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Vanda Pharmaceuticals Reports First Quarter 2015 Financial Results

- HETLIOZ® net product sales increased by 24% over the prior quarter to $7.5 million, patients on active treatment grew by 22% over the prior quarter

- Fanapt® net product sales reach $14.7 million in the first quarter since regaining rights

- Vanda reaffirms full year net product sales guidance of $95 million to $110 million

Conference call scheduled for 4:30 p.m. ET today


News provided by

Vanda Pharmaceuticals Inc.

May 06, 2015, 04:01 ET

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WASHINGTON, May 6, 2015 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ: VNDA), today announced financial and operational results for the first quarter ended March 31, 2015.

"The first quarter of 2015 was a record quarter for product sales driven by HETLIOZ and Fanapt.  As we are just at the beginning of accessing the 80,000 Non-24 patients in the U.S., the growth potential for HETLIOZ remains ahead.  Similarly, the expanded patent exclusivity for Fanapt underscores the growth potential of this product through the coming decade and beyond.  We are looking to further drive revenue growth through both geographic expansion and the disciplined life cycle management of our commercial products." said Mihael H. Polymeropoulos M.D., Vanda's President and CEO.

Financial Highlights

  • First quarter of 2015 Total net product sales increased by 268% over the prior quarter to $22.2 million, driven by the growth in HETLIOZ® sales and the acquisition of the Fanapt® product rights.
  • Net loss for the first quarter of 2015 was $10.2 million, or $0.24 per share, compared with a net loss of $26.5 million, or $0.79 per share, for the same period in 2014.
  • Cash, cash equivalents and marketable securities increased by $4.5 million to $134.3 million as of March 31, 2015, as compared to $129.8 million as of December 31, 2014.

HETLIOZ® (tasimelteon)

  • HETLIOZ® net product sales grew to $7.5 million the first quarter of 2015, a 24% increase compared to $6.0 million in the fourth quarter of 2014.  As of March 31, 2015, patients on active HETLIOZ® treatment grew by 22%, compared to the fourth quarter of 2014.
  • In April 2015, the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use adopted a positive opinion for HETLIOZ® for the treatment of Non-24-Hour Sleep-Wake Disorder (Non-24). A final decision is expected by the end of the second quarter of 2015.
  • HETLIOZ® life cycle management activities continue to progress with a HETLIOZ® interventional study for the treatment of Smith-Magenis Syndrome and a HETLIOZ® pediatric pharmacokinetic study each expected to begin by the end of 2015.

Fanapt® (iloperidone)

  • Fanapt® U.S. net product sales reached $14.7 million in the first quarter since regaining rights.  Vanda's field sales force began promotion of Fanapt® in the U.S. in April 2015.
  • During 2015, three additional Fanapt® patents were listed in the U.S. Food and Drug Administration's (FDA) Orange Book.  Fanapt® patents 8,586,610, 8,652,776 and 8,999,638 expire in November 2027, August 2030 and October 2030, respectively.

Tradipitant (VLY-686)

  • Vanda expects to initiate a Phase II study in chronic pruritus in patients with atopic dermatitis in the fourth quarter of 2015, seeking to confirm the exploratory efficacy findings reported in the Phase II proof of concept study (2101).

Non-GAAP Financial Results

Vanda Non-GAAP Total revenues for the first quarter of 2015 were $22.2 million, compared to Non-GAAP Total revenues of $1.7 million for the first quarter of 2014. 

For the first quarter of 2015, Non-GAAP net loss was $4.1 million, or $0.10 per share, compared with a Non-GAAP net loss of $32.0 million, or $0.95 per share, for the same period in 2014.

Vanda provides Non-GAAP financial information, which it believes can enhance an overall understanding of its financial performance when considered together with GAAP figures.   Refer to the sections of this press entitled "Non-GAAP Financial Information" and "Reconciliation of GAAP to Non-GAAP Financial Information".

2015 Financial Guidance

Vanda affirms its prior 2015 financial guidance and expects to achieve the following financial objectives in 2015:

  • Combined net product sales from both HETLIOZ® and Fanapt® of between $95 million and $110 million.
  • HETLIOZ® net product sales of between $40 million to $45 million and Fanapt® net product sales of between $55 million to $65 million. 
  • Non-GAAP Operating expenses, excluding cost of sales, of between $105 million and $120 million.   

Non-GAAP Operating expenses also excludes:

  • Intangible asset amortization expense of $13.0 million.
  • Stock-based compensation of between $8.5 million and $10.5 million.

Full HETLIOZ® Prescribing Information can be found at: www.hetlioz.com.

Full Fanapt® Prescribing Information, including Boxed Warnings and Important Safety Information can be found at: www.fanapt.com.

