Vanda Pharmaceuticals Reports Fourth Quarter and Full Year 2019 Financial Results
WASHINGTON, Feb. 25, 2020 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (Nasdaq: VNDA) today announced financial and operational results for the fourth quarter and full year ended December 31, 2019.
"We had another year of outstanding commercial growth," said Mihael H. Polymeropoulos, M.D., Vanda's President and CEO. "I have never been more excited about the opportunities ahead with our relentless focus on developing innovative therapies for patients in need."
Key Financial Highlights
-- Total revenues were $60.9 million in the fourth quarter of 2019, a 15%
increase compared to $53.0 million in the fourth quarter of 2018. Total
revenues were $227.2 million for the full year 2019, an 18% increase
compared $193.1 million for the full year 2018.
-- HETLIOZ(®) net product sales were $38.6 million in the fourth quarter
of 2019, a 19% increase compared to $32.4 million in the fourth quarter
of 2018. HETLIOZ(®) net product sales were $143.0 million for the full
year 2019, a 23% increase compared to $115.8 million for the full year
2018.
-- Fanapt(®) net product sales were $22.3 million in the fourth quarter of
2019, an 8% increase compared to $20.6 million in the fourth quarter of
2018. Fanapt(®) net product sales were $84.2 million for the full year
2019, a 9% increase compared to $77.3 million for the full year 2018.
-- Cash, cash equivalents and marketable securities (Cash) were $312.1
million as of December 31, 2019, representing an increase to Cash of
$54.8 million compared to December 31, 2018.
Key Product and Pipeline Highlights
Tradipitant
-- Results from the EPIONE study of tradipitant in the treatment of
pruritus in atopic dermatitis were reported today. Vanda will reassess
EPIONE 2 and determine next steps.
-- Enrollment in the Phase III study of tradipitant in gastroparesis
(VP-VLY-686-3301) is ongoing.
-- Vanda expects to complete the Phase III program of tradipitant in motion
sickness and file a New Drug Application with the U.S. Food and Drug
Administration (FDA) in 2020.
-- Vanda continues to engage with the FDA over the requirement of a 9-month
dog toxicity study.
HETLIOZ(®) (tasimelteon)
-- Vanda submitted a supplemental New Drug Application (sNDA) for
HETLIOZ(®) in Smith-Magenis Syndrome (SMS), including data for a liquid
formulation, and expects regulatory action by the FDA in 2020.
-- Vanda continues to pursue approval for HETLIOZ(®) in the treatment of
jet lag disorder (JLD).
-- A clinical program for HETLIOZ(®) in delayed sleep phase disorder
(DSPD) is ongoing.
Fanapt(®) (iloperidone)
-- A Phase III study of Fanapt(®) in bipolar disorder is ongoing.
-- Development of the long acting injectable (LAI) formulation of
Fanapt(®) is ongoing.
GAAP Financial Results
Net income was $4.2 million for the fourth quarter of 2019, compared to net income of $10.4 million for the fourth quarter of 2018. Diluted net income per share was $0.08 in the fourth quarter of 2019, compared to $0.19 in the fourth quarter of 2018.
Net income was $115.6 million for the full year 2019, compared to net income of $25.2 million, for the full year 2018. Diluted net income per share was $2.11 for the full year 2019, compared to $0.48 for the full year 2018. The income tax benefit of $86.5 million reflected in the financial results for the full year 2019 includes the favorable impact of the release of Vanda's deferred tax asset valuation allowance.
2020 Financial Guidance
Vanda expects to achieve the following financial objectives in 2020:
Full Year 2020
Financial Objectives
Full Year 2020
Guidance
---
Total revenues
$240 to $260 million
---
HETLIOZ(R) net product sales
$155 to $165 million
---
Fanapt(R) net product sales
$85 to $95 million
---
Year-end 2020 Cash Greater than $320 million
---
Conference Call
Vanda has scheduled a conference call for today, Tuesday, February 25, 2020, at 4:30 PM ET. During the call, Vanda's management will discuss the fourth quarter and full year 2019 financial results and other corporate activities. Investors can call 1-866-688-9426 (domestic) or 1-409-216-0816 (international) and use passcode 2149683. A replay of the call will be available on Tuesday, February 25, 2020, beginning at 7:30 PM ET and will be accessible until Tuesday, March 3, 2020, at 7:30 PM ET. The replay call-in number is 1-855-859-2056 for domestic callers and 1-404-537-3406 for international callers. The passcode number is 2149683.
The conference call will be broadcast simultaneously on Vanda's website, www.vandapharma.com. Investors should click on the Investors 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 is a leading global biopharmaceutical company focused on the development and commercialization of innovative therapies to address high unmet medical needs and improve the lives of patients. For more on Vanda Pharmaceuticals Inc., please visit www.vandapharma.com.
