WASHINGTON, July 31, 2013 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ: VNDA), a biopharmaceutical company focused on the development and commercialization of products for the treatment of central nervous system disorders, today announced financial and operational results for the second quarter ended June 30, 2013.
SECOND QUARTER 2013 REPORTED RESULTSTotal revenues for the second quarter of 2013 were $8.3 million, compared to $8.4 million for the same period in 2012. Second quarter 2013 revenues included $1.6 million in Fanapt® royalties received from Novartis as compared to royalties of $1.7 million for the second quarter of 2012.
Total operating expenses for the second quarter of 2013 were $11.4 million, compared to $16.5 million for the second quarter of 2012. The primary driver of the lower expenses in the second quarter of 2013 was the completion of the tasimelteon Non-24 and Major Depressive Disorder efficacy studies.
Vanda recorded a net loss of $3.1 million for the second quarter of 2013, compared to a net loss of $8.0 million for the same period in 2012. Diluted net loss per share for the second quarter of 2013 was $0.11, compared to a diluted net loss per share of $0.28 for the second quarter of 2012.
Cash, cash equivalents and marketable securities (Cash) decreased by $7.3 million in the second quarter of 2013, compared to decreases of $12.5 million in the second quarter of 2012 and $9.5 million in the first quarter of 2013. Vanda's Cash as of June 30, 2013 totaled $103.6 million.
Year to Date June 30, 2013 Key Financial Figures1
Six Months EndedJune 30June 30($ in thousands, except per share amounts)20132012 Change ($)Change (%)Total revenues
(132)(1%)Research & development expenses
13,94224,670(10,728)(43%)General & administrative expenses
9,0327,5101,52220%Non-cash stock-based compensation2
(7,252)(15,969)8,71755%Diluted net loss per share
Second Quarter 2013 Key Financial Figures1
Three Months EndedJune 30March 31($ in thousands, except per share amounts)20132013 Change ($)Change (%)Total revenues
2513%Research & development expenses
5,9827,960(1,978)(25%)General & administrative expenses
5,0743,9581,11628%Non-cash stock-based compensation2
(3,079)(4,173)1,09426%Diluted net loss per share
Select Cash Flow Data1 Six Months EndedJune 30June 30($ in thousands)20132012Net cash provided by (used in)Operating activities
Select Balance Sheet Data1 June 30March 31June 30($ in thousands)201320132012Total cash and marketable securities
44,701(1) Unaudited (2) Non-cash stock-based compensation is allocated to both Research & development and General & administrative expenses
OPERATIONAL HIGHLIGHTSOn July 29, 2013, Vanda announced that the FDA accepted the filing and granted a priority review classification to Vanda's NDA for tasimelteon, a circadian regulator for the treatment of Non-24 in the totally blind. Currently, there is no approved treatment for Non-24 and tasimelteon has the potential to address this unmet medical need. The FDA determined the action target date under Prescription Drug User Fee Act (PDUFA-V), to be January 31, 2014. The FDA has also tentatively scheduled an advisory committee meeting to discuss the tasimelteon application on November 14, 2013.
Vanda continues to expand its activities in support of Non-24 disease awareness and education with professional, advocacy and patient groups. In June 2013, Vanda presented data from the SET and RESET studies at the 27th Annual Meeting of the Associated Professional Sleep Societies, SLEEP 2013, and the 95th Annual Endocrine Society Meeting, ENDO 2013.Vanda recorded second quarter 2013 revenue of $8.3 million including $6.7 million in licensing revenue related to the amortization of the upfront payment received from Novartis for U.S. and Canadian commercial rights to Fanapt® and Fanapt® royalties of $1.6 million. Fanapt® prescriptions, as reported by IMS, were approximately 41,400 for the second quarter of 2013. This represents a 11% increase over second quarter 2012 prescriptions and a 7% increase versus first quarter 2013 prescriptions.AFFIRMS 2013 FINANCIAL GUIDANCEConsistent with prior guidance, 2013 expenses are expected to reflect lower research and development spending as compared to 2012 and an increase in commercial spending.
CONFERENCE CALLVanda has scheduled a conference call for today, Wednesday, July 31, 2013, at 10:00 AM ET. During the call, Vanda's management will discuss the second quarter 2013 financial results and other corporate activities. Investors can call 1-888-895-5479 (domestic) and 1-847-619-6250 (international) and use passcode 35347357. A replay of the call will be available beginning Wednesday, July 31, 2013 at 12:00 PM ET and will be accessible until Wednesday, August 7, 2013, at 5:00 PM ET. The replay call-in number is 1-888-843-7419 for domestic callers and 1-630-652-3042 for international callers. The access number is 35347357.
