ng trodusquemine (MSI-1436),
the IL-9 antibody program, LOMUCIN(TM), or squalamine may be
delayed or may not be successful; the risk that Genaera may not
obtain regulatory approval for its products, whether due to
adequacy of the development program, the conduct of the clinical
trials, changing regulatory requirements, different methods of
evaluating and interpreting data, regulatory interpretations of
clinical risk and benefit, or otherwise; Genaera's reliance on its
collaborators, in connection with the development and
commercialization of Genaera's product candidates; market
acceptance of Genaera's products, if regulatory approval is
achieved; competition; general financial, economic, regulatory and
political conditions affecting the biotechnology and pharmaceutical
industry; and the other risks and uncertainties discussed in this
announcement and in Genaera's filings with the U.S. Securities and
Exchange Commission, all of which are available from the Commission
in its EDGAR database at
http://www.sec.gov as well as other
sources. You are encouraged to read these reports. Given the
uncertainties affecting development stage pharmaceutical companies,
you are cautioned not to place undue reliance on any such
forward-looking statements, any of which may turn out to be wrong
due to inaccurate assumptions, unknown risks, uncertainties or
other factors. Genaera does not intend (and it is not obligated) to
publicly update, revise or correct these forward-looking statements
or the risk factors that may relate thereto.
CONTACT: investor relations, Genaera Corporation,
+1-610-941-5675; ormedia, Susan Neath of Porter Novelli Life
Sciences, +1-619-849-6007, sneath@pnlifesciences.com
Web site: http://www.genaera.com/
Ticker Symbol: (NASDAQ-NMS:GENR)
Terms and conditi
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