SECURITIES AND EXCHANGE COMMISSION
Washington, D.C.  20549
 
FORM 8-K
 
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
 
Date of report (Date of earliest event reported):  August 4, 2021
 
IONIS PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Charter)
 
Delaware
(State or Other Jurisdiction of Incorporation)
 
000-19125
33-0336973
(Commission File No.)
(IRS Employer Identification No.)

2855 Gazelle Court
Carlsbad, CA 92010
(Address of Principal Executive Offices and Zip Code)
 
Registrant’s telephone number, including area code: (760) 931-9200


Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:


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))
 
Securities registered pursuant to Section 12(b) of the Act:

Title of each class
 
Trading symbol
 
Name of each exchange on which registered
Common Stock, $.001 Par Value
 
IONS
 
The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (Section 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (Section 240.12b-2 of this chapter).

  Emerging growth company               
 
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.            ☐
 


Item 2.02
Results of Operations and Financial Condition.
 
On August 4, 2021, Ionis Pharmaceuticals, Inc. (the “Company”) issued a press release announcing the Company’s financial results for the quarter ended June 30, 2021.  In addition to disclosing results that are determined in accordance with Generally Accepted Accounting Principles (GAAP), the Company also discloses pro forma or non-GAAP results of operations, which are adjusted from GAAP to exclude non-cash compensation expense related to equity awards, expenses related to the Company’s acquisition of Akcea Therapeutics, Inc. (“Akcea”), and expenses related to the Company’s restructured commercial operations and the related tax effects.  The Company is presenting pro forma information excluding non-cash compensation expense related to equity awards, expenses related to the Akcea acquisition, and expenses related to the restructured commercial operations and related tax effects because the Company believes it is useful for investors in assessing the Company’s operating results compared to the prior year.  A copy of the release is furnished with this report as an exhibit pursuant to “Item 2.02. Results of Operations and Financial Condition” of Form 8-K in accordance with SEC Release Nos. 33-8216 and 34-47583.
 
The information in this Current Report on Form 8-K and the Exhibit attached hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, regardless of any general incorporation language in such filing.
 
Item 9.01.
Financial Statements and Exhibits.
 
(d) Exhibits.
 
Exhibit No.
Description
Press Release dated August 4, 2021.
   
104
Cover Page Interactive Data File (embedded within the Inline XBRL document).


SIGNATURE
 
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
 
Ionis Pharmaceuticals, Inc.
 
Dated:  August 4, 2021
By:
/s/ Patrick R. O’Neil
 
Patrick R. O’Neil
 
Executive Vice President, Legal, General Counsel and Chief Compliance Officer




Exhibit 99.1


Ionis reports second quarter 2021 financial results and recent business achievements

Key Phase 3 milestones move tofersen, eplontersen and pelacarsen closer to the market
 
Exclusive license to Bicycle Therapeutics’ technology potentially expands LICA technology capabilities
 
Webcast today, August 4, 2021, at 11:30 a.m. Eastern Time
 
CARLSBAD, Calif., August 4, 2021 – Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today reported its financial results for the second quarter of 2021 and recent business achievements.
 
“Since our last quarterly update, we continued to execute on our strategic objectives to prepare for multiple Ionis commercial launches, expand our drug delivery capabilities and advance new products towards the market. Biogen completed dosing in the tofersen Phase 3 VALOR study and began offering tofersen to SOD1-ALS patients on an individual compassionate use basis. We achieved full enrollment in the eplontersen Phase 3 NEURO-TTRansform study and 50 percent enrollment in the pelacarsen Phase 3 Lp(a) HORIZON study. Additionally, we licensed Bicycle Therapeutics’ technology to expand the capabilities of our LICA technology,” said Brett P. Monia, Ph.D., chief executive officer of Ionis. “Looking ahead, we expect data from multiple pipeline programs, including additional data supporting the potential for our IONIS-PKK-LRx program to change the standard of care for patients with hereditary angioedema. And by this fall, we expect data from the Phase 3 VALOR study of tofersen in patients with SOD1-ALS. If results from the VALOR study are positive, we expect tofersen to be our next commercial medicine. These key recent achievements and upcoming catalysts keep us on track for a regular cadence of Phase 3 data and new drug applications, leading to 12 or more products on the market in 2026.”
 