Conference Call

Vanda has scheduled a conference call for today, Wednesday, May 6, 2015, at 4:30 PM ET.  During the call, Vanda's management will discuss the first quarter 2015 financial results and other corporate activities.  Investors can call 1-800-708-4540 (domestic) or 1-847-619-6397 (international) and use passcode 39503340. A replay of the call will be available beginning Wednesday, May 6, 2015 at 7:00 PM ET and will be accessible until Tuesday, May 12, 2015, at 11:59 PM ET.  The replay call-in number is 1-888-843-7419 for domestic callers and 1-630-652-3042 for international callers. The passcode number is 39503340.

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.

Non-GAAP Financial Information

Vanda believes that the Non-GAAP financial information provided in this release can assist investors in understanding and assessing the ongoing economics of Vanda's business and reflect how it manages the business internally and sets operational goals. Vanda's "Non-GAAP Total revenues" excludes the Fanapt® licensing revenue. Vanda's "Non-GAAP Selling, general and administrative  expenses" and "Non-GAAP Research and development  expenses" exclude stock-based compensation.  Vanda's "Non-GAAP Net income (loss)" and "Non-GAAP net income (loss) per share" excludes the Fanapt® licensing revenue, stock-based compensation, intangible asset amortization and gain on arbitration settlement.

Vanda believes that excluding the impact of these items better reflects the recurring economic characteristics of its business, as well as Vanda's use of financial resources and its long-term performance. 

This press release includes a projection of 2015 Non-GAAP Operating expenses, excluding cost of goods sold, a forward-looking Non-GAAP financial measure under the heading "2015 Financial Guidance".  This Non-GAAP financial measure is determined by excluding cost of goods sold, stock-based compensation and intangible asset amortization.  Vanda is unable to reconcile this Non-GAAP guidance to GAAP because it is difficult to predict the future impact of these adjustments.

These Non-GAAP financial measures, as presented, may not be comparable to similarly titled measures reported by other companies since not all companies may calculate these measures in an identical manner and, therefore, they are not necessarily an accurate measure of comparison between companies. 

The presentation of these Non-GAAP financial measures is not intended to be considered in isolation or as a substitute for guidance prepared in accordance with GAAP. The principal limitation of these Non-GAAP financial measures is that they exclude significant elements that are required by GAAP to be recorded in Vanda's financial statements. In addition, they are subject to inherent limitations as they reflect the exercise of judgments by management in determining these Non-GAAP financial measures. In order to compensate for these limitations, Vanda presents its Non-GAAP financial guidance in connection with its GAAP guidance. Investors are encouraged to review the reconciliation of the Non-GAAP financial measures to their most directly comparable GAAP financial measure.

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.

Forward-Looking Statements

Various statements in this release, including, but not limited to, the guidance provided in the heading of this press release and under "2015 Financial Guidance" above, 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 Vanda's forward-looking statements include, among others: Vanda's ability to successfully commercialize HETLIOZ® for the treatment of Non-24 in the U.S.; uncertainty as to the market awareness of Non-24 and the market acceptance of HETLIOZ®; Vanda's ability to generate U.S. sales of Fanapt® for the treatment of schizophrenia; the timing and costs of Vanda's establishment of a sales and marketing, supply chain, distribution, pharmacovigilance, compliance and safety infrastructure to promote Fanapt® in the U.S.; Vanda's dependence on third-party manufacturers to manufacture HETLIOZ® and Fanapt® in sufficient quantities and quality; Vanda's limited sales and marketing infrastructure; the regulatory status of HETLIOZ® and Fanapt® in Europe; Vanda's ability to successfully commercialize HETLIOZ® and Fanapt® outside the U.S.; Vanda's ability to obtain the capital necessary to fund its research and development or commercial activities; the timing and costs of complying with the remaining post-marketing commitments and post-marketing requirements established in connection with the FDA's approval of Fanapt®; delays in the completion of Vanda's or its partners' clinical trials; a failure of Vanda's products to be demonstrably safe and effective; Vanda's expectations regarding trends with respect to its revenues, costs, expenses and liabilities; Vanda's failure to identify or obtain rights to new products; a loss of any of Vanda's key scientists or management personnel; limitations on Vanda's ability to utilize some or all of its prior net operating losses and orphan drug and research and development credits; the costs and effects of litigation; losses incurred from product liability claims made against Vanda; use of existing cash, cash equivalents and marketable securities 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, 2014 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, current reports on Form 8-K and other filings with the SEC, 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 






Three Months Ended




March 31


March 31


($ in thousands, except per share amounts)


2015


2014










Revenues:








   HETLIOZ®product sales, net


$

7,460


$

-


   Fanapt®product sales, net 



14,690



-


   Fanapt®royalty revenue



-



1,691


   Fanapt®licensing revenue



-



7,452


      Total revenues



22,150



9,143










Operating expenses:








