Primary Endpoint of Pivotal Phase III Clinical Trial Achieved for ...(limited to difficulties or delaysin deve...),Health

Date:12/6/2007

limited to, difficulties or delays in development, testing, regulatory approval, production and marketing of Remoxy and other potential ORADUR-based products, unexpected delays in the filing of a New Drug Application for Remoxy with the FDA, unexpected adverse side effects or inadequate therapeutic efficacy of Remoxy or other potential ORADUR-based products that could slow or prevent product approval or market acceptance (including the risk that current and past results of clinical trials are not necessarily indicative of future results of clinical trials), the uncertainty of patent protection for Remoxy and other potential ORADUR-based products and unanticipated research and development and other costs. Further information regarding these and other risks is included in DURECT's Form 10-Q dated November 8, 2007 under the heading "Risk Factors."

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