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DURECT Corporation to Announce 2020 Financial Results and Provide Business Update on March 4

CUPERTINO, Calif., Feb. 25, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that it will report its fourth quarter and year ended December 31, 2020 financial results and host a conference call after the market close on Thursday, March 4, 2021. Thursday, March 4 @ 4:30pm Eastern Time / 1:30 p.m. Pacific Time Toll Free: 877-407-0784 International:  […]

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DURECT Corporation Announces Pricing of $42.5 Million Public Offering of Common Stock

CUPERTINO, Calif., Feb. 4, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) (“DURECT“), a biopharmaceutical company committed to transforming the treatment of acute organ injury and chronic liver diseases by advancing novel and potentially lifesaving therapies based on its endogenous epigenetic regulator program, today announced the pricing of its underwritten public offering of 17,708,333 shares of its

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DURECT Corporation Announces Proposed Offering of Common Stock

CUPERTINO, Calif., Feb. 3, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) (“DURECT“), a biopharmaceutical company committed to transforming the treatment of acute organ injury and chronic liver diseases by advancing novel and potentially lifesaving therapies based on its endogenous epigenetic regulator program, today announced that it is commencing an underwritten public offering of its common stock

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DURECT Corporation Announces U.S. FDA Approval of POSIMIR® For Post-Surgical Pain Reduction for up to 72 Hours Following Arthroscopic Subacromial Decompression

POSIMIR is the only approved sustained-release bupivacaine product indicated for up to 72 hours of post-surgical analgesia from a single application Conference Call Today, February 2, 2021 at 4:30pm ET CUPERTINO, Calif., Feb. 2, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that the U.S. Food and Drug Administration (FDA) has approved POSIMIR® (bupivacaine solution)

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DURECT Corporation Announces First Patient Dosed in Phase 2b AHFIRM Study of DUR-928 in Severe Alcohol-Associated Hepatitis

CUPERTINO, Calif., Jan. 25, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced it has dosed the first patient in its AHFIRM randomized, double-blind, placebo-controlled, multi-center Phase 2b study to evaluate the safety and efficacy of DUR-928 in severe alcohol-associated hepatitis (AH) patients. “We are excited to have begun dosing severe AH patients in the AHFIRM

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DURECT Corporation Appoints Two New Board Members

CUPERTINO, Calif., Jan. 5, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced the appointment of two new members to its board of directors, Gail J. Maderis, MBA and Mohammad Azab, M.D., M. Sc., MBA, two senior industry veterans with extensive drug development, clinical research and medical affairs experience. “We are pleased to welcome Ms. Maderis

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DURECT Corporation Announces Closing of LACTEL® Absorbable Polymer Product Line Sale to Evonik and Receipt of $15 Million

CUPERTINO, Calif., Jan. 4, 2021 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that the sale of the LACTEL product line to Evonik closed and the $15 million payment was received on December 31, 2020. About DURECT CorporationDURECT is a biopharmaceutical company committed to transforming the treatment of acute organ injury and chronic liver diseases by advancing novel and

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DURECT Corporation to Participate in Investor Conferences in January 2021

H.C. Wainwright BioConnect 2021 Conference and LifeSci Advisors Corporate Access Event CUPERTINO, Calif., Dec. 21, 2020 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that it will participate in the forthcoming H.C. Wainwright BioConnect 2021 Conference and Annual LifeSci Advisors Corporate Access Event. Both conferences will take place virtually.  H.C. Wainwright BioConnect 2021 Conference (January 11-14) DURECT

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DURECT Corporation Announces DUR-928 Granted FDA Fast Track Designation for Treatment of Alcoholic Hepatitis

CUPERTINO, Calif., Dec. 16, 2020 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation to DUR-928 for the treatment of alcoholic hepatitis (AH, also known as alcohol-associated hepatitis). AH is an acute, life-threatening form of alcohol-associated liver disease (ALD). DUR-928 is the lead investigational product

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DURECT Corporation to Sell its LACTEL® Absorbable Polymer Product Line to Evonik for $15 Million

CUPERTINO, Calif., Dec. 7, 2020 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced that it has signed an agreement to sell its LACTEL Absorbable Polymer (LACTEL) product line to Evonik, a global leader in specialty chemicals. Under the terms of the agreement, Evonik will pay DURECT $15 million in exchange for certain assets and liabilities associated with LACTEL

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