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Actionable news in ALXN: Alexion Pharmaceuticals, Inc.,

Alexion Reports First Quarter 2016 Results

The following excerpt is from the company's SEC filing.

- Total Revenues of $701 Million; Increased 17 Percent Year-on-Year; 22 Percent Increase Year-on-Year on a Constant Currency Basis -

- Soliris

(eculizumab) Revenues Driven by Steady Number of New Patients Treated in the U.S., Europe and Japan -

- Strensiq

(asfotase alfa) Launch Off to a Strong Start in Initial Countries -

- Kanuma

(sebelipase alfa) U.S. Launch Under Way -

- Exceeded Target Enrollment for Two Initial Studies of ALXN1210 in Patients with PNH -

- Commenced Dose Escalation for SBC-103 in Phase 1/2 Study in Patients with MPS IIIB -

- Pr ogressed Three Registration Studies of Eculizumab: Data from gMG Expected Mid-Year; Data from DGF Expected Second Half 2016; On Track to Complete Enrollment in NMOSD This Year -

-Alexion Pharmaceuticals, Inc. (NASDAQ: ALXN) today announced financial results for the first quarter of 2016. Total revenues grew to $701 million, a 17 percent increase, compared to $600 million for the same period in 2015. In the first quarter, the negative impact of currency on total revenue was 5 percent or $30 million, net of hedging activities, compared to the same quarter last year. First quarter revenue growth was further negatively impacted by increased macroeconomic weakness in Latin American countries, primarily Brazil and Argentina. Non-GAAP diluted earnings per share (EPS) for the first quarter of 2016 was $1.11 per share, compared to $1.28 per share in the first quarter of 2015. On a GAAP basis, diluted EPS for the first quarter of 2016 was $0.41 per share, compared to $0.45 per share in the first quarter of 2015.

“In Q1 2016, we grew our core Soliris business by serving a steady number of new patients with PNH and aHUS in the U.S., Europe and Japan, partially offset by the increased impact of macroeconomic weakness in Latin America. We are very pleased with the strong start to the Strensiq launches in initial countries and have now commenced the U.S. launch of Kanuma,” said David Hallal, Chief Executive Officer of Alexion. “We look forward to 2016 being another transformative year for Alexion as we serve an increasing number of patients with four devastating, ultra-rare diseases and progress multiple milestones in our robust rare disease pipeline.”

First Quarter 2016 Financial Highlights

(eculizumab) net product sales were $665 million compared to $600 million in Q1 2015. Net product sales increased 11 percent year-on-year, despite continued currency headwinds as well as increased macroeconomic weakness in Latin American countries, primarily Brazil and Argentina. Soliris volume increased 18 percent year-on-year.

(asfotase alfa) net product sales were $33 million.

net product sales were $2.5 million.

Non-GAAP R&D expense was $158 million, compared to $97 million in the same quarter last year. GAAP R&D expense was $176 million, compared to $221 million in the same quarter last year.

Non-GAAP SG&A expense was $194 million, compared to $157 million in the same quarter last year. GAAP SG&A expense was $233 million, compared to $187 million in the same quarter last year.

Non-GAAP diluted EPS was $1.11 per share, compared to $1.28 per share in the same quarter last year. On a GAAP basis, diluted EPS was $0.41 per share, compared to $0.45 per share in the same quarter last year.

Product and Pipeline Updates

Complement Portfolio

Eculizumab-Generalized Myasthenia Gravis (gMG):

Enrollment is complete in the REGAIN study, a single, multinational, placebo-controlled registration trial of eculizumab in refractory gMG, and data are expected in mid-2016.

Eculizumab-Neuromyelitis Optica Spectrum Disorder (NMOSD):

Alexion expects to complete enrollment this year in the PREVENT study, a single, multinational, placebo-controlled registration trial of eculizumab in patients with relapsing NMOSD.

