Recent Highlights
- 2005 nine-month financial highlights:
- Total revenue increased 11 percent to $752 million
- Worldwide Synagis(R) sales increased 16 percent to $624 million
- Net earnings grew to $6 million, or $0.02 per diluted share
- Bought out Abbott's U.S. Synagis co-promotion rights following
2005-2006 RSV season
- CAIV-T, the refrigerator-stable formulation of FluMist(R), submitted
to FDA for approval
- Phase 2 anti-Staphylococcal antibody program in-licensed from
GlaxoSmithKline
- Pipeline expanded through acquisition of Cellective Therapeutics, new
collaborations with VasGene Therapeutics and Avidia, and in-licensing
of technology from Georgetown University
- Collaboration with NIH formalized to develop pandemic influenza
vaccines
- IND submitted for antibody targeting interferon-alpha as a potential
lupus treatment
- Repurchased $106 million of common stock in the first nine months of
2005
GAITHERSBURG, Md., Oct. 20 /PRNewswire-FirstCall/ -- MedImmune, Inc.
(Nasdaq: MEDI) announced today that for the 2005 third quarter, total revenue
increased to $154 million from $93 million in the 2004 third quarter. Revenue
growth in the 2005 third quarter was primarily driven by a 66-percent increase
of worldwide sales of Synagis (palivizumab) to $101 million, from $61 million
in the 2004 third quarter. Sales of Synagis in the U.S. for the 2005 third
quarter were $43 million versus $42 million in the 2004 quarter while
international sales of Synagis to Abbott in the 2005 quarter were $58 million
versus $19 million in the 2004 quarter. Changes in sales of Synagis in the
third quarter primarily reflect fluctuations in stocking patterns by
distributors and wholesalers in advance of the respiratory syncytial virus
(RSV) season. Worldwide sales of Ethyol(R) (amifostine) in the 2005 third
quarter increased 15 percent to $25 million from $21 million in the 2004
quarter. Sales of FluMist(R) (influenza virus vaccine live, intranasal) and
CytoGam(R) (cytomegalovirus immune globulin intravenous (human)) were
$10 million each for the 2005 third quarter. In the 2004 third quarter, sales
of CytoGam were $11 million, while last season's shipments of FluMist did not
begin until the fourth quarter.
Total revenue for the first nine months of 2005 grew 11 percent to
$752 million from $675 million in the first nine months of 2004. The growth in
revenues is primarily due to a 16-percent increase in worldwide sales of
Synagis in 2005 to $624 million from $539 million in the 2004 period. Sales of
Synagis in the U.S. in the 2005 period increased 11 percent to $526 million
from $472 million in the 2004 period. International sales of Synagis to Abbott
grew 46 percent in the first nine months of 2005 to $98 million from
$67 million in the first nine months of 2004. Worldwide sales of Ethyol and
CytoGam in the first nine months of 2005 were $70 million and $32 million,
respectively, compared to $71 million and $28 million, respectively, in the
first nine months of 2004. Sales of FluMist in the first nine months of 2005
totaled $13 million compared to $27 million in the 2004 period. FluMist sales
recorded in the first nine months of 2004 were from sales recognized in the
first and second quarters of 2004 for vaccine distributed for the 2003-2004
flu season.
"In the first nine months of 2005, we have made substantial progress
toward achieving our long term objectives," stated David M. Mott, president
and chief executive officer. "Buying out Abbott's U.S. Synagis co-promotion
rights, increasing our financial participation in the ex-U.S. markets through
our expanded distribution agreement with Abbott outside the U.S. and amending
our HPV vaccine license agreement with GlaxoSmithKline to enable the
cross-licensing of Merck together have the potential to drive our financial
growth over the next several years. The maturation of our late stage R&D
pipeline and the substantial expansion of our overall R&D portfolio promise to
drive longer term growth. And the investments we are making in building the
leadership team, the facilities and the systems ensure that we are building
the business on a strong foundation."
In connection with the dissolution in last year's second quarter of
MedImmune's relationship with Wyeth for the development and marketing of the
company's influenza vaccine technology, certain charges impacted results for
2004 and 2005. In the discussion below, MedImmune has provided the overall
results for both the third quarter and nine months ended September 30 with and
without the impact of these charges, as well as a reconciliation in the
accompanying schedules so that the underlying trends in the operations of the
business can be more readily identified.
