Intercell AG to Acquire Iomai Corporation to Expand Late Stage Product Pipeline and Strengthen Leadership in Vaccine Innovation
13 Mai 2008 - 2:18AM
PR Newswire (US)
- Intercell AG ('Intercell') to acquire Iomai Corporation ('Iomai')
in a fully recommended share/cash transaction for USD 6.60 per
share of Iomai's common stock representing a fully diluted equity
value of Iomai of approximately USD 189 million (EUR 122 million).
Acquisition to be accomplished through stock-for-stock exchange for
approximately 41 percent of Iomai's current shares outstanding held
by major shareholders for approximately 1.7 million Intercell
shares (representing approximately four percent of Intercell's
total outstanding shares), and an all-cash merger for the remaining
fully diluted outstanding shares of Iomai's common stock for
approximately USD 119 million (EUR 77 million). VIENNA, Austria and
GAITHERSBURG, Md., May 12 /PRNewswire-FirstCall/ -- Intercell AG
(VSE: ICLL) and Iomai Corporation (NASDAQ:IOMI) announced today
that they have entered into a definitive agreement pursuant to
which Intercell will acquire Iomai for USD 6.60 per share
representing a fully diluted equity value of approximately USD 189
million (EUR 122 million). The transaction has been unanimously
approved by the Boards of Directors of both companies and is
subject to customary closing conditions including antitrust
clearances, clearance by the Committee on Foreign Investment in the
United States and the approval of the holders of a majority of
Iomai's shares. Shareholders holding over 50 percent of Iomai's
total shares outstanding have entered into agreements to vote in
favour of the combination. Intercell will gain full rights to
Iomai's late stage Travelers' Diarrhea vaccine which is based on
Iomai's proprietary needle-free patch delivery vaccine technology
and has shown positive interim Phase II efficacy data. The
Travelers' Diarrhea vaccine is expected to enter pivotal Phase III
trials in the first half of 2009. If approved, the medical use of
Iomai's Travelers' Diarrhea vaccine will be highly complementary
with Intercell's Japanese Encephalitis vaccine for which a
Biologics License Application was successfully submitted to the US
Food and Drug Administration in December 2007, and for which
Intercell expects market approvals in the US, Europe and Australia
in 2008. Together, both vaccines create an extremely attractive
Traveler's Vaccine franchise which will target a combined market
opportunity of over USD 1 billion in sales per year. Commenting on
the transaction, Gerd Zettlmeissl, CEO of Intercell, said: "This
transaction further expands our leadership in vaccine innovation,
greatly enhances Intercell's R&D technology base and further
strengthens our late stage vaccine portfolio. Building on our
proven experience in industrialization and in moving novel products
to the market, Intercell is fully committed to becoming the leading
pure play vaccine company globally. We look forward to welcoming
Iomai's employees to Intercell and are excited by the potential of
the combined group to create significant value for all
stakeholders." Stanley C. Erck, President and CEO of Iomai, said:
"We have built a dynamic and scientifically driven organisation.
This strategic combination with Intercell will create a stronger,
more diversified vaccine company and will accelerate the
development of Iomai's vaccine programs and fully leverage our
innovative TCI technology. We believe this transaction is in the
best interest of all parties, including shareholders, employees and
ultimately patients." Intercell will also gain full rights to two
additional clinical and three preclinical programs under
development, the most advanced being an immunostimulant vaccine
patch in Phase II for pandemic influenza. This patch is designed to
enhance the immune response compared to injected pandemic influenza
vaccines. If successful, it would have the effect of expanding
limited vaccine supplies by allowing public health officials to use
fewer or lower doses of the vaccine. The vaccine patch has recently
generated positive interim immunogenicity data in a 500-subject
Phase I/II study with a one-dose application. The program is funded
by a grant from the United States Department of Health and Human
Services. Iomai's pioneering work in transcutaneous immunization
(TCI) technology has led to the development of a simple and
promising needle-free vaccine patch. This highly innovative vaccine
delivery system provides a potential future alternative to current
injected vaccines. TCI technology has the potential to enhance the
efficacy of existing vaccines, replace current vaccines that have a
cumbersome mode of administration and enable the development of new
vaccines that are not viable to be delivered via an injection.
