UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): July 31, 2013
VANDA PHARMACEUTICALS INC.
(Exact name of Registrant as specified in its charter)
Delaware
(State or other jurisdiction of incorporation)
001-34186 | 03-0491827 | |
(Commission File No.) | (IRS Employer Identification No.) |
2200 Pennsylvania Avenue NW
Suite 300E
Washington, DC 20037
(Address of principal executive offices and zip code)
Registrants telephone number, including area code: (202) 734-3400
Not Applicable
(Former Name or Former Address, if Changed Since Last Report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
¨ | Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ | Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ | Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ | Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 2.02. | Results of Operations and Financial Condition. |
On July 31, 2013, Vanda Pharmaceuticals Inc. (the Company or Vanda) issued a press release and is holding a conference call regarding its results of operations and financial condition for the quarter ended June 30, 2013. The press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated by reference herein.
Various statements to be made during the conference call 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 Companys forward-looking statements include, among others: Vandas failure to obtain regulatory approval for its products or product candidates, particularly tasimelteon for the treatment of Non-24-Hour Disorder, or to comply with ongoing regulatory requirements; Vandas loss of rights to develop and commercialize its products, product candidates or partnered products under its license and sublicense agreements; Vandas failure to develop or obtain sales, marketing and distribution resources and expertise or to otherwise manage its growth; Vandas ability to successfully commercialize tasimelteon following regulatory approval, if any; the extent and effectiveness of the development, sales and marketing and distribution support Fanapt® receives; Vandas ability to successfully commercialize Fanapt® outside of the U.S. and Canada; delays in the completion of Vandas or its partners clinical trials; a failure of Vandas products, product candidates or partnered products to be demonstrably safe and effective; a lack of acceptance of Vandas products, product candidates or partnered products in the marketplace, or a failure to become or remain profitable; Vandas expectations regarding trends with respect to its revenues, costs, expenses and liabilities; Vandas inability to obtain the capital necessary to fund its research and development or commercial activities; the costs and effects of current or potential litigation; Vandas failure to identify or obtain rights to new products or product candidates; limitations on Vandas ability to utilize some or all of its prior net operating losses and research and development credits; a loss of any of Vandas key scientists or management personnel; losses incurred from product liability claims made against Vanda and other factors that are described in the Risk Factors and Managements Discussion and Analysis of Financial Condition and Results of Operations sections of Vandas 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 SECs website at www.sec.gov. In addition to the risks described above and in Vandas annual report on Form 10-K and quarterly reports on Form 10-Q, other unknown or unpredictable factors also could affect Vandas 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 conveyed on the conference call will be provided only as of the date of the call, and Vanda undertakes no obligation, and specifically declines any obligation, to update or revise publicly any forward-looking statements made during the call after the date thereof, whether as a result of new information, future events or otherwise.
The information in Item 2.02 of this Current Report on Form 8-K and the Exhibit attached hereto shall not be deemed filed for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the Exchange Act) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.
Item 9.01. | Financial Statements and Exhibits. |
(d) | Exhibits |
Exhibit |
Description | |
99.1 | Press release of Vanda Pharmaceuticals Inc. dated July 31, 2013. |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
VANDA PHARMACEUTICALS INC. | ||||
By: | /s/ James P. Kelly | |||
Name: | James P. Kelly | |||
Title: | Senior Vice President, Chief Financial Officer, Secretary, and Treasurer |
Dated: July 31, 2013
Exhibit 99.1
Vanda Pharmaceuticals Reports Second Quarter 2013 Results
WASHINGTON July 31, 2013 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.
Key Highlights:
| On July 29, 2013 Vanda announced that the U.S. Food and Drug Administration (FDA) accepted the filing and granted priority review classification to Vandas New Drug Application (NDA) for tasimelteon, a circadian regulator for the treatment of Non-24-Hour Disorder (Non-24) in the totally blind. |
| 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. |
| Full year 2013 decrease in cash, cash equivalents and marketable securities (Cash) is expected to be between $45.0 and $50.0 million, consistent with prior guidance. |
| Vanda recorded second quarter 2013 revenue of $8.3 million including 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 over first quarter 2013 prescriptions. |
Page 1 of 7
SECOND QUARTER 2013 REPORTED RESULTS
Total 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. Vandas Cash as of June 30, 2013 totaled $103.6 million.
