Gilead Sciences Announces Second Quarter 2019 Financial Results

July 30, 2019 4:01 PM

- Product Sales of $5.6 billion -

-
Diluted EPS of $1.47 per share -

- Non-GAAP Diluted EPS of $1.82 per share -

- Revised Full Year 2019 Guidance -

FOSTER CITY, Calif.--(BUSINESS WIRE)-- Gilead Sciences, Inc. (Nasdaq: GILD) announced today its results of operations for the second quarter ended June 30, 2019. The financial results that follow represent a year-over-year comparison of the second quarter of 2019 to the second quarter of 2018. Total revenues were $5.7 billion in 2019 compared to $5.6 billion in 2018. Net income was $1.9 billion or $1.47 per diluted share in 2019 compared to $1.8 billion or $1.39 per diluted share in 2018. Non-GAAP net income was $2.3 billion or $1.82 per diluted share in 2019 compared to $2.5 billion or $1.91 per diluted share in 2018.

“I am very pleased with Gilead’s performance and our ability to continue to reach patients around the world with our medicines. I am also very excited about the progress we are making to strengthen our pipeline, including the recently announced Galapagos collaboration, to bring forward our next generation of products,” said Daniel O’Day, Chairman and Chief Executive Officer, Gilead Sciences. “We saw strong revenue growth quarter-over-quarter, primarily driven by our HIV medicines and the rapid adoption of Biktarvy. Based on this momentum and our confidence in the outlook for the coming months, we are raising our full-year product sales guidance for 2019.”

Three Months Ended

Six Months Ended

June 30,

June 30,

(In millions, except per share amounts)

2019

2018

2019

2018

Product sales

$

5,607

$

5,540

$

10,807

$

10,541

Royalty, contract and other revenues

78

108

159

195

Total revenues

$

5,685

$

5,648

$

10,966

$

10,736

Net income attributable to Gilead

$

1,880

$

1,817

$

3,855

$

3,355

Non-GAAP net income

$

2,331

$

2,494

$

4,589

$

4,452

Diluted earnings per share

$

1.47

$

1.39

$

3.01

$

2.55

Non-GAAP diluted earnings per share

$

1.82

$

1.91

$

3.58

$

3.39

___________________________________

Note: Non-GAAP financial information excludes acquisition-related, up-front collaboration and licensing, stock-based compensation and other expenses, fair value adjustments of equity securities and discrete tax charges or benefits associated with changes in tax related laws and guidelines. A reconciliation between GAAP and non-GAAP financial information is provided in the tables on pages 9 through 11.

Product Sales

Total product sales for the second quarter of 2019 were $5.6 billion compared to $5.5 billion for the same period in 2018. For the second quarter of 2019, product sales in the United States, Europe and other locations were $4.1 billion, $1.0 billion and $512 million, respectively. For the second quarter of 2018, product sales in the United States, Europe and other locations were $4.1 billion, $1.0 billion and $466 million, respectively. Product sales in Europe for the second quarter of 2019 benefited from approximately $160 million of adjustments for statutory rebates related primarily to HCV and HIV sales made in prior years.

Operating Expenses

Three Months Ended

Six Months Ended

June 30,

June 30,

(In millions)

2019

2018

2019

2018

Research and development expenses (R&D)

$

1,160

$

1,192

$

2,217

$

2,129

Non-GAAP R&D expenses

$

916

$

921

$

1,787

$

1,735

Selling, general and administrative expenses (SG&A)

$

1,095

$

980

$

2,125

$

1,977

Non-GAAP SG&A expenses

$

1,015

$

840

$

1,977

$

1,724

During the second quarter of 2019, compared to the same period in 2018:

Effective Tax Rate

The effective tax rate and non-GAAP effective tax rate in the second quarter of 2019 were 22.2% and 21.5%, respectively, compared to 12.8% and 13.4% for the same period in 2018, respectively. The increases were primarily due to the 2018 impact of a favorable settlement of a tax examination.

