08.05.2008 11:00:00
|
King Pharmaceuticals Reports First-Quarter 2008 Financial Results
King Pharmaceuticals, Inc. (NYSE:KG) announced today that total revenues
were $432 million during the first quarter ended March 31, 2008,
compared to $516 million in the first quarter of 2007. This decrease was
primarily due to the market entry of the first generic substitute for
ALTACE® (ramipril) in
December 2007. Reported net earnings equaled $88 million and diluted
earnings per share equaled $0.36 during the first quarter of 2008,
compared to net earnings of $116 million and diluted earnings per share
of $0.48 in the first quarter of the prior year. Excluding special
items, net earnings equaled $90 million and diluted earnings per share
equaled $0.37 during the first quarter ended March 31, 2008, compared to
net earnings of $118 million and diluted earnings per share of $0.48 in
the first quarter of 2007.
Brian A. Markison, Chairman, President and Chief Executive Officer of
King, stated, "We are focused on the continued
successful execution of our strategy for long-term growth, which
includes the submission of three important New Drug Applications (NDAs)
with the U.S. Food and Drug Administration (FDA) by the end of this
year. Once approved, these new products have the potential to provide
additional significant value for our shareholders.”
The three NDAs King plans to submit are REMOXY™ (long-acting oral oxycodone), ACUROX™
(short-acting oral oxycodone HCl, niacin, and other functional inactive
ingredients), and CORVUE™ (binodenoson, a
pharmacologic stress imaging agent for injection). Importantly, the
REMOXY™ NDA remains
on schedule for submission by the end of June 2008.
As of March 31, 2008, the Company’s cash and
cash equivalents totaled approximately $827 million. During the first
quarter of 2008, the Company generated cash flow from operations of
approximately $100 million. Additionally, the fair value of King’s
investments in debt securities equaled approximately $589 million as of
the end of the first quarter of 2008.
Joseph Squicciarino, King’s Chief Financial
Officer, emphasized, "We have taken the
necessary steps to realize an expected SG&A cost savings of $75 to $90
million this year. Accordingly, we are on track to meet our annual cash
flow from operations goal of $400 to $450 million for 2008.”
Commenting on the net sales performance of the Company’s
marketed products, Steve Andrzejewski, Chief Commercial Officer of King,
said, "We are particularly pleased with the
continued strong performance of THROMBIN-JMI®,
especially considering the market entry of multiple new competitors
since October 2007.”
Net revenue from branded pharmaceuticals totaled $369 million for the
first quarter of 2008, compared to $449 million during the first quarter
of 2007.
Net sales of SKELAXIN®
(metaxalone) totaled $116 million during the first quarter of 2008,
compared to $112 million during the same period of the prior year.
THROMBIN-JMI®
(thrombin, topical, bovine, USP) net sales totaled $67 million during
the first quarter of 2008, compared to $64 million during the first
quarter of 2007.
Net sales of AVINZA®
(morphine sulfate extended release) totaled $32 million during the first
quarter of 2008, compared to $9 million during the first quarter of
2007. This increase is primarily due to the fact that the Company did
not acquire AVINZA®
until February 26, 2007 and is not due to an increase in demand.
LEVOXYL®
(levothyroxine sodium tablets, USP) net sales totaled $16 million during
the first quarter ended March 31, 2008, compared to $22 million during
the first quarter of 2007. This decrease was primarily due to a
reduction in the level of inventory held by the Company’s
wholesale customers during the most recent quarter from that which
existed on December 31, 2007.
ALTACE® net sales
totaled $80 million during the first quarter of 2008, compared to $157
million during the first quarter of 2007.
King’s Meridian Auto-Injector business
contributed revenue of $43 million during each of the first quarters of
2008 and 2007.
Royalty revenues, derived primarily from ADENOSCAN®
(adenosine), totaled $19 million during the first quarter ended March
31, 2008.
About REMOXY™
REMOXY™, an investigational drug, is an
innovative formulation of extended-release, long-acting oxycodone, a
strong opioid painkiller for the treatment of moderate to severe chronic
pain. It is designed to resist common methods of abuse that are reported
with respect to other long-acting opioids. REMOXY™
is a proposed brand name that is subject to FDA approval.