Year to Date June 30, 2013 Key Financial Figures1
Six Months Ended | ||||||||||||||||
June 30 | June 30 | |||||||||||||||
($ in thousands, except per share amounts) | 2013 | 2012 | Change ($) | Change (%) | ||||||||||||
Total revenues |
$ | 16,387 | $ | 16,519 | $ | (132 | ) | (1 | %) | |||||||
Research & development expenses |
13,942 | 24,670 | (10,728 | ) | (43 | %) | ||||||||||
General & administrative expenses |
9,032 | 7,510 | 1,522 | 20 | % | |||||||||||
Non-cash stock-based compensation2 |
1,782 | 2,595 | (813 | ) | (31 | %) | ||||||||||
Net loss |
(7,252 | ) | (15,969 | ) | 8,717 | 55 | % | |||||||||
Diluted net loss per share |
$ | (0.26 | ) | $ | (0.57 | ) | $ | 0.31 | 54 | % |
Second Quarter 2013 Key Financial Figures1
Three Months Ended | ||||||||||||||||
June 30 | March 31 | |||||||||||||||
($ in thousands, except per share amounts) | 2013 | 2013 | Change ($) | Change (%) | ||||||||||||
Total revenues |
$ | 8,319 | $ | 8,068 | $ | 251 | 3 | % | ||||||||
Research & development expenses |
5,982 | 7,960 | (1,978 | ) | (25 | %) | ||||||||||
General & administrative expenses |
5,074 | 3,958 | 1,116 | 28 | % | |||||||||||
Non-cash stock-based compensation2 |
830 | 952 | (122 | ) | (13 | %) | ||||||||||
Net loss |
(3,079 | ) | (4,173 | ) | 1,094 | 26 | % | |||||||||
Diluted net loss per share |
$ | (0.11 | ) | $ | (0.15 | ) | $ | 0.04 | 27 | % |
Page 2 of 7
Select Cash Flow Data1
Six Months Ended | ||||||||
June 30 | June 30 | |||||||
($ in thousands) | 2013 | 2012 | ||||||
Net cash provided by (used in) |
||||||||
Operating activities |
$ | (17,168 | ) | $ | (20,904 | ) | ||
Investing activities |
31,428 | 27,369 | ||||||
Financing activities |
601 | |
Select Balance Sheet Data1
($ in thousands) | June 30 2013 |
March 31 2013 |
June 30 2012 |
|||||||||
Total cash and marketable securities |
$ | 103,633 | $ | 110,932 | $ | 144,701 |
(1) | Unaudited |
(2) | Non-cash stock-based compensation is allocated to both Research & development and General & administrative expenses |
OPERATIONAL HIGHLIGHTS
On July 29, 2013, Vanda announced that the FDA accepted the filing and granted a priority review classification to Vandas 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.
Page 3 of 7
AFFIRMS 2013 FINANCIAL GUIDANCE
Consistent with prior guidance, 2013 expenses are expected to reflect lower research and development spending as compared to 2012 and an increase in commercial spending.
| Full year 2013 decrease in Cash is expected to be between $45.0 and $50.0 million, compared to $47.5 million for 2012. |
| Total 2013 operating expenses are expected to be between $57.0 and $62.0 million. This includes Fanapt® intangible asset amortization of $1.5 million and $4.0 to $6.0 million of non-cash stock based compensation. Total 2012 operating expenses were $61.0 million. |
| 2013 operating expense guidance includes $3.5 million in milestone payments due upon the acceptance by the FDA of a tasimelteon NDA submission and assumes $4.0 to $5.0 million in NDA filing-related expenses. |
CONFERENCE CALL
Vanda has scheduled a conference call for today, Wednesday, July 31, 2013, at 10:00 AM ET. During the call, Vandas 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 Vandas 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 Vandas 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.
Page 4 of 7
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 companys forward-looking statements include, among others: Vandas 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 Managements Discussion and Analysis of Financial Condition and Results of Operations sections of Vandas 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 SECs website at www.sec.gov. In addition to the risks described above and in Vandas annual report on Form 10-K and quarterly reports on Form 10-Q, other unknown or unpredictable factors also could affect Vandas 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.