Cash, Cash Equivalents and Marketable Debt Securities

As of June 30, 2019, Gilead had $30.2 billion of cash, cash equivalents and marketable debt securities, compared to $31.5 billion as of December 31, 2018. During the second quarter of 2019, Gilead generated $2.2 billion in operating cash flow, repaid $500 million of debt, paid cash dividends of $800 million and utilized $588 million on stock repurchases.

Revised Full Year 2019 Guidance

Gilead revised its full year 2019 guidance, initially provided on February 4, 2019. The updated guidance for product sales reflects favorable demand trends observed in the first half of 2019 across Gilead’s product portfolio, the adjustments for statutory rebates related to Europe sales made in prior years, a greater impact from generic versions of Letairis in the second half of 2019 and the full year impact from generic products containing tenofovir disoproxil fumarate in certain European countries. The guidance for diluted EPS impact of acquisition-related, up-front collaboration and licensing, stock-based compensation and other expense was updated as a result of the collaboration agreement with Galapagos NV (Galapagos).

(In millions, except percentages and per share amounts)

Initially Provided
February 4, 2019
Reiterated
May 2, 2019

Updated
July 30, 2019

Product Sales

$21,300 - $21,800

$21,600 - $22,100

Non-GAAP

Product Gross Margin

85% - 87%

85% - 87%

R&D Expenses

$3,600 - $3,800

$3,600 - $3,800

SG&A Expenses

$3,900 - $4,100

$3,900 - $4,100

Effective Tax Rate

20.0% - 21.0%

20.0% - 21.0%

Diluted EPS Impact of Acquisition-related, Up-front Collaboration and Licensing, Stock-based Compensation and Other Expenses

$1.40 - $1.50

$3.90 - $4.00

Corporate Highlights, Including the Announcement of:

Product and Pipeline Updates, Including the Announcement of:

HIV and Liver Diseases Programs

Inflammation Program

Cell Therapy Program

Non-GAAP Financial Information

The information presented in this document has been prepared in accordance with U.S. generally accepted accounting principles (GAAP), unless otherwise noted as non-GAAP. Management believes non-GAAP information is useful for investors, when considered in conjunction with Gilead’s GAAP financial information, because management uses such information internally for its operating, budgeting and financial planning purposes. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of Gilead’s operating results as reported under GAAP. Non-GAAP measures may be defined and calculated differently by other companies in the same industry. A reconciliation between GAAP and non-GAAP financial information is provided in the tables on pages 9 through 11.

Conference Call

The live webcast of the call can be accessed at Gilead’s Investors page at http://investors.gilead.com/. Please connect to the website at least 15 minutes prior to the start of the call to allow adequate time for any software download that may be required to listen to the webcast. Alternatively, please call 877-359-9508 (U.S.) or 224-357-2393 (international) and dial the conference ID 8696029 to access the call. Telephone replay will be available approximately two hours after the call through 8:00 p.m. Eastern Time, August 1, 2019. To access the replay, please call 855-859-2056 (U.S.) or 404-537-3406 (international) and dial the conference ID 8696029. The webcast will be archived on www.gilead.com for one year.

About Gilead Sciences

Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. The company strives to transform and simplify care for people with life-threatening illnesses around the world. Gilead has operations in more than 35 countries worldwide, with headquarters in Foster City, California.

