EXTON, Pa., Aug. 1, 2013 /PRNewswire/ -- VIROPHARMA INCORPORATED (Nasdaq: VPHM) today announced financial results for the second quarter of 2013. Net sales were $104 million for the second quarter ended June 30, 2013 as compared to $95 million in the comparative period of 2012. The increase in net sales quarter over quarter was driven by the commercial product growth of both Cinryze in the U.S. and higher European product sales. During the second quarter of 2013 U.S. Cinryze net sales grew by 22 percent over the second quarter of 2012 to $91 million. The quarterly U.S. Cinryze sales reflect $96 million of patient demand offset by approximately $5 million of wholesaler channel inventory drawdown. The patient demand represents an increase of approximately $5 million from the $91 million of patient demand reported in the first quarter of 2013.
"The second quarter of 2013 represented a period of strong commercial execution coupled with significant progress in our clinical development pipeline, despite this morning's news related to our combination efforts with Halozyme," stated Vincent Milano, ViroPharma's chief executive officer. "In addition to the positive maribavir interim data update we shared last month and the continued advancement of enrollment in the two studies, we also are approaching critical data milestones heading into the second half of 2013, including our antibody mediated rejection study with Cinryze in kidney transplant patients and analysis of the completed subjects from the Cinryze subcutaneous administration study which we updated this morning."
Continued Milano, "On the commercial front, the continued growth trajectory of U.S. Cinryze remains strong, with early signs of positive impact from our sales force optimization and continued progress with our European operations. Overall, we believe ViroPharma is well positioned to continue generating growth and strong momentum."
Our GAAP net income was $0.6 million in the second quarter of 2013 compared to a GAAP net loss of $6 million in the second quarter of 2012. GAAP diluted earnings per share was $0.01 for the second quarter of 2013 compared to GAAP diluted loss per share of $0.08 for the same period in 2012.
Non-GAAP adjusted net income for the three months ended June 30, 2013 was $11 million, compared to $5 million for the same period in 2012. Non-GAAP adjusted diluted net earnings per share was $0.15 for the second quarter of 2013 compared to $0.07 for the same period in 2012. A reconciliation between GAAP and non-GAAP adjusted measures is provided in the Selected Financial Information – Non-GAAP Financial Measures Reconciliation table included with this release.
Operating HighlightsCinryze global net sales during the second quarter of 2013 were $95 million, a 23 percent increase over the same period in 2012 driven by demand growth and net realized price growth, partially offset by a reduction in channel inventories. Vancocin net sales during the second quarter of 2013 were $4 million compared to $16 million for the same period in 2012. During the second quarter of 2013, we generated net sales of approximately $8 million from our European operations compared to $4 million during the second quarter of 2012.
Cost of sales for the three months ended June 30, 2013 was flat as compared to the three months ended June 30, 2012.
Research and development costs incurred during the second quarter of 2013 were relatively flat compared to the same period in 2012 as advancements in our clinical development programs, including the subcutaneous Cinryze and maribavir development programs were offset by lower spending in our VP20621 program due to the completion of our Phase 2 trial. The increase in selling, general and administrative expenses for the second quarter of 2013 compared to the same period in 2012 was driven by the growth of our global organization and our commercialization efforts.
We recognized a tax benefit of $0.8 million in the second quarter ended June 30, 2013 compared to a tax benefit of $2.9 million in the second quarter ended June 30, 2012.
Working Capital HighlightsAt June 30, 2013, our working capital was $379 million, which included cash, cash equivalents and short term investments of $259 million. During the first half of 2013 we generated $9 million net cash from operations. Financial Highlights ($ in millions, except per share data)Q2 2013Q2 2012PercentChangeTotal net product sales
+10%Cinryze U.S. net product sales
+22%EU net product sales
+118%Vancocin net product sales
-75%GAAP net income (loss)
(5.8)Non-GAAP adjusted net income
5.1GAAP diluted net income (loss) per
(0.08)Non-GAAP adjusted diluted EPS
0.07Non-GAAP DisclosuresThe Company is reporting both GAAP net income (loss) and non-GAAP adjusted results for the three and six months ended June 30, 2013 and 2012. Non-GAAP adjusted net income is GAAP net income (loss) excluding (1) non-cash interest expense, (2) amortization related to intangible assets acquired, (3) share-based compensation expenses, (4) changes in contingent consideration, (5) option amortization and (6) certain non-recurring events, including impairment losses. Non-GAAP adjusted diluted net income per share reflects the Non-GAAP adjusted net income, after the incremental effect of applying the "if converted" method of accounting to the senior convertible notes, and the diluted shares used in determining our GAAP diluted net income (loss) per share. A reconciliation between GAAP and non-GAAP adjusted measures is provided in the Selected Financial Information – Non-GAAP Financial Measures Reconciliation table included with this release. The Company believes that its presentation of historical non-GAAP financial measures provides useful supplementary information to and facilitates additional analysis by investors. These historical non-GAAP financial measures are in addition to, not a substitute for, or superior to, measures of financial performance prepared in accordance with U.S. Generally Accepted Accounting Principles.
