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    Navidea Appoints Michael M. Goldberg, M.D. President and Chief Executive Officer

    Chelsea Pratt
    Sep. 27, 2016 12:50AM PST
    Biotech Investing

    Navidea Biopharmaceuticals today announced that its Board of Directors has appointed Michael M. Goldberg, M.D. as President and Chief Executive Officer effective September 22, 2016.

    Navidea Biopharmaceuticals, Inc. (NYSE MKT: NAVB) today announced that its Board of Directors has appointed Michael M. Goldberg, M.D. as President and Chief Executive Officer effective September 22, 2016. The Board of Directors has also appointed Eric K. Rowinsky M.D., a Navidea board member since 2010, as Chairman of Navidea’s Board, a position previously held by Dr. Goldberg, who will remain a board member.
    “We are delighted to announce the appointment of Michael as Navidea’s
    CEO,” said Dr. Rowinsky, Chairman of Navidea’s Compensation, Nominating
    and Governance committee and newly appointed Chairman. “Dr. Goldberg is
    a visionary leader with a deep knowledge and appreciation for the
    potential of Navidea’s macrophage targeting technology platform and its
    wide range of diagnostic and therapeutic applications. At this important
    transition point for the Company, we will benefit greatly from his
    expertise as we drive the development of our Manocept™ clinical
    immunodiagnostic and immunotherapeutic programs to deliver targeted
    products to improve patient outcomes.”
    “I look forward to spearheading the growth of both Navidea and
    Macrophage Therapeutics as we execute our mission to not only diagnose
    but treat disease,” said Michael M. Goldberg, M.D. “The combination of
    exceptional technology, a strong leadership team as well as our
    expectation of improved financial stability will allow us to effectively
    execute on our strategy to more rapidly advance on numerous development
    programs with our ground-breaking proprietary technology for multiple
    high value indications.”
    Michael M. Goldberg, M.D. has been a member of the Navidea Board of
    Directors since November 2013, serving as interim Chief Executive
    Officer from May to October 2014. Dr. Goldberg is currently a Managing
    Partner of Montaur Capital Partners. Prior to this role, he served as
    the Chairman of the Board and Chief Executive Officer of Emisphere
    Technologies, Inc., the pioneer in the development of oral delivery
    technologies for macromolecules. Prior to Emisphere, he served as Vice
    President in Investment Banking of The First Boston Corporation, where
    he was a founding member of the Healthcare Banking Group. Dr. Goldberg
    graduated from the accelerated six year combined BS/MD program from
    Rensselaer Polytechnic Institute and the Albany Medical College in 1982,
    and obtained an M.B.A. from the Graduate School of Business, Columbia
    University, in 1985.
    Eric K. Rowinsky, M.D. has extensive research and drug development
    experience, oncology expertise, corporate strategy and broad scientific
    and medical knowledge and has served as a director of Navidea since July
    2010. He is currently Executive Chairman and President, of Rgenix, Inc.
    During his career, Dr. Rowinsky has held executive positions at Stemline
    Therapeutics, Inc., Primrose Therapeutics, and ImClone Systems
    Incorporated. Prior to that, Dr. Rowinsky held several positions at the
    Cancer Therapy & Research Center’s Institute of Drug Development,
    including Director of the Institute, Director of Clinical Research and
    SBC Endowed Chair for Early Drug Development, and 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. Dr. Rowinsky is a member of the boards of
    directors of Biogen Inc. and Fortress Biosciences, Inc., publicly-held
    life sciences companies. He is also an Adjunct Professor of Medicine at
    New York University.
    About Navidea
    Navidea Biopharmaceuticals, Inc. (NYSE MKT: NAVB) is a biopharmaceutical
    company focused on the development and commercialization of precision
    immunodiagnostic agents and immunotherapeutics. Navidea is developing
    multiple precision-targeted products and platforms including Manocept™
    and NAV4694 to help identify the sites and pathways of undetected
    disease and enable better diagnostic accuracy, clinical decision-making,
    targeted treatment and, ultimately, patient care. Lymphoseek®
    (technetium Tc 99m tilmanocept) injection, Navidea’s first commercial
    product from the Manocept platform, was approved by the FDA in March
    2013 and in Europe in November 2014. The development activities of the
    Manocept immunotherapeutic platform will be conducted by Navidea in
    conjunction with its subsidiary, Macrophage Therapeutics. Navidea’s
    strategy is to deliver superior growth and shareholder return by
    bringing to market novel products and advancing the Company’s pipeline
    through global partnering and commercialization efforts. For more
    information, please visit www.navidea.com.
    The Private Securities Litigation Reform Act of 1995 (the Act)
    provides a safe harbor for forward-looking statements made by or on
    behalf of the Company. 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 within the meaning of the Act. 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, our ability to
    repay our debt, the outcome of the CRG litigation, 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.

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