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IMMEDIATE
RELEASE
CONTACTS:
Brent
Larson,
Vice
President / CFO
614
822 2330
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May
26, 2010
Tim
Ryan,
The
Shoreham Group
212
242 7777
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NEOPROBE
NOMINATES BRENDAN FORD AND DR. ERIC ROWINSKY TO BOARD
Nominees
to Serve as Directors Through 2013
DUBLIN,
OHIO – May 26, 2010 - Neoprobe Corporation (OTCBB: NEOP), a diversified
developer of innovative biomedical surgical oncology products, today announced
that its Board of Directors has nominated Brendan A. Ford and Eric K. Rowinsky,
M.D. to serve as members of Neoprobe’s Board of Directors. Mr. Ford and Dr.
Rowinsky have been nominated to stand for election at Neoprobe’s 2010 Annual
Meeting of Stockholders scheduled for July 16th in
Dublin, Ohio. Both Mr. Ford and Dr. Rowinsky have been nominated to serve as
directors through Neoprobe’s stockholders’ meeting in 2013.
Mr. Ford is a partner in Talisman
Capital Partners, a private investment partnership focusing on middle-market
companies. From 1991
through 2007, Mr. Ford served in various executive positions including Executive
Vice President, Business
Development and Corporate Strategy with Cardinal Health, Inc., primarily
in capacities related to
mergers, acquisitions and related strategic activities, and was involved
in over $19 billion in acquisition and disposition transactions for Cardinal.
Prior to his service with Cardinal Health, Mr. Ford practiced law with the firm of Baker and Hostetler
from 1986 to 1991. From 1980 to 1983, Mr. Ford was employed by Touche Ross LLP
as a certified public accountant. Mr. Ford has a B.S. in Business from Miami
University and a J.D. from
The Ohio State University. Mr. Ford serves as a director and board committee
member for several privately-held companies.
Dr.
Rowinsky has been an independent consultant since January 2010. From
2005 to December 2009, he served as the Chief Medical Officer and Executive Vice
President of Clinical Development and Regulatory Affairs of ImClone Systems
Incorporated, a life sciences company. Prior to that, Dr. Rowinsky held
several positions at the Cancer Therapy & Research Center’s Institute of
Drug Development in San Antonio, Texas, including Director of the Institute,
Director of Clinical Research and SBC Endowed Chair for Early Drug Development,
and he concurrently served as Clinical Professor of Medicine in the Division of
Medical Oncology at the University of Texas Health Science Center at
San Antonio. Dr. Rowinsky was an Associate Professor of Oncology
at the Johns Hopkins University School of Medicine and on active staff at the
Johns Hopkins School of Medicine from 1987 to 1996. Dr. Rowinsky
is a member of the boards of directors of Biogen Idec, Inc. and ADVENTRX
Pharmaceuticals, Inc. Dr. Rowinsky has extensive research and drug
development experience, oncology expertise and broad scientific and medical
knowledge.
“We are
delighted to have Brendan and Eric become directors of Neoprobe,” said David
Bupp, Neoprobe’s President and CEO. “Both provide Neoprobe with outstanding
development, commercial and strategic business experience regarding the
development and commercialization of pharmaceutical and medical products that
will be invaluable to the Neoprobe management team as we commercialize
Lymphoseek® and as
we continue to pursue our development and commercialization strategy for the
RIGS®
technology. We believe that adding Brendan and Eric to the Board is very
positive for Neoprobe and its stockholders and we look forward to working with
them.”
In
connection with the nomination of the new directors, Neoprobe also announced
that Reuven Avital and J. Frank Whitley, Jr., both longtime Neoprobe directors,
will retire from the Board following the 2010 Annual Meeting of
Stockholders.
NEOPROBE
CORPORATION
ADD
- - 2
"Reuven
and Frank will be greatly missed on our Board," stated Carl J. Aschinger, Jr.,
Neoprobe’s Chairman. "Their years of wisdom, insight and guidance have been of
enormous value to Neoprobe, and our work has been enriched as a result.
During their tenure on the Board, Neoprobe reinvented itself into a
biomedical company with tremendous commercial and development potential in the
field of radiopharmaceuticals. That success is in no small part due to the
perspectives and engagement that Reuven and Frank brought to the Board. We
are all grateful for their service to the organization and we wish them
well."
About
Neoprobe
Neoprobe is a biomedical company focused
on enhancing patient care and improving patient outcome by meeting the critical
intraoperative diagnostic information needs of physicians and therapeutic
treatment needs of patients. Neoprobe currently markets the neoprobe® GDS line of gamma detection systems
that are widely used by cancer surgeons. In addition, Neoprobe holds significant
interests in the development of related biomedical systems and
radiopharmaceutical agents including Lymphoseek® and RIGScan™ CR. Neoprobe’s subsidiary,
Cira Biosciences, Inc., is also advancing a patient-specific cellular therapy
technology platform called ACT. Neoprobe’s strategy is to deliver
superior growth and shareholder return by maximizing its strong position in
gamma detection technologies and diversifying into new, synergistic biomedical
markets through continued investment and selective acquisitions. www.neoprobe.com
Statements
in this news release, which relate to other than strictly historical facts, such
as statements about the Company’s plans and strategies, expectations for future
financial performance, new and existing products and technologies, anticipated
clinical and regulatory pathways, and markets for the Company’s products are
forward-looking statements The words “believe,” “expect,”
“anticipate,” “estimate,” “project,” and similar expressions identify
forward-looking statements that speak only as of the date
hereof. Investors are cautioned that such statements involve risks
and uncertainties that could cause actual results to differ materially from
historical or anticipated results due to many factors including, but not limited
to, the Company’s continuing operating losses, uncertainty of market acceptance
of its products, reliance on third party manufacturers, accumulated deficit,
future capital needs, uncertainty of capital funding, dependence on limited
product line and distribution channels, competition, limited marketing and
manufacturing experience, risks of development of new products, regulatory risks
and other risks detailed in the Company’s most recent Annual Report on Form 10-K
and other Securities and Exchange Commission filings. The Company
undertakes no obligation to publicly update or revise any forward-looking
statements.