   Cost of goods sold



5,015



-


   Research and development



4,478



7,263


   Selling, general and administrative



18,806



27,893


   Intangible asset amortization(1)



4,144



565


      Total operating expenses



32,443



35,721










Income (loss) from operations



(10,293)



(26,578)


   Other income



72



45


Net income (loss)


$

(10,221)


$

(26,533)










Net income (loss) per share:








 

   Basic and diluted


$

(0.24)


$

(0.79)










Weighted average shares outstanding:








 

   Basic and diluted



41,744,948



33,678,706











(1)    A new intangible asset was recorded in the first quarter of 2015 related to the $25.0 million milestone obligation to Bristol-Myers Squibb due upon cumulative global net product sales of HETLIOZ® reaching $250.0 million. The HETLIOZ® intangible asset and related amortization is recognized when reaching that sales amount is deemed probable while the actual payment will occur once the sales are realized. 

VANDA PHARMACEUTICALS INC.


 CONDENSED CONSOLIDATED BALANCE SHEETS 













($ in thousands)


March 31,
 2015


December 31,
 2014






ASSETS








   Current assets:








      Cash and cash equivalents


$

32,809


$

60,901


      Marketable securities



101,520



68,921


      Accounts receivable, net



20,120



3,654


      Inventory



5,215



5,170


      Prepaid expenses and other current assets



2,503



3,084


         Total current assets



162,167



141,730










   Property and equipment, net



3,080



2,437


   Intangible assets, net



47,580



26,724


   Restricted cash and other



813



813


         Total assets


$

213,640


$

171,704


















LIABILITIES AND STOCKHOLDERS' EQUITY








   Current liabilities:








      Accounts payable


$

1,490


$

835


      Accrued and other current liabilities



30,299



6,951


         Total current liabilities



31,789



7,786










      Milestone obligation under license agreement



25,000



-


      Other non-current liabilities



4,378



3,101


         Total liabilities



61,167



10,887










   Stockholders' equity:








      Common stock



42



41


      Additional paid-in capital



450,609



448,744


      Accumulated other comprehensive income



27



16


      Accumulated deficit



(298,205)



(287,984)


         Total stockholders' equity



152,473



160,817


         Total liabilities and stockholders' equity


$

213,640


$

171,704


Reconciliation of GAAP to Non-GAAP Financial Information

 

VANDA PHARMACEUTICALS INC.


Reconciliation of GAAP to Non-GAAP Financial Information










Three Months Ended




March 31


March 31


($ in thousands, except per share amounts)


2015


2014










Net income (loss)


$

(10,221)


$

(26,533)


Adjustments:








   Fanapt®licensing revenue



-



(7,452)


   Stock-based compensation



1,945



1,393


   Intangible asset amortization(1)



4,144



565










Non-GAAP Net loss


$

(4,132)


$

(32,027)










Non-GAAP Net loss per share:








   Basic and diluted


$

(0.10)


$

(0.95)










Weighted average shares outstanding:








   Basic and diluted



41,744,948



33,678,706


















Total revenues


$

22,150


$

9,143


Adjustment:








   Fanapt®licensing revenue



-



(7,452)










Non-GAAP Total revenues


$

22,150


$

1,691


















Operating expenses


$

32,443


$

35,721


Adjustments:








   Cost of goods sold



(5,015)



-


   Stock-based compensation



(1,945)



(1,393)


   Intangible asset amortization(1)



(4,144)



(565)










Non-GAAP Operating expenses


$

21,339


$

33,763


excluding Cost of goods sold
























Research and development


$

4,478


$

7,263


Adjustment:








   Stock-based compensation



(624)



(480)










Non-GAAP Research and development


$

3,854


$

6,783


















Selling, general and administrative


$

18,806


$

27,893


Adjustment:








   Stock-based compensation



(1,321)



(913)











Non-GAAP Selling, general and administrative

$

17,485


$

26,980


COMPANY CONTACT: 
Jim Kelly
Senior Vice President & Chief Financial Officer
Vanda Pharmaceuticals Inc.
(202) 734-3428
[email protected]

SOURCE Vanda Pharmaceuticals Inc.

Related Links

http://www.vandapharma.com

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Vanda Pharmaceuticals announces the publication in PLOS One of an article titled "Melatonin agonist tasimelteon (HETLIOZ®) improves sleep in patients with primary insomnia: A multicenter, randomized, double-blind, placebo-controlled trial"

Vanda Pharmaceuticals announces the publication in PLOS One of an article titled "Melatonin agonist tasimelteon (HETLIOZ®) improves sleep in patients with primary insomnia: A multicenter, randomized, double-blind, placebo-controlled trial"

Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced the publication of an article titled "Melatonin agonist tasimelteon (HETLIOZ®)...

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