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PDL BioPharma Announces First Quarter 2009 Financial Results
- Revenues From Continuing Operations Increase 25 Percent to
- Conference Call Today at
Total revenues from continuing operations for the first quarter of 2009 were
"We were pleased to begin fulfilling the goal of income distribution to stockholders by paying our first post-spin-off dividend in April, a result of the revenues and profits PDL is generating from royalties on a diversified portfolio of successful products," said
Total general and administrative expenses from continuing operations in the first quarter of 2009 were
Net income for the first quarter of 2009 was
Net cash provided by operating activities was
2009 Dividends
PDL previously announced that it would pay two dividends to its stockholders in 2009 of
Recent Developments
-- Elected Frederick Frank and Jody Lindell to the Company's Board of
Directors in March 2009 and subsequently designated Mr. Frank as Lead
Director.
-- As a result of the April 1, 2009 dividend payment, we announced
An adjustment to the conversion rate for the Company's 2.75%
Convertible Subordinated Notes due August 16, 2023 (the "2023 Notes").
The conversion rate, as adjusted, is 123.715 shares of common stock per
$1,000 principal amount of the 2023 Notes, effective March 17, 2009.
The conversion rate for the 2023 Notes was previously 114.153 shares
of common stock per $1,000 principal amount of the 2023 Notes.
-- As a result of the April 1, 2009 dividend payment, we announced an
adjustment to the conversion rate for the Company's 2.00% Convertible
Senior Notes due February 15, 2012 (the "2012 Notes"). The conversion
rate, as adjusted, is 89.165 shares of common stock per $1,000
principal amount of the 2012 Notes, effective March 17, 2009. The
conversion rate for the 2012 Notes was previously 82.162 shares of
common stock per $1,000 principal amount of the 2012 Notes.
-- Alexion agreed to pay PDL $25 million, of which it paid $12.5 million
in January 2009 and is obligated to pay the second installment of
$12.5 million in June 2009.
-- In February of 2009, we received a letter from MedImmune asserting that
it may be entitled to pay a lower royalty rate on sales of Synagis
because of our settlement with Alexion. In April of 2009, we sent a
letter notifying MedImmune of the exercise of certain of our rights
under our license agreement, the exercise of which we believe precludes
MedImmune from being entitled to a lower royalty rate based on the
Alexion settlement.
-- Approval for Raptiva(R) was suspended in the European Union and in
Canada in February of 2009 and product was withdrawn from the U.S.
market in April of 2009 because of safety concerns. In 2008, royalties
attributable to sales of Raptiva were $3.9 million or 1.3% of total
revenue from continuing operations.
2009 Financial Guidance
PDL reaffirms its previous revenue guidance and continues to anticipate strong revenue growth in 2009 increasing from 2008 to a range of
PDL continues to expect its general and administrative expenses for 2009 to range from
Conference Call Details
To access the live conference call today,
To access the live and subsequently archived webcast of the conference call, go to the company's Web site at http://www.pdl.com and click "Investors." Please connect to the web site at least 15 minutes prior to the call to allow for any software download that may be necessary.
About PDL BioPharma
PDL BioPharma, Inc. pioneered the humanization of monoclonal antibodies and, by doing so, enabled the discovery of a new generation of targeted treatments for cancer and autoimmune diseases. PDL is focused on maximizing the value of our antibody humanization patents and related assets. PDL receives royalties on sales of a number of humanized antibody products marketed today and also may receive royalty payments on additional humanized antibody products launched before patent expiry in late 2014. This press release and further information about PDL BioPharma, Inc. can be found at www.pdl.com.
Forward-looking Statements
This press release contains forward-looking statements, including regarding PDL's expectations with respect to its 2009 royalty revenues, expenses, net income and cash provided by operating activities.
