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Alexion Reports Third Quarter 2019 Results

October 23, 2019

BOSTON--(BUSINESS WIRE)--Oct 23, 2019--

Alexion Pharmaceuticals, Inc. (NASDAQ:ALXN) today announced financial results for the third quarter of 2019. Total revenues in the third quarter were $1,263.1 million, a 23 percent increase compared to the same period in 2018. The negative impact of foreign currency on total revenues year-over-year was less than 1 percent, or $2.5 million, inclusive of hedging activities. On a GAAP basis, diluted EPS in the quarter was $2.08, a 41 percent increase versus the prior year. Non-GAAP diluted EPS for the third quarter of 2019 was $2.79, a 38 percent increase versus the third quarter of 2018.

“With consistent and strong execution, we have delivered another record performance in the third quarter, building on our momentum from the first half of 2019. Our teams continued to demonstrate launch excellence across the globe, with very rapid starts to the German and Japanese ULTOMIRIS PNH launches, where conversion is progressing ahead of the best-in-class U.S. launch at the same time points, as well as a strong start to the SOLIRIS NMOSD launch in the U.S.,” said Ludwig Hantson, Ph.D., Chief Executive Officer of Alexion. “We also continued to expand our portfolio with two additional approvals - ULTOMIRIS for atypical HUS in the U.S. and SOLIRIS for NMOSD in the EU - and three new business development transactions that further diversify our pipeline, including an agreement to acquire Achillion. By continuing to deliver on the ambitious transformation plan we laid out two-and-a-half years ago, we have successfully established a strong foundation for the future and look forward to building on this progress as we advance our mission of delivering life-changing therapies to people with rare diseases.”

Third Quarter 2019 Financial Highlights

Research and Development

PHASE 3

PHASE 1/2

PRE-CLINICAL

Share Repurchase Authorization

In October 2019, the Board of Directors approved a new share repurchase authorization of $1 billion. The repurchase program does not have an expiration date and we are not obligated to acquire a particular number of shares of common stock.

2019 Financial Guidance

Alexion is increasing revenues and EPS guidance. Full guidance updates are outlined below.

 

Previous (as of July 24, 2019)

Updated (as of October 23, 2019)

Total revenues

$4,750 to $4,800 million

$4,860 to $4,890 million

SOLIRIS/ULTOMIRIS revenues

$4,095 to $4,130 million

$4,180 to $4,200 million

Metabolic revenues

$655 to $670 million

$680 to $690 million

R&D (% total revenues)

 

 

GAAP

17% to 19%

17% to 18%

Non-GAAP

14% to 16%

14% to 15%

SG&A (% total revenues)

 

 

GAAP

23% to 24%

24% to 25%

Non-GAAP

20% to 21%

21% to 22%

Operating margin

 

 

GAAP

42% to 43%

41% to 42%

Non-GAAP

55% to 56%

55% to 56%

Earnings per share

 

 

GAAP

$8.13 to $8.41

$8.58 to $8.78

Non-GAAP

$9.65 to $9.85

$10.25 to $10.40

Updated 2019 financial guidance assumes a GAAP effective tax rate of 5 to 6 percent and a non-GAAP effective tax rate of 13 to 14 percent for the year.

Updated guidance excludes the financial impact of the recently announced agreement to acquire Achillion as it is anticipated to close in the first half of 2020.

Alexion’s financial guidance is based on current foreign exchange rates net of hedging activities and does not include the effect of acquisitions, license and collaboration agreements, intangible asset impairments, litigation charges, changes in fair value of contingent consideration or restructuring and related activity outside of the previously announced activities that may occur after the issuance of this press release.

Conference Call/Webcast Information:

Alexion will host a conference call/audio webcast to discuss the third quarter 2019 results today at 8:00 a.m. Eastern Time. To participate in the call, dial 866-762-3111 (USA) or 210-874-7712 (International), conference ID 6281803 shortly before 8:00 a.m. Eastern Time. A replay of the call will be available for a limited period following the call. The audio webcast can be accessed on the Investor page of Alexion’s website at: http://ir.alexion.com.