Second Quarter 2021 and Recent Summary Financial Results
 

Second quarter results reflect focus on Ionis’ strategic objectives

o
$126 million in total revenues

o
$154 million of operating expenses on a non-GAAP basis(1) and $199 million on a GAAP basis

o
Net loss of $36 million on a non-GAAP basis(1) and $81 million on a GAAP basis


Well capitalized with cash and investments of $2.1 billion at the end of the second quarter

“In addition to advancing our pipeline and expanding our drug discovery capabilities, we have taken multiple steps to streamline our operations in support of our wholly owned medicines. We have completed the integration of Akcea, entered distribution arrangements with Sobi and restructured our commercial operations. These steps enabled us to unlock significant resources that we are redirecting towards our highest priority programs,” said Elizabeth L. Hougen, chief financial officer of Ionis. “We remain on track to achieve our 2021 revenue guidance of more than $600 million. We continue to expect increased R&D revenue in the second half of this year. Already in the third quarter, we earned $25 million from Novartis for the pelacarsen enrollment milestone. We are revising our 2021 operating expense and net loss guidance because of our license of Bicycle’s technology. Importantly, we remain well-capitalized with the resources we need to achieve our strategic objectives.

1

Revised 2021 Financial Guidance
 

Updated operating expense and net loss guidance because of Ionis’ license of Bicycle’s technology(1)
 
 
Prior 2021 Guidance
Revised 2021 Guidance
Revenue
>$600 million
Unchanged
Operating Expenses (1)
$675 million to $725 million
$710 million to $750 million
Net Loss (1)
<$75 million
<$110 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 commercial operations and the related tax effects. Please refer to the section below titled “Financial Impacts of Akcea Acquisition 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 release.
 
Second Quarter 2021 Marketed Products Highlights
 

SPINRAZA®: The global market leader for the treatment of spinal muscular atrophy (SMA) patients of all ages
 

o
$500 million in worldwide sales in the second quarter
 

o
More than 11,000 patients worldwide on therapy at the end of the second quarter across commercial, expanded access and clinical trial settings
 

o
New data presented at CureSMA reinforce the potential for higher-dose SPINRAZA to improve SMA patient outcomes and further support SPINRAZA’s potential long-term benefit for SMA patients of all ages
 

TEGSEDI® and WAYLIVRA®: important medicines approved for the treatment of patients with severe rare diseases
 

o
Successfully completed the transition of North American TEGSEDI operations to Swedish Orphan Biovitrum AB (Sobi)
 
Second Quarter 2021 and Recent Events
 

Phase 3 Pipeline: Six Phase 3 studies on track for a regular cadence of data readouts beginning this year
 

o
Completed dosing in the Phase 3 VALOR study of tofersen in patients with SOD1-ALS, with data expected by this fall
 

Opened individual compassionate use access for SOD1-ALS patients with the most rapidly progressive disease
 

o
Achieved full enrollment in the Phase 3 NEURO-TTRansform study of eplontersen in patients with TTR polyneuropathy, with data expected by mid-2022
 

o
Achieved 50 percent enrollment in the Phase 3 Lp(a) HORIZON study of pelacarsen for patients at risk for Lp(a)-driven cardiovascular disease, resulting in a $25 million payment from Novartis
 

o
Advanced ION363 into a Phase 3 study in patients with FUS-ALS
 

Mid-stage Pipeline: multiple medicines with potential to change the standard of care for patients with severe diseases
 

o
Continued to advance the Phase 2b RE-THINc ESRD study of IONIS-FXI-LRx, with data expected in the first half of 2022
 

o
Reported data from the 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
 

o
Advanced the ongoing Phase 2 study of ION541 in patients with ALS regardless of family history, resulting in a $10 million payment from Biogen
 

o
Advanced ION224 into a Phase 2b study in patients with non-alcoholic steatohepatitis (NASH)
 

o
Advanced ION373 into the Phase 2 portion of a pivotal study in patients with Alexander disease
 
