e8vk
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): August 10, 2009
VANDA PHARMACEUTICALS INC.
(Exact name of Registrant as specified in its charter)
Delaware
(State or other jurisdiction of incorporation)
|
|
|
000-51863
(Commission File No.)
|
|
03-0491827
(IRS Employer Identification No.) |
9605 Medical Center Drive
Suite 300
Rockville, Maryland 20850
(Address of principal executive offices and zip code)
Registrants telephone number, including area code: (240) 599-4500
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:
o Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
o Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
o Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17
CFR 240.14d-2(b))
o 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 August 10, 2009, Vanda Pharmaceuticals Inc. issued a press release relating to its results
of operations and financial condition for the second quarter ended June 30, 2009. The full text of
this press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
The information in Item 2.02 of this 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 No. |
|
Description |
99.1
|
|
Press release of Vanda Pharmaceuticals Inc. dated August 10, 2009. |
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/ STEPHANIE R. IRISH
|
|
|
|
Name: |
Stephanie R. Irish |
|
|
|
Title: |
Acting Chief Financial Officer and Treasurer |
|
|
Dated: August 10, 2009
exv99w1
Exhibit 99.1
For Immediate Release
Company Contact:
Stephanie R. Irish
Acting Chief Financial Officer
Vanda Pharmaceuticals Inc.
(240) 599-4500
stephanie.irish@vandapharma.com
Vanda Pharmaceuticals Reports Second Quarter 2009 Results
FDA GRANTS U.S. MARKETING APPROVAL OF FANAPT (ILOPERIDONE)
ROCKVILLE, MD. August 10, 2009 Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ: VNDA), a
biopharmaceutical company focused on the development and commercialization of clinical-stage
products for central nervous system disorders, today announced financial and operational results
for the second quarter ended June 30, 2009.
Vanda reported a net loss of $12.4 million for the second quarter of 2009, compared to $6.5 million
for the first quarter of 2009 and $13.5 million for the second quarter of 2008. Total expenses for
the second quarter of 2009 were $12.4 million, compared to $6.6 million for the first quarter of
2009 and $13.9 million for the second quarter of 2008. Research and development (R&D) expenses for
the second quarter of 2009 were $7.2 million, compared to $2.3 million for the first quarter of
2009 and $5.5 million for the second quarter of 2008. The increase in R&D expenses in the second
quarter of 2009 relative to the first quarter of 2009 and second quarter of 2008 is primarily due
to the regulatory consulting fees paid and/or accrued as a result of the approval of Fanapt
(iloperidone) by the U.S. Food and Drug Administration (FDA). In addition, the Company recorded a
$12.0 million milestone payment due to Novartis as an intangible asset. Of the $12.0 million
milestone payment, $7.0 million was paid in May 2009 and the remaining $5.0 million is due in
November 2009; however, Novartis has the right to accelerate the due date in its sole discretion.
As of June 30, 2009, Vandas cash, cash equivalents, and marketable securities totaled
approximately $29.0 million. As of June 30, 2009, a total of approximately 27.1 million shares of
Vanda common stock were outstanding. Net loss per common share for the second quarter of 2009 was
$0.46, compared to $0.24 for the first quarter of 2009 and $0.51 for the second quarter of 2008.
OPERATIONAL HIGHLIGHTS
On May 6, 2009, the FDA granted U.S. marketing approval of Fanapt for the acute treatment of
schizophrenia in adults. Vanda expects to make Fanapt available in U.S. pharmacies later this
year. Holders of a New Drug Application (NDA) have 60 days after approval to file for
Page 1 of 8
patent term restoration under the Hatch-Waxman Act. Vanda submitted its application for patent
term restoration with respect to Fanapt on June 9, 2009.
Vanda also continues to pursue its clinical development plan for tasimelteon for the treatment of
circadian rhythm sleep disorders. On June 26, 2009, Vanda met with the FDA to discuss the clinical
development plan in an End of Phase II Meeting. Vanda will continue to work with the FDA to
characterize the path to an NDA for tasimelteon.
