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Accentia Biopharmaceuticals Announces Favorable Interim Blinded,Data on SinuNase in Its Fast-Tracked Pivotal Phase 3 Clinical Trial,for Chronic Sinusitis

er factors that may cause the actual results of Accentia to be materially different from historical results or from any results expressed or implied by such forward-looking statements. These factors include, but are not limited to, risks and uncertainties related to the progress, timing, cost, and results of clinical trials and product development programs; difficulties or delays in obtaining regulatory approval for product candidates; competition from other pharmaceutical or biotechnology companies; and the additional risks discussed in filings with the Securities and Exchange Commission. All forward-looking statements are qualified in their entirety by this cautionary statement, and Accentia undertakes no obligation to revise or update this news release to reflect events or circumstances after the date hereof.

Contact

Accentia Biopharmaceuticals, Inc., Tampa, FL
Susan Bonitz, Ph.D., 813-864-2554-Extension 277
sbonitz@accentia.net
or
Investors:
The Investor Relations Group, New York
Adam S. Holdsworth, 212-825-3210
aholdsworth@investorrelationsgroup.com
or
Media:
Janet Vasquez, 212-825-3210
jvasqyez@investorrelationsgroup.com


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