Astellas Pharma conducts R&D and marketing efforts focused in the urology, cardiology,
immunology, dermatology, infectious diseases, and neurology therapeutic
sectors.
Full press
release below about FDA Advisory Committee recommending approval of mirabegron for the treatment of overactive bladder (OAB).
SOURCE: www.astellas.us.
FDA Advisory Committee
Recommends Approval of Mirabegron - Investigational Overactive Bladder
Treatment from Astellas
DEERFIELD, Ill., April 5,
2012 /PRNewswire/ -- Astellas Pharma US, Inc. ("Astellas"), a U.S.
subsidiary of Tokyo-based Astellas Pharma Inc. (Tokyo: 4503), announced today
that the Reproductive Health Drugs Advisory Committee of the U.S. Food and Drug
Administration (FDA) voted that the overall risk/benefit assessment supports
approval of mirabegron (YM178) for the treatment of overactive bladder (OAB)
(Yes: 7, No: 4, Abstain: 1).
Today's committee
recommendation, although not binding, will be considered by the FDA as it
reviews the New Drug Application (NDA). The FDA is expected to issue an action
letter on the mirabegron application by June 29, 2012.
Mirabegron is a once daily
oral selective B3-adrenoceptor agonist discovered and developed by Astellas.
Mirabegron has been studied extensively in more than 10,000 individuals over
the last 10 years.
"We are pleased with
the committee's recommendation, which marks an important step in bringing a new
treatment option to the more than 42 million Americans living with overactive
bladder," said Steven Ryder, MD, president, Astellas Pharma Global
Development. "If approved, mirabegron will offer patients and physicians
the first new oral mechanism of action in OAB treatment since the launch of the
first anticholinergic agent 30 years ago. Mirabegron and other pipeline
products are part of Astellas' commitment to advancing urological health."
Mirabegron uses a distinct
mechanism of action versus antimuscarinics, the current treatment standard.
Antimuscarinics work by binding to muscarinic receptors in the bladder and
inhibiting involuntary bladder contractions. Mirabegron works by stimulating
the B3 receptors in the detrusor muscle of the bladder, causing relaxation of
the bladder muscle during the storage phase of the micturition (urination)
cycle. This improves the storage capacity of the bladder without diminishing
bladder contraction during bladder voiding.
Astellas submitted a New
Drug Application for mirabegron to the FDA on Aug. 26, 2011. Regulatory
applications for mirabegron are also under review in several other countries.
In July 2011, mirabegron was granted marketing approval in Japan and was
launched in September 2011.
About Overactive Bladder
According to the National Association for Continence, one in five
adults has overactive bladder. However, recent studies have found that
many more people may be affected, but have not talked to their physicians out
of embarrassment or belief that OAB cannot be treated. For people with OAB,
inappropriate signals are sent to the muscles in the bladder causing them to
contract before the bladder is full. These bladder contractions may cause
strong, sudden urges, and a frequent need to go to the bathroom, sometimes
without any advance warning. Many patients cope with their symptoms by
restricting fluids, carrying extra clothing and "mapping" bathroom
locations wherever they go.
About Astellas
Astellas Pharma US, Inc., located in Deerfield, Illinois, is a U.S.
affiliate of Tokyo-based Astellas Pharma Inc. Astellas is a pharmaceutical
company dedicated to improving the health of people around the world through
the provision of innovative and reliable pharmaceutical products. For more
information about Astellas Pharma US, Inc., please visit our website at www.astellas.us.
SOURCE Astellas Pharma US,
Inc.
CONTACT: Jenny M. Kite of
Astellas, +1-847-317-5405 office, or +1-847-682-4530 cell,
Jenny.Kite@us.Astellas.com; or Paula Mavroudis of Edelman, +1-312-240-2709
office, or +1-312-434-4145 cell, Paula.Mavroudis@Edelman.com, for Astellas
Pharma US, Inc.
Web Site: http://www.us.astellas.com
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