Research and Development ProgramsViroPharma is investing in research and development programs to ensure growth for the future. The current pipeline includes programs in various stages of clinical and pre-clinical development focused on rare diseases and serious unmet medical needs.
2013 Guidance ViroPharma is providing guidance for the year 2013 as a convenience to investors. The following guidance provided by ViroPharma are projections, based upon numerous assumptions, all of which are subject to certain risks and uncertainties. For a discussion of the risks and uncertainties associated with these forward looking statements, please see the Disclosure Notice below.
For the year 2013, ViroPharma is reiterating the following:
Conference Call and WebcastViroPharma is hosting a live teleconference and webcast with senior management to discuss the financial announcement, guidance, and all other operational results of the first quarter and discuss developments in the subcutaneous Cinryze clinical development program on August 1, 2013 at 9:00 a.m. Eastern. To participate in the conference call, please dial (800) 874-4559 (domestic) and (302) 607-2019 (international). After placing the call, please tell the operator you wish to join the ViroPharma investor conference call.
Alternatively, the live webcast of the conference call can be accessed via ViroPharma's website at http://www.viropharma.com. Windows Media or Real Player will be needed to access the webcast. An audio archive will be available at the same address until August 15, 2013.
About ViroPharma IncorporatedViroPharma Incorporated is an international biopharmaceutical company committed to developing and commercializing novel solutions for physician specialists to address unmet medical needs of patients living with diseases that have few if any clinical therapeutic options. ViroPharma is developing a portfolio of therapeutics for rare and Orphan diseases including C1 esterase inhibitor deficiency, cytomegalovirus (CMV), Friedreich's Ataxia, eosinophilic esophagitis (EoE) and adrenal insufficiency. Our goal is to provide rewarding careers to employees, to create new standards of care in the way serious diseases are treated, and to build international partnerships with the patients, advocates, and health care professionals we serve. ViroPharma's commercial products address diseases including hereditary angioedema (HAE), seizures in children and adolescents, adrenal insufficiency and C. difficile-associated diarrhea (CDAD). For full U.S. prescribing information on our products, please download the package inserts at http://www.viropharma.com/Products.aspx; the prescribing information for other countries can be found at www.viropharma.com.
ViroPharma routinely posts information, including press releases, which may be important to investors in the investor relations and media sections of our company's web site, www.viropharma.com. The company encourages investors to consult these sections for more information on ViroPharma and our business.
Disclosure Notice Certain statements in this press release contain forward-looking statements that involve a number of risks and uncertainties. Forward-looking statements provide our current expectations or forecasts of future events. Forward looking statements in this press release include our financial guidance for 2013, forecasted future tax rates, our ability to continue to successfully commercialize our products in the United States and Europe, the timing and results of anticipated events in our clinical development programs, and our ability to identify and execute upon business development opportunities.
Our actual results may vary depending on a variety of factors, including:
There can be no assurance that we will conduct additional studies or that we will be successful in gaining regulatory approval of Cinryze for additional indications, routes of administration or in additional territories. Biologics such as Cinryze require processing steps that are more difficult than those required for most chemical pharmaceuticals, and as a result, Sanquin, our manufacturer of Cinryze has received observations on Form 483 which require us to continue to meet commitments made to the FDA related to various manufacturing issues. In the event Sanquin fails to meet these commitments, the FDA may take actions that limit our ability to manufacture Cinryze. In the event Sanquin is not able to manufacture the anticipated volume of product at the industrial scale as a result of either FDA requirements, batch failures, variability in batch yields, required maintenance or other causes, we may not be able to satisfy patient demand or build safety stock. Our inability to obtain adequate product supplies to satisfy our patient demand may create opportunities for our competitors and we will suffer a loss of potential future revenues. Clinical data presented regarding studies with maribavir are interim data as the studies are ongoing. There can be no assurance that interim data will be representative of the final clinical data from the studies or that the results of the studies will support future clinical studies of maribavir. These factors, and other factors, including, but not limited to those described in ViroPharma's Annual report on Form 10-K for the year ended December 31, 2012 and Quarterly report on form 10-Q for the period ended March 31, 2013 could cause future results to differ materially from the expectations expressed in this press release. The forward-looking statements contained in this press release may become outdated over time. ViroPharma does not assume any responsibility for updating any forward-looking statements. VIROPHARMA INCORPORATEDSelected Financial Information(unaudited)(unaudited)Consolidated Statements of Operations:Three months endedSix months ended(in thousands, except per share data)