FINANCIAL DETAILS
|
|
Operating Expenses. Second quarter 2009 R&D expenses of $7.2 million consisted primarily of
$5.4 million of consulting fees, as well as $0.6 million of salaries and benefits, $0.6
million of non-cash stock based compensation costs for R&D personnel, and $0.3 million of
pre-clinical work. This compares to $2.3 million for the first quarter of 2009 and $5.5
million for the second quarter of 2008. The increase in R&D expenses in the second quarter of
2009 relative to the first quarter of 2009 and second quarter of 2008 is primarily due to the
$5.0 million in regulatory consulting fees paid and/or accrued as a result of the approval of
Fanapt by the FDA. |
|
|
General and administrative (G&A) expenses of $5.0 million for the second quarter of 2009
consisted primarily of $0.5 million of salaries and benefits and $2.2 million of non-cash
stock based compensation costs for G&A personnel, as well as $0.6 million of legal fees, $0.7
million of commercial costs and $0.2 million of insurance costs. This compares to $4.2
million for the first quarter of 2009 and $8.5 million for the second quarter of 2008. The
increase in G&A expenses in the second quarter of 2009 relative to the first quarter of 2009
is primarily due to an increase in professional fees and commercial costs related to Vandas
participation at the American Psychiatric Associations Annual Meeting in May. The decrease
in G&A expenses in the second quarter of 2009 relative to the second quarter of 2008 is
primarily due to lower stock-based compensation and commercial expenses. |
|
|
|
Employee stock-based compensation expense recorded in the second quarter of 2009 totaled $2.8
million. Of these non-cash charges, $0.6 million was recorded as R&D expense and $2.2 million
was recorded as G&A expense. For the first quarter of 2009 and the second quarter of 2008,
total stock-based compensation expense was $2.3 million and $4.0 million, respectively. The
increase in stock-based compensation expense in the second quarter of 2009 relative to the first
quarter of 2009 is the result of the issuance of additional non-qualified stock options in the
second quarter, as well as the expense related to the vesting of restricted stock units upon the
approval of Fanapt by the FDA. The decrease in stock-based compensation expense in the second
quarter of 2009 relative to the second quarter of 2008 is primarily due to a lower stock-based
compensation expense resulting from the workforce reduction in the fourth quarter of 2008. |
|
|
Cash and marketable securities decreased by $13.6 million during the second quarter of
2009. Changes included $12.4 million of net losses, increases of $1.3 million in inventory
and $7.0 million in intangible assets offset by increases in accrued expenses and accounts
payable of $2.9 million, $3.4 million in non-cash depreciation, amortization, and stock-based
compensation expense, $0.9 million in proceeds from the exercise of stock options and $0.1
million of other working capital outflows. |
|
|
Vandas cash, cash equivalents and marketable securities as of June 30, 2009 totaled
approximately $29.0 million, compared to approximately $46.5 million as of December 31, 2008. |
Page 2 of 8
|
|
Net loss for the second quarter of 2009 was $12.4 million, compared to a net loss of $6.5
million for the first quarter of 2009 and a net loss of $13.5 million for the second quarter
of 2008. |
|
|
Net loss per common share for the second quarter of 2009 was $0.46, compared to $0.24 for
the first quarter of 2009 and $0.51 for the second quarter of 2008. |
FINANCIAL GUIDANCE
Based on its current operating plans, Vanda believes that its existing cash, cash equivalents and
marketable securities, will be sufficient to meet its anticipated operating needs through 2009.
However, given the recent approval by the FDA of the NDA for Fanapt, Vanda is currently evaluating
alternative commercial strategies for the product. These strategies include, in addition to Vanda
launching Fanapt on its own, entering into one or more partnerships, other collaboration
agreements or strategic transactions that may provide capital to support Vandas operations.
CONFERENCE CALL
Vanda has scheduled a conference call for today, Monday, August 10, 2009, at 10:00 AM ET. During
the call, Mihael H. Polymeropoulos, M.D., President and CEO, and Stephanie Irish, Acting CFO, will
discuss quarterly results and other corporate activities. Investors can call 1-800-599-9829
(domestic) and 1-617-847-8703 (international) prior to the 10:00 AM start time and ask for the
Vanda Pharmaceuticals conference call hosted by Dr. Polymeropoulos (participant passcode 93125446).
A replay of the call will be available Monday, August 10, 2009, at 1:00 PM ET and will be
accessible until Monday, August 17, 2009, at 5:00 PM ET. The replay call-in number is
1-888-286-8010 for domestic callers and 1-617-801-6888 for international callers. The access
number is 78449791.
The conference call will be broadcast simultaneously on the companys Web site,
http://www.vandapharma.com. Investors should click on the Investor Relations tab and are advised
to go to the Web site at least 15 minutes early to register, download, and install any necessary
software. The call will also be archived on the Vanda Web site for a period of 30 days, through
September 9, 2009.
