Y-mAbs Therapeutics, Inc.
Investors that purchased the Company’s securities and have suffered a loss, please fill in transaction information below, or email to firstname.lastname@example.org.
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The investigation focuses on whether the Company issued false and/or misleading statements and/or failed to disclose information pertinent to investors. Y-mAbs is the subject of briefing documents posted to the FDA website on October 26, 2022. According to the documents, FDA scientists have identified concerns with the data submitted as part of the Company’s Biologics License Application (BLA) for omburtamab. The FDA identified multiple issues with the Company’s data, including the differences between its study and control populations. Based on this news, shares of Y-mAbs fell by more than 23% in intraday trading on the same day.