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DURECT Provides an Update to the Memryte Program Under Development,by Voyager Pharmaceutical Corp

nt, and manufacturing process development of Memryte, obtain regulatory and manufacturing approvals from regulatory agencies, and manufacture and commercialize Memryte, as well as marketplace acceptance of Memryte. Further information regarding these and other risks is included in DURECT's Form 10-Q dated May 9, 2007 under the heading "Risk Factors."

NOTE: Memryte is under development and has not been submitted or approved for commercialization by the US Food and Drug Administration or other health authorities.

CONTACT: Jeremiah Hall, Senior Vice President of Feinstein KeanHealthcare, +1-415-677-2700, or jeremiah.hall@fkhealth.com

Web site: http://www.durect.com//

Ticker Symbol: (NASDAQ-NMS:DRRX)

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