Eculizumab-Delayed Graft Function (DGF):

Enrollment is complete in the PROTECT study, a single, multinational, placebo-controlled registration trial of eculizumab in the prevention of DGF, and data are expected in the second half of 2016.

ALXN1210:

Alexion exceeded target enrollment in both a Phase 1/2 study and a Phase 2 study of ALXN1210, our highly innovative longer-acting C5 antibody, in patients with paroxysmal nocturnal hemoglobinuria (PNH), and we expect data from the Phase 1/2 study to be presented in mid-2016. Alexion also expects to initiate a clinical program in patients with atypical hemolytic uremic syndrome (aHUS) later this year.

ALXN1007:

Alexion is continuing to advance the development of ALXN1007, a complement inhibitor that targets C5a, in patients with graft-versus-host disease involving the lower gastrointestinal tract (GI-GVHD). Interim Phase 2 data reported in the fourth quarter of 2015 support the evaluation of higher doses of ALXN1007 in additional patients with acute GI-GVHD.

Metabolic Portfolio

Strensiq:

New long-term data presented at the Endocrine Society’s 98

Annual Meeting and Expo (ENDO) in April showed sustained improvements in survival rates, bone healing, respiratory support, and growth and mobility in children with HPP treated with Strensiq. In addition, the data presented at ENDO showed that adolescent and adult patients treated with Strensiq reduced or eliminated their need of ambulatory assistive devices and had improvements in physical function as measured by the Six Minute Walk Test.

Kanuma:

Kanuma received marketing approval from Japan’s Ministry of Health, Labour and Welfare on March 28, 2016. Additionally, new data presented by researchers at the WORLD

Symposium

meeting in March showed a substantial survival benefit beyond 2 years of age in infants with LAL-D treated with Kanuma.

SBC-103:

Alexion has commenced the planned dose escalation in the Phase 1/2 trial of SBC-103, a recombinant form of the NAGLU enzyme, in patients with mucopolysaccharidosis IIIB, or MPS IIIB. Patients are now being randomized to either a 5 mg/kg or 10 mg/kg dose. Six-month data presented at the WORLD

meeting in March showed continued reductions in heparan sulfate cerebrospinal fluid with a mean reduction of 26% in the highest dose studied, 3 mg/kg.

cPMP Replacement Therapy (ALXN1101):

Alexion is progressing a pivotal study to evaluate ALXN1101 in neonates with Molybdenum Cofactor Deficiency (MoCD) Type A. Alexion received Breakthrough Therapy designation for its cPMP replacement therapy.

Preclinical Portfolio

Alexion has more than 30 diverse preclinical programs across a range of therapeutic modalities, with four of these programs expected to enter the clinic in 2016.

2016 Financial Guidance

Alexion expects 2016 total revenues to be at the low end of our previously guided range of $3,050 million to $3,100 million, primarily due to increased macroeconomic weakness in Latin America, partially offset by an increase in Strensiq revenues and the strengthening of foreign currencies.

R&D and SG&A expenses are expected to be at the high end of guidance primarily due to continued investment in key programs in our R&D pipeline and the commercial launches of Strensiq and Kanuma, as well as the strengthening of foreign currencies.

Alexion expects 2016 non-GAAP EPS to be at the low end of the previously guided range of $5.00 to $5.20 per share.

Updated 2016 non-GAAP financial guidance is as follows:

Updated Guidance (1)

Prior Guidance (1)

Low end of $3,050 to $3,100 million

Soliris revenues

$2,835 to $2,875 million

$2,900 to $2,925 million

Metabolic revenues

$180 to $200 million

$150 to $175 million

Cost of sales

8% to 9%

Research and development expense

High end of $650 to $680 million

Selling, general and administrative expense

High end of $760 to $790 million

Interest expense

$100 million

Effective tax rate

7% to 8%

Earnings per share

Low end of $5.00 to $5.20

Diluted shares outstanding

230 million

(1) Financial guidance is based on forecasted results at current spot rates net of hedging activities.