2


Strategic and Business Events
 

o
Entered a license agreement with Bicycle Therapeutics for exclusive rights to Bicycle’s peptide technology to expand the capabilities of Ionis’ LICA technology
 

o
Announced changes to the Ionis board of directors
 

Joseph Loscalzo, M.D., Ph.D., appointed as chairman and Allene M. Diaz as a member of the board
 

Joseph Wender appointed as lead independent director
 

Ionis founder and executive chairman, Stanley T. Crooke M.D., Ph.D. and Breaux B. Castleman retired from the board
 
Upcoming 2021 Pipeline Catalysts(2)

 
Anticipated Key 2021 Data Readouts
 
Program
 
Phase
 
Anticipated Indication
H1
H2
 
IONIS-PKK-LRx
 
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
 
 
Vupanorsen
 
2b
 
sHTG/CVD risk reduction
 
 
IONIS-PKK-LRx
 
2
 
Hereditary angioedema (full data)
 
 
IONIS-GHR-LRx
 
2 + OLE
 
Acromegaly
 

Anticipated Key 2021 Study Initiations
 
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
 
2b
 
Resistant hypertension
 
 
IONIS-AGT-LRx
 
2
 
Heart failure with reduced ejection fraction
 
 
ION373
 
2/3
 
Alexander disease
 
 
ION224
 
2b
 
NASH
 
 
IONIS-APOCIII-LRx
 
3
 
Second TG indication (sHTG)
 
 
ION582
 
2
 
Angelman Syndrome
 

(2) Timing of partnered program catalysts based on partners’ most recent publicly available disclosures

Second Quarter 2021 Financial Results

Revenue

Ionis' revenue was comprised of the following (amounts in millions):
 
   
Three months ended,
June 30,
   
Six months ended
June 30,
 
   
2021
   
2020
   
2021
   
2020
 
Revenue:
                 
Commercial revenue:
                       
SPINRAZA royalties
 
$
72
   
$
72
   
$
132
   
$
138
 
TEGSEDI and WAYLIVRA revenue, net
   
12
     
16
     
31
     
32
 
Licensing and royalty revenue
   
2
     
2
     
7
     
4
 
Total commercial revenue
   
86
     
90
     
170
     
174
 
R&D Revenue:
                               
Amortization from upfront payments
   
20
     
28
     
40
     
49
 
Milestone payments
   
15
     
7
     
20
     
30
 
License fees
   
-
     
15
     
-
     
15
 
Other services
   
5
     
6
     
7
     
11
 
Total R&D revenue
   
40
     
56
     
67
     
105
 
Total revenue
 
$
126
   
$
146
   
$
237
   
$
279
 

3

In the second quarter of 2021, the Company successfully completed the transition of its TEGSEDI operations in North America to Sobi. As a result, the Company’s commercial revenue from product sales shifted to distribution fees based on net sales generated by Sobi.

The Company’s R&D revenue decreased in the second quarter of 2021 compared to the same period last year primarily because the Company earned more milestone payments in the second quarter of 2020 than the same period this year. The Company expects its R&D revenue to increase in the second half of 2021 compared to the first half as its partnered programs advance. Already in the third quarter of 2021, the Company earned a $25 million milestone payment from Novartis when Novartis achieved 50 percent enrollment in the Phase 3 Lp(a) HORIZON study of pelacarsen.

Financial Impacts of Akcea Acquisition and Restructured Commercial Operations
 
In the second quarter of 2021, the Company incurred $15 million of costs in conjunction with the Akcea acquisition and restructuring of the Company’s commercial operations. The Company excluded these costs from its non-GAAP amounts for the period. Refer to the detailed reconciliation of non-GAAP and GAAP measures that is provided later in this release.

