Kessler Topaz Meltzer & Check, LLP: Securities Fraud Class Action Lawsuit Filed Against Revance Therapeutics, Inc. (RVNC) on Their Behalf |
Monday, 17. January 2022 15:51 |
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RADNOR, Pa., Jan. 17, 2022 (GLOBE NEWSWIRE) -- The law firm of Kessler Topaz Meltzer & Check, LLP informs investors that a securities class action lawsuit has been filed in the United States District Court for the Northern District of California against Revance Therapeutics, Inc. (“Revance”) (NASDAQ: RVNC). The action charges Revance with violations of the federal securities laws, including omissions and fraudulent misrepresentations relating to the company’s business, operations, and prospects. As a result of Revance’s materially misleading statements to the public, Revance investors have suffered significant losses. CANNOT VIEW THIS VIDEO? PLEASE CLICK HERE CLICK HERE TO SUBMIT YOUR REVANCE LOSSES LEAD PLAINTIFF DEADLINE: February 8, 2022 CLASS PERIOD: November 25, 2019 through October 11, 2021 CONTACT AN ATTORNEY TO DISCUSS YOUR RIGHTS: REVANCE’S ALLEGED MISCONDUCT On November 25, 2019, Revance issued a press release announcing that it had submitted a Biologics License Application (“BLA”) to the FDA for DAXI. Then, on October 12, 2021, Revance issued a press release revealing that on July 2, 2021, the FDA had issued a Form 483 informing Revance of serious concerns it had discovered while inspecting one of Revance’s manufacturing facilities. Among other things, the Form 483 indicated that “[t]he current manufacturing process is not the process proposed for licensure,” and “[t]he firm’s Quality Unit lacks the responsibility and authority for the control, review, and approval of outsourced activities which includes defining the responsibilities and communication processes for quality-related activities in a written agreement.” Following this news, Revance’s stock price fell $6.85 per share, or 25%, to close at $20.45 per share on October 12, 2021. Then, on October 15, 2021, Revance issued another press release disclosing that “[i]n a communication received on October 15, [2021,] the FDA has determined it is unable to approve the BLA in its present form, and indicated that there are deficiencies related to the FDA’s onsite inspection at Revance’s manufacturing facility.” Following this news, Revance’s stock price fell $8.90 per share, or 39.19%, to close at $13.81 per share on October 18, 2021. WHAT CAN I DO? CLICK HERE TO SIGN UP FOR THE CASE WHO CAN BE A LEAD PLAINTIFF? ABOUT KESSLER TOPAZ MELTZER & CHECK, LLP CONTACT: Video accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/ecebd236-1d0d-4040-b180-2aee1773108e ![]() |
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