Forward-Looking Statement

Statements included in this press release that are not historical in nature are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Gilead cautions readers that forward-looking statements are subject to certain risks and uncertainties that could cause actual results to differ materially. These risks and uncertainties include: Gilead’s ability to achieve its anticipated full year 2019 financial results; Gilead’s ability to sustain growth in revenues for its antiviral and other programs; the risk that private and public payers may be reluctant to provide, or continue to provide, coverage or reimbursement for new products; austerity measures in European countries that may increase the amount of discount required on Gilead’s products; an increase in discounts, chargebacks and rebates due to ongoing contracts and future negotiations with commercial and government payers; a larger than anticipated shift in payer mix to more highly discounted payer segments and geographic regions and decreases in treatment duration; availability of funding for state AIDS Drug Assistance Programs (ADAPs); continued fluctuations in ADAP purchases driven by federal and state grant cycles as well as purchases by retail pharmacies and other non-wholesaler locations with whom Gilead has no inventory management agreements may not mirror patient demand and may cause fluctuations in Gilead’s earnings; market share and price erosion caused by the introduction of generic versions of our products; an uncertain global macroeconomic environment; potential amendments to the Affordable Care Act or other government action that could have the effect of lowering prices or reducing the number of insured patients; Gilead’s ability to initiate clinical trials in its currently anticipated timeframes; the levels of inventory held by wholesalers and retailers which may cause fluctuations in Gilead’s earnings; Gilead’s ability to realize the potential benefits of collaborations or licensing arrangements, including with Galapagos, Novartis, Carna, Nurix, Humanigen, Goldfinch, Insitro and Novo Nordisk; Gilead’s ability to submit new drug applications for new product candidates in the timelines currently anticipated, including a new drug application to FDA for filgotinib for the treatment of rheumatoid arthritis; Gilead’s ability to receive regulatory approvals in a timely manner or at all, for new and current products, including FDA approval for Descovy for PrEP; Gilead’s ability to successfully commercialize its products, including Yescarta; the risk that physicians and patients may not see advantages of these products over other therapies and may therefore be reluctant to prescribe the products; safety and efficacy data from clinical studies may not warrant further development of Gilead’s product candidates, including filgotinib, selonsertib, GS-9674, GS-0976 and KTE-X19; Gilead’s ability to pay dividends or complete its share repurchase program due to changes in its stock price, corporate or other market conditions; fluctuations in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead’s future revenues and pre-tax earnings; and other risks identified from time to time in Gilead’s reports filed with the U.S. Securities and Exchange Commission (the SEC). In addition, Gilead makes estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses and related disclosures. Gilead bases its estimates on historical experience and on various other market specific and other relevant assumptions that it believes to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. There may be other factors of which Gilead is not currently aware that may affect matters discussed in the forward-looking statements and may also cause actual results to differ significantly from these estimates. Further, results for the quarter ended June 30, 2019 are not necessarily indicative of operating results for any future periods. You are urged to consider statements that include the words may, will, would, could, should, might, believes, estimates, projects, potential, expects, plans, anticipates, intends, continues, forecast, designed, goal or the negative of those words or other comparable words to be uncertain and forward-looking. Gilead directs readers to its press releases, Quarterly Report on Form 10-Q for the quarter ended March 31, 2019 and other subsequent disclosure documents filed with the SEC. Gilead claims the protection of the Safe Harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements.

All forward-looking statements are based on information currently available to Gilead and Gilead assumes no obligation to update or supplement any such forward-looking statements other than as required by law. Any forward-looking statements speak only as of the date hereof or as of the dates indicated in the statements.

Gilead owns or has rights to various trademarks, copyrights and trade names used in its business, including the following: GILEAD®, GILEAD SCIENCES®, AMBISOME®, ATRIPLA®, BIKTARVY®, CAYSTON®, COMPLERA®, DESCOVY®, EMTRIVA®, EPCLUSA®, EVIPLERA®, GENVOYA®, HARVONI®, HEPSERA®, LETAIRIS®, ODEFSEY®, RANEXA®, SOVALDI®, STRIBILD®, TRUVADA®, TRUVADAFORPREP®, TYBOST®, VEMLIDY®, VIREAD®, VOSEVI®, YESCARTA® and ZYDELIG®.

LEXISCAN® is a registered trademark of Astellas U.S. LLC. MACUGEN® is a registered trademark of Eyetech, Inc. SYMTUZA® is a registered trademark of Janssen Sciences Ireland UC. TAMIFLU® is a registered trademark of Hoffmann-La Roche Inc.

For more information on Gilead Sciences, Inc., please visit www.gilead.com or call the Gilead Public Affairs Department at 1-800-GILEAD-5 (1-800-445-3235).

GILEAD SCIENCES, INC.

