- MedImmune Continues its Commitment to Protecting Public Health by Creating
More Reliable and Efficiently Developed Influenza Vaccines -
GAITHERSBURG, Md., Dec. 7 /PRNewswire-FirstCall/ -- MedImmune, Inc.
(Nasdaq: MEDI), maker of the intranasal influenza vaccine FluMist(R)
(Influenza Virus Vaccine Live, Attenuated), announced today that it has taken
another step towards becoming the world leader in advancing the development of
new, more reliable and efficiently developed vaccines that prevent influenza.
Toward this end, MedImmune has acquired exclusive worldwide rights to certain
intellectual property owned by Mount Sinai School of Medicine for reverse
genetics, including U.S. Patent Nos. 6,544,785 and 6,649,372. With this
license, MedImmune has further strengthened its patent estate to now either
own or have exclusive licenses to all of the key intellectual property (listed
below) for this technology:
* Mount Sinai School of Medicine Plasmid Rescue Portfolio (WO 01/04333)
* MedImmune Fundamental Reverse Genetics Portfolio (WO 91/03552)
* Wisconsin Alumni Research Foundation Plasmid Rescue Portfolio
(WO 00/60050)
* St. Jude Children's Research Hospital Dual Promoter Plasmid Rescue
Portfolio (WO 01/83794)
"The use of reverse genetics will allow MedImmune to improve the
efficiency of producing new influenza vaccine strains on an annual basis,
ultimately resulting in more reliable delivery of the vaccine to the public,"
said George W. Kemble, Ph.D., MedImmune's vice president of research and
development, vaccines. "When used to produce pandemic influenza vaccine seeds,
reverse genetics has the added benefit of enabling scientists to remove
potentially pathogenic portions of the virus, thereby making the vaccine and
its production safer."
Reverse genetics is a method of altering the influenza genome to produce
vaccine seeds that are then used to produce the vaccine. Reverse genetics is
an important breakthrough for manufacturing all influenza vaccines, because it
is more efficient and reliable than current methods used to produce vaccine
seeds. For pandemic vaccines, reverse genetics is even more important because
it does not require vaccine manufacturers to work directly with the
infectious, circulating pandemic strain, rather only segments of its genome.
Due to these benefits, the technology is now being used by most manufacturing
companies and the U.S. government in their development of pandemic vaccines.
"As a long time leader in the field of virology, our goal is to ensure
that this important technology continues to be widely used to prepare for
potential pandemics, while at the same time ensuring that research continues
to find new and innovative uses for reverse genetics," said Dennis Charney,
M.D., Dean for Academic and Scientific Affairs at Mount Sinai School of
Medicine. "At MedImmune, we found partners who share this vision."
"MedImmune remains committed to making sure that the reverse genetics
technology is accessible to public health officials in their efforts to
protect people from pandemic strains of influenza," said Edward T. Mathers,
MedImmune's senior vice president of corporate development. "Toward this goal,
we will continue to work with government institutions and industry
manufacturers to provide licenses to our entire intellectual property estate
for both pandemic and interpandemic purposes to allow for the use of this
critical technology in the commercialization of influenza vaccines."
Under the terms of today's agreement, Mount Sinai will receive an upfront
fee, milestone payments and royalties on future product sales.
About Influenza
In the U.S., influenza causes seasonal epidemics of disease resulting in
approximately 36,000 deaths each year, according the U.S. Centers for Disease
Control and Prevention. A pandemic occurs when a novel strain of influenza
virus circulates widely in the human population that has no prior immunity and
is highly susceptible. Recent outbreaks of avian influenza in Asia emphasize
the need for the United States to be prepared in the event of a pandemic.
MedImmune is actively involved in applying its technologies, including
reverse genetics, as well as its expertise to pandemic preparedness. In
September, MedImmune finalized a Cooperative Research and Development
Agreement (CRADA) with the National Institutes of Health (NIH) to produce and
test versions of the company's attenuated, live intranasal influenza vaccine
against pandemic influenza strains.
Recent Progress with Influenza Vaccine Franchise
In September 2005, MedImmune submitted a supplemental Biologics License
Application (sBLA) with the U.S. Food and Drug Administration (FDA) for
approval to use its refrigerator-stable formulation of FluMist, known as
CAIV-T (cold adapted influenza vaccine, trivalent) in healthy individuals 5 to
49 years of age. The sBLA was based on results from a Phase 3 study comparing
the immunogenicity of FluMist to CAIV-T, as well as additional preclinical and
clinical data supporting the comparability of the two formulations.