Iomai's TCI technology strengthens Intercell's position as an
innovative vaccine company and is highly complementary with its
proprietary antigen identification and adjuvant vaccine technology
platforms (AIP(R) and IC31(R)). TCI adds an important third arm to
Intercell's leading vaccine technologies, specifically a delivery
platform for antigens and adjuvants that can facilitate the
development of a broad range of in-house and partnered vaccine
products. Both companies have already partnered technologies with
Merck & Co., Inc., the most recent one being Iomai's agreement
to conduct proof-of-principle preclinical studies evaluating the
use of its needle-free immunostimulant patch. Intercell plans to
further leverage the TCI technology by applying it to other
vaccines in its development pipeline, such as its Pneumococcus
vaccine candidate. Furthermore, Iomai's vaccine patch has the
potential to provide cheaper and more effective medication to those
living in endemic areas, in particular high risk groups such as
children and the elderly located in developing countries in Africa,
Asia and Latin America. Transaction Terms: Under the terms of the
merger agreement, Intercell will acquire Iomai for USD 6.60 per
share of Iomai's common stock representing a fully diluted equity
value of Iomai of approximately USD 189 million (EUR 122 million).
The consideration will be paid in cash and stock. Iomai's public
shareholders, representing approximately 59 percent of Iomai's
outstanding common stock will receive cash. Certain of Iomai's
largest shareholders, together representing approximately 41
percent of Iomai's outstanding common stock, have agreed to
exchange their shares for Intercell stock at an exchange ratio
corresponding to a value of USD 6.60 per share of Iomai common
stock upon closing. The combination is structured as a share
exchange together with a merger of Iomai and a US subsidiary of
Intercell. Certain of Iomai's largest shareholders (and their
affiliates), which together represent over 50 percent of Iomai's
outstanding common stock, have agreed pursuant to a voting
agreement with Intercell that they will vote their shares in favour
of the merger. The transaction has been unanimously approved by the
Boards of Directors of both companies and is subject to customary
closing conditions, including the approval of the merger by a
majority of shareholders of Iomai at a special shareholder meeting
to be held as soon as practical, receipt of antitrust clearances
and clearance by the Committee on Foreign Investment in the United
States. Intercell and Iomai expect the transaction to close before
the end of the third quarter of 2008. Based on Intercell's closing
share price as of 9 May 2008, Intercell would issue approximately
1.7 million Intercell shares from authorized capital as
consideration, the final number of Intercell shares to be
determined shortly before the closing of the transaction. Intercell
will fund the cash component of the transaction from existing cash
reserves and expects to maintain profitability in 2008. Merrill
Lynch International acted as exclusive financial adviser to
Intercell and Cowen and Company provided a financial fairness
opinion to Iomai's Board of Directors. Analyst/Shareholder
Conference Call: A conference call on the transaction together with
Intercell's Q1 2008 results will be held by Intercell and Iomai's
senior managements on May 13, 2008 at 8:30 a.m. CET (7:30 a.m.
GMT). A webcast replay of the conference call will be made
available on Intercell's website. For further information please go
to http://www.intercell.com/. Ad-hoc Information About Travelers'
Diarrhea: This year, approximately 55 million international
travelers will visit countries where bacteria that cause travelers'
diarrhea are endemic, particularly Africa, Asia and Latin America.
The Centers for Disease Control and Prevention estimate that
between 20 and 50 percent of international travelers contract
diarrhea. The effects go beyond the acute symptoms of the disease;
between 10 and 30 percent of those who develop travelers' diarrhea
will develop the chronic symptoms of irritable bowel syndrome.