About Alexion

Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases through the discovery, development and commercialization of life-changing therapies. As the global leader in complement biology and inhibition for more than 20 years, Alexion has developed and commercializes two approved complement inhibitors to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), as well as the first and only approved complement inhibitor to treat anti-acetylcholine receptor (AchR) antibody-positive generalized myasthenia gravis (gMG) and neuromyelitis optica spectrum disorder (NMOSD). Alexion also has two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia (HPP) and lysosomal acid lipase deficiency (LAL-D). In addition, the company is developing several mid-to-late-stage therapies, including a second complement inhibitor, a copper-binding agent for Wilson disease and an anti-neonatal Fc receptor (FcRn) antibody for rare Immunoglobulin G (IgG)-mediated diseases as well as several early-stage therapies, including one for light chain (AL) amyloidosis and a second anti-FcRn therapy. Alexion focuses its research efforts on novel molecules and targets in the complement cascade and its development efforts on the core therapeutic areas of hematology, nephrology, neurology and metabolic disorders. Alexion has been named to the Forbes’ list of the World’s Most Innovative Companies seven years in a row and is headquartered in Boston, Massachusetts’ Innovation District. The company also has offices around the globe and serves patients in more than 50 countries. This press release and further information about Alexion can be found at: www.alexion.com.

[ALXN-E]

Forward-Looking Statement

This press release contains forward-looking statements, including statements related to: guidance regarding anticipated financial results for 2019 (and the assumptions related to such guidance); the strength of our business and continued growth; plans to expand the Company’s pipeline; Company’s goal of continuing to build on momentum as the year progresses; future plans for, and the timing for, the commencement of future clinical trials and the expected timing of the receipt of results of certain clinical trials and studies, including clinical programs for ULTOMIRIS in aHUS, NMOSD, HSCT-TMA, ALS, PPMS and a subcutaneous administration in PNH and aHUS and for ALXN1830 in WAIHA and gMG; potential benefits of current products and products under development and in clinical trials; plans for development programs with third parties including, Eidos, Affibody, Dicerna, Zealand, Stealth and Complement Pharma; the potential to treat a broad range of complement mediated diseases with the product to be developed with Zealand; the anticipated closings of the Achillion acquisition and the Immune Pharma asset acquisition; and Alexion’s future clinical, regulatory, and commercial plans for ULTOMIRIS and other products and product candidates. Forward-looking statements are subject to factors that may cause Alexion’s results and plans to differ materially from those forward-looking statements, including for example: our dependence on sales from our principal product (SOLIRIS); our ability to facilitate the timely conversion from SOLIRIS to ULTOMIRIS; payer, physician and patient acceptance of ULTOMIRIS as an alternative to SOLIRIS; appropriate pricing for ULTOMIRIS; future competition from biosimilars and novel products; decisions of regulatory authorities regarding the adequacy of our research, marketing approval or material limitations on the marketing of our products; delays or failure of product candidates to obtain regulatory approval; delays or the inability to launch product candidates due to regulatory restrictions, anticipated expense or other matters; interruptions or failures in the manufacture and supply of our products and our product candidates; failure to satisfactorily address matters raised by the FDA and other regulatory agencies; results in early stage clinical trials may not be indicative of full results or results from later stage or larger clinical trials (or broader patient populations) and do not ensure regulatory approval; the possibility that results of clinical trials are not predictive of safety and efficacy and potency of our products (or we fail to adequately operate or manage our clinical trials) which could cause us to halt trials, delay or prevent us from making regulatory approval filings or result in denial of approval of our product candidates; unexpected delays in clinical trials; unexpected concerns that may arise from additional data or analysis obtained during clinical trials; future product improvements may not be realized due to expense or feasibility or other factors; uncertainty of long-term success in developing, licensing or acquiring other product candidates or additional indications for existing products; inability to complete planned acquisitions due to failure of regulatory approval or material changes in target or otherwise; inability to complete acquisitions and investments due to increased competition for technology; the possibility that current rates of adoption of our products are not sustained; the adequacy of our pharmacovigilance and drug safety reporting processes; failure to protect and enforce our data, intellectual property and proprietary rights and the risks and uncertainties relating to intellectual property claims, lawsuits and challenges against us (including intellectual property lawsuits relating to ULTOMIRIS brought by third parties against Alexion and inter partes review petitions submitted by third parties); the risk that third party payors (including governmental agencies) will not reimburse or continue to reimburse for the use of our products at acceptable rates or at all; failure to realize the benefits and potential of investments, collaborations, licenses and acquisitions; the possibility that expected tax benefits will not be realized; assessment of impact of recent accounting pronouncements; potential declines in sovereign credit ratings or sovereign defaults in countries where we sell our products; delay of collection or reduction in reimbursement due to adverse economic conditions or changes in government and private insurer regulations and approaches to reimbursement; uncertainties surrounding legal proceedings, company investigations and government investigations, including investigations of Alexion by the U.S. Securities and Exchange Commission (SEC) and U.S. Department of Justice; the risk that estimates regarding the number of patients with PNH, aHUS, gMG, NMOSD, HPP and LAL-D and other future indications we are pursuing are inaccurate; the risks of changing foreign exchange rates; risks relating to the potential effects of the Company’s restructuring; risks related to the acquisition of companies and co-development and collaboration efforts; and a variety of other risks set forth from time to time in Alexion’s filings with the SEC, including but not limited to the risks discussed in Alexion’s Quarterly Report on Form 10-Q for the period ended June 30, 2019 and in our other filings with the SEC. Alexion disclaims any obligation to update any of these forward-looking statements to reflect events or circumstances after the date hereof, except when a duty arises under law.