Additional Results for the 2005 Third Quarter
For the third quarter of 2005, MedImmune reported a net loss of
$64 million, or $0.26 per share, compared to a net loss of $65 million, or
$0.26 per share, for the third quarter of 2004. Excluding the charges
associated with the termination of the Wyeth agreements, the net loss for the
2005 third quarter was $61 million, or $0.25 per share, compared to
$55 million, or $0.22 per share, in the 2004 quarter. MedImmune's quarterly
results are heavily impacted by the seasonal use of two of its four marketed
products, Synagis and FluMist, both of which are used to help prevent serious
respiratory viruses that most commonly occur in the fall and winter months.
Gross margins on product sales were 67 percent in the 2005 quarter and
56 percent in the 2004 quarter. Excluding the impact of FluMist, gross margins
were 72 percent in the 2005 third quarter and 69 percent in the 2004 second
quarter, primarily reflecting the favorable impact of higher international
sales of Synagis during the 2005 third quarter, as well as a $4.9 million
recoupment of past royalty overpayments that was recognized as a reduction to
cost of sales during the 2005 third quarter. Gross margins for FluMist reduced
overall gross margins by five percentage points in the 2005 quarter and
13 percentage points in the 2004 third quarter. The lower negative impact of
FluMist on gross margins for the 2005 third quarter was due primarily to
reduced production costs and the anticipated ability to utilize certain
semi-finished inventory components for the next production season.
Research and development (R&D) expenses increased to $119 million in the
2005 quarter from $73 million in the 2004 quarter. The growth in R&D expenses
is primarily due to a higher level of activity from new and ongoing
collaboration agreements, preclinical research and process development
activities and clinical trials for product candidates, including Numax and
CAIV-T. Included in the 2005 quarter were upfront fees and milestones payments
under licensing agreements and research collaborations totaling $36 million,
including collaborations with GlaxoSmithKline for the anti-Staphylococcal
antibody collaboration and VasGene Therapeutics for the EphB4 and EphrinB2, as
compared to upfront fees and milestones payments of approximately $1 million
in the prior year quarter.
Selling, general and administrative (SG&A) costs increased to $81 million
in the 2005 third quarter from $68 million in the 2004 quarter. The increase
is due primarily to the 2005 expansion of the pediatric commercial
organization, new marketing and medical education programs related to Synagis
and FluMist, and amortization expense of $3.9 million associated with the
intangible asset that was recorded during the 2005 third quarter as a result
of reacquiring full promotion rights for Synagis in the U.S., effective July
2006.
The effective tax rate used to calculate the benefit for income taxes
associated with the 2005 third quarter pretax loss was 29 percent compared to
37 percent in the 2004 period. During the quarter, the company made a
correction to the prior accounting for the reversal of approximately
$5 million of valuation allowances associated with the utilization of certain
acquired income tax carryforwards. The correction was comprised of relatively
small amounts related to reporting periods dating back to the acquisition of
Aviron in January 2002. The correction reduced the amount of benefit available
from income taxes in the quarter on the income statement and also reduced
goodwill on the balance sheet, both by approximately $5 million.
Additional Results for Nine-Month Period Ended September 30, 2005
For the first nine months of 2005, MedImmune reported net income of
$6 million, or $0.02 per diluted share, compared to net loss of $54 million,
or $0.22 per share in the first nine months of 2004. Excluding the charges
associated with the termination of the Wyeth agreements, MedImmune's net
earnings in the first nine months of 2005 were $10 million, or $0.04 per
diluted share, compared to $27 million or $0.11 per diluted share in the 2004
period.
Gross margins on product sales for the 2005 nine-month period were
73 percent compared to 65 percent for the corresponding 2004 period. Excluding
the impact of FluMist, gross margins were 75 percent and 74 percent in the
first nine months of 2005 and 2004 respectively. Gross margins for FluMist
reduced overall gross margins by two percentage points for the 2005 nine-month
period and by nine percentage points for the 2004 nine-month period. The lower
negative impact of FluMist on gross margins for the 2005 nine-month period was
due primarily to lower manufacturing cost estimates for the 2005-2006
influenza season and the ability to utilize certain semi-finished inventory
components for the next production season.