ABOUT VANDA PHARMACEUTICALS INC.:
Vanda Pharmaceuticals Inc. is a biopharmaceutical company focused on the development and
commercialization of clinical-stage products for central nervous system disorders. For more on
Vanda Pharmaceuticals Inc., please visit http://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,
targets, likely, will, would, and could, 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. Vanda Pharmaceuticals Inc.
is at an early stage of development and may not ever have any products that generate significant
revenue. Important factors that could cause actual results to differ materially from those
reflected in the companys forward-looking statements include, among others: delays in the
completion of Vandas clinical trials; a failure of Vandas products to be demonstrably safe and
effective; Vandas failure to obtain regulatory approval for its products or to comply with ongoing
regulatory requirements for its products; a lack of acceptance of Vandas products in the
marketplace, or a failure to become or remain profitable; Vandas expectations
Page 3 of 8
regarding trends
with respect to its costs and expenses; Vandas inability to obtain the capital
necessary to fund its commercial and research and development activities; Vandas failure to
identify or obtain rights to new products; Vandas failure to develop or obtain sales, marketing
and distribution resources and expertise or to otherwise manage its growth; a loss of any of
Vandas key scientists or management personnel; losses incurred from product liability claims made
against Vanda; a loss of rights to develop and commercialize Vandas products under its license and
sublicense agreements and other factors that are described in the Risk Factors section (Part II,
Item 1A) of Vandas quarterly report on Form 10-Q for the fiscal quarter ended March 31, 2009 (File
No. 001-34186). In addition to the risks described above and in Part II, Item 1A of Vandas
quarterly report 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 4 of 8
VANDA PHARMACEUTICALS INC.
(A Development Stage Enterprise)
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Three Months Ended |
|
|
Six Months Ended |
|
|
|
June 30, |
|
|
June 30, |
|
|
June 30, |
|
|
June 30, |
|
|
|
2009 |
|
|
2008 |
|
|
2009 |
|
|
2008 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Revenue |
|
$ |
|
|
|
$ |
|
|
|
$ |
|
|
|
$ |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of Sales |
|
|
229,352 |
|
|
|
|
|
|
|
229,352 |
|
|
|
|
|
Research and development |
|
|
7,195,595 |
|
|
|
5,480,909 |
|
|
|
9,528,934 |
|
|
|
16,583,574 |
|
General and administrative |
|
|
4,988,317 |
|
|
|
8,454,985 |
|
|
|
9,212,351 |
|
|
|
17,414,199 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total operating expenses |
|
|
12,413,264 |
|
|
|
13,935,894 |
|
|
|
18,970,637 |
|
|
|
33,997,773 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Loss from operations |
|
|
(12,413,264 |
) |
|
|
(13,935,894 |
) |
|
|
(18,970,637 |
) |
|
|
(33,997,773 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income |
|
|
21,163 |
|
|
|
441,012 |
|
|
|
74,549 |
|
|
|
1,306,762 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net loss |
|
$ |
(12,392,101 |
) |
|
$ |
(13,494,882 |
) |
|
$ |
(18,896,088 |
) |
|
$ |
(32,691,011 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Basic and diluted net loss per
share attributable to
common stockholders |
|
$ |
(0.46 |
) |
|
$ |
(0.51 |
) |
|
$ |
(0.71 |
) |
|
$ |
(1.23 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Shares used in calculation of
basic and diluted net loss
per share attributable to
common stockholders |
|
|
26,900,841 |
|
|
|
26,649,439 |
|
|
|
26,777,159 |
|
|
|
26,648,892 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Page 5 of 8
VANDA PHARMACEUTICALS INC.
(A Development Stage Enterprise)
CONDENSED CONSOLIDATED BALANCE SHEETS (Unaudited)
|
|
|
|
|
|
|
|
|
|
|
June 30, 2009 |
|
|
December 31, 2008 |
|
|
|
|
|
|
|
|
|
|
ASSETS |
|
|
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
24,014,203 |
|
|
$ |
39,079,304 |
|
Marketable securities |
|
|
5,008,623 |
|
|
|
7,378,798 |
|
Prepaid expenses, deposits and other current assets |
|
|
1,129,194 |
|
|
|
1,287,400 |
|
Inventory |
|
|
1,272,240 |
|
|
|
|
|
|
|
|
|
|
|
|
Total current assets |
|
|
31,424,260 |
|
|
|
47,745,502 |
|
|
|
|
|
|
|
|
|
|
Property and equipment, net |
|
|
1,518,442 |
|
|
|
1,758,111 |
|
Restricted cash |
|
|
430,230 |
|
|
|
430,230 |
|
Intangible asset, net |
|
|
11,770,648 |
|
|
|
|
|
|
|
|
|
|
|
|
Total assets |
|
$ |
45,143,580 |
|
|
$ |
49,933,843 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
LIABILITIES AND STOCKHOLDERS EQUITY |
|
|
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
|
|
Accounts payable |
|
$ |
6,916,901 |
|
|
$ |
512,382 |
|
Accrued expenses |
|
|
4,415,231 |
|
|
|
2,898,417 |
|
|
|
|
|
|
|
|
Total current liabilities |
|
|
11,332,132 |
|
|
|
3,410,799 |
|
|
|
|
|
|
|
|
|
|
Long-term liabilities: |
|
|
|
|
|
|
|
|
Deferred rent |
|
|
504,811 |
|
|
|
502,770 |
|
|
|
|
|
|
|
|
Total liabilities |
|
|
11,836,943 |
|
|
|
3,913,569 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Stockholders equity: |
|
|
|
|
|
|
|
|
Common stock |
|
|
27,140 |
|
|
|
26,653 |
|
Additional paid-in capital |
|
|
277,149,879 |
|
|
|
270,988,157 |
|
Accumulated other comprehensive income (loss) |
|
|
213 |
|
|
|
(20,029 |
) |
Deficit accumulated during the development stage |
|
|
(243,870,595 |
) |
|
|
(224,974,507 |
) |
|
|
|
|
|
|
|
Total stockholders equity |
|
|
33,306,637 |
|
|
|
46,020,274 |
|
|
|
|
|
|
|
|
|
Total liabilities and stockholders equity |
|
$ |
45,143,580 |
|
|
$ |
49,933,843 |
|
|
|
|
|
|
|
|
Page 6 of 8
VANDA PHARMACEUTICALS INC.
