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Humacyte, Inc. Class Action Lawsuit Alert: Johnson Fistel Announces Shareholders with Losses Should Contact the Law Firm for More Information

Key Takeaway: A class action lawsuit has been filed against Humacyte, Inc. on behalf of investors who experienced losses between May 10, 2024, and October 17, 2024. The lawsuit claims that the company made misleading statements regarding its manufacturing practices and the status of its FDA approval process. Investors are encouraged to apply for lead plaintiff status by January 17, 2025. The situation is primarily driven by allegations of compliance failures at the company's facility in Durham, North Carolina.

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CONCERNS & RISKS

  • Humacyte's Durham facility allegedly violated good manufacturing practices.
  • FDA review of Humacyte's Biologics License Application is delayed due to remediation needs.
  • Significant risks to the FDA approval of Acellular Tissue Engineered Vessel arise from the current issues.
  • Investors learned that previous positive statements from Humacyte were materially misleading.

Full Press Release Details

SAN DIEGO, Nov. 25, 2024 (GLOBE NEWSWIRE) -- Shareholder rights law firm Johnson Fistel, LLP announces that a class action lawsuit has commenced on behalf of investors of Humacyte, Inc. (NASDAQ: HUMA). The lawsuit seeks to recover losses on behalf of investors who acquired securities between May 10, 2024 and October 17, 2024. Investors have until January 17, 2025, to apply to the Court to be appointed as lead plaintiff in the lawsuit.
If you incurred significant losses and want to act as the lead plaintiff in the Humacyte class action lawsuit or determine if you are eligible to receive a potential recovery of your losses, please submit your details here: https://www.johnsonfistel.com/investigations/humacyte
Contact for More Information: James Baker, (619) 814-4471, jimb@johnsonfistel.com or fjohnson@johnsonfistel.com
According to the lawsuit, during the Class Period, defendants made false and/or misleading statements and/or failed to disclose that: (1) Humacyte’s Durham, North Carolina facility failed to comply with good manufacturing practices, including quality assurance and microbial testing; (2) the Food and Drug Administration’s (“FDA”) review of the Biologics License Application (“BLA”) would be delayed while Humacyte remediated these deficiencies; and (3) as a result, there was a substantial risk to FDA approval of Acellular Tissue Engineered Vessel (“ATEV”) for vascular trauma; and (4) as a result of the foregoing, defendants’ positive statements about Humacyte’s business, operations, and prospects were materially misleading and/or lacked a reasonable basis. When the true details entered the market, the lawsuit claims that investors suffered damages.
Investor Action Steps: Shareholders who incurred losses during the class period, have until January 17, 2025, to move the court to become a lead plaintiff in this action. A lead plaintiff will act on behalf of all other class members in directing the class-action lawsuit. The lead plaintiff can select a law firm of its choice to litigate the class-action lawsuit. An investor's ability to share any potential future recovery of the class action lawsuit is not dependent upon serving as lead plaintiff.
About Johnson Fistel, LLP | Top Law Firm, Securities Fraud, Investors Rights:
Johnson Fistel, LLP is a nationally recognized shareholder rights law firm with offices in California, New York, Georgia, and Colorado. The firm represents individual and institutional investors in shareholder derivative and securities class action lawsuits. We also extend our services to foreign investors who have purchased on US exchanges. Stay updated with news on stock drops and learn how Johnson Fistel, LLP can help you recover your losses. For more information about the firm and its attorneys, please visit http://www.johnsonfistel.com.
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Johnson Fistel, LLP has paid for the dissemination of this promotional communication, and Frank J. Johnson is the attorney responsible for its content.
501 W. Broadway, Suite 800, San Diego, CA 92101
James Baker, Investor Relations or Frank J. Johnson, Esq., (619) 814-4471

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Frequently Asked Questions

What is the Humacyte class action lawsuit about?

The lawsuit addresses losses for investors who acquired Humacyte securities from May 10 to October 17, 2024.

How can I become a lead plaintiff in the lawsuit?

To act as a lead plaintiff, submit your details by January 17, 2025.

What misstatements does the lawsuit claim were made?

It claims Humacyte failed to disclose manufacturing compliance issues and FDA review delays.

What is the deadline for class members to act?

Investors must act by January 17, 2025, to be considered for lead plaintiff status.

Who can investors contact for more information?

Investors can contact James Baker at (619) 814-4471 or via email.

Last updated: Nov 25, 2024