####
Page 5 of 7
VANDA PHARMACEUTICALS INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
Three Months Ended | Six Months Ended | |||||||||||||||
($ in thousands, except per share amounts) | June 30 2013 |
June 30 2012 |
June 30 2013 |
June 30 2012 |
||||||||||||
Revenues: |
||||||||||||||||
Licensing agreement |
$ | 6,678 | $ | 6,678 | $ | 13,284 | $ | 13,284 | ||||||||
Royalty revenue |
1,641 | 1,700 | 3,103 | 3,235 | ||||||||||||
|
|
|
|
|
|
|
|
|||||||||
Total revenues |
8,319 | 8,378 | 16,387 | 16,519 | ||||||||||||
Operating expenses: |
||||||||||||||||
Research and development |
5,982 | 12,490 | 13,942 | 24,670 | ||||||||||||
General and administrative |
5,074 | 3,601 | 9,032 | 7,510 | ||||||||||||
Intangible asset amortization |
372 | 372 | 741 | 741 | ||||||||||||
|
|
|
|
|
|
|
|
|||||||||
Total operating expenses |
11,428 | 16,463 | 23,715 | 32,921 | ||||||||||||
|
|
|
|
|
|
|
|
|||||||||
Loss from operations |
(3,109 | ) | (8,085 | ) | (7,328 | ) | (16,402 | ) | ||||||||
Other income |
30 | 78 | 76 | 433 | ||||||||||||
|
|
|
|
|
|
|
|
|||||||||
Loss before tax benefit |
(3,079 | ) | (8,007 | ) | (7,252 | ) | (15,969 | ) | ||||||||
Tax benefit |
| | | | ||||||||||||
|
|
|
|
|
|
|
|
|||||||||
Net loss |
$ | (3,079 | ) | $ | (8,007 | ) | $ | (7,252 | ) | $ | (15,969 | ) | ||||
|
|
|
|
|
|
|
|
|||||||||
Net loss per share: |
||||||||||||||||
Basic |
$ | (0.11 | ) | $ | (0.28 | ) | $ | (0.26 | ) | $ | (0.57 | ) | ||||
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|
|
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|
|
|
|||||||||
Diluted |
$ | (0.11 | ) | $ | (0.28 | ) | $ | (0.26 | ) | $ | (0.57 | ) | ||||
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|
|
|
|
|
|||||||||
Shares used in calculations of net loss per share: |
||||||||||||||||
Basic |
28,377,254 | 28,226,743 | 28,361,340 | 28,226,743 | ||||||||||||
|
|
|
|
|
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|
|
|||||||||
Diluted |
28,377,254 | 28,226,743 | 28,361,340 | 28,226,743 | ||||||||||||
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|
|
|
|
Page 6 of 7
VANDA PHARMACEUTICALS INC.
CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited)
($ in thousands) | June 30, 2013 | December 31, 2012 | ||||||
ASSETS |
||||||||
Current assets: |
||||||||
Cash and cash equivalents |
$ | 103,633 | $ | 88,772 | ||||
Marketable securities |
| 31,631 | ||||||
Accounts receivable |
1,641 | 1,168 | ||||||
Prepaid expenses and other current assets |
2,651 | 3,967 | ||||||
Restricted cash, current |
430 | 430 | ||||||
|
|
|
|
|||||
Total current assets |
108,355 | 125,968 | ||||||
Property and equipment, net |
2,208 | 2,348 | ||||||
Intangible asset, net |
5,791 | 6,532 | ||||||
Restricted cash, non-current |
600 | 600 | ||||||
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|
|
|||||
Total assets |
$ | 116,954 | $ | 135,448 | ||||
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LIABILITIES AND STOCKHOLDERS EQUITY |
||||||||
Current liabilities: |
||||||||
Accounts payable |
$ | 1,167 | $ | 287 | ||||
Accrued liabilities |
3,770 | 5,187 | ||||||
Deferred rent, current |
209 | | ||||||
Deferred revenues, current |
26,789 | 26,789 | ||||||
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|
|
|
|||||
Total current liabilities |
31,935 | 32,263 | ||||||
Deferred rent, non-current |
3,002 | 3,005 | ||||||
Deferred revenues, non-current |
76,991 | 90,275 | ||||||
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Total liabilities |
111,928 | 125,543 | ||||||
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Stockholders equity: |
||||||||
Common stock |
28 | 28 | ||||||
Additional paid-in capital |
303,357 | 300,974 | ||||||
Accumulated other comprehensive income |
| 10 | ||||||
Accumulated deficit |
(298,359 | ) | (291,107 | ) | ||||
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|
|
|||||
Total stockholders equity |
5,026 | 9,905 | ||||||
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|
|
|||||
Total liabilities and stockholders equity |
$ | 116,954 | $ | 135,448 | ||||
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|
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COMPANY CONTACT:
Jim Kelly
Senior Vice President & Chief Financial Officer
Vanda Pharmaceuticals Inc.
(202) 734-3428
jim.kelly@vandapharma.com
SOURCE Vanda Pharmaceuticals Inc.
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