Each of these forward-looking statements involves risks and uncertainties. Actual results may differ materially from those, express or implied, in these forward-looking statements. Factors that may cause differences between current expectations and actual results include, but are not limited to, the following:
-- The expected rate of growth in royalty-bearing product sales by PDL's
existing licensees;
-- The relative mix of royalty-bearing products manufactured and sold
outside the U.S. versus manufactured or sold in the U.S.;
-- The ability of our licensees to receive regulatory approvals to
market and launch new
royalty-bearing products and whether such products, if launched, will
be commercially successful;
-- Changes in any of the other assumptions on which PDL's projected
royalty revenues are based;
-- The outcome of pending litigation or disputes; and
-- The failure of licensees to comply with existing license agreements,
including any failure to pay royalties due.
Other factors that may cause PDL's actual results to differ materially from those expressed or implied in the forward-looking statements in this press release are discussed in PDL's filings with the SEC, including the "Risk Factors" sections of its annual and quarterly reports filed with the SEC. Copies of PDL's filings with the SEC may be obtained at the "Investors" section of PDL's website at www.pdl.com. PDL expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in PDL's expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based for any reason, except as required by law, even as new information becomes available or other events occur in the future. All forward-looking statements in this press release are qualified in their entirety by this cautionary statement.
NOTE: PDL BioPharma and the PDL BioPharma logo are considered trademarks of PDL BioPharma, Inc.
~financial statements to follow~
PDL BIOPHARMA, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share amounts)
(unaudited)
Three Months Ended March 31,
2009 2008
Revenues $62,622 $50,205
General and administrative expenses 4,693 12,709
Operating income 57,929 37,496
Interest and other income, net 336 4,864
Interest expense (3,574) (3,555)
Income from continuing
operations before income
taxes 54,691 38,805
Income tax expense 17,234 1,034
Income from continuing
operations 37,457 37,771
Loss from discontinued
operations, net of income
taxes (1) - (99,646)
Net income (loss) $37,457 $(61,875)
Income (loss) per basic share
Continuing operations $0.31 $0.32
Discontinued operations - (0.85)
Net income (loss) per basic
share $0.31 $(0.53)
Income (loss) per diluted
share
Continuing operations $0.23 $0.29
Discontinued operations - (0.71)
Net income (loss) per diluted
share $0.23 $(0.42)
Cash dividends declared per
common share $1.00 $-
Shares used to compute income
(loss) per basic share 119,327 117,525
Shares used to compute income
(loss) per diluted share 172,570 141,232
(1) The financial results associated with both PDL's former
commercial operations which were sold in March 2008 and PDL's
former biotechnology operations which were spun off in December
2008 have been presented as discontinued operations for the three
months ended March 31, 2008.
PDL BIOPHARMA, INC.
CONDENSED CONSOLIDATED BALANCE SHEET DATA
(in thousands)
(unaudited)
March 31, December 31,
2009 2008
Cash, cash equivalents,
short-term investments
and restricted cash $193,192 $147,527
Total assets $219,065 $191,142
Total stockholders'
deficit $(422,297) $(352,569)
PDL BIOPHARMA, INC.
CONDENSED CONSOLIDATED STATEMENT OF CASH FLOW DATA
(in thousands)
(unaudited)
Three Months Ended
March 31,
2009 2008
Net income (loss) $37,457 $(61,875)
Adjustments to reconcile net income
(loss) to net cash provided by (used
in) operating activities (3,596) 33,769
Changes in assets and liabilities (6,148) (1,225)
Net cash provided by (used in) operating
activities $27,713 $(29,331)
PDL BIOPHARMA, INC.
SUPPLEMENTAL INFORMATION ON DISCONTINUED OPERATIONS (1)
(in thousands)
(unaudited)
Biotechnology Operations Three Months
Ended March 31,
2009 2008
Net revenues $- $7,124
Total costs and expenses - (15,325)
Income tax expense (benefit) - (30)
Loss from discontinued operations $- $(8,171)
Commercial Operations Three Months
Ended March 31,
2009 2008
Net revenues $- $39,359
Total costs and expenses - (102,807)
Income tax expense (benefit) - 28,027
Loss from discontinued operations $- $(91,475)
(1) The financial results associated with both PDL's former
commercial operations which were sold in March 2008 and PDL's
former biotechnology operations which were spun off in December
2008 have been presented as discontinued operations for the
three months ended March 31, 2008.
SOURCE PDL BioPharma, Inc.