Because of the extent of the problem and the lack of safe and
effective prophylaxis, market studies suggest that there is a large
market for an effective travelers' diarrhea vaccine, potentially
exceeding USD 750 million annually. If approved, the Iomai vaccine
would be the first vaccine for travelers' diarrhea available in the
United States. About Pandemic Influenza: Three influenza pandemics
have occurred in the 20th century leading to the death of more than
50 million people globally. By US government estimates, pandemic
influenza has a greater potential to cause deaths and illnesses
than virtually any other natural health threat. Signs of a pandemic
influenza have emerged in Southeast Asia, as lethal infections of
poultry and humans with avian influenza virus continue. The current
virus is now endemic in bird populations, having spread to more
than 40 countries and causing the deaths of hundreds of millions of
birds. Furthermore, the World Health Organization reports that the
number of avian flu cases in humans has reached more than 370 cases
in 14 countries. In November 2005, the US government announced a
USD 7.1 billion initiative to prevent and prepare for a pandemic
influenza outbreak. In January 2007, Iomai entered into a USD 128
million contract with the US government to develop a dose-sparing
patch for use with a pandemic influenza vaccine. About Japanese
Encephalitis: With over three billion people living in endemic
areas, Japanese Encephalitis, a mosquito-borne flaviviral
infection, is the leading cause of childhood encephalitis and viral
encephalitis in Asia. The Japanese Encephalitis virus remains
virulent in this region and has recently spread to countries not
previously affected. About Intercell AG: Intercell AG is a growing
biotechnology company which focuses on the design and development
of novel vaccines for the prevention and treatment of infectious
diseases with substantial unmet medical need. The Company develops
antigens and adjuvants which are derived from its proprietary
technology platforms and has in-house GMP manufacturing
capabilities. Based on these technologies, Intercell has strategic
partnerships with a number of global pharmaceutical companies,
including Novartis, Merck & Co., Inc., Wyeth, Sanofi Pasteur,
Kirin, and the Statens Serum Institut. The Company's leading
product, a prophylactic vaccine against Japanese Encephalitis,
successfully concluded pivotal Phase III clinical trials in 2006.
The Market Authorization Application (MAA) in Europe as well as the
Biological License Application (BLA) with the US Food and Drug
Administration (FDA) for the use of the vaccine to prevent Japanese
Encephalitis were submitted in December of 2007. The licensure
application to TGA (Therapeutic Goods Administration) in Australia
was submitted in February of 2008. The Company's broad development
pipeline includes a partnered S. aureus vaccine in Phase II, a
therapeutic vaccine against Hepatitis C in Phase II, a Pseudomonas
vaccine in Phase II, a partnered Tuberculosis vaccine (Phase I/II),
and five products focused on infectious diseases in preclinical
development. Intercell is listed on the Prime Market of the Vienna
Stock Exchange under the symbol "ICLL". ISIN: AT0000612601 For more
information on Intercell, please visit: http://www.intercell.com/
About Iomai Corporation: Iomai Corporation has approximately 110
employees and discovers and develops vaccines and immune system
stimulants, delivered via a novel, needle-free technology called
transcutaneous immunization (TCI). TCI, discovered by researchers
at the Walter Reed Army Institute of Research, taps into the unique
benefits of a major group of antigen-presenting cells found in the
outer layers of the skin to generate an enhanced immune response.
Iomai is leveraging TCI to enhance the efficacy of existing
vaccines, develop new vaccines that are viable only through
transcutaneous administration and expand the global vaccine market.
Iomai currently has four product candidates in development: one to
prevent traveler's diarrhea and three targeting influenza and
pandemic flu. Iomai is listed on the NASDAQ Global Market under the
symbol "IOMI". For more information on Iomai, please visit:
http://www.iomai.com/ Additional Information and Where to Find It:
In connection with the proposed transaction, Iomai Corporation will
be filing a proxy statement for its stockholders and other
documents regarding the proposed transaction with the Securities
and Exchange Commission (SEC). BEFORE MAKING ANY VOTING OR
INVESTMENT DECISION, IOMAI STOCKHOLDERS AND INVESTORS ARE URGED TO
READ THE PROXY STATEMENT AND OTHER RELEVANT MATERIALS CAREFULLY IN
THEIR ENTIRETY WHEN THEY BECOME AVAILABLE BECAUSE THE DOCUMENTS
WILL CONTAIN IMPORTANT INFORMATION ABOUT THE PROPOSED TRANSACTION
AND IOMAI. Investors and stockholders may obtain copies of the
proxy statement and other relevant documents filed with the SEC by
Iomai free of charge at the SEC's web site at http://www.sec.gov/.
In addition, investors and stockholders may obtain copies of the
proxy statement and other relevant documents filed with the SEC by
Iomai (when they are available) by going to Iomai's Investor
Relations page on its corporate website at http://www.iomai.com/.
