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Pfizer's anti-smoking drug wins priority review
Pfizer's anti-smoking drug wins priority review
Date published: 29/12/2005
Pfizer
has been granted a six-month priority review for the New Drug Application for
its smoking cessation medicine, varenicline tartrate, which the company intends
to market under the brand name Champix.
The Food and Drug
Administration (FDA) assigns priority review status to medicines that may
provide a significant therapeutic advance over existing therapies. Once the FDA
formally determines the application is sufficiently complete for review, the
filing will move forward under priority review.
According to the World
Health Organisation, every eight seconds a person dies of a smoking-related
disease. At present, less than seven per cent of smokers who try to quit on
their own achieve more than one year of abstinence and most relapse within a
few days of attempting to quit.
"If current smoking patterns continue,
the annual number of people dying of smoking-related diseases globally will
double from five to ten million deaths by 2020," said Hank McKinnell, chairman
and chief executive officer of Pfizer.
"Pfizer's research and
development effort for Champix represents the best of what medical innovation
can bring to patients and families struggling to overcome tobacco
addiction."
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