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Editorial Advisory Board

  • Professor Andrea M. Armani, University of Southern California
  • Ruti Ben-Shlomi, Ph.D., LightSolver
  • James Butler, Ph.D., Hamamatsu
  • Natalie Fardian-Melamed, Ph.D., Columbia University
  • Justin Sigley, Ph.D., AmeriCOM
  • Professor Birgit Stiller, Max Planck Institute for the Science of Light, and Leibniz University of Hannover
  • Professor Stephen Sweeney, University of Glasgow
  • Mohan Wang, Ph.D., University of Oxford
  • Professor Xuchen Wang, Harbin Engineering University
  • Professor Stefan Witte, Delft University of Technology

SHAREHOLDER ALERT: Robbins LLP Reminds Investors that Provention Bio, Inc. (PRVB) is Being Sued for Misleading Shareholders

Shareholder rights law firm Robbins LLP reminds investors that a class action has been filed on behalf of all purchasers of Provention Bio, Inc. (NASDAQ: PRVB) securities between November 2, 2020 and April 8, 2021, against the Company and certain of its officers for remedies under the Securities Exchange Act of 1934. Provention is a clinical stage biopharmaceutical company that focuses on the development and commercialization of therapeutics and solutions to intercept and prevent immune-mediated diseases. The Company's product candidates include PRV-103 teplizumad and mAb, in Phase III clinical trial for interception of Type 1 diabetes ("T1D").

If you suffered a loss due to Provention Bio, Inc.'s misconduct, click here.

Provention Bio, Inc. (PRVB) Made Misstatements Regarding its Deteriorating Financial Condition

According to the complaint, during the class period, the Company touted the FDA's submission of a Biologics License Application ("BLA") for teplizumab for the delay or prevention of T1D in at-risk individuals, and granted Provention's request for Priority Review and assigned a user fee goal date of July 2, 2021, under the Prescription Drug User-Fee Act. However, these statements were false and/or misleading in that they failed to disclose that: (i) the teplizumab BLA was deficient in its submitted form and would require additional data to secure FDA approval; (ii) the teplizumab BLA lacked the evidentiary support the Company had led investors to believe it possessed; and (iii) the Company had overstated the teplizumab BLA's approval prospects and the commercialization timeline for the drug.

On April 8, 2021, Provention issued a press release announcing that it had received "notification on April 2, 2021 from the [FDA], stating that, as part of its ongoing review of the Company's [BLA] for teplizumab for the delay or prevention of clinical [T1D], the FDA has identified deficiencies that preclude discussion of labeling and post-marketing requirements/commitments at this time." On this news, Provention's stock price fell $1.73 per share, or almost 18%, to close at $8.00 per share on April 9, 2021.

If you purchased shares of Provention Bio, Inc. (PRVB) between November 2, 2020 and April 8, 2021, you have until July 23, 2021, to ask the court to appoint you lead plaintiff for the class.

All representation is on a contingency fee basis. Shareholders pay no fees or expenses.

Contact us to learn more:

Lauren Levi

(800) 350-6003

llevi@robbinsllp.com

Shareholder Information Form

Robbins LLP is a nationally recognized leader in shareholder rights law. To be notified if a class action against Provention Bio, Inc. settles or to receive free alerts about companies engaged in wrongdoing, sign up for Stock Watch today.

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