R&D expenses for the first nine months of 2005 were $266 million versus
$179 million in the 2004 period. The increase in R&D expenses is due to new
and ongoing collaboration activities, preclinical research and process
development activities and clinical trials for product candidates, including
Numax and CAIV-T. Included in the 2005 nine-month period were upfront and
milestone payments totaling approximately $42 million, compared to $4 million
in the prior year period. MedImmune's R&D expenditures in the first nine
months of 2005 were 36 percent of product sales versus 27 percent in the
comparable 2004 period, reflecting the continuing investment to bring new
products to market as part of the company's long-range plan.
SG&A expenses in the 2005 nine-month period increased to $300 million from
$250 million in the 2004 nine-month period, due primarily to additional costs
associated with expanding the pediatric sales organization, increased
co-promotion expenses related to sales of Synagis in the U.S. and amortization
expense of $3.9 million associated with the intangible asset that was recorded
during the 2005 third quarter as a result of reacquiring full promotion rights
for Synagis in the U.S., effective July 2006.
The effective tax rate used to calculate income tax expense for the 2005
nine-month period was 65 percent compared to the effective rate of 34 percent
used to calculate the benefit from income taxes in the 2004 period. The
correction to the prior accounting for reversal of the valuation allowances
discussed above increased income tax expense, which also had the impact of
increasing the effective tax rate for the nine-month period.
Cash and marketable securities at September 30, 2005 were $1.4 billion as
compared to $1.7 billion at December 31, 2004. The decrease is primarily due
to payments related to the amended Abbott agreement, upfront fees and
milestone payments related to collaborations and licensing agreements, and
repurchases of approximately four million shares of our common stock at a
total cost of $106 million.
Looking Ahead in 2005
On February 3, 2005, MedImmune provided its overall financial guidance for
2005. On August 31, the company reduced its earnings-per-share guidance by
$0.10 to $0.11 to a range of $0.24 to $0.30 based upon the revised
co-promotion agreement with Abbott that had the impact in 2005 of primarily
increasing selling, general and administrative costs. On September 14, 2005,
the company further updated its earnings-per-share guidance with the
acquisition of Cellective Therapeutics. This transaction, which closed on
October 14, will result in a one-time nondeductible in-process research and
development (IPR&D) charge in the fourth quarter that is expected to reduce
the company's 2005 diluted earnings-per-share by approximately $0.20 to a
range of $0.04 to $0.10. The effective tax rate for the year is expected to be
approximately 94 percent. Were we to exclude the impact of the nondeductible
IPR&D charge for Cellective, the effective rate would be approximately
43 percent. Today, MedImmune is reconfirming the guidance given in February
2005 for revenues, gross margin and R&D expenses, and reconfirms the revised
guidance given in September 2005 for earnings per share. The company's
guidance is provided as a convenience to investors. Guidance and objectives
provided by the company are forward-looking statements and are based upon
numerous assumptions, many of which MedImmune cannot control and that may not
develop as MedImmune expects. For a discussion of the risks associated with
these projections, see the Disclosure Notice below.
Conference Call & Webcast
MedImmune is offering a live webcast of a discussion by MedImmune
management of its earnings and other business results on Thursday, October 20,
2005 at 8:00 a.m. eastern time. The live webcast may be accessed in the
investor section of MedImmune's website, http://www.medimmune.com. A replay of
the webcast will also be available via the MedImmune website until October 27,
2005. An audio replay of the webcast will be available beginning at 10:00 a.m.
eastern time on October 20, 2005 and ending at midnight October 27, 2005 by
calling (888) 286-8010. The passcode for the audio replay is 91740140.
About MedImmune, Inc.
MedImmune strives to provide better medicines to patients, new medical
options for physicians, rewarding careers to employees, and increased value to
shareholders. Dedicated to advancing science and medicine to help people live
better lives, the company is focused on the areas of infectious disease,
cancer and inflammatory diseases. With more than 2,000 employees worldwide,
MedImmune is headquartered in Maryland. For more information, visit the
company's website.
DISCLOSURE NOTICE: This announcement contains historical financial
information as of and for the three-month and nine-month periods ended
September 30, 2005 and September 30, 2004 that is unaudited and certain
audited balance sheet information as of December 31, 2004. MedImmune assumes
no obligation to update this information based on new information or future
performance except as may be specifically required by applicable law or
regulation.