In addition to financial information prepared in accordance with GAAP, this press release also contains non-GAAP financial measures that Alexion believes, when considered together with the GAAP information, provide investors and management with supplemental information relating to performance, trends and prospects that promote a more complete understanding of our operating results and financial position during different periods. The non-GAAP results exclude the impact of the following GAAP items (see reconciliation tables below for additional information): share-based compensation expense, fair value adjustment of inventory acquired, amortization of purchased intangible assets, changes in fair value of contingent consideration, restructuring and related expenses, upfront payments related to licenses and collaborations, acquired in-process research and development assets, impairment of intangible assets, change in value of strategic equity investments, litigation charges, gain or loss on sale of a business or asset and certain adjustments to income tax expense. These non-GAAP financial measures are not intended to be considered in isolation or as a substitute for, or superior to, the financial measures prepared and presented in accordance with GAAP, and should be reviewed in conjunction with the relevant GAAP financial measures. Please refer to the attached Reconciliations of GAAP to non-GAAP Financial Results and GAAP to non-GAAP 2019 Financial Guidance for explanations of the amounts adjusted to arrive at non-GAAP net income and non-GAAP earnings per share amounts for the three and nine month periods ended September 30, 2019 and 2018 and projected twelve months ending December 31, 2019.

(Tables Follow)

ALEXION PHARMACEUTICALS, INC.

TABLE 1: CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(in millions, except per share amounts)

(unaudited)

 

Three months ended

 

Nine months ended

 

September 30,

 

September 30,

 

2019

 

2018

 

2019

 

2018

Net product sales

$

1,263.1

 

 

$

1,026.5

 

 

$

3,605.8

 

 

$

3,001.6

 

Other revenue

 

 

 

 

1.0

 

 

0.8

 

Total revenues

1,263.1

 

 

1,026.5

 

 

3,606.8

 

 

3,002.4

 

Cost of sales

95.2

 

 

90.6

 

 

280.2

 

 

277.5

 

Operating expenses:

 

 

 

 

 

 

 

Research and development

232.9

 

 

174.8

 

 

616.4

 

 

524.8

 

Selling, general and administrative

299.3

 

 

258.7

 

 

880.1

 

 

793.1

 

Acquired in-process research and development

 

 

 

 

(4.1

)

 

803.7

 

Amortization of purchased intangible assets

75.6

 

 

80.0

 

 

235.7

 

 

240.1

 

Change in fair value of contingent consideration

29.8

 

 

53.5

 

 

7.2

 

 

110.9

 

Restructuring expenses

0.3

 

 

10.3

 

 

11.9

 

 

26.4

 

Total operating expenses

637.9

 

 

577.3

 

 

1,747.2

 

 

2,499.0

 

Operating income

530.0

 

 

358.6

 

 

1,579.4

 

 

225.9

 

Other income and expense:

 

 

 

 

 

 

 

Investment income

23.0

 

 

5.9

 

 

50.6

 

 

119.4

 

Interest expense

(17.9

)

 

(24.6

)

 

(56.1

)

 

(73.7

)

Other income and (expense)

0.4

 

 

2.2

 

 

2.9

 

 

3.5

 

Income before income taxes

535.5

 

 