About ACUROX™ Tablets
ACUROX™ Tablets, an investigational drug, is
an orally administered immediate-release tablet containing oxycodone HCl
as an active analgesic ingredient, niacin as an active ingredient in
subtherapeutic amounts, and a proprietary composition of functional
inactive ingredients. ACUROX™ Tablets are
intended to relieve moderate to severe pain while resisting or deterring
common methods of prescription drug abuse, including intravenous
injection of dissolved tablets, nasal snorting of crushed tablets and
intentional swallowing of excessive numbers of tablets. ACUROX™
is a proposed brand name subject to FDA approval.
About CORVUE™
CORVUE™, a selective adenosine A2a receptor
agonist, is being developed as an alternative to exercise prior to
cardiac perfusion imaging for the diagnosis of coronary artery disease.
CORVUE™ is designed to minimize side effects
such as dyspnea, nausea, heart block, flushing and chest pain. For ease
of administration, CORVUE™ is being developed
for dosing as a single IV injection with a fast onset while providing a
sufficient duration of coronary blood vessel dilation for flexibility in
diagnostic imaging. CORVUE™ is an
investigational drug that has not been approved by the FDA.
Additionally, CORVUE™ is a proposed brand
name subject to FDA approval.
Webcast Information
King will conduct a webcast today which may include discussion of the
Company’s marketed products, pipeline,
strategy for growth, financial results and expectations, and other
matters relating to its business. Interested persons may listen to the
webcast on Thursday, May 8, 2008, at 11:00 a.m., E.D.T., by clicking the
following link to register and then joining the live event with the same
URL:
http://www.kingpharm.com/web_casts.asp
If you are unable to participate during the live event, the webcast will
be archived on King’s web site at the same
link for not less than 30 days after the webcast.
About Special Items
Under Generally Accepted Accounting Principles ("GAAP”),
reported "net earnings”
and "diluted earnings per share”
include special items. In addition to the reported results determined in
accordance with GAAP, King provides its net earnings and diluted
earnings per share results for the quarters ended March 31, 2008 and
2007, excluding special items. These non-GAAP financial measures exclude
special items which are those particular material income or expense
items that King considers to be unrelated to the Company’s
ongoing, underlying business, non-recurring, or not generally
predictable. Such items include, but are not limited to, merger and
restructuring expenses; non-capitalized expenses associated with
acquisitions, such as in-process research and development charges and
inventory valuation adjustment charges; charges resulting from the early
extinguishment of debt; asset impairment charges; expenses of drug
recalls; and gains and losses resulting from the divestiture of assets.
King believes the identification of special items enhances the analysis
of the Company’s ongoing, underlying business
and the analysis of the Company’s financial
results when comparing those results to that of a previous or subsequent
like period. However, it should be noted that the determination of
whether to classify an item as a special item involves judgments by King’s
management. A reconciliation of non-GAAP financial measures referenced
herein and King’s reported financial results
determined in accordance with GAAP is provided below.
About King Pharmaceuticals
King, headquartered in Bristol, Tennessee, is a vertically integrated
branded pharmaceutical company. King, an S&P 500 Index company, seeks to
capitalize on opportunities in the pharmaceutical industry through the
development, including through in-licensing arrangements and
acquisitions, of novel branded prescription pharmaceutical products in
attractive markets and the strategic acquisition of branded products
that can benefit from focused promotion and marketing and product
life-cycle management.