CONDENSED CONSOLIDATED STATEMENTS OF INCOME

(unaudited)

(in millions, except per share amounts)

Three Months Ended

Six Months Ended

June 30,

June 30,

2019

2018

2019

2018

Revenues:

Product sales

$

5,607

$

5,540

$

10,807

$

10,541

Royalty, contract and other revenues

78

108

159

195

Total revenues

5,685

5,648

10,966

10,736

Costs and expenses:

Cost of goods sold

1,000

1,196

1,957

2,197

Research and development expenses

1,160

1,192

2,217

2,129

Selling, general and administrative expenses

1,095

980

2,125

1,977

Total costs and expenses

3,255

3,368

6,299

6,303

Income from operations

2,430

2,280

4,667

4,433

Interest expense

(248

)

(266

)

(502

)

(556

)

Other income (expense), net

228

72

595

242

Income before provision for income taxes

2,410

2,086

4,760

4,119

Provision for income taxes

535

267

917

761

Net income

1,875

1,819

3,843

3,358

Net income (loss) attributable to noncontrolling interest

(5

)

2

(12

)

3

Net income attributable to Gilead

$

1,880

$

1,817

$

3,855

$

3,355

Net income per share attributable to Gilead common stockholders - basic

$

1.48

$

1.40

$

3.03

$

2.58

Shares used in per share calculation - basic

1,270

1,298

1,273

1,302

Net income per share attributable to Gilead common stockholders - diluted

$

1.47

$

1.39

$

3.01

$

2.55

Shares used in per share calculation - diluted

1,277

1,308

1,280

1,314

Cash dividends declared per share

$

0.63

$

0.57

$

1.26

$

1.14

GILEAD SCIENCES, INC.

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION

(unaudited)

(in millions, except percentages and per share amounts)

Three Months Ended

Six Months Ended

June 30,

June 30,

2019

2018

2019

2018

Cost of goods sold reconciliation:

GAAP cost of goods sold

$

1,000

$

1,196

$

1,957

$

2,197

Acquisition-related – amortization of purchased intangibles

(273

)

(300

)

(556

)

(601

)

Stock-based compensation expenses(1)

(13

)

(21

)

(27

)

(34

)

Non-GAAP cost of goods sold

$

714

$

875

$

1,374

$

1,562

Product gross margin reconciliation:

GAAP product gross margin

82.2

%

78.4

%

81.9

%

79.2

%

Acquisition-related – amortization of purchased intangibles

4.9

%

5.4

%

5.1

%

5.7

%

Stock-based compensation expenses

0.2

%

0.4

%

0.2

%

0.3

%

Non-GAAP product gross margin(4)

87.3

%

84.2

%

87.3

%

85.2

%

Research and development expenses reconciliation:

GAAP research and development expenses

$

1,160

$

1,192

$

2,217

$

2,129

Up-front collaboration and licensing expenses

(165

)

(160

)

(291

)

(160

)

Acquisition-related – other costs

(9

)

(25

)

Stock-based compensation expenses(1)

(80

)

(102

)

(141

)

(205

)

Other(2)

1

2

(4

)

Non-GAAP research and development expenses

$

916

$

921

$

1,787

$

1,735

Selling, general and administrative expenses reconciliation:

GAAP selling, general and administrative expenses

$

1,095

$

980

$

2,125

$

1,977

Acquisition-related – other costs

(9

)

(15

)

Stock-based compensation expenses(1)

(81

)

(129

)

(149

)

(233

)

Other(2)

1

(2

)

1

(5

)

Non-GAAP selling, general and administrative expenses

$

1,015

$

840

$

1,977

$

1,724

Operating margin reconciliation:

GAAP operating margin

42.7

%

40.4

%

42.6

%

41.3

%

Up-front collaboration and licensing expenses

2.9

%

2.8

%

2.7

%

1.5

%

Acquisition-related – amortization of purchased intangibles

4.8

%

5.3

%

5.1

%

5.6

%

Acquisition-related – other costs

%

0.3

%

%

0.4

%

Stock-based compensation expenses

3.1

%

4.5

%

2.9

%

4.4

%

Other(2)

%

%

%

0.1

%

Non-GAAP operating margin(4)

53.5

%

53.3

%

53.1

%

53.2

%

Other income (expense), net reconciliation:

GAAP other income (expense), net

$

228

$

72

$

595

$

242

Unrealized (gains) losses from equity securities, net

(57

)

64

(254

)

19

Non-GAAP other income (expense), net

$

171

$

136

$

341

$

261

GILEAD SCIENCES, INC.

