSK9)
|
1 (MAD)
|
Dyslipidemia
|
•
|
||||
Vupanorsen
|
2b
|
sHTG/CVD risk reduction
|
•
|
Program
|
Phase
|
Anticipated Indication
|
H1
|
H2
|
|||
SPINRAZA
|
4 (RESPOND)
|
SMA, suboptimal gene therapy response
|
|||||
Tofersen
|
3 (ATLAS)
|
Presymptomatic SOD1-ALS
|
|||||
ION363
|
3
|
FUS-ALS
|
|||||
IONIS-AGT-LRx
|
2 & 2b
|
Heart failure & resistant hypertension
|
|||||
ION373
|
2/3
|
Alexander disease
|
|||||
ION224
|
2b
|
NASH
|
|||||
Olezarsen
|
3 (CORE)
|
Severe hypertriglyceridemia (sHTG)
|
|||||
Donidalorsen
|
3
|
Hereditary angioedema
|
•
|
||||
SPINRAZA
|
3b (ASCEND)
|
SMA, previous risdiplam treatment
|
•
|
||||
ION582
|
2
|
Angelman syndrome
|
•
|
Three months ended,
September 30,
|
Nine months ended
September 30,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
67
|
$
|
74
|
$
|
199
|
$
|
212
|
||||||||
TEGSEDI and WAYLIVRA revenue, net
|
15
|
19
|
47
|
51
|
||||||||||||
Licensing and royalty revenue
|
3
|
2
|
9
|
6
|
||||||||||||
Total commercial revenue
|
85
|
95
|
255
|
269
|
||||||||||||
R&D revenue:
|
||||||||||||||||
Amortization from upfront payments
|
17
|
19
|
57
|
68
|
||||||||||||
Milestone payments
|
28
|
44
|
48
|
73
|
||||||||||||
License fees
|
-
|
-
|
-
|
15
|
||||||||||||
Other services
|
3
|
2
|
10
|
14
|
||||||||||||
Total R&D revenue
|
48
|
65
|
115
|
170
|
||||||||||||
Total revenue
|
$
|
133
|
$
|
160
|
$
|
370
|
$
|
439
|
Three months ended, ended,
September 30,
|
Nine months ended,
September 30,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
(as revised*)
|
(as revised*)
|
|||||||||||||||
(unaudited)
|
||||||||||||||||
Revenue:
|
||||||||||||||||
Commercial revenue:
|
||||||||||||||||
SPINRAZA royalties
|
$
|
67
|
$
|
74
|
$
|
199
|
$
|
212
|
||||||||
TEGSEDI and WAYLIVRA revenue, net
|
15
|
19
|
47
|
51
|
||||||||||||
Licensing and royalty revenue
|
3
|
2
|
9
|
6
|
||||||||||||
Total commercial revenue
|
85
|
95
|
255
|
269
|
||||||||||||
Research and development revenue under collaborative agreements
|
48
|
65
|
115
|
170
|
||||||||||||
Total revenue
|
133
|
160
|
370
|
439
|
||||||||||||
Expenses:
|
||||||||||||||||
Cost of sales
|
3
|
3
|
9
|
9
|
||||||||||||
Research, development and patent
|
185
|
125
|
464
|
364
|
||||||||||||
Selling, general and administrative
|
31
|
69
|
148
|
215
|
||||||||||||
Total operating expenses
|
219
|
197
|
621
|
588
|
||||||||||||
Loss from operations
|
(86
|
)
|
(37
|
)
|
(251
|
)
|
(149
|
)
|
||||||||
Other income (expense):
|
||||||||||||||||
Loss on early retirement of debt
|
-
|
-
|
(9
|
)
|
-
|
|||||||||||
Other income, net
|
2
|
5
|
6
|
29
|
||||||||||||
Loss before income tax benefit (expense)
|
(84
|
)
|
(32
|
)
|
(254
|
)
|
(120
|
)
|
||||||||
Income tax benefit (expense)
|
2
|
(5
|
)
|
1
|
(4
|
)
|
||||||||||
Net loss
|
$
|
(82
|
)
|
$
|
(37
|
)
|
$
|
(253
|
)
|
$
|
(124
|
)
|
||||
Net loss attributable to noncontrolling interest in Akcea Therapeutics, Inc.