Forward-looking Statements
This release contains forward-looking statements which reflect management’s
current views of future events and operations, including, but not
limited to, statements pertaining to the expected timetable for REMOXY™,
ACUROX™ Tablets and
CORVUE™ NDA submissions with the FDA;
statements pertaining to the Company’s
expected SG&A expense and cash flow from operations in 2008; and
statements pertaining to the Company’s
planned webcast to discuss its first-quarter 2008 results. These
forward-looking statements involve certain significant risks and
uncertainties, and actual results may differ materially from the
forward-looking statements. Some important factors which may cause
actual results to differ materially from the forward-looking statements
include dependence on the future level of demand for and net sales of
King’s branded pharmaceutical products;
dependence on King’s ability to successfully
market its branded pharmaceutical products; dependence on King’s
ability to increase its presence in its targeted, specialty-driven
markets; dependence on King’s ability to
continue to acquire branded pharmaceutical products, including products
in development; dependence on King’s ability
to continue to successfully execute the Company’s
strategy and to continue to capitalize on strategic opportunities in the
future for sustained long-term growth; dependence on King’s
ability to successfully integrate its acquisitions; dependence on King’s
ability to control its SG&A expense as planned; dependence on whether
the Company encounters unexpected events which could affect its SG&A
expense; dependence on the Company’s ability
to continue to advance the development of its pipeline products as
planned; dependence on the high cost and uncertainty of research,
clinical trials, and other development activities involving
pharmaceutical products in which King has an interest; dependence on
whether the NDAs for REMOXY™,
ACUROX™ Tablets and
CORVUE™ are submitted to the FDA during the
planned timeframe; dependence on the unpredictability of the duration
and results of the FDA’s review of
Investigational New Drug applications ("IND”),
NDAs, and Abbreviated New Drug Applications ("ANDA”)
and/or the review of other regulatory agencies worldwide that relate to
projects in King’s development pipeline;
dependence on the availability and cost of raw materials; dependence on
no material interruptions in supply by contract manufacturers of King’s
products; dependence on the potential effect on sales of the Company’s
existing branded pharmaceutical products as a result of the potential
development and approval of a generic substitute for any such product or
other new competitive products; dependence on the potential effect of
future acquisitions and other transactions pursuant to the Company’s
growth strategy; dependence on King’s
compliance with FDA and other government regulations that relate to the
Company’s business; dependence on King’s
ability to conduct its webcast as currently planned on May 8, 2008;
dependence on changes in general economic and business conditions;
changes in current pricing levels; changes in federal and state laws and
regulations; changes in competition; unexpected changes in technologies
and technological advances; and manufacturing capacity constraints.
Other important factors that may cause actual results to differ
materially from the forward-looking statements are discussed in the "Risk
Factors” section and other sections of King’s
Form 10-K for the year ended December 31, 2007, which is on file with
the U.S. Securities and Exchange Commission. King does not undertake to
publicly update or revise any of its forward-looking statements even if
experience or future changes show that the indicated results or events
will not be realized.
KING PHARMACEUTICALS, INC.
CONSOLIDATED BALANCE SHEETS
(in thousands, except share data)
March 31,
December 31,
2008
2007
ASSETS
Current assets:
Cash and cash equivalents
$
826,582
$
20,009
Investments in debt securities
589,107
1,344,980
Marketable securities
1,589
1,135
Accounts receivable, net
186,787
183,664
Inventories
110,561
110,308
Deferred income tax assets
95,836
100,138
Income tax receivable
-
20,175
Prepaid expenses and other current assets
40,311
39,245
Total current assets
1,850,773
1,819,654
Property, plant and equipment, net
264,789
257,093
Intangible assets, net
733,847
780,974
Goodwill
129,150
129,150
Deferred income tax assets
351,983
343,700
Other assets
88,827
96,251
Total assets
$
3,419,369
$
3,426,822
LIABILITIES AND SHAREHOLDERS’ EQUITY
Current liabilities:
Accounts payable
$
59,342
$
76,481
Accrued expenses
293,304
376,604
Income taxes payable
17,180
-
Total current liabilities
369,826
453,085
Long-term debt
400,000
400,000
Other liabilities
62,331
62,980
Total liabilities
832,157
916,065
Commitments and contingencies
Shareholders’ equity:
Common shares no par value, 600,000,000 shares authorized,
246,544,435 and 245,937,709 shares issued and outstanding,
respectively
1,290,079
1,283,440
Retained earnings
1,312,993
1,225,360