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL INFORMATION - (Continued)

(unaudited)

(in millions, except percentages and per share amounts)

Three Months Ended

Six Months Ended

June 30,

June 30,

2019

2018

2019

2018

Effective tax rate reconciliation:

GAAP effective tax rate

22.2

%

12.8

%

19.3

%

18.5

%

Up-front collaboration and licensing expenses

%

0.7

%

0.2

%

0.1

%

Acquisition-related – amortization of purchased intangibles

(1.5

)%

(0.8

)%

(1.2

)%

(1.5

)%

Acquisition-related – other costs

%

0.1

%

%

%

Stock-based compensation expenses(1)

%

0.7

%

0.1

%

0.5

%

Unrealized (gains) losses from equity securities, net

0.8

%

(0.4

)%

1.1

%

(0.1

)%

Tax Reform adjustments(3)

%

0.5

%

%

0.2

%

Non-GAAP effective tax rate(4)

21.5

%

13.4

%

19.2

%

17.8

%

Net income attributable to Gilead reconciliation:

GAAP net income attributable to Gilead

$

1,880

$

1,817

$

3,855

$

3,355

Up-front collaboration and licensing expenses

128

125

226

125

Acquisition-related – amortization of purchased intangibles

252

281

512

562

Acquisition-related – other costs

14

32

Stock-based compensation expenses(1)

135

202

252

362

Unrealized (gains) losses from equity securities, net

(63

)

63

(254

)

18

Tax Reform adjustments(3)

(10

)

(10

)

Other(2)

(1

)

2

(2

)

8

Non-GAAP net income attributable to Gilead

$

2,331

$

2,494

$

4,589

$

4,452

Diluted earnings per share reconciliation:

GAAP diluted earnings per share

$

1.47

$

1.39

$

3.01

$

2.55

Up-front collaboration and licensing expenses

0.10

0.10

0.18

0.10

Acquisition-related – amortization of purchased intangibles

0.20

0.21

0.40

0.43

Acquisition-related – other costs

0.01

0.02

Stock-based compensation expenses(1)

0.11

0.15

0.20

0.28

Unrealized (gains) losses from equity securities, net

(0.05

)

0.05

(0.20

)

0.01

Tax Reform adjustments(3)

(0.01

)

(0.01

)

Other(2)

0.01

Non-GAAP diluted earnings per share(4)

$

1.82

$

1.91

$

3.58

$

3.39

Non-GAAP adjustment summary:

Cost of goods sold adjustments

$

286

$

321

$

583

$

635

Research and development expenses adjustments

244

271

430

394

Selling, general and administrative expenses adjustments

80

140

148

253

Other income (expense), net adjustments

(57

)

64

(254

)

19

Total non-GAAP adjustments before tax

553

796

907

1,301

Income tax effect

(102

)

(109

)

(173

)

(194

)

Tax Reform adjustments(3)

(10

)

(10

)

Total non-GAAP adjustments after tax

$

451

$

677

$

734

$

1,097

Notes:

(1)

The decreases were primarily due to stock-based compensation expenses incurred in 2018 following Gilead’s acquisition of Kite Pharma, Inc.

(2)

Amounts represent restructuring, contingent consideration and/or other individually insignificant amounts

(3)

Amounts represent measurement period adjustments relating to the enactment of the 2017 Tax Cuts and Jobs Act (Tax Reform)

(4)

Amounts may not sum due to rounding

GILEAD SCIENCES, INC.

RECONCILIATION OF GAAP TO NON-GAAP 2019 FULL YEAR GUIDANCE

(unaudited)

(in millions, except percentages and per share amounts)

Initially Provided
February 4, 2019
Reiterated
May 2, 2019

Updated
July 30, 2019

Projected product gross margin GAAP to non-GAAP reconciliation:

GAAP projected product gross margin

80% - 81%

80% - 81%

Acquisition-related expenses

5% - 6%

5% - 6%

Non-GAAP projected product gross margin(1)

85% - 87%

85% - 87%

Projected research and development expenses GAAP to non-GAAP reconciliation:

GAAP projected research and development expenses(2)