342.1

 

 

1,576.8

 

 

275.1

 

Income tax expense

67.9

 

 

11.2

 

 

61.5

 

 

152.5

 

Net income

$

467.6

 

 

$

330.9

 

 

$

1,515.3

 

 

$

122.6

 

Earnings per common share

 

 

 

 

 

 

 

Basic

$

2.09

 

 

$

1.48

 

 

$

6.77

 

 

$

0.55

 

Diluted

$

2.08

 

 

$

1.47

 

 

$

6.72

 

 

$

0.55

 

Shares used in computing earnings per common share

 

 

 

 

 

 

 

Basic

223.3

 

 

222.9

 

 

223.8

 

 

222.5

 

Diluted

224.5

 

 

224.6

 

 

225.4

 

 

224.2

 

 

 

 

 

 

 

 

 

ALEXION PHARMACEUTICALS, INC.

TABLE 2: RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL RESULTS

(in millions, except per share amounts)

(unaudited)

 

Three months ended

 

Nine months ended

 

September 30,

 

September 30,

 

2019

 

2018

 

2019

 

2018

GAAP net income

$

467.6

 

 

$

330.9

 

 

$

1,515.3

 

 

$

122.6

 

Before tax adjustments:

 

 

 

 

 

 

 

Cost of sales:

 

 

 

 

 

 

 

Share-based compensation

3.4

 

 

3.3

 

 

10.7

 

 

12.2

 

Restructuring related expenses (1)

 

 

 

 

 

 

5.8

 

Research and development expense:

 

 

 

 

 

 

 

Share-based compensation

16.7

 

 

12.5

 

 

45.9

 

 

42.5

 

Upfront payments related to licenses and collaborations (2)

30.1

 

 

 

 

76.3

 

 

 

Restructuring related expenses (1)

 

 

 

 

 

 

0.1

 

Selling, general and administrative expense:

 

 

 

 

 

 

 

Share-based compensation

38.9

 

 

29.8

 

 

120.1

 

 

96.2

 

Restructuring related expenses (1)

 

 

7.9

 

 

 

 

18.0

 

Litigation charges

 

 

 

 

0.1

 

 

7.1

 

Gain on sale of asset

 

 

(3.5

)

 

 

 

(3.5

)

Acquired in-process research and development (3)

 

 

 

 

(4.1

)

 

803.7

 

Amortization of purchased intangible assets

75.6

 

 

80.0

 

 

235.7

 

 

240.1

 

Change in fair value of contingent consideration (4)

29.8

 

 

53.5

 

 

7.2

 

 

110.9

 

Restructuring expenses (1)

0.3

 

 

10.3

 

 

11.9

 

 

26.4

 

Investment income:

 

 

 

 

 

 

 

Change in value of strategic equity investments (5)

(12.0

)

 

 

 

(20.6

)

 

(100.8

)

Other income:

 

 

 

 

 

 

 

Restructuring related expenses (1)

 

 

 

 

 

 

(0.1

)

Adjustments to income tax expense (6)

(14.6

)

 

(64.6

)

 

(212.1

)

 

(68.9

)

Non-GAAP net income

$

635.8

 

 

$

460.1

 

 

$

1,786.4

 

 

$

1,312.3

 

 

 

 

 

 

 

 

 

GAAP earnings per common share - diluted

$

2.08

 

 

$

1.47

 

 

$

6.72

 

 

$

0.55

 

Non-GAAP earnings per common share - diluted

$

2.79

 

 

$

2.02

 

 

$

7.83

 

 

$

5.78

 

 

 

 

 

 

 

 

 

Shares used in computing diluted earnings per common share (GAAP)

224.5

 

 

224.6

 

 

225.4

 

 

224.2

 

Shares used in computing diluted earnings per common share (non-GAAP)

227.7

 

 

227.4

 

 

228.2

 

 

227.0

 

(1) The following table summarizes the total restructuring and related expenses recorded by type of activity and the classification within the Reconciliation of GAAP to non-GAAP Financial Results:

 

Three months ended September 30,

 

Three months ended September 30,

 

2019

 

2018

 

Employee
Separation
Costs

 

Asset-
Related
Charges

 

Other

 

Total

 

Employee
Separation
Costs

 

Asset-
Related
Charges

 

Other

 

Total

Cost of sales

$

 

 