(A Development Stage Enterprise)
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited)
|
|
|
|
|
|
|
|
|
|
|
Six Months Ended |
|
|
|
June 30, |
|
|
June 30, |
|
|
|
2009 |
|
|
2008 |
|
|
|
|
|
|
|
|
|
|
Cash flows from operating activities: |
|
|
|
|
|
|
|
|
Net loss |
|
$ |
(18,896,088 |
) |
|
$ |
(32,691,011 |
) |
Adjustments to reconcile net income to net cash used
in operating activities: |
|
|
|
|
|
|
|
|
Depreciation and amortization |
|
|
239,669 |
|
|
|
259,707 |
|
Stock-based compensation |
|
|
5,279,366 |
|
|
|
9,074,594 |
|
Gain on disposal of assets |
|
|
|
|
|
|
211 |
|
Amortization of net discounts on short-term investments |
|
|
96,599 |
|
|
|
(195,911 |
) |
Amortization of intangible assets |
|
|
229,352 |
|
|
|
|
|
Changes in assets and liabilities: |
|
|
|
|
|
|
|
|
Prepaid expenses and other current assets |
|
|
158,206 |
|
|
|
(247,729 |
) |
Inventory |
|
|
(1,272,240 |
) |
|
|
|
|
Accounts payable |
|
|
1,404,519 |
|
|
|
2,425,921 |
|
Accrued expenses |
|
|
1,516,814 |
|
|
|
(5,979,353 |
) |
Other liabilities |
|
|
2,041 |
|
|
|
136,734 |
|
|
|
|
|
|
|
|
Net cash used in operating activities |
|
|
(11,241,762 |
) |
|
|
(27,216,837 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash flows from investing activities: |
|
|
|
|
|
|
|
|
Acquisition of intangible asset |
|
|
(7,000,000 |
) |
|
|
|
|
Purchases of property and equipment |
|
|
|
|
|
|
(479,581 |
) |
Purchases of marketable securities |
|
|
(8,082,729 |
) |
|
|
(2,081,121 |
) |
Proceeds from sales of marketable securities |
|
|
126,547 |
|
|
|
4,875,076 |
|
Maturities of marketable securities |
|
|
10,250,000 |
|
|
|
39,460,000 |
|
|
|
|
|
|
|
|
Net cash provided by (used in) investing activities |
|
|
(4,706,182 |
) |
|
|
41,774,374 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash flows from financing activities: |
|
|
|
|
|
|
|
|
Proceeds from exercise of stock options and warrants |
|
|
882,843 |
|
|
|
|
|
|
|
|
|
|
|
|
Net cash provided by financing activities |
|
|
882,843 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Effect of foreign currency translation |
|
|
|
|
|
|
16,745 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net change in cash and cash equivalents |
|
|
(15,065,101 |
) |
|
|
14,574,282 |
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents, beginning of period |
|
|
39,079,304 |
|
|
|
41,929,533 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cash and cash equivalents, end of period |
|
$ |
24,014,203 |
|
|
$ |
56,503,815 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Supplemental disclosure of non-cash investing activities |
|
|
|
|
|
|
|
|
Intangible asset acquisition included in accounts payable |
|
$ |
5,000,000 |
|
|
|
|
|
Page 7 of 8
SOURCE Vanda Pharmaceuticals Inc.
08/XX/2009
CONTACT: Stephanie R. Irish, Acting Chief Financial Officer of Vanda Pharmaceuticals Inc.,
+1-240-599-4500
Web site: http://www.vandapharma.com
(VNDA)
CO: Vanda Pharmaceuticals Inc.
Page 8 of 8