This announcement also contains forward-looking statements regarding
MedImmune's future financial performance and business prospects. Those
statements involve substantial risks and uncertainties and are present in the
section captioned "Looking Ahead in 2005," as well as other sections
containing statements with words such as "anticipate," "believe," "estimate,"
"expect," "intend," "project" or other terms of similar meaning. Those
statements reflect management's current beliefs and are based on numerous
assumptions, which MedImmune cannot control and which may not develop as
MedImmune expects for reasons set forth in MedImmune's Annual Report on Form
10-K for the year ended December 31, 2004, its subsequent quarterly reports on
Form 10-Q, its current reports on Form 8-K filed for events occurring in 2005
and other public disclosures and filings with the U.S. Securities and Exchange
Commission. Consequently, actual results may differ materially from those
projected in the forward-looking statements.
MedImmune is also developing several products for potential future
marketing and the overall success of these development efforts is important
for the company's long-term prospects. There can be no assurance that such
development efforts will succeed, that such products will receive required
regulatory clearance or that, even if such regulatory clearance is received,
such products will ultimately achieve commercial success.
This press release, including the reconciliation of certain data presented
in this release to their most comparable GAAP measures, can be found on
MedImmune's website at http://www.medimmune.com in the box marked "News" or
with the archived press releases on the Investor Summary page.
MedImmune, Inc.
Consolidated Statements of Operations (Unaudited)
(in millions, except per share data)
Three Months Ended Nine Months Ended
September 30, September 30,
2005 2004 2005 2004
Revenues:
Product sales $146.0 $92.3 $739.4 $666.2
Other revenue 7.6 0.4 12.5 9.1
153.6 92.7 751.9 675.3
Costs and expenses:
Cost of sales 48.7 40.4 196.5 235.9
Research and development 118.6 72.6 265.8 179.5
Selling, general and
administrative (1) 81.1 67.9 299.5 249.7
Other operating expenses 3.8 2.4 9.3 6.3
Impairment of intangible asset - - - 73.0
Acquired in-process research
and development (IPR&D) 4.7 3.8 4.7 28.5
Technology transfer and
transition expenses 0.5 12.0 1.9 23.5
257.4 199.1 777.7 796.4
Interest income, net 12.8 15.3 43.2 43.7
Gain (loss) on investment
activities 0.4 (12.0) (0.5) (4.7)
Earnings (loss) before
income taxes (90.6) (103.1) 16.9 (82.1)
Provision (benefit) for
income taxes (26.5) (38.1) 11.1 (27.8)
Net earnings (loss) $(64.1) $(65.0) $5.8 $(54.3)
Basic earnings (loss)
per share $(0.26) $(0.26) $0.02 $(0.22)
Shares used in computing
basic earnings (loss)
per share 245.9 248.9 247.1 248.6
Diluted earnings (loss)
per share (2) $(0.26) $(0.26) $0.02 $(0.22)
Shares used in computing
diluted earnings (loss)
per share (2) 245.9 248.9 249.4 248.6
(1) In August 2005, the Company amended its co-promotion agreement with
Abbott Laboratories ("Abbott") for sales of Synagis(R) in the United
States. In connection with this transaction, the Company recorded an
intangible asset of $360.4 million which represents the fair value of
the exclusive promotion rights, determined as the aggregate value of
the probable additional payments to be made as a result of the
amended terms of the agreement in excess of the value of the co-
promotion services to be rendered, as determined under the previous
agreement. Amortization expense of $3.9 million was recognized
during the third quarter of 2005, and is included in selling, general
& administrative expense in the consolidated statement of operations.
(2) In accordance with EITF No. 04-8, "The Effect of Contingently
Convertible Debt on Diluted Earnings per Share," which became
effective during the fourth quarter of 2004, the company's 1%
Convertible Senior Notes, which represent 7.3 million potential
shares of common stock, are now included in diluted earnings per
share using the if-converted method, regardless of whether the market
price trigger has been met, unless the effect is anti-dilutive. For
all periods presented, the 1% Convertible Senior Notes were excluded
from dilutive earnings per share as they were anti-dilutive.
MedImmune, Inc.