Conference Call/Webcast Information:

Alexion will host a conference call/audio webcast to discuss matters mentioned in this release. The call is scheduled for today, April 28, at 10:00 a.m., Eastern Time. To participate in this call, dial 888-576-4397 (USA) or 719-325-2301 (International), passcode 4785731 shortly before 10:00 a.m., Eastern Time. A

replay of the call will be available for a limited period following the call, beginning at 1:00 p.m., Eastern Time. The replay number is 888-203-1112 (USA) or 719-457-0820 (International), passcode 4785731. The audio webcast can be accessed on the Investor page of Alexion’s website at:

http://ir.alexionpharm.com

About Alexion

Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with devastating and rare disorders. Alexion developed and commercializes Soliris

(eculizumab), the first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS), two life-threatening ultra-rare disorders. As the global leader in complement inhibition, Alexion is strengthening and broadening its portfolio of complement inhibitors, including evaluating potential indications for eculizumab in additional severe and ultra-rare disorders. Alexion’s metabolic franchise includes two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare disorders, Strensiq

(asfotase alfa) to treat patients with hypophosphatasia (HPP) and Kanuma

(sebelipase alfa) to treat patients with lysosomal acid lipase deficiency (LAL-D). In addition, Alexion is advancing the most robust rare disease pipeline in the biotech industry with highly innovative product candidates in multiple therapeutic areas. This press release and further information about Alexion can be found at: www.alexion.com.

[ALXN-E]

This news release contains forward-looking statements, including statements related to guidance regarding anticipated financial results for 2016, assessment of the Company's financial position and commercialization efforts, medical benefits and commercial potential for Soliris, Strensiq and Kanuma, medical and commercial potential of each of Alexion's product candidates, launch expectations for Strensiq and Kanuma, and plans for clinical programs for our product candidates. Forward-looking statements are subject to factors that may cause Alexion's results and plans to differ from those expected, including for example, decisions of regulatory authorities regarding marketing approval or material limitations on the marketing of our products, delays, interruptions or failures in the manufacture and supply of our products and our product candidates, progress in establishing and developing commercial infrastructure, failure to satisfactorily address matters raised by the FDA and other regulatory agencies, the possibility that results of clinical trials are not predictive of safety and efficacy results of our products in broader patient populations in the disease studied or other diseases, the risk that strategic transactions will not result in short-term or long-term benefits, the possibility that current results of commercialization are not predictive of future rates of adoption of Soliris in PNH, aHUS or other diseases, the possibility that clinical trials of our product candidates could be delayed or that additional research and testing is required by regulatory agencies, the adequacy of our pharmacovigilance and drug safety reporting processes, 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, risks regarding government investigations, including the SEC and DOJ investigations, the risk that estimates regarding the number of patients with PNH, aHUS, HPP and LAL-D are inaccurate, the risks of shifting foreign exchange rates, and a variety of other risks set forth from time to time in Alexion's filings with the U.S. Securities and Exchange Commission, including but not limited to the risks discussed in Alexion's Annual Report on Form 10-K for the period ended December 31, 2015 and in our other filings with the U.S. Securities and Exchange Commission. Alexion does not intend 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 news 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: share-based compensation expense, fair value adjustment of inventory acquired, amortization of purchased intangible assets, changes in fair value of contingent consideration, acquisition-related costs, restructuring expenses, upfront and milestone payments related to license and collaboration agreements, and non-cash taxes. 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 Reconciliation of GAAP to non-GAAP Financial Results for explanations of the amounts adjusted to arrive at non-GAAP net income and non-GAAP earnings per share amounts for the three month periods ended March 31, 2016 and 2015.