$

 

 

$

 

 

$

 

 

$

 

 

$

 

 

$

 

 

$

 

Research and
development

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Selling, general and
administrative

 

 

 

 

 

 

 

 

 

 

7.9

 

 

 

 

7.9

 

Restructuring expense

(2.8

)

 

 

 

3.1

 

 

0.3

 

 

2.8

 

 

 

 

7.5

 

 

10.3

 

Other (income) expense

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

$

(2.8

)

 

$

 

 

$

3.1

 

 

$

0.3

 

 

$

2.8

 

 

$

7.9

 

 

$

7.5

 

 

$

18.2

 

 

Nine months ended September 30,

 

Nine months ended September 30,

 

2019

 

2018

 

Employee
Separation
Costs

 

Asset-
Related
Charges

 

Other

 

Total

 

Employee
Separation
Costs

 

Asset-
Related
Charges

 

Other

 

Total

Cost of sales

$

 

 

$

 

 

$

 

 

$

 

 

$

 

 

$

5.8

 

 

$

 

 

$

5.8

 

Research and
development

 

 

 

 

 

 

 

 

 

 

0.1

 

 

 

 

0.1

 

Selling, general and
administrative

 

 

 

 

 

 

 

 

 

 

18.0

 

 

 

 

18.0

 

Restructuring expense

8.7

 

 

 

 

3.2

 

 

11.9

 

 

6.9

 

 

 

 

19.5

 

 

26.4

 

Other (income) expense

 

 

 

 

 

 

 

 

 

 

 

 

(0.1

)

 

(0.1

)

 

$

8.7

 

 

$

 

 

$

3.2

 

 

$

11.9

 

 

$

6.9

 

 

$

23.9

 

 

$

19.4

 

 

$

50.2

 

(2) During the three months ended September 30, 2019, we recorded an upfront license payment of $30.1 million in connection with an agreement that we entered into with Eidos Therapeutics, Inc. (Eidos). During the nine months ended September 30, 2019, we recorded upfront license payments of $76.3 million in connection with agreements that we entered into with Eidos, Affibody AB and Zealand Pharma A/S.

(3) In connection with the agreement of the final working capital adjustment for the Syntimmune acquisition, we recognized a benefit of $4.1 million associated with previously acquired in-process research and development in the second quarter of 2019.

(4) Changes in the fair value of contingent consideration expense for the three and nine months ended September 30, 2019 include the impact of changes in the expected timing of achieving contingent milestones, in addition to the interest component related to the passage of time. For the three and nine months ended September 30, 2018, changes in the fair value of contingent consideration expense was primarily due to amending certain contingent milestone payments due under our prior merger agreement with Enobia Pharma Corp. in September 2018 as well as due to increases in the likelihood and anticipated timing of payments for contingent consideration.

(5) During the three and nine months ended September 30, 2019, we recognized an unrealized gain of $12.0 million and $20.6 million, respectively, in investment income to adjust our strategic equity investments to fair value. The nine months ended September 30, 2018 included the recognition of an unrealized gain of $100.8 million on our investment in Moderna Therapeutics, Inc. following the completion of a new round of equity financing in the first quarter 2018.

(6) Alexion’s non-GAAP income tax expense for the three and nine months ended September 30, 2019 and 2018 excludes the tax effect of pre-tax adjustments to GAAP profit. Non-GAAP income tax expense for the three and nine months ended September 30, 2019 excludes a one-time tax expense of $10.2 million related to the July 1, 2019 integration of Wilson Therapeutics intellectual property into the Alexion corporate structure. Non-GAAP income tax expense for the nine months ended September 30, 2019 also excludes certain one-time tax benefits of $95.7 million and $30.3 million associated with a tax election made with respect to intellectual property of Wilson Therapeutics and a release of an existing valuation allowance, respectively. Non-GAAP income tax expense for the three and nine months ended September 30, 2018 excludes adjustments to provisional estimates of the impact of Tax Cuts and Jobs Act we recorded in fourth quarter 2017.

ALEXION PHARMACEUTICALS, INC.