Consolidated Statements of Operations (Unaudited)
(in millions, except per share data)
Presented in the following table is a reconciliation of reported net
earnings (loss) under GAAP to net earnings (loss) excluding items related to
the termination of the Wyeth collaboration for FluMist during 2004. The
transition activities associated with Wyeth's exit from the collaboration are
substantially complete. MedImmune's management excludes the impact of the
charges associated with the termination of the Wyeth collaboration when
evaluating the company's ongoing performance, and provides the following
reconciliation to aid investors in their understanding of underlying
performance trends.
Three Months Ended Nine Months Ended
September 30, September 30,
2005 2004 2005 2004
Item:
Net earnings (loss),
as reported (1) $(64.1) $(65.0) $5.8 $(54.3)
Impairment of intangible
asset (2) - - - 73.0
Acquired in-process research
and development (3) 4.7 3.8 4.7 28.5
Technology transfer and
transition expenses (4) 0.5 12.0 1.9 23.5
Income taxes (5) (1.9) (5.9) (2.4) (43.8)
Net earnings (loss),
as adjusted $(60.8) $(55.1) $10.0 $26.9
Basic earnings (loss)
per share, as reported (0.26) (0.26) 0.02 (0.22)
Diluted earnings (loss)
per share, as reported (0.26) (0.26) 0.02 (0.22)
Basic earnings (loss)
per share, as adjusted (0.25) (0.22) 0.04 0.11
Diluted earnings (loss)
per share, as adjusted (6) (0.25) (0.22) 0.04 0.11
Shares used to compute earnings
(loss) per share:
Basic, as reported 245.9 248.9 247.1 248.6
Diluted, as reported 245.9 248.9 249.4 248.6
Basic, as adjusted 245.9 248.9 247.1 248.6
Diluted, as adjusted 245.9 248.9 249.4 251.1
(1) Prepared in accordance with accounting principles generally accepted
in the United States (GAAP).
(2) Represents the addback of the noncash impairment charge associated
with the termination of our collaboration with Wyeth for the
unamortized portion of the intangible asset initially recorded upon
our acquisition of MedImmune Vaccines, Inc.
(3) Represents the addback of the portion of the amounts paid to Wyeth
for the reacquisition of the influenza vaccines franchise that was
allocated to in-process research and development (IPR&D).
(4) Represents the addback of the payments for certain transition
activities, largely comprised of amounts paid to Wyeth for the
manufacture of CAIV-T clinical trial materials, transition of
clinical trial data, and transfer of manufacturing technology
knowledge.
(5) Represents the adjustment to income taxes associated with the
impairment of intangible asset, IPR&D and the technology transfer and
transition charges.
(6) The convertible notes were anti-dilutive for all periods presented.
MedImmune, Inc.
Condensed Consolidated Balance Sheets
(in millions)
September 30, December 31,
2005 2004
(unaudited)
Assets:
Cash and marketable securities $1,419.4 $1,706.1
Trade and contract receivables, net 141.5 206.6
Inventory, net 91.7 64.1
Deferred taxes, net 179.0 177.9
Property and equipment, net 354.8 310.9
Goodwill and intangible assets, net (1) 383.0 37.9
Other assets 65.3 60.9
$2,634.7 $2,564.4
Liabilities and shareholders' equity:
Accounts payable $64.8 $15.1
Accrued expenses 143.4 337.3
Other liabilities (1) 331.0 30.3
Debt 506.4 507.1
Shareholders' equity 1,589.1 1,674.6
$2,634.7 $2,564.4
Common shares outstanding 245.7 248.5
(1) In August 2005, the Company amended its co-promotion agreement with
Abbott for sales of Synagis(R) in the United States. In connection
with this transaction, the Company recorded an intangible asset of
$360.4 million which represents the fair value of the exclusive
promotion rights, determined as the aggregate value of the probable
additional payments to be made as a result of the amended terms of
the agreement in excess of the value of the co-promotion services to
be rendered, as determined under the previous agreement. In
addition, certain of the additional payments under the agreement
totaling $290.4 million that the Company deems probable have been
aggregated and recorded as liabilities in the consolidated balance
sheet.
SOURCE MedImmune, Inc.
CONTACT:
Investors:
Peter Vozzo, +1-301-398-4358
John Filler,
+1-301-398-4086
Media:
Jamie Lacey, +1-301-398-4035
all for MedImmune,
Inc.