|
$
|
-
|
$
|
13
|
$
|
-
|
$
|
34
|
||||||||
Net loss attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
$
|
(82
|
)
|
$
|
(24
|
)
|
$
|
(253
|
)
|
$
|
(90
|
)
|
||||
Basic and diluted net loss per share
|
$
|
(0.58
|
)
|
$
|
(0.18
|
)
|
$
|
(1.80
|
)
|
$
|
(0.64
|
)
|
||||
Shares used in computing basic and diluted net loss per share
|
141
|
140
|
141
|
139
|
Three months ended,
September 30,
|
Nine months ended,
September 30,
|
|||||||||||||||
2021
|
2020
|
2021
|
2020
|
|||||||||||||
(as revised*)
|
(as revised*)
|
|||||||||||||||
(unaudited)
|
||||||||||||||||
As reported research, development and patent expenses according to GAAP
|
$
|
185
|
$
|
125
|
$
|
464
|
$
|
364
|
||||||||
Excluding compensation expense related to equity awards
|
(23
|
)
|
(25
|
)
|
(72
|
)
|
(77
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(2
|
)
|
-
|
(8
|
)
|
-
|
||||||||||
Non-GAAP research, development and patent expenses
|
$
|
160
|
$
|
100
|
$
|
384
|
$
|
287
|
||||||||
As reported selling, general and administrative expenses according to GAAP
|
$
|
31
|
$
|
69
|
$
|
148
|
$
|
215
|
||||||||
Excluding compensation expense related to equity awards
|
(7
|
)
|
(20
|
)
|
(26
|
)
|
(57
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(1
|
)
|
-
|
(16
|
)
|
-
|
||||||||||
Non-GAAP selling, general and administrative expenses
|
$
|
23
|
$
|
49
|
$
|
106
|
$
|
158
|
||||||||
As reported operating expenses according to GAAP
|
$
|
219
|
$
|
197
|
$
|
621
|
$
|
588
|
||||||||
Excluding compensation expense related to equity awards
|
(31
|
)
|
(46
|
)
|
(98
|
)
|
(135
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(3
|
)
|
-
|
(24
|
)
|
-
|
||||||||||
Non-GAAP operating expenses
|
$
|
185
|
$
|
151
|
$
|
499
|
$
|
453
|
||||||||
As reported loss from operations according to GAAP
|
$
|
(86
|
)
|
$
|
(37
|
)
|
$
|
(251
|
)
|
$
|
(149
|
)
|
||||
Excluding compensation expense related to equity awards
|
(31
|
)
|
(46
|
)
|
(98
|
)
|
(135
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(3
|
)
|
-
|
(24
|
)
|
-
|
||||||||||
Non-GAAP income (loss) from operations
|
$
|
(52
|
)
|
$
|
9
|
$
|
(129
|
)
|
$
|
(14
|
)
|
|||||
As reported net loss attributable to Ionis Pharmaceuticals, Inc. common stockholders according to GAAP
|
$
|
(82
|
)
|
$
|
(24
|
)
|
$
|
(253
|
)
|
$
|
(90
|
)
|
||||
Excluding compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
|
(31
|
)
|
(42
|
)
|
(98
|
)
|
(126
|
)
|
||||||||
Excluding Akcea merger and restructured commercial operation costs**
|
(3
|
)
|
-
|
(24
|
)
|
-
|
||||||||||
Income tax effect related to compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common
stockholders
|
-
|
6
|
-
|
18
|
||||||||||||
Non-GAAP net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders according to GAAP
|
$
|
(48
|
)
|
$
|
12
|
$
|
(131
|
)
|
$
|
18
|
September 30,
|
December 31,
|
|||||||
2021
|
2020
|
|||||||
(as revised*)
|
||||||||
(unaudited)
|
||||||||
Assets:
|
||||||||
Cash, cash equivalents and short-term investments
|
$
|
1,987
|
$
|
1,892
|
||||
Contracts receivable
|
9
|
76
|
||||||
Other current assets
|
160
|
162
|
||||||
Property, plant and equipment, net
|
180
|
181
|
||||||
Other assets
|
79
|
79
|
||||||
Total assets
|
$
|
2,415
|
$
|
2,390
|
||||
Liabilities and stockholders’ equity:
|
||||||||
Other current liabilities
|
$
|
120
|
$
|
183
|
||||
Current portion of 1% convertible senior notes, net
|
62
|
309
|
||||||
Current portion of deferred contract revenue
|
98
|
108
|
||||||
0% convertible senior notes, net
|
618
|
-
|
||||||
0.125% convertible senior notes, net
|
542
|
540
|
||||||
Long-term obligations, less current portion
|
81
|
83
|
||||||
Long-term deferred contract revenue
|
363
|
424
|
||||||
Total stockholders’ equity
|
531
|
743
|
||||||
Total liabilities and stockholders’ equity
|
$
|
2,415
|
$
|
2,390
|