FORM 6-K
SECURITIES AND EXCHANGE COMMISSION
Washington D.C. 20549
Report of Foreign Issuer
Pursuant to Rule 13a-16 or 15d-16 of
the Securities Exchange Act of 1934
For period ending June 30, 2008
GlaxoSmithKline plc
(Name of registrant)
980 Great West Road, Brentford, Middlesex, TW8 9GS
(Address of principal executive offices)
Indicate by check mark whether the registrant files or
will file annual reports under cover Form 20-F or Form 40-F
Form 20-F x Form 40-F
--
Indicate by check mark whether the registrant by furnishing the
information contained in this Form is also thereby furnishing the
information to the Commission pursuant to Rule 12g3-2(b) under the
Securities Exchange Act of 1934.
Yes No x
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Issued – Monday 30
June 2008, London, UK & Philadelphia, US
Glaxo
S
mith
K
line Responds to FDA on CERVARIX®
and Plans to Submit Final Study Data for Approval
GlaxoSmithKline today provided
the following update regarding its application to the U.S. Food and Drug
Administration (FDA) for approval of CERVARIX®, its vaccine to prevent cervical
cancer.
GSK has submitted its response to questions raised by the FDA in their Complete
Response Letter, received in December, 2007. In addition, given that final data
from GSK’s Phase III pivotal efficacy study, HPV-008, are expected to be
available later this year, GSK has decided to augment its application for approval
with these data to ensure they are included in the U.S. label. GSK anticipates
submitting these data in the first half of 2009. The timing depends on reaching a
certain number of cases in order to conduct the final analysis. An FDA action on
the application is expected to take up to six months following this submission.
Interim data from this study were filed in the original application for the vaccine
in March, 2007. The company does not expect that new clinical studies will be
required for approval.
"Study 008 is a key study that will be completing later this year, and we expect
the final results will strengthen the U.S. label for CERVARIX®,” said
Barbara Howe, M.D., Vice President and Director, North American Vaccine
Development, GlaxoSmithKline. “We continue to have positive and productive
discussions with the FDA and remain confident in the vaccine’s safety and
efficacy profile. We look forward to bringing this important new cervical cancer
vaccine to girls and women in the U.S.”
To date, GSK’s cervical cancer vaccine has been approved in 67 countries
around the world including the 27 member countries of the European Union, Mexico,
Australia, Singapore and the Philippines. Licensing applications have been
submitted in more than 35 additional countries including Japan. GSK also submitted
the vaccine to the World Health Organization (WHO) for prequalification in
September 2007.
Notes to Editors
Burden of Cervical Cancer
Worldwide, more than 500,000
women will be newly diagnosed with cervical cancer and over 280,000 women will die
from it each
year.1
In the United States, after
breast cancer, cervical cancer is the second leading cause of cancer death in women
ages 20 to
39.2
About GlaxoSmithKline
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, please visit www.gsk.com/media.
GlaxoSmithKline Biologicals (GSK Biologicals) is a leading global vaccine
manufacturer committed to preventing disease in people of all ages with innovative
vaccines and delivery systems. The division, headquartered in Belgium, is active in
vaccine research, development and production with more than 30 vaccines currently
available globally and 20 more in development. In 2007 GSK Biologicals distributed
1.1 billion doses of vaccines – an average of 3 million doses a day.
CERVARIX® is a registered trademark of the GlaxoSmithKline group of
companies.
GSK cautionary statement regarding forward-looking statements
Under the safe harbour
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 'Business Review' in the company's Annual Report on Form 20-F for
2007.
References:
1. World Health Organization.
Initiative for Vaccine Research.
http://www.who.int/vaccine_research/diseases/hpv/en/ Accessed on May 2, 2007.
2. Jemal A, Murray T, Ward E, Sammuels A et al. Cancer Statistics, 2005. Cancer
Journal for Clinicians 2005; 55; 10-30
Enquiries:
UK Media enquiries: |
Philip Thomson |
(020) 8047 5502 |
Alice Hunt |
(020) 8047 5502 |
|
Gwenan White |
(020) 8047 5502 |
|
Claire Brough |
(020) 8047 5502 |
|
US Media enquiries: |
Nancy Pekarek |
(919) 483 2839 |
Mary Anne Rhyne |
(919) 483 2839 |
|
Liad Diamond |
(919) 483 2839 |
|
Sarah Alspach |
(919) 483 2839 |
|
European Analyst/Investor enquiries: |
David Mawdsley |
(020) 8047 5564 |
Sally Ferguson |
(020) 8047 5543 |
|
Gary Davies |
(020) 8047 5503 |
|
US Analyst/ Investor enquiries: |
Frank Murdolo |
(215) 751 7002 |
Tom Curry |
(215) 751 5419 |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has
duly caused this report to be signed on its behalf by the undersigned, thereunto duly
authorised.
GlaxoSmithKline plc
(Registrant)
Date: June 30, 2008
By: VICTORIA WHYTE
------------------
Victoria Whyte
Authorised Signatory for and on
behalf of GlaxoSmithKline plc