TABLE 3: RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL GUIDANCE

(in millions, except per share amounts and percentages)

(unaudited)

Twelve months ending

December 31, 2019

Low

High

 
GAAP net income

$

1,926

 

$

1,970

 

 
Before tax adjustments:
Share-based compensation

 

251

 

 

234

 

Upfront payments related to licenses and collaborations

 

96

 

 

96

 

Acquired in-process research and development

 

(4

)

 

(4

)

Amortization of purchased intangible assets

 

309

 

 

309

 

Change in fair value of contingent consideration

 

12

 

 

12

 

Restructuring expenses

 

20

 

 

20

 

Change in value of strategic equity investments

 

(21

)

 

(21

)

Adjustments to income tax expense

 

(257

)

 

(250

)

Non-GAAP net income

$

2,332

 

$

2,366

 

 
Diluted GAAP earnings per common share

$

8.58

 

$

8.78

 

Diluted non-GAAP earnings per common share

$

10.25

 

$

10.4

 

 

Operating expense and margin (% total revenues)

 

 

GAAP research and development expense

 

18

%

 

17

%

Share-based compensation

 

1

%

 

1

%

Upfront payments related to licenses and collaborations

 

2

%

 

2

%

Non-GAAP research and development expense

 

15

%

 

14

%

 

GAAP selling, general and administrative expense

 

25

%

 

24

%

Share-based compensation

 

3

%

 

3

%

Non-GAAP selling, general and administrative expense

 

22

%

 

21

%

 

GAAP operating margin

 

41

%

 

42

%

Share-based compensation

 

5

%

 

5

%

Upfront payments related to licenses and collaborations

 

2

%

 

2

%

Acquired in-process research and development

 

0

%

 

0

%

Amortization of purchased intangible assets

 

6

%

 

6

%

Change in fair value of contingent consideration

 

0

%

 

0

%

Restructuring expenses

 

0

%

 

0

%

Non-GAAP operating margin

 

55

%

 

56

%

 

Income tax expense (% of income before income taxes)

 

 

GAAP income tax expense

 

6

%

 

5

%

Tax effect of pre-tax adjustments to GAAP net income and other one-time items associated with intellectual property

 

8

%

 

8

%

Non-GAAP income tax expense

 

14

%

 

13

%

 

Amounts may not foot due to rounding.

ALEXION PHARMACEUTICALS, INC.

TABLE 4: NET PRODUCT SALES BY GEOGRAPHY

(in millions)

(unaudited)

 

 

Three months ended

 

Nine months ended

 

 

September 30,

 

September 30,

 

 

2019

 

2018

 

2019

 

2018

SOLIRIS

 

 

 

 

 

 

 

 

United States

 

$

496.8

 

 

$

404.5

 

 

$

1,456.8

 

 

$

1,136.3

 

Europe

 

255.5

 

 

262.1

 

 

800.2

 

 

766.3

 

Asia Pacific

 

118.0

 

 

98.2

 

 

329.2

 

 

277.3

 

Rest of World

 

120.2

 

 

123.2

 

 

347.1

 

 

406.4

 

Total Soliris

 

$

990.5

 

 

$

888.0

 

 

$

2,933.3

 

 

$

2,586.3

 

ULTOMIRIS

 

 

 

 

 

 

 

 

United States

 

$

65.1

 

 

$

 

 

$

143.9

 

 

$

 

Europe

 

21.1

 

 

 

 

21.1

 

 

 

Asia Pacific

 

3.7

 

 

 

 

3.7

 

 

 

Rest of World

 

 

 

 

 

 

 

 

Total Ultomiris

 

$

89.9

 

 

$

 

 

$

168.7

 

 

$

 

STRENSIQ

 

 

 

 

 

 

 

 

United States

 

$

118.0

 

 

$

86.6

 

 

$

323.7

 

 

$

275.7

 

Europe

 

19.0

 

 

16.6

 

 

56.0

 

 

47.0

 

Asia Pacific

 

14.0

 

 

7.2

 

 

36.0

 

 

19.2

 

Rest of World

 

3.3

 

 

2.8

 

 

10.0

 

 

7.1

 

Total Strensiq

 

$

154.3

 

 

$

113.2

 

 

$

425.7

 

 

$

349.0

 

KANUMA

 

 

 

 

 

 

 

 

United States

 

$

16.0

 

 

$

13.7

 

 

$

45.1

 

 

$

38.6

 

Europe

 

6.3

 

 

4.7

 

 

19.4

 

 

16.4

 

Asia Pacific

 

1.3

 

 

0.8

 

 

3.4

 