The conference call will be broadcast simultaneously on Vanda's website, www.vandapharma.com. Investors should click on the Investor Relations tab and are advised to go to the website at least 15 minutes early to register, download, and install any necessary software or presentations. The call will also be archived on Vanda's website for a period of 30 days.
ABOUT VANDA PHARMACEUTICALS INC.:Vanda Pharmaceuticals Inc. is a biopharmaceutical company focused on the development and commercialization of products for the treatment of central nervous system disorders. For more on Vanda, please visit www.vandapharma.com.
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
Various statements in this release are "forward-looking statements" under the securities laws. Words such as, but not limited to, "believe," "expect," "anticipate," "estimate," "intend," "plan," "project," "target," "goal," "likely," "will," "would," and "could," or the negative of these terms and similar expressions or words, identify forward-looking statements. Forward-looking statements are based upon current expectations that involve risks, changes in circumstances, assumptions and uncertainties. Important factors that could cause actual results to differ materially from those reflected in the company's forward-looking statements include, among others: Vanda's failure to obtain, or any delay in obtaining, regulatory approval for tasimelteon for the treatment of Non-24-Hour Disorder or to comply with ongoing regulatory requirements; the costs and effects of current or potential litigation and other factors that are described in the "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of Vanda's annual report on Form 10-K for the fiscal year ended December 31, 2012 which is on file with the SEC and available on the SEC's website at www.sec.gov. In addition to the risks described above and in Vanda's annual report on Form 10-K and quarterly reports on Form 10-Q, other unknown or unpredictable factors also could affect Vanda's results. There can be no assurance that the actual results or developments anticipated by Vanda will be realized or, even if substantially realized, that they will have the expected consequences to, or effects on, Vanda. Therefore, no assurance can be given that the outcomes stated in such forward-looking statements and estimates will be achieved.
All written and verbal forward-looking statements attributable to Vanda or any person acting on its behalf are expressly qualified in their entirety by the cautionary statements contained or referred to herein. Vanda cautions investors not to rely too heavily on the forward-looking statements Vanda makes or that are made on its behalf. The information in this release is provided only as of the date of this release, and Vanda undertakes no obligation, and specifically declines any obligation, to update or revise publicly any forward-looking statements, whether as a result of new information, future events or otherwise.
VANDA PHARMACEUTICALS INC.CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)Three Months EndedSix Months EndedJune 30June 30June 30June 30($ in thousands, except per share amounts)
13,284Royalty revenue1,6411,7003,1033,235Total revenues8,3198,37816,38716,519Operating expenses:Research and development5,98212,49013,94224,670General and administrative5,0743,6019,0327,510Intangible asset amortization372372741741Total operating expenses11,42816,46323,71532,921Loss from operations(3,109)(8,085)(7,328)(16,402)Other income307876433Loss before tax benefit(3,079)(8,007)(7,252)(15,969)Tax benefit----Net loss$
(15,969)Net loss per share:Basic$
(0.57)Shares used in calculations of net lossper share:Basic 28,377,25428,226,74328,361,34028,226,743Diluted28,377,25428,226,74328,361,34028,226,743
VANDA PHARMACEUTICALS INC. CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited)($ in thousands)June 30, 2013December 31, 2012ASSETSCurrent assets:Cash and cash equivalents$
88,772Marketable securities-31,631Accounts receivable1,6411,168Prepaid expenses and other current assets2,6513,967Restricted cash, current430430Total current assets108,355125,968Property and equipment, net2,2082,348Intangible asset, net5,7916,532Restricted cash, non-current600600Total assets$
135,448LIABILITIES AND STOCKHOLDERS' EQUITYCurrent liabilities:Accounts payable$
287Accrued liabilities3,7705,187Deferred rent, current209-Deferred revenues, current26,78926,789Total current liabilities31,93532,263Deferred rent, non-current3,0023,005Deferred revenues, non-current76,99190,275Total liabilities111,928125,543Stockholders' equity:Common stock2828Additional paid-in capital303,357300,974Accumulated other comprehensive income-10Accumulated deficit(298,359)(291,107)Total stockholders' equity5,0269,905Total liabilities and stockholders' equity$
Senior Vice President & Chief Financial Officer
Vanda Pharmaceuticals Inc.
|SOURCE Vanda Pharmaceuticals Inc.|
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