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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 initiated against Humacyte, Inc. on behalf of investors who purchased shares between May 10, 2024, and October 17, 2024. Johnson Fistel, LLP is leading the action, which alleges that Humacyte misled investors regarding its manufacturing practices and the FDA approval process for its Acellular Tissue Engineered Vessel. Affected investors are encouraged to apply by January 17, 2025, to be appointed as lead plaintiff in the case. The lawsuit cites significant compliance issues at Humacyte's Durham, North Carolina facility that could impact the company's future success.

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CONCERNS & RISKS

  • Humacyte's facility failed to comply with good manufacturing practices.
  • The FDA review of Humacyte's BLA will be delayed due to these deficiencies.
  • There is a substantial risk to FDA approval of Acellular Tissue Engineered Vessel for vascular trauma.
  • Misleading statements by defendants about Humacyte's business and operations.

Full Press Release Details

SAN DIEGO, Dec. 19, 2024 (GLOBE NEWSWIRE) -- 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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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 lawsuit against Humacyte about?

The lawsuit claims Humacyte made misleading statements about its manufacturing practices and FDA approval risks.

Who can become a lead plaintiff in the lawsuit?

Investors who suffered losses from May 10, 2024, to October 17, 2024, can apply to be lead plaintiff.

What is the deadline for lead plaintiff applications?

The deadline to apply as a lead plaintiff is January 17, 2025.

How can I participate in the class action lawsuit?

Investors can submit their details online to determine eligibility for potential recovery.

What law firm is handling the Humacyte case?

Johnson Fistel, LLP is representing investors in the Humacyte class action lawsuit.

Last updated: Dec 19, 2024