$4,195 - $4,480

$8,290 - $8,595

Stock-based compensation expenses

(345) - (380)

(290) - (325)

Up-front collaboration and licensing expenses(2)

(250) - (300)

(4,400) - (4,470)

Non-GAAP projected research and development expenses

$3,600 - $3,800

$3,600 - $3,800

Projected selling, general and administrative expenses GAAP to non-GAAP reconciliation:

GAAP projected selling, general and administrative expenses

$4,255 - $4,490

$4,205 - $4,440

Stock-based compensation expenses

(355) - (390)

(305) - (340)

Non-GAAP projected selling, general and administrative expenses

$3,900 - $4,100

$3,900 - $4,100

Projected effective tax rate GAAP to non-GAAP reconciliation:

GAAP projected effective tax rate(3)

21.5% - 22.5%

21.5% - 22.5%

Tax rate effect of adjustments noted above(3)

(1.5%) - (1.5%)

(1.5%) - (1.5%)

Non-GAAP projected effective tax rate

20.0% - 21.0%

20.0% - 21.0%

Projected diluted EPS impact of acquisition-related, up-front collaboration and licensing, stock-based compensation and other expenses(2)(3):

Acquisition-related expenses / up-front collaboration and licensing expenses(2)

$0.93 - $0.97

$3.47 - $3.51

Stock-based compensation expenses

$0.47 - $0.53

$0.43 - $0.49

Projected diluted EPS impact of acquisition-related, up-front collaboration and licensing, stock-based compensation and other expenses(2)(3)

$1.40 - $1.50

$3.90 - $4.00

____________________
Notes:

(1)

Total stock-based compensation expenses have a less than one percent impact on non-GAAP projected product gross margin

(2)

Updates made primarily for the collaboration with Galapagos, which is expected to close late in the third quarter of 2019, subject to a number of closing conditions, including antitrust clearances required by the U.S. Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended, and the rules and regulations promulgated thereunder and receipt of merger control approval from the Austrian Federal Competition Authority.

(3)

Excludes fair value adjustments of equity securities and the associated income tax effect, as Gilead is unable to project future fair value adjustments, and other discrete tax charges or benefits

GILEAD SCIENCES, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(unaudited)

(in millions)

June 30,

December 31,

2019

2018

Cash, cash equivalents and marketable securities

$

30,234

$

31,512

Accounts receivable, net

3,396

3,327

Inventories

884

814

Property, plant and equipment, net

4,249

4,006

Intangible assets, net

15,152

15,738

Goodwill

4,117

4,117

Other assets

5,178

4,161

Total assets

$

63,210

$

63,675

Current liabilities

$

8,961

$

10,605

Long-term liabilities

31,498

31,536

Stockholders’ equity(1)

22,751

21,534

Total liabilities and stockholders’ equity

$

63,210

$

63,675

____________________
Note:

(1)

As of June 30, 2019, there were 1,267 million shares of common stock issued and outstanding

GILEAD SCIENCES, INC.

PRODUCT SALES SUMMARY

(unaudited)

(in millions)

Three Months Ended

Six Months Ended

June 30,

June 30,

2019

2018

2019

2018

Atripla – U.S.

$

122

$

274

$

255

$

502

Atripla – Europe

26

39

42

90

Atripla – Other International

4

36

26

71

152

349

323

663

Biktarvy – U.S.

1,023

183

1,762

218

Biktarvy – Europe

73

2

121

2

Biktarvy – Other International

20

26

1,116

185

1,909

220

Complera / Eviplera – U.S.

42

82

86

149

Complera / Eviplera – Europe

72

103

134

212

Complera / Eviplera – Other International

9

14

18

28

123

199

238

389

Descovy – U.S.

246

311

479

585

Descovy – Europe

69

78

137

153

Descovy – Other International

43

14

84

26

358

403

700

764

Genvoya – U.S.

733

904

1,461

1,757

Genvoya – Europe

177

207

370

393

Genvoya – Other International

70

49

164

92

980

1,160

1,995

2,242

Odefsey – U.S.

266

303

548

582

Odefsey – Europe

111

77

217

135

Odefsey – Other International

10

5

19

10

387

385

784

727

Stribild – U.S.