Operating Expenses
 
Ionis’ operating expenses for the second quarter of 2021 increased slightly compared to the same period last year driven by an increase in R&D expenses, partially offset by a decrease in SG&A expenses. Ionis’ increased R&D expenses were primarily driven by the Company’s investments in advancing its late-stage wholly owned pipeline. Ionis’ decreased SG&A expenses were primarily from operating efficiencies achieved from integrating Akcea and restructuring the Company’s commercial operations.

Net Loss Attributable to Ionis Common Stockholders

Ionis’ net loss attributable to Ionis’ common stockholders for the second quarter of 2021 increased compared to the same period in the prior year for the reasons discussed above. Additionally, the Company recognized an $8.6 million non-cash loss from the early retirement of a significant portion of its 1 percent senior convertible notes.

Balance Sheet

Ionis ended June 2021 with cash, cash equivalents and short-term investments of $2.1 billion, compared to $1.9 billion at December 31, 2020. In April 2021, Ionis issued $632.5 million of 0 percent senior convertible notes due in April 2026 and repurchased $247.9 million of its 1 percent senior convertible notes. The Company’s remaining $62 million of 1 percent senior convertible notes mature in November 2021.

The Company revised its 2020 amounts to reflect the simplified convertible instruments guidance the Company adopted retrospectively on January 1, 2021.

Webcast

Today, at 11:30 a.m. Eastern Time, Ionis will conduct a live webcast to discuss this earnings release and related activities. Interested parties may access the webcast here. A webcast replay will be available for a limited time at the same address.

4

About Ionis Pharmaceuticals, Inc.
 
For more than 30 years, Ionis has been the leader in RNA-targeted therapy, pioneering new markets and changing the standards of care with its novel antisense technology. Ionis currently has three marketed medicines and a premier late-stage pipeline highlighted by industry leading neurological and cardiometabolic franchises. Our scientific innovation began and continues with the knowledge that sick people depend on us, which fuels our vision of becoming one of the most successful biotechnology companies.

To learn more about Ionis visit www.ionispharma.com or follow us on Twitter @ionispharma.

Ionis’ Forward-looking Statement
 
This press release includes forward-looking statements regarding Ionis’ business, financial guidance and the therapeutic and commercial potential of SPINRAZA (nusinersen), TEGSEDI (inotersen) and WAYLIVRA (volanesorsen) and Ionis' technologies and products in development. Any statement describing Ionis’ goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties, including those related to the impact COVID-19 could have on our business, and including those inherent in the process of discovering, developing and commercializing medicines that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such medicines. Ionis’ forward-looking statements also involve assumptions that, if they never materialize or prove correct, could cause its results to differ materially from those expressed or implied by such forward-looking statements. Although Ionis’ forward-looking statements reflect the good faith judgment of its management, these statements are based only on facts and factors currently known by Ionis. As a result, you are cautioned not to rely on these forward-looking statements. These and other risks concerning Ionis' programs are described in additional detail in Ionis' annual report on Form 10-K for the year ended December 31, 2020, and the most recent Form 10-Q quarterly filing, which are on file with the SEC. Copies of these and other documents are available from the Company.

In this press release, unless the context requires otherwise, “Ionis,” “Company,” “we,” “our,” and “us” refers to Ionis Pharmaceuticals and its subsidiaries.

Ionis Pharmaceuticals is a trademark of Ionis Pharmaceuticals, Inc. Akcea Therapeutics® is a registered trademark of Akcea Therapeutics, Inc. TEGSEDI® is a registered trademark of Akcea Therapeutics, Inc. WAYLIVRA® is a registered trademark of Akcea Therapeutics, Inc. SPINRAZA® is a registered trademark of Biogen.