Iomai and its directors, executive officers and other members of
management may be deemed to be participants in the solicitation of
proxies from Iomai's stockholders with respect to the proposed
transaction. Information regarding Iomai's executive officers and
directors, and their beneficial ownership of Iomai's common stock
as of March 26, 2008 is available in Iomai's proxy statement for
its 2008 Annual Meeting of Stockholders, which was filed with the
SEC on April 4, 2008. Other information regarding the interests of
such potential participants in the proxy solicitation will be
contained in the proxy statement and other relevant materials to be
filed with the SEC when they become available. Forward Looking
Statements for Intercell AG: This communication expressly or
implicitly contains certain advance statements concerning Intercell
AG and its business. Such statements involve certain known and
unknown risks, uncertainties and other factors which could cause
the actual results, financial condition, performance or
achievements of Intercell AG to be materially different from any
future results, performance or achievements expressed or implied by
such advance statements. Intercell AG is providing this
communication as of this date and does not update any advance
statements contained herein as a result of new information, future
events or otherwise. Forward Looking Statements for Iomai
Corporation: Some matters discussed in this press release
constitute "forward-looking statements" that involve known and
unknown risks and uncertainties that could cause actual results to
differ materially from those expressed or implied by the
forward-looking statements. Such forward-looking statements include
statements about the anticipated acquisition of Iomai by Intercell
and timing of and potential benefits of the anticipated
acquisition; the potential synergies between the combination of
Iomai and Intercell's product technologies; expectations regarding
the timing of clinical trials and product development; the ability
of Iomai's adjuvant patches to provide protective immune responses;
the significance of clinical results described in this press
release; expectations that the clinical trial data from a clinical
trial will be sufficient to proceed with future clinical trials;
estimates of potential markets for Iomai's product candidates; the
potential for Iomai's product candidates to be lower cost or more
effective for specific patient populations; expectations that the
characteristics of Iomai's adjuvant patch for pandemic influenza
would make the product ideal for stockpile and rapid distribution;
expectations that TCI technology will enhance the efficacy of or
replace or be an alternative to current injected vaccines,
expectations that TCI technology can facilitate development of a
broad range of vaccine products; and expectations for further
collaboration with Merck & Co., Inc. or any other potential
collaborations. These statements are subject to risks and
uncertainties that could cause actual results to differ materially
from those projected in these forward-looking statements.
Applicable risks and uncertainties include, among others, that the
proposed acquisition does not close or that the companies may be
required to modify aspects of the transaction to achieve regulatory
approval; that prior to the closing of the acquisition, Iomai's
business suffers due to uncertainty; that the companies are unable
to successfully execute their integration strategies, or achieve
planned synergies; that future clinical trials may not replicate
results seen in the trials described in this press release; that
the U.S. Food and Drug Administration or other regulatory
authorities may not concur with Iomai's analysis of the trial
results described in this press release; that Iomai may not be able
to enroll sufficient numbers of subjects in future clinical trials;
that Iomai may be unable to obtain the regulatory approvals or
financing necessary to conduct additional clinical trials; that
competitors may develop products that are safer, more effective, or
more convenient to use; that future clinical results may not
support regulatory approval to commercialize Iomai's product
candidates, which will depend on the outcome of additional clinical
trials and analysis by regulatory authorities of data Iomai
submits; that development costs may exceed expectations; that Iomai
may fail to adequately protect its intellectual property or may be
determined to infringe on the intellectual property of others; and
the risks identified under the heading "Risk Factors" in our Annual
Report on Form 10-K for the year ended December 31, 2007 and filed
with the Securities and Exchange Commission. Iomai cautions
investors and others not to place undue reliance on the
forward-looking statements contained in this press release. These
statements speak only as of the date of this document and we
undertake no obligation to update or revise the statements. You are
encouraged to read Iomai's filings for a discussion of these and
other risks and uncertainties which are filed with the U.S.
Securities and Exchange Commission and are available at
http://www.sec.gov/. DATASOURCE: Iomai Corporation CONTACT: Lucia
Malfent, Head of Corporate Communications of Intercell AG,
+43-1-20620-303, ; or Russell P. Wilson, SVP, Chief Financial
Officer and General Counsel of Iomai Corporation, +1-301-556-4478,
; or Brian Reid of WeissComm Partners, Inc., +1-703-402-3626, , for
Iomai Corporation Web site: http://www.iomai.com/
http://www.intercell.com/
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