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St. Jude Medical, Inc. Investor Relations Angela Craig, 651-481-7789 or
Media Relations Kathleen Janasz, 651-415-7042 or St. Jude Medical, ANS
Division Media Relations Denise Landry, 972-309-8085 St. Jude Medical,
Inc. (NYSE:STJ) today announced it has received an Investigational
Device Exemption (IDE) from the U.S. Food and Drug Administration (FDA)
to begin enrollment in a controlled, multi-site, blinded, clinical
study of deep brain stimulation for major depressive disorder, a severe
form of depression.
The BROADEN(TM) (BROdmann Area 25 DEep brain Neuromodulation)
study will evaluate the safety and effectiveness of deep brain
stimulation in patients with depression for whom currently-available
treatments are not effective. The study will build upon the pioneering
depression work of a research team from the University of Toronto, led
by neurologist Helen S. Mayberg, M.D. (now with Emory University School
of Medicine), and neurosurgeon Andres Lozano, M.D.
"Major depressive disorder is severely disabling," said Dr.
Lozano. "Currently, there are no widely-accepted treatment options for
patients with this condition once multiple medications, psychotherapy
and electroconvulsive therapy have failed."
Drs. Mayberg and Lozano conducted the first study of deep brain
stimulation (DBS) for depression in Toronto, Canada, in 2003 and
published their findings in Neuron in March 2005. As reported in this
journal article, imaging studies led them to an area of the brain
thought to be involved in depression called Brodmann Area 25. This area
appears to become overactive when people are profoundly sad and
depressed.
St. Jude Medical owns the intellectual property rights and has
various patents pending for the use of neurostimulation at Brodmann
Area 25. The Libra(R) Deep Brain Stimulation System, which is being
evaluated in this study, is designed to deliver mild electrical pulses
from a device implanted near the collarbone and connected to small
electrical leads placed at specific targets in the brain.
In the U.S., more than 21 million adults suffer from some kind of
depressive disorder, according to the National Institute of Mental
Health. Of these, only about 80 percent can be effectively treated with
currently available therapies, according to the National Advisory
Mental Health Council. Unfortunately, that means approximately 4
million adult Americans live with depression that does not respond to
medications, psychotherapy and, in certain cases, electroconvulsive
therapy.
"St. Jude Medical is dedicated to researching and developing
neuromodulation therapies for people who live with conditions such as
severe depression," said Chris Chavez, president of St. Jude Medical's
ANS Division. "We are hopeful that this trial will lead to the
successful development of a sustainable therapy for those patients who
have exhausted other treatment options."
To be eligible for the study, participants must:
-- Currently be diagnosed with major depressive disorder
-- Be between 21 and 70 years old, with onset of first episode before age 45
-- Have tried at least four treatments in their current episode,
such as different medications, various combinations of medications or
electroconvulsive therapy
-- Have been depressed for at least one year
For more information about this study, call toll-free 866-787-4332 or visit www.BROADENstudy.com.
About St. Jude Medical
St. Jude Medical is dedicated to making life better for cardiac,
neurological and chronic pain patients worldwide through excellence in
medical device technology and services. The Company has five major
focus areas that include: cardiac rhythm management, atrial
fibrillation, cardiac surgery, cardiology and neuromodulation.
Headquartered in St. Paul, Minn., St. Jude Medical employs
approximately 12,000 people worldwide. For more information, please
visit www.sjm.com.
About the ANS Division of St. Jude Medical
The ANS Division (Advanced Neuromodulation Systems) became a part
of St. Jude Medical in 2005. The ANS Division is an innovative
technology leader dedicated to the design, development, manufacturing
and marketing of implantable neuromodulation systems to improve the
quality of life for people suffering from disabling chronic pain and
other nervous system disorders (www.ans-medical.com).
Forward-Looking Statements
This news release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995 that
involve risks and uncertainties. Such forward-looking statements
include the expectations, plans and prospects for the Company,
including potential clinical successes, anticipated regulatory
approvals and future product launches, and projected revenues, margins,
earnings, and market shares. The statements made by the Company are
based upon management's current expectations and are subject to certain
risks and uncertainties that could cause actual results to differ
materially from those described in the forward-looking statements.
These risks and uncertainties include market conditions and other
factors beyond the Company's control and the risk factors and other
cautionary statements described in the Company's filings with the SEC,
including those described in the Company's Annual Report on Form 10-K
filed on February 28, 2007 (see pages 13-20) and Quarterly Reports on
Form 10-Q filed on August 9, 2007 (see pages 28-29) and November 2,
2007 (see pages 23-24). The Company does not intend to update these
statements and undertakes no duty to any person to provide any such
update under any circumstance.
Research to focus on the Brodmann Area 25 region of the brain