 

2.9

 

Rest of World

 

4.8

 

 

6.1

 

 

10.2

 

 

8.4

 

Total Kanuma

 

$

28.4

 

 

$

25.3

 

 

$

78.1

 

 

$

66.3

 

 

 

 

 

 

 

 

 

 

Net Product Sales

 

 

 

 

 

 

 

 

United States

 

$

695.9

 

 

$

504.8

 

 

$

1,969.5

 

 

$

1,450.6

 

Europe

 

301.9

 

 

283.4

 

 

896.7

 

 

829.7

 

Asia Pacific

 

137.0

 

 

106.2

 

 

372.3

 

 

299.4

 

Rest of World

 

128.3

 

 

132.1

 

 

367.3

 

 

421.9

 

Total Net Product Sales

 

$

1,263.1

 

 

$

1,026.5

 

 

$

3,605.8

 

 

$

3,001.6

 

ALEXION PHARMACEUTICALS, INC.

TABLE 5: CONDENSED CONSOLIDATED BALANCE SHEETS

(in millions)

(unaudited)

 

September 30,

 

December 31

 

2019

 

2018

Cash and cash equivalents

$

2,171.3

 

 

$

1,365.5

 

Marketable securities

44.4

 

 

198.3

 

Trade accounts receivable, net

1,116.3

 

 

922.3

 

Inventories

576.7

 

 

472.5

 

Prepaid expenses and other current assets (1)

432.5

 

 

426.4

 

Property, plant and equipment, net (1)

1,148.0

 

 

1,471.5

 

Intangible assets, net

3,410.1

 

 

3,641.3

 

Goodwill

5,037.4

 

 

5,037.4

 

Right of use operating assets (1)

206.9

 

 

 

Other assets

671.4

 

 

396.7

 

Total assets

$

14,815.0

 

 

$

13,931.9

 

 

 

 

 

Accounts payable and accrued expenses

$

868.2

 

 

$

698.2

 

Revolving credit facility

 

 

250.0

 

Current portion of long-term debt

126.6

 

 

93.8

 

Current portion of contingent consideration

 

 

97.6

 

Other current liabilities (1)

96.4

 

 

34.4

 

Long-term debt, less current portion

2,406.7

 

 

2,501.7

 

Contingent consideration

188.0

 

 

183.2

 

Facility lease obligations (1)

 

 

361.0

 

Deferred tax liabilities

314.7

 

 

391.1

 

Noncurrent operating lease liabilities (1)

166.8

 

 

 

Other liabilities (1)

280.4

 

 

155.6

 

Total liabilities

4,447.8

 

 

4,766.6

 

Total stockholders' equity (1)

10,367.2

 

 

9,165.3

 

Total liabilities and stockholders' equity

$

14,815.0

 

 

$

13,931.9

 

(1) In February 2016, the Financial Accounting Standards Board issued a new standard that requires lessees to recognize leases on-balance sheet. We adopted the new standard on January 1, 2019 using the modified retrospective approach. The September 30, 2019 condensed consolidated balance sheet is presented under the new standard, while the December 31, 2018 condensed consolidated balance sheet is not adjusted and continues to be reported under the accounting standards in effect for that period. Upon adoption of the new lease standard, we derecognized $472.8 million of property, plant and equipment and other assets and $372.2 million of facility lease obligations associated with previously existing build-to-suit arrangements which resulted in a decrease of $90.3 million to retained earnings, net of tax. In addition, we capitalized $326.1 million and $255.3 million of right of use assets and lease liabilities, respectively, within our condensed consolidated balance sheet upon adoption.

View source version on businesswire.com:https://www.businesswire.com/news/home/20191023005211/en/

CONTACT: Alexion:

Media

Megan Goulart, 857-338-8634

Senior Director, Corporate Communications

Investors

Susan Altschuller, Ph.D., 857-338-8788

Vice President, Investor Relations

KEYWORD: UNITED STATES NORTH AMERICA MASSACHUSETTS

INDUSTRY KEYWORD: BIOTECHNOLOGY PHARMACEUTICAL HEALTH

SOURCE: Alexion Pharmaceuticals, Inc.

Copyright Business Wire 2019.

PUB: 10/23/2019 06:30 AM/DISC: 10/23/2019 06:30 AM

http://www.businesswire.com/news/home/20191023005211/en