(Tables Follow)

ALEXION PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(in thousands, except per share amounts)

(unaudited)

Three months ended

700,425

600,333

Other revenue

701,038

58,986

69,399

Operating expenses:

176,290

221,080

232,561

187,116

Amortization of purchased intangible assets

80,094

Change in fair value of contingent consideration

(14,800

11,979

Acquisition-related costs

Restructuring expenses

Total operating expenses

476,206

427,227

Operating income

165,846

103,707

Other income and expense:

Investment income

(23,890

Foreign currency gain

Income before income taxes

143,598

106,945

Income tax provision

51,432

15,622

Net income

92,166

91,323

Earnings per common share

Shares used in computing earnings per common share

225,060

199,361

226,873

202,034

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL RESULTS

Net income reconciliation:

Share-based compensation expense

56,889

42,797

Fair value adjustment of inventory acquired (1)

Amortization of purchased intangible assets (2)

Change in fair value of contingent consideration (3)

Acquisition-related costs (4)

Restructuring expenses (5)

Upfront and milestone payments related to license and collaboration agreements

112,500

Non-cash taxes (6)

33,784

(3,672

Non-GAAP net income

253,775

261,979

GAAP earnings per share - diluted

Non-GAAP earnings per share - diluted

Shares used in computing diluted earnings per share (GAAP)

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

229,174

204,383

Cost of sales reconciliation:

GAAP cost of sales

(3,403

(1,409

Non-GAAP cost of sales

55,052

67,990

Research and development expense reconciliation:

GAAP research and development

(15,185

(11,084

(3,050

(112,500

Non-GAAP research and development expense

158,055

97,496

Selling, general and administrative expense reconciliation:

GAAP selling, general and administrative expense

(38,301

(30,304

Non-GAAP selling, general and administrative expense

194,260

156,812

Income tax provision reconciliation:

GAAP income tax provision

(33,784

Non-GAAP income tax provision

17,648

19,294

Inventory fair value adjustment associated with the amortization of Kanuma inventory step-up related to the purchase accounting for Synageva.

In the third quarter of 2015, the Company initiated amortization of its purchased intangible assets due to the regulatory approvals for Strensiq and Kanuma.

In the first quarter of 2016, the Company realized a change in fair value of contingent consideration due to decreases in the likelihood of payments for contingent consideration associated with our prior business combinations.

The following table summarizes acquisition-related costs:

Acquisition-related costs:

Transaction costs

Integration costs

First quarter 2016 restructuring expenses of $0.7 million includes $1.6 million related to the European headquarters relocation, offset by a $0.9 million benefit resulting from the acquisition of Synageva due to changes in estimates associated with employee costs.

Non-cash taxes represents the adjustment from GAAP tax expense to the taxes payable in cash on current period operations.

REVENUES

(in thousands)

664,656

33,242

Total net product sales

Royalty revenue

Total other revenue

CONDENSED CONSOLIDATED BALANCE SHEETS

Cash and cash equivalents

710,198

1,010,111

Marketable securities

317,354

374,904

Trade accounts receivable, net

586,249

532,832

Inventories

293,962

289,874

Prepaid expenses and other current assets

219,746

208,993

Property, plant and equipment, net

749,295

697,025

Intangible assets, net

4,627,817

4,707,914

Goodwill

5,049,321

5,047,885

Other assets

248,503

228,343

Total assets

12,802,445

13,097,881

Accounts payable and accrued expenses

401,974

460,708

Deferred revenue

78,416

20,504

Current portion of long-term debt

35,358

166,365

Other current liabilities

87,865

62,038

Long-term debt, less current portion

3,212,772

3,254,536

Contingent consideration

107,085

121,424

Facility lease obligation

172,970

151,307

Deferred tax liabilities

535,910

528,990

Other liabilities

107,818

73,393

Total liabilities

4,740,168

4,839,265

Total stockholders' equity

8,062,277

8,258,616

Total liabilities and stockholders' equity

Alexion Contacts:

Stephanie Fagan, 203-271-8223

Senior Vice President, Corporate Communications

Investors

Elena Ridloff, CFA, 203-699-7722

Vice President, Investor Relations

The above information was disclosed in a filing to the SEC. To see the filing, click here.

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