Ionis Pharmaceuticals Investor Contact:
760-603-2331

Ionis Pharmaceuticals Media Contact:
Roslyn Patterson
Vice President, Marketing and Communications
760-603-2681

5

IONIS PHARMACEUTICALS, INC.
SELECTED FINANCIAL INFORMATION
Condensed Consolidated Statements of Operations
(In Millions, Except Per Share Data)

   
Three months ended, ended,
June 30,
   
Six months ended,
June 30,
 
   
2021
   
2020
   
2021
   
2020
 
   
(as revised*)
   
(as revised*)
 
   
(unaudited)
 
Revenue:
                       
Commercial revenue:
                       
SPINRAZA royalties
 
$
72
   
$
72
   
$
132
   
$
138
 
TEGSEDI and WAYLIVRA revenue, net
   
12
     
16
     
31
     
32
 
Licensing and royalty revenue
   
2
     
2
     
7
     
4
 
Total commercial revenue
   
86
     
90
     
170
     
174
 
Research and development revenue under collaborative agreements
   
40
     
56
     
67
     
105
 
Total revenue
   
126
     
146
     
237
     
279
 
Expenses:
                               
Cost of sales
   
3
     
3
     
6
     
6
 
Research, development and patent
   
139
     
122
     
279
     
239
 
Selling, general and administrative
   
57
     
73
     
117
     
147
 
Total operating expenses
   
199
     
198
     
402
     
392
 
Loss from operations
   
(73
)
   
(52
)
   
(165
)
   
(113
)
                                 
Other income (expense):
                               
Loss on early retirement of debt
   
(8
)
   
-
     
(8
)
   
-
 
Other income, net
   
-
     
17
     
3
     
25
 
Loss before income tax (expense) benefit
   
(81
)
   
(35
)
   
(170
)
   
(88
)
                                 
Income tax (expense) benefit
   
-
     
(3
)
   
(1
)
   
1
 
                                 
Net loss
 
(81
)
 
(38
)
 
(171
)
 
(87
)
Net loss attributable to noncontrolling interest in Akcea Therapeutics, Inc.
   
-
     
12
     
-
     
22
 
Net loss attributable to Ionis Pharmaceuticals, Inc. common stockholders
 
(81
)
 
(26
)
 
(171
)
 
(65
)
                                 
Basic and diluted net loss per share
 
(0.57
)
 
(0.18
)
 
(1.21
)
 
(0.47
)
Shares used in computing basic and diluted net loss per share
   
141
     
139
     
141
     
139
 

*The Company revised its 2020 amounts to reflect the simplified convertible instruments guidance the Company adopted retrospectively on January 1, 2021.
 
6

IONIS PHARMACEUTICALS, INC.
Reconciliation of GAAP to Non-GAAP Basis:
Condensed Consolidated Operating Expenses, Loss From Operations, and Net Income (Loss)
(In Millions)

   
Three months ended,
June 30,
   
Six months ended,
June 30,
 
   
2021
   
2020
   
2021
   
2020
 
   
(as revised*)
   
(as revised*)
 
   
(unaudited)
 
As reported research, development and patent expenses according to GAAP
 
$
139
   
$
122
   
$
279
   
$
239
 
Excluding compensation expense related to equity awards
   
(23
)
   
(26
)
   
(49
)
   
(52
)
Excluding Akcea acquisition and restructured commercial operation costs
   
(4
)
   
-
     
(6
)
   
-
 
                                 
Non-GAAP research, development and patent expenses
 
$
112
   
$
96
   
$
224
   
$
187
 
As reported selling, general and administrative expenses according to GAAP
 
$
57
   
$
73
   
$
117
   
$
147
 
Excluding compensation expense related to equity awards
   
(7
)
   
(22
)
   
(19
)
   
(37
)
Excluding Akcea acquisition and restructured commercial operation costs
   
(11
)
   
-
     
(16
)
   
-
 
                                 
Non-GAAP selling, general and administrative expenses
 
$
39
   
$
51
   
$
82
   
$
110
 
As reported operating expenses according to GAAP
 
$
199
   
$
198
   
$
402
   
$
392
 
Excluding compensation expense related to equity awards
   
(30
)
   
