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DURECT Announces Launch of First FDA Approved SABER™-Injectable Peptide Product
Date:2/8/2011

oMate™ Equine and that regulate the ovulation in sows and mares, respectively.

DURECT Forward-Looking Statement

The statements in this press release regarding SucroMate, the potential royalty and other payments that may be received by DURECT from SucroMate and other described products and applications of the SABER technology are forward-looking statements involving risks and uncertainties that can cause actual results to differ materially from those in such forward-looking statements. Potential risks and uncertainties include, but are not limited to, the potential that SucroMate may not achieve meaningful commercial sales or that other SABER-based products may not be successfully developed and approved by the FDA or other regulatory agencies. Further information regarding these and other risks is included in DURECT's Form 10-Q dated November 4, 2010 under the heading "Risk Factors."


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