HOUSTON, Oct. 1 /PRNewswire-FirstCall/ --
Cyberonics, Inc. (Nasdaq:
CYBX -
News)
today announced that it has completed a comprehensive process with
respect to
an effort to identify a partner for the depression indication related
to the
company's Vagus Nerve Stimulation (VNS) Therapy(TM) System.
Cyberonics announced in February a plan to identify a partner
to assist
with the activities required to obtain broad reimbursement coverage for
the
depression indication, including completion of the post-market studies
mandated by the FDA in order to maintain approval of VNS Therapy(TM)
for
depression and the initiation of a new randomized clinical trial. The
process
undertaken over the last six months has not resulted in the receipt of
an
offer that provides sufficient value to the company's shareholders.
Accordingly, Cyberonics is evaluating alternative actions intended to
maintain
the current regulatory approval, while minimizing the company's
required
investment, as well as ensuring that this valuable treatment continues
to be
available to patients in the United States and certain international
markets.
"As we review alternatives, we remain committed to supporting
patients and
clinical partners while continuing to drive shareholder value,"
commented Dan
Moore, President and Chief Executive Officer. "We previously stated
that
Cyberonics would not undertake a new clinical trial without a partner,
and
that continues to be our position. For the second half of fiscal 2009,
costs
related to the two post-market depression clinical programs are
expected to be
in the range of $3.5 million to $4.0 million. These costs are
consistent with
our previously provided guidance. In fiscal 2010, these costs are not
expected to exceed $4.0 million and are anticipated to be less than
$2.0
million in 2011, as the FDA-mandated clinical programs conclude. We are
currently generating revenue of approximately $3.0 million per annum
from the
depression indication. We expect to continue the momentum we have
experienced
within our epilepsy business and the financial progress we have
achieved over
the last 12 months."
About VNS Therapy(TM) and Cyberonics
Cyberonics, Inc. (NASDAQ: CYBX - News) is a medical
technology company with core
expertise in neuromodulation. The company developed and markets the
Vagus
Nerve Stimulation (VNS) Therapy(TM) System, which is FDA-approved for
the
treatments of epilepsy and depression. The VNS Therapy System uses a
surgically implanted medical device that delivers electrical pulsed
signals to
the vagus nerve. Cyberonics markets the VNS Therapy System in selected
markets worldwide.
Additional information on Cyberonics, Inc. and VNS Therapy(TM)
is
available at http://www.cyberonics.com
and http://www.vnstherapy.com.
Safe harbor statement
This press release contains forward-looking statements within
the meaning
of Section 27A of the Securities Act of 1933, as amended and Section
21E of
the Securities Exchange Act of 1934, as amended. These statements can
be
identified by the use of forward-looking terminology, including "may,"
"believe," "will," "expect," "anticipate," "estimate," "plan,"
"intend," and
"forecast," or other similar words. Statements contained in this press
release are based upon information presently available to us and
assumptions
that we believe to be reasonable. We are not assuming any duty to
update this
information should those facts change or should we no longer believe
the
assumptions to be reasonable. Investors are cautioned that all such
statements involve risks and uncertainties, including without
limitation,
statements concerning maintaining the current regulatory approval for
depression, minimizing the company's investment in the depression
indication,
ensuring that VNS Therapy continues to be available to depression
patients,
costs related to the two post-market depression clinical programs in
the range
of $3.5 million to $4.0 million in fiscal 2009, not in excess of $4.0
million
in fiscal 2010, less than $2.0 million in 2011, and continuing the
momentum we
have experienced within our epilepsy business and the financial
progress we
have achieved over the last 12 months. Our actual results may differ
materially. Important factors that may cause actual results to differ
include, but are not limited to: continued market acceptance of VNS
Therapy
and sales of our product; the development and satisfactory completion
of
clinical trials and/or market test and/or regulatory approval of VNS
Therapy
for the treatment of other indications; satisfactory completion of
post-market
studies required by the U.S. Food and Drug Administration as a
condition of
approval for the treatment-resistant depression indication; adverse
changes in
coverage or reimbursement amounts by third-parties; intellectual
property
protection and potential infringement claims; maintaining compliance
with
government regulations and obtaining necessary government approvals for
new
indications; product liability claims and potential litigation;
reliance on
single suppliers and manufacturers for certain components; the accuracy
of
management's estimates of future expenses and sales; the results of the
previously disclosed governmental inquiries; the potential
identification of
material weaknesses in our internal controls over financial reporting;
risks
and costs associated with such governmental inquiries and any
litigation
relating thereto or to our stock option grants, procedures, and
practices
(including the previously disclosed private litigation); uncertainties
associated with stockholder litigation; and other risks detailed from
time to
time in our filings with the Securities and Exchange Commission (SEC).
For a
detailed discussion of these and other cautionary statements, please
refer to
our most recent filings with the SEC, including our Annual Report on
Form 10-K
for the fiscal year ended April 25, 2008.
Contact information
Greg Browne, CFO
Cyberonics, Inc.
100 Cyberonics Blvd.
Houston, TX 77058
Main: (281) 228-7262
Fax: (281) 218-9332
ir@cyberonics.com