(48
)
   
(68
)
   
(89
)
Excluding Akcea acquisition and restructured commercial operation costs
   
(15
)
   
-
     
(22
)
   
-
 
                                 
Non-GAAP operating expenses
 
$
154
   
$
150
   
$
312
   
$
303
 
                                 
As reported loss from operations according to GAAP
 
$
(73
)
 
$
(52
)
 
$
(165
)
 
(113
)
Excluding compensation expense related to equity awards
   
(30
)
   
(48
)
   
(68
)
   
(89
)
Excluding Akcea acquisition and restructured commercial operation costs
   
(15
)
   
-
     
(22
)
   
-
 
Non-GAAP loss from operations
 
$
(28
)
 
(4
)
 
$
(75
)
 
(24
)
As reported net loss attributable to Ionis Pharmaceuticals, Inc. common stockholders according to GAAP
 
$
(81
)
 
$
(26
)
 
$
(171
)
 
(65
)
Excluding compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
   
(30
)
   
(45
)
   
(68
)
   
(84
)
Excluding Akcea acquisition and restructured commercial operation costs
   
(15
)
   
-
     
(22
)
   
-
 
Income tax effect related to compensation expense related to equity awards attributable to Ionis Pharmaceuticals, Inc. common stockholders
   
-
     
4
     
-
     
12
 
Non-GAAP net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders according to GAAP
 
$
(36
)
 
$
15
   
$
(81
)
 
$
7
 

*The Company revised its 2020 amounts to reflect the simplified convertible instruments guidance the Company adopted retrospectively on January 1, 2021.
 
7

Reconciliation of GAAP to Non-GAAP Basis
 
As illustrated in the Selected Financial Information in this press release, non-GAAP operating expenses, non-GAAP income (loss) from operations, and non-GAAP net income (loss) attributable to Ionis Pharmaceuticals, Inc. common stockholders were adjusted from GAAP to exclude compensation expense related to equity awards and costs related to the Akcea acquisition and restructured commercial operations and the related tax effects. Compensation expense related to equity awards are non-cash. Costs related to the Akcea acquisition and restructured commercial operations include: severance costs, retention costs and other costs related to commercial operations. Ionis has regularly reported non-GAAP measures for operating results as non-GAAP results. These measures are provided as supplementary information and are not a substitute for financial measures calculated in accordance with GAAP. Ionis reports these non-GAAP results to better enable financial statement users to assess and compare its historical performance and project its future operating results and cash flows. Further, the presentation of Ionis' non-GAAP results is consistent with how Ionis' management internally evaluates the performance of its operations.

8

IONIS PHARMACEUTICALS, INC.
Condensed Consolidated Balance Sheets
(In Millions)
 
     
June 30,
2021
     
December 31,
2020
  
         
(as revised*)
 
   
(unaudited)
 
Assets:
           
Cash, cash equivalents and short-term investments
 
$
2,059
   
$
1,892
 
Contracts receivable
   
24
     
76
 
Other current assets
   
155
     
162
 
Property, plant and equipment, net
   
179
     
181
 
Other assets
   
80
     
79
 
Total assets
 
$
2,497
   
$
2,390
 
                 
Liabilities and stockholders’ equity:
               
Other current liabilities
 
$
130
   
$
183
 
Current portion of 1% convertible senior notes, net
   
62
     
309
 
Current portion of deferred contract revenue
   
102
     
108
 
0% convertible senior notes, net
   
617
     
-
 
0.125% convertible senior notes, net
   
541
     
540
 
Long-term obligations, less current portion
   
82
     
83
 
Long-term deferred contract revenue
   
380
     
424
 
Total stockholders’ equity
   
583
     
743
 
Total liabilities and stockholders’ equity
 
$
2,497
   
$
2,390
 

*The Company revised its 2020 amounts to reflect the simplified convertible instruments guidance the Company adopted retrospectively on January 1, 2021.
 

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