Recent Updates
Recently added Catalysts
HUMA Negative Sentiment Score: 15/100

HUMACYTE ALERT: Bragar Eagel & Squire, P.C. Announces that a Class Action Lawsuit Has Been Filed Against Humacyte, Inc. and Encourages Investors to Contact the Firm

Key Takeaway: A class action lawsuit has been filed against Humacyte, Inc. by Bragar Eagel & Squire, alleging that the company made misleading statements and failed to disclose important adverse information regarding its operations and prospects. The lawsuit targets investors who acquired Humacyte securities between May 10, 2024, and October 17, 2024. Key allegations include non-compliance with good manufacturing practices at its Durham facility and delays in FDA review due to remediation needs. Investors are encouraged to participate in the lawsuit, with a deadline to apply as lead plaintiff set for January 17, 2025.

Market Sentiment Analysis

CONCERNS & RISKS

  • Class action lawsuit filed against Humacyte over material misstatements.
  • Allegations include failure to comply with good manufacturing practices.
  • FDA review of the BLA delayed due to remediation of deficiencies.
  • Substantial risk to FDA approval of ATEV for vascular trauma.

Full Press Release Details

NEW YORK, Dec. 10, 2024 (GLOBE NEWSWIRE) -- Bragar Eagel & Squire, P.C., a nationally recognized stockholder rights law firm, announces that a class action lawsuit has been filed against Humacyte, Inc. (“Humacyte” or the “Company”) (NASDAQ: HUMA) in the United States District Court for the Middle District of North Carolina on behalf of all persons and entities who purchased or otherwise acquired Humacyte securities between May 10, 2024 and October 17, 2024, both dates inclusive (the “Class Period”). Investors have until January 17, 2025 to apply to the Court to be appointed as lead plaintiff in the lawsuit.
Click here to participate in the action.
The Complaint alleges that throughout the Class Period, Defendants made materially false and/or misleading statements, as well as failed to disclose material adverse facts about the Company's business, operations, and prospects. Specifically, the Complaint alleges that Defendants failed to disclose to investors: (1) that the Company's Durham, North Carolina facility failed to comply with good manufacturing practices, including quality assurance and microbial testing; (2) that the FDA's review of the BLA would be delayed while Humacyte remediated these deficiencies; and (3) that, as a result, there was a substantial risk to FDA approval of ATEV for vascular trauma; and (4) that, as a result of the foregoing, Defendants' positive statements about the Company's business, operations, and prospects were materially misleading and/or lacked a reasonable basis.
If you purchased or otherwise acquired Humacyte shares and suffered a loss, are a long-term stockholder, have information, would like to learn more about these claims, or have any questions concerning this announcement or your rights or interests with respect to these matters, please contact Brandon Walker or Marion Passmore by email at investigations@bespc.com, telephone at (212) 355-4648, or by filling out this contact form. There is no cost or obligation to you.
About Bragar Eagel & Squire, P.C.:
Bragar Eagel & Squire, P.C. is a nationally recognized law firm with offices in New York, California, and South Carolina. The firm represents individual and institutional investors in commercial, securities, derivative, and other complex litigation in state and federal courts across the country. For more information about the firm, please visit www.bespc.com. Attorney advertising. Prior results do not guarantee similar outcomes.
Contact Information:
Bragar Eagel & Squire, P.C.
Brandon Walker, Esq.
Marion Passmore, Esq.

Tags

Bragar Eagel & Squire

Frequently Asked Questions

What is the class action lawsuit against Humacyte about?

The lawsuit alleges that Humacyte made false statements and omitted key information regarding its business practices and FDA approval process.

Who can participate in the Humacyte class action?

All persons and entities who purchased Humacyte securities between May 10, 2024, and October 17, 2024, may participate.

When is the deadline to apply as lead plaintiff?

Investors have until January 17, 2025, to apply to the Court as lead plaintiff.

What issues did Humacyte fail to disclose?

Humacyte failed to disclose compliance issues at their manufacturing facility affecting FDA review.

How can I contact Bragar Eagel & Squire for more information?

You can email investigations@bespc.com or call (212) 355-4648 for inquiries.

Last updated: Dec 11, 2024