Accumulated other comprehensive (loss) income
(15,860
)
1,957
Total shareholders’ equity
2,587,212
2,510,757
Total liabilities and shareholders’
equity
$
3,419,369
$
3,426,822
KING PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share data)
(Unaudited)
Three Months Ended
March 31,
2008
2007
REVENUES:
Total revenues
$
432,033
$
516,030
OPERATING COSTS AND EXPENSES:
Cost of revenues, exclusive of depreciation and amortization shown
below
91,461
111,454
Selling, general and administrative, exclusive of co-promotion fees
109,041
121,210
Special legal and professional fees
2,860
1,144
Co-promotion fees
17,957
45,958
Total selling, general, and administrative expense
129,858
168,312
Depreciation and amortization
59,075
34,178
Accelerated depreciation
623
1,500
Research and development
28,508
32,271
Restructuring charges
1,059
460
Total operating costs and expenses
310,584
348,175
OPERATING INCOME
121,449
167,855
OTHER INCOME:
Interest expense
(1,804
)
(2,025
)
Interest income
13,629
9,266
Other, net
(704
)
(543
)
Total other income
11,121
6,698
INCOME FROM CONTINUING OPERATIONS BEFORE INCOME TAXES
132,570
174,553
Income tax expense
44,937
58,499
INCOME FROM CONTINUING OPERATIONS
87,633
116,054
DISCONTINUED OPERATIONS
Loss from discontinued operations
-
(220
)
Income tax benefit
-
(79
)
Total loss from discontinued operations
-
(141
)
NET INCOME
$
87,633
$
115,913
Basic net income per common share
$
0.36
$
0.48
Diluted net income per common share
$
0.36
$
0.48
Shares used in basic net income per share
243,290
242,390
Shares used in diluted net income per share
244,689
243,671
KING PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS
EXCLUDING SPECIAL ITEMS - NON GAAP
(in thousands, except per share data)
(Unaudited)
Three Months Ended
March 31,
2008
2007
REVENUES:
Total revenues
$
432,033
$
516,030
OPERATING COSTS AND EXPENSES:
Cost of revenues , exclusive of depreciation and amortization shown
below
91,461
111,454
Selling, general and administrative, exclusive of co-promotion fees
109,041
121,210
Co-promotion fees
17,957
45,958
Total selling, general, and administrative expense
126,998
167,168
Depreciation and amortization
59,075
34,178
Research and development
28,508
32,271
Total operating costs and expenses
306,042
345,071
OPERATING INCOME
125,991
170,959
OTHER INCOME:
Interest expense
(1,804
)
(2,025
)
Interest income
13,629
9,266
Other, net
(704
)
(543
)
Total other income
11,121
6,698
INCOME BEFORE INCOME TAXES
137,112
177,657
Income tax expense
46,644
59,659
NET INCOME
$
90,468
$
117,998
Basic net income per common share
$
0.37
$
0.49
Diluted net income per common share
$
0.37
$
0.48
Shares used in basic net income per share
243,290
242,390
Shares used in diluted net income per share
244,689
243,671
KING PHARMACEUTICALS, INC.
RECONCILIATION OF NON-GAAP MEASURES
(in thousands, except per share data)
(Unaudited)
The following tables reconcile Non-GAAP measures to amounts reported
under GAAP:
Three Months Ended March 31, 2008
EPS
Net income, excluding special items
$
90,468
Diluted income per common share, excluding special items
$
0.37
SPECIAL ITEMS:
Special legal and professional fees (selling, general, and
administrative)
(2,860
)
(0.01
)
Accelerated depreciation (other operating costs and expenses)
(623
)
(0.00
)
Restructuring charges (other operating costs and expenses)
(1,059
)
(0.01
)
Total special items before income taxes
(4,542
)
(0.02
)
Income tax benefit from special items
1,707
0.01
Net income
$
87,633
Diluted income per common share, as reported under GAAP
$
0.36
Three Months Ended March 31, 2007
EPS
Net income, excluding special items
$
117,998
Diluted income per common share, excluding special items
$
0.48
SPECIAL ITEMS:
Special legal and professional fees (selling, general, and
administrative)
(1,144
)
(0.00
)
Accelerated depreciation (other operating costs and expenses)
(1,500
)
(0.01
)
Restructuring charges (other operating costs and expenses)
(460
)
(0.00
)
Loss from discontinued operations
(220
)
(0.00
)
Total special items before income taxes
(3,324
)
(0.01
)
Income tax benefit from special items
1,239
0.01
Net income
$
115,913
Diluted income per common share, as reported under GAAP
$
0.48
KING PHARMACEUTICALS, INC. SUMMARY RECONCILIATION OF SPECIAL ITEMS FOR THE FIRST QUARTERS ENDED MARCH 31, 2008 AND 2007
King recorded special items during the first quarter ended March 31,
2008 resulting in a net charge of $5 million, or $3 million net of tax,
primarily due to professional fees associated with previously disclosed
government inquiries and private plaintiff securities litigation.
During the first quarter ended March 31, 2007, King recorded special
items resulting in a net charge of $3 million, or $2 million net of tax,
primarily due to accelerated depreciation and restructuring charges in
connection with the transfer of the production of LEVOXYL®
from the Company’s St. Petersburg, Florida
facility to its Bristol, Tennessee facility.
EXECUTIVE OFFICES KING PHARMACEUTICALS, INC. 501 FIFTH STREET, BRISTOL, TENNESSEE 37620
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