Humacyte Prices $50 Million Public Offering to Support Commercialization of Symvess and Pipeline Development

June 16th, 2026 4:25 PM
By: Newsworthy Staff

Humacyte announced the pricing of a $50 million public offering of 47.6 million shares at $1.05 per share, with proceeds earmarked for the commercialization of Symvess, a Biologics License Application supplement for hemodialysis, and pipeline advancement.

Humacyte Prices $50 Million Public Offering to Support Commercialization of Symvess and Pipeline Development

Humacyte Inc. (NASDAQ: HUMA) has announced the pricing of an underwritten public offering of 47.6 million shares of common stock at $1.05 per share, with expected gross proceeds of approximately $50 million before underwriting discounts, commissions and offering expenses. The company also granted underwriters a 30-day option to purchase up to an additional 7.1 million shares at the public offering price. The offering is expected to close on or about June 12, 2026, subject to customary closing conditions.

Humacyte said it intends to use the net proceeds to support commercialization of Symvess(R), advance a planned Biologics License Application supplement filing for a hemodialysis indication, fund development of pipeline candidates and provide working capital for general corporate purposes. Barclays, BTIG and Titan Partners, a division of American Capital Partners, are serving as joint book-running managers for the offering. For more details, visit the full press release at https://ibn.fm/k6T1b.

Humacyte is a commercial-stage biotechnology platform company developing universally implantable, bioengineered human tissues at commercial scale. In the first quarter of 2025, the company commenced the United States commercial launch of Symvess, its first FDA-approved product. Humacyte is pioneering the development and manufacture of off-the-shelf, universally implantable, bioengineered human tissues, advanced tissue constructs and organ systems with the goal of improving the lives of patients and transforming the practice of medicine. The company is leveraging its novel, scalable technology platform to develop proprietary, bioengineered, acellular human tissues for use in the treatment of diseases and conditions across a range of anatomic locations in multiple therapeutic areas.

For uses other than the U.S. Food and Drug Administration approval in the extremity vascular trauma indication, the acellular tissue engineered vessel is an investigational product and has not been approved for sale by the FDA or any other regulatory agency. For further information, visit the company’s website at https://humacyte.com/.

Source Statement

This news article relied primarily on a press release disributed by InvestorBrandNetwork (IBN). You can read the source press release here,

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