DURECT is a biopharmaceutical company actively developing therapeutics based on its Epigenetic Regulator Program and proprietary drug delivery platforms. DUR 928, a new chemical entity in Phase 2 development, is the lead candidate in DURECT’s Epigenetic Regulator Program. An endogenous, orally bioavailable small molecule, DUR-928 has been shown in preclinical studies to play an important regulatory role in lipid homeostasis, inflammation, and cell survival. Human applications may include acute organ injury, as seen in alcoholic hepatitis; other hepatic diseases, such as nonalcoholic steatohepatitis (NASH) and primary sclerosing cholangitis; renal diseases; and inflammatory skin conditions such as psoriasis and atopic dermatitis. DURECT’s advanced oral and injectable delivery technologies are designed to enable new indications and enhanced attributes for small-molecule and biologic drugs. Late-stage product candidates in this category include POSIMIR® (bupivacaine extended-release solution), an investigational locally-acting, non-opioid analgesic intended to provide up to 3 days of continuous pain relief after surgery, and ORADUR®-Methylphenidate ER, an investigational formulation of methylphenidate that has been approved in Taiwan for the treatment of attention deficit hyperactivity disorder (ADHD) as Methydur Sustained Release Capsules. In addition, for the assignment of certain patent rights related to its drug delivery technology, DURECT is set to receive single digit sales-based earn-out payments from U.S. net sales of PERSERIS™ (risperidone), which was approved by FDA in July 2018 for the treatment of schizophrenia in adults and is owned and marketed by Indivior PLC.

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DURECT to Present at the 20th Annual B. Riley FBR Institutional Investor Conference on May 22, 2019

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DURECT Corporation Announces Preliminary Data from the Ongoing DUR-928 Alcoholic Hepatitis Phase 2a Trial

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