June 30,June 30,2013201220132012Revenue:Net product sales
210,860$ 230,439Costs and Expenses:Cost of sales (excluding amortization of product
28,15828,08958,01760,167Research and development
17,16516,62134,36132,020Selling, general and administrative
--104,245-Other operating expenses
6848582,7672,054Total costs and expenses
99,92595,238304,930190,901Operating income (loss)
3,786(599)(94,070)39,538Other Income (Expense):Interest income
(3,681)(3,518)(7,290)(6,965)Other expense, net
(493)(4,783)(4,648)(3,548)Income (loss) before income tax expense (benefit)
(235)(8,758)(105,689)29,303Income tax expense (benefit)
(833)(2,928)(42,291)15,142Net income (loss)
4,161Basic net income (loss) per share
.20Diluted net income (loss) per share
.19Shares used in computing net income (loss) per
68,91769,39065,28173,028 Selected Financial InformationReconciliation of GAAP Net Income (Loss) to Adjusted Non-GAAP Net IncomeAn itemized reconciliation between net income (loss) and adjusted net
income on a non-GAAP basis is as follows:(in thousands, except per share data)
Three months endedSix months endedJune 30,June 30,2013201220132012(unaudited)(unaudited)GAAP net income (loss)
598$ (5,830)$ (63,398)$
4,161Adjustments:Non-cash interest expense
--104,245-Tax effect of the above
(6,692)(6,971)(54,683)(14,053)Non-GAAP adjusted net income
36,141Computation of Non-GAAP Adjusted Diluted Net Income per ShareNon-GAAP adjusted net income
36,141Add interest expense on senior
convertible notes, net of income tax
6256341,2511,269Non-GAAP adjusted diluted net income
37,410Shares used in computing GAAP diluted
net income (loss) per share
68,91769,39065,28173,028Shares used in computing Non-GAAP
adjusted diluted net income per share
79,78082,81279,43883,892GAAP diluted net income (loss) per share
.19Non-GAAP adjusted diluted net income
.45Use of Non-GAAP Financial Measures Our "non-GAAP adjusted net income" excludes the following items from GAAP net income (loss):
1. Non-cash interest expense: Non-GAAP adjusted net income excludes non-cash interest expense on our convertible notes. We believe that excluding the non-cash portion of our interest expense allows management and investors an alternative view of our financial results "as if" our net income reflected only the cash portion of our interest expense.
2. Purchase accounting and product acquisition related adjustments: Non-GAAP adjusted net income excludes certain items related to our acquisitions. The excluded items may include among other adjustments; charges related to amortization of intangible assets arising from acquisitions and changes in the fair value of future contingent consideration or significant transaction costs.
3. Share-based compensation expense: Non-GAAP adjusted net income excludes the impact of our non-cash share-based compensation expense. We believe that excluding the impact of expensing share-based compensation better reflects the recurring economic characteristics of our business.
Non-GAAP net income may exclude unusual or non-recurring items that are evaluated on an individual basis. Our evaluation of whether to exclude an item for purposes of determining our non-GAAP financial measures considers both the quantitative and qualitative aspects of the item, including, among other things (i) its size and nature, (ii) whether or not it relates to our ongoing business operations, and (iii) whether or not we expect it to occur as part of our normal business on a regular basis. For purposes of determining non-GAAP net income, items such as asset impairment or upfront fees or milestone payments under license agreements, may be excluded, among others, which will be evaluated on an individual basis.VIROPHARMA INCORPORATEDSelected Financial InformationSelected Consolidated Balance Sheet DataJune 30,December 31,(in thousands) 20132012(unaudited)AssetsCurrent assets:Cash and cash equivalents$
75,518Short-term investments67,33571,338Inventory87,83464,384Total current assets468,527453,418Intangible assets, net494,392617,539Goodwill96,26496,759Total assets1,113,1061,219,952Liabilities and Stockholders' EquityTotal current liabilities$
4,028Deferred tax liabilities120,050167,484Long-term debt166,205161,793Total liabilities403,328462,913Total stockholders' equity709,778757,039Total liabilities and stockholders' equity1,113,1061,219,952 Six Months Ended June 30,June 30,Statement of Cash Flows:20132012(in thousands)(unaudited)Net cash provided by operating activities$
74,878Net cash provided by investing activities2,28112,110Net cash provided by (used in) financing activities4,666(60,744)
|SOURCE ViroPharma Incorporated|
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