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GlaxoSmithKline Submits Biologics License Application for FDA Approval of FluLaval(TM

Snowy Owl

Retired in 2010, In Memoriam
GlaxoSmithKline Submits Biologics License Application for FDA Approval of FluLaval(TM)

PHILADELPHIA, March 23 /PRNewswire-FirstCall/ -- GlaxoSmithKline
(NYSE: GSK) today announced it has submitted a Biologics License Application
(BLA) for FluLaval(TM) (Influenza Virus Vaccine) to the U.S. Food and Drug
Administration (FDA). If licensed, FluLaval will be used for the active
immunization of adults 18 years of age and older against influenza disease
caused by influenza virus types A and B, which are contained in the vaccine.

"GSK is committed to increasing the supply of seasonal flu vaccine to help
keep Americans healthy during the flu season," said Christopher Viehbacher,
President, U.S. Pharmaceuticals, GSK. "Influenza is a serious threat to
public health and the U.S. has faced recent shortages of vaccine to prevent
it. Following last year's approval of Fluarix, today's announcement is
another important step toward ensuring adequate availability of a critical
weapon to fight the flu."

Fluarix(R) (Influenza Virus Vaccine) was approved by the U.S. FDA on
August 31, 2005. GSK added FluLaval to its portfolio of flu products when it
acquired the Canadian vaccine manufacturer ID Biomedical Corporation in
December 2005. FluLaval was granted fast-track status by the U.S. FDA in July
2005 and is marketed in Canada under the name Fluviral(TM). If granted U.S.
marketing approval for FluLaval, GlaxoSmithKline expects to provide up to 30
million doses of seasonal influenza vaccine (FluLaval and Fluarix) to the U.S.
market for the 2006/2007 flu season.

About Influenza

Influenza is a highly contagious and potentially fatal virus that affects
five to 20 percent of the total U.S. population during each influenza season.
Between 1990 and 1999, approximately 36,000 people died in the United States
each year from complications of influenza infection; more than 90 percent of
these deaths occurred in persons 65 years of age and older. Influenza can
reach epidemic levels and poses a significant threat to public health,
particularly among the nation's oldest and youngest citizens.

Influenza vaccination is the primary method for preventing influenza and
its severe complications. Influenza is easily passed from one person to
another through the air by tiny droplets and particles released when an
infected individual coughs or sneezes. Most people recover fully within a
week or two.

The risk of complications is elevated in very young, very old and
chronically ill persons. The genetic makeup of the influenza virus and the
rapid mutations that can occur make annual vaccination necessary.

GlaxoSmithKline: A Leader in Preventing and Treating Influenza

GlaxoSmithKline has an active research and development program targeted at
both seasonal and pandemic influenza and has recently committed over $2
billion to expand capacity for manufacturing flu vaccine and its antiviral
influenza treatment Relenza(R) (zanamivir for inhalation).

GlaxoSmithKline - one of the world's leading research-based pharmaceutical
and healthcare companies - is committed to improving the quality of human life
by enabling people to do more, feel better and live longer. For company
information, visit GlaxoSmithKline at http://www.gsk.com.

GlaxoSmithKline Forward-Looking Statements

Cautionary statement regarding forward-looking statements under the safe
harbor provisions of the U.S. Private Securities Litigation Reform Act of
1995: the company cautions investors that any forward-looking statements or
projections made by the company, including those made in this Announcement,
are subject to risks and uncertainties that may cause actual results to differ
materially from those projected. Factors that may affect the Group's
operations are described under 'Risk Factors' in the Operating and Financial
Review and Prospects in the company's Annual Report 2005.

http://www.prnewswire.com/cgi-bin/s...06/0004325936&EDATE=THU+Mar+23+2006,+11:43+AM
 
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