CAUTIONARY NOTE REGARDING FORWARD LOOKING STATEMENTS
Various statements in this release, including, but not limited to, the guidance provided under "2020 Financial Guidance" above, are "forward-looking statements" under the securities laws. 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 assumptions regarding its ability to continue to grow its business in the U.S., Vanda's ability to complete the clinical development and obtain regulatory approval for tradipitant in the treatment of motion sickness, gastroparesis and/or atopic dermatitis, Vanda's discussion and potential resolution of the deficiencies that the FDA believes are contained in the sNDA for HETLIOZ(®) for the treatment of JLD and Vanda's ability to obtain marketing approval for the use of HETLIOZ(®) in the treatment of JLD following any such resolution, Vanda's ability to complete the clinical development, submit an sNDA and obtain regulatory approval for tasimelteon in the treatment of sleep disorders in patients with SMS, Vanda's ability to complete the clinical development and obtain regulatory approval for Fanapt(®) in bipolar disorder and Fanapt(® )LAI in schizophrenia, 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, 2018 and quarterly report on Form 10-Q for the quarter ended September 30, 2019, which are on file with the SEC and available on the SEC's website at www.sec.gov. Additional factors may be described in those sections of Vanda's annual report on Form 10-K for the year ended December 31, 2019, to be filed with the SEC in the first quarter of 2020. 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
(in thousands, except for share and per share amounts)
(unaudited)
Three Months Ended Twelve Months Ended
December 31 December 31 December 31 December 31
2019 2018 2019 2018
Revenues:
HETLIOZ(R)product sales, net $
38,599 $
32,444 $
142,980 $
115,835
Fanapt(R)product sales, net 22,331 20,597 84,208 77,283
Total revenues 60,930 53,041 227,188 193,118
Operating expenses:
Cost of goods sold excluding
amortization 6,225 5,667 24,488 20,508
Research and development 13,074 12,922 48,649 43,594
Selling, general and
administrative 37,018 24,922 129,736 105,751
Intangible asset amortization 370 380 1,505 1,527
Total operating expenses 56,687 43,891 204,378 171,380
Income from operations 4,243 9,150 22,810 21,738
Other income 1,567 1,168 6,218 3,608
Income before income taxes 5,810 10,318 29,028 25,346
Provision (benefit) for income taxes 1,594 (42) (86,525) 138
Net income $
4,216 $
10,360 $
115,553 $
25,208
Net income per share, basic $
0.08 $
0.20 $
2.17 $
0.50
Net income per share, diluted $
0.08 $
0.19 $
2.11 $
0.48
Weighted average shares outstanding, basic 53,389,950 52,457,275 53,137,562 50,859,947
Weighted average shares outstanding, diluted 54,973,952 55,216,507 54,847,060 53,045,257
VANDA PHARMACEUTICALS INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands)
(unaudited)
December 31 December 31
2019 (1) 2018 (1)
ASSETS
Current
assets:
Cash and cash
equivalents $
45,072 $
61,005
Marketable
securities 267,057 196,355
Accounts
receivable, net 26,367 28,780
Inventory 1,140 994
Prepaid expenses and
other current assets 14,500 11,998
Total current
assets 354,136 299,132
Property and
equipment, net 3,864 4,417
Operating lease right-
of-use assets 11,180
Intangible
assets, net 23,037 24,542
Deferred tax
assets 87,680 -
Non-current
inventory and other 3,851 4,039
Total assets $
483,748 $
332,130
LIABILITIES AND
STOCKHOLDERS' EQUITY
Current
liabilities:
Accounts payable and
accrued liabilities $
27,590 $
21,584
Product revenue
allowances 31,915 31,231
Milestone
obligations
under license
agreements 200
Total current
liabilities 59,505 53,015
Operating lease
non-current
liabilities 12,455
Other non-
current
liabilities 843 3,693
Total
liabilities 72,803 56,708
Stockholders'
equity:
Common stock 54 52
Additional
paid-in
capital 631,307 611,587
Accumulated other
comprehensive income 249 1
Accumulated
deficit (220,665) (336,218)
Total
stockholders'
equity 410,945 275,422
Total liabilities and
stockholders' equity $
483,748 $
332,130
(1) With the adoption of Accounting Standards Codification
Subtopic ASC 842, Leases, on January 1, 2019, Vanda
recognized operating lease liabilities and right-of-use
assets. Prior period financial statements were not recast for
the new leasing standard. For more information, please refer
to footnote 2 in the annual report on Form 10-K for the year
ended December 31, 2019, to be filed in the first quarter of
2020.
Corporate Contact:
AJ Jones II
Chief Corporate Affairs and Communications Officer
Vanda Pharmaceuticals Inc.
202-734-3400
pr@vandapharma.com
Elizabeth Van Every
Head of Corporate Affairs
Vanda Pharmaceuticals Inc.
202-734-3400
pr@vandapharma.com
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SOURCE Vanda Pharmaceuticals Inc.