MedImmune is nearing completion of a large Phase 3 clinical trial directly
comparing the relative efficacy and safety of CAIV-T with the standard
injectable vaccine. The goal of the study is to provide the pivotal data to
seek regulatory approval for use of the intranasal vaccine in children down to
6 months of age. This prospective, controlled, Phase 3 trial includes
approximately 8,500 children between the ages of six months and 59 months,
including those with a history of asthma and wheezing. It has been conducted
at approximately 250 sites in North America, Europe and Asia. Efficacy in the
trial will be measured by the reduction in the incidence of symptomatic
culture-confirmed influenza that matched the strains in the vaccines. The
primary safety comparison in the trial will be measured by the rate of
medically significant wheezing after vaccination.
About CAIV-T
CAIV-T is an investigational intranasal, cold-adapted trivalent influenza
vaccine. It is the next generation, refrigerator-stable formulation of
FluMist, which is a frozen, live attenuated cold-adapted trivalent influenza
vaccine. To date, the safety, tolerability and efficacy of CAIV-T has been
studied in both healthy and at-risk populations between the ages of 6 weeks
and 98 years. Some of these data were presented in October 2003 at the Fifth
Annual Options for the Control of Influenza Conference in Okinawa, Japan.
About FluMist
FluMist is indicated for active immunization for the prevention of disease
caused by influenza A and B viruses in healthy children and adolescents, 5 to
17 years of age, and healthy adults, 18 to 49 years of age. There are risks
associated with all vaccines, including FluMist. Like any vaccine, FluMist
does not protect 100 percent of individuals vaccinated. In studies of people
between the ages of 5 and 49 years, runny nose was the most commonly reported
side effect. Other common side effects included various cold-like symptoms,
such as headache, cough, sore throat, tiredness/weakness, irritability, and
muscle aches.
FluMist should not be used, under any circumstances, in anyone with an
allergy to any part of the vaccine, including eggs; in children and
adolescents receiving aspirin therapy; in people who have a history of
Guillain-Barre syndrome; and in people with known or suspected immune system
problems. Pregnant women and people with certain medical conditions, asthma,
or reactive airways disease should not get FluMist.
Please see the Prescribing Information at
http://www.flumist.com/pdf/prescribinginfo.pdf, visit http://www.flumist.com,
or call 1-877-633-4411 for additional information.
About Mount Sinai School of Medicine
Located in Manhattan, Mount Sinai School of Medicine (MSSM) is
internationally recognized for ground-breaking clinical and basic-science
research, and innovative approaches to medical education. Through the Mount
Sinai Graduate School of Biological Sciences, Mount Sinai trains biomedical
researchers with an emphasis on the rapid translation of discoveries of basic
research into new techniques for fighting disease. For example, the FDA has
recently approved two therapeutic products and one medical device based on
MSSM technology and there are six products based on MSSM technology in
clinical development. Further indication of Mount Sinai's leadership in
scientific investigation is its receipt during fiscal year 2004 of
$153.2 million. Mount Sinai now ranks 25th among the nation's medical schools
in receipt of research support from NIH. Mount Sinai School of Medicine also
is known for unique educational programs such as the Humanities in Medicine
program, which creates opportunities for liberal arts students to pursue
medical school, and instructional innovations like. Long dedicated to
improving its community, the School extends its boundaries to work with East
Harlem and surrounding communities to provide access to health care and
educational programs to at risk populations.
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 diseases,
cancer and inflammatory diseases. With more than 2,200 employees worldwide,
MedImmune is headquartered in Maryland. For more information, visit the
company's Web site at http://www.medimmune.com .
This announcement contains, in addition to historical information, certain
forward-looking statements that involve risks and uncertainties, in
particular, related to the development of CAIV-T as well as potential
influenza vaccines using reverse genetics. Such statements reflect
management's current views and are based on certain assumptions. Actual
results could differ materially from those currently anticipated as a result
of a number of factors, including risks and uncertainties discussed in
MedImmune's filings with the U.S. Securities and Exchange Commission. There
can be no assurance that such development efforts will succeed, that such
vaccines will receive required regulatory clearance or that, even if such
regulatory clearance is received, such vaccines will ultimately achieve
commercial success. There can be no assurance that even if such a vaccine is
commercially available, that it will protect against a particular influenza
strain or prevent a pandemic.
SOURCE MedImmune, Inc.
CONTACT:
Media:
Clarencia Stephen, +1-301-398-4073
Jamie Lacey,
+1-301-398-4035
Investors:
Peter Vozzo, +1-301-398-4358
John Filler,
+1-301-398-4086
all of MedImmune