78

144

145

277

Stribild – Europe

24

34

42

63

Stribild – Other International

6

9

17

21

108

187

204

361

Truvada – U.S.

657

649

1,208

1,156

Truvada – Europe

41

86

74

183

Truvada – Other International

20

30

42

78

718

765

1,324

1,417

Other HIV(1) – U.S.

9

11

20

20

Other HIV(1) – Europe

1

3

2

4

Other HIV(1) – Other International

5

5

10

8

15

19

32

32

Revenue share – Symtuza(2) – U.S.

55

97

Revenue share – Symtuza(2) – Europe

29

13

53

20

Revenue share – Symtuza(2) – Other International

84

13

150

20

Total HIV – U.S.

3,231

2,861

6,061

5,246

Total HIV – Europe

623

642

1,192

1,255

Total HIV – Other International

187

162

406

334

4,041

3,665

7,659

6,835

AmBisome – U.S.

10

14

18

31

AmBisome – Europe

60

55

117

111

AmBisome – Other International

35

34

63

68

105

103

198

210

GILEAD SCIENCES, INC.

PRODUCT SALES SUMMARY - (Continued)

(unaudited)

(in millions)

Three Months Ended

Six Months Ended

June 30,

June 30,

2019

2018

2019

2018

Ledipasvir/Sofosbuvir(3) – U.S.

$

86

$

230

$

203

$

464

Ledipasvir/Sofosbuvir(3) – Europe

22

22

49

78

Ledipasvir/Sofosbuvir(3) – Other International

85

79

166

137

193

331

418

679

Letairis – U.S.

204

244

401

448

Ranexa – U.S.

19

208

174

403

Sofosbuvir/Velpatasvir(4) – U.S.

219

239

449

508

Sofosbuvir/Velpatasvir(4) – Europe

156

168

310

366

Sofosbuvir/Velpatasvir(4) – Other International

118

93

225

162

493

500

984

1,036

Vemlidy – U.S.

71

59

136

106

Vemlidy – Europe

5

3

9

6

Vemlidy – Other International

40

14

72

22

116

76

217

134

Viread – U.S.

9

16

21

23

Viread – Europe

28

32

42

62

Viread – Other International

38

34

84

94

75

82

147

179

Vosevi – U.S.

53

86

98

172

Vosevi – Europe

15

20

31

36

Vosevi – Other International

7

3

9

8

75

109

138

216

Yescarta – U.S.

99

68

189

108

Yescarta – Europe

21

27

Yescarta – Other International

120

68

216

108

Zydelig – U.S.

12

17

23

31

Zydelig – Europe

14

22

29

40

Zydelig – Other International

1

1

26

39

53

72

Other(5) – U.S.

41

27

77

56

Other(5) – Europe

97

41

117

56

Other(5) – Other International

2

47

8

109

140

115

202

221

Total product sales – U.S.

4,054

4,069

7,850

7,596

Total product sales – Europe

1,041

1,005

1,923

2,010

Total product sales – Other International

512

466

1,034

935

$

5,607

$

5,540

$

10,807

$

10,541

____________________
Notes:

(1)

Includes Emtriva and Tybost

(2)

Represents Gilead’s revenue from cobicistat (C), emtricitabine (FTC) and tenofovir alafenamide (TAF) in Symtuza (darunavir/C/FTC/TAF), a fixed dose combination product commercialized by Janssen Sciences Ireland UC

(3)

Amounts consist of sales of Harvoni and the authorized generic version of Harvoni sold by Gilead’s separate subsidiary, Asegua Therapeutics LLC

(4)

Amounts consist of sales of Epclusa and the authorized generic version of Epclusa sold by Gilead’s separate subsidiary, Asegua Therapeutics LLC

(5)

Includes Cayston, Hepsera and Sovaldi. In Europe, the increase for both the three and six months ended June 30, 2019 was primarily due to approximately $80 million of favorable adjustments for statutory rebates related to sales of Sovaldi made in prior years

Investors

Robin Washington

(650) 522-5688



Sung Lee

(650) 524-7792

Media

Amy Flood

(650) 522-5643

Source: Gilead Sciences, Inc.

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