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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of
the Securities Exchange
Act of 1934
Date of Report (Date of earliest event reported):
June 10, 2026
Humacyte, Inc.
(Exact name of registrant as specified in its charter)
| Delaware |
|
001-39532 |
|
85-1763759 |
(State or other jurisdiction of
incorporation or organization) |
|
(Commission File Number) |
|
(I.R.S. Employer
Identification Number) |
|
2525 East North Carolina Highway 54
Durham, NC |
|
27713 |
| (Address of principal executive offices) |
|
(Zip code) |
(919) 313-9633
(Registrant’s telephone number, including
area code)
Not Applicable
(Former name or former address, if changed since
last report)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
| ¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class |
|
Trading Symbol(s) |
|
Name of each exchange on which
registered |
| Common
Stock, par value $0.0001 per share |
|
HUMA |
|
The Nasdaq Stock Market LLC |
| Redeemable
Warrants, each whole warrant exercisable for one share of Common Stock at an exercise price of $11.50 |
|
HUMAW |
|
The Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant
is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the
Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ¨
| If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period
for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨ |
Item 1.01. Entry into a Material Definitive Agreement.
On
June 10, 2026, Humacyte, Inc. (the “Company”) entered into an underwriting agreement (the “Underwriting Agreement”)
with Barclays Capital Inc., BTIG, LLC and Titan Partners Group LLC, a division of American Capital Partners, LLC, as representatives of
the several underwriters named therein (collectively, the “Underwriters”), relating to the issuance and sale in an underwritten
offering (the “Offering”), pursuant to which the Company agreed to issue and sell 47,619,048 shares of the Company’s
common stock, $0.0001 par value per share, at a price to the public of $1.05 per share (the “Firm Shares”). The Company also
granted the Underwriters a 30-day option to purchase up to an additional 7,142,857 shares of the Company’s common stock at the same
price as the Firm Shares (the “Option Shares” and, together with the Firm Shares, the “Shares”).
The
net proceeds to the Company from the Offering are expected to be approximately $46.80 million, after deducting the underwriting discounts
and commissions and estimated Offering expenses payable by the Company, or approximately $53.85 million if the Underwriters exercise in
full their option to purchase the Option Shares. The Offering is expected to close on or about June 12, 2026, subject to the satisfaction
of customary closing conditions.
The Offering is being made pursuant to the Company’s
effective shelf registration statement on Form S-3 (File No. 333-290231), which was previously filed with the U.S. Securities and Exchange
Commission (the “Commission”) on September 12, 2025 and declared effective by the Commission on September 22, 2025.
The Underwriting
Agreement contains customary representations, warranties and agreements by the Company, customary conditions to closing, indemnification
obligations of the Company and the Underwriters, including for liabilities under the Securities Act of 1933, as amended (the “Securities
Act”), and termination provisions. The representations, warranties and covenants contained in the Underwriting
Agreement were made only for purposes of such agreement and are as of specific dates, are
not for the benefit of any party other than the parties thereto, and are not intended as
documents for investors and the public to obtain factual information about the current state of affairs of the parties thereto. Rather,
investors and the public should look to other disclosures contained in the Company’s annual, quarterly and current reports the Company
may file with the Commission.
The Underwriting Agreement is filed as Exhibit
1.1 hereto and is incorporated herein by reference. The foregoing description of the terms of the Underwriting Agreement is qualified
in its entirety by reference to the Underwriting Agreement.
The legal opinion of Covington & Burling LLP
relating to the Shares is filed herewith as Exhibit 5.1.
Item 7.01. Regulation FD Disclosure.
On
June 10, 2026, the Company issued press releases announcing the commencement of the Offering and the pricing of the Offering. Copies
of the press releases are furnished as Exhibit 99.1 and Exhibit 99.2, respectively, to this Current Report on Form 8-K and are incorporated
by reference herein.
The information contained in this Item 7.01 shall
not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”),
or incorporated by reference in any filing under the Securities Act, or the Exchange Act, except as shall be expressly set forth by specific
reference in such a filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
|
Exhibit
Number |
|
Description |
| 1.1 |
|
Underwriting Agreement, dated June 10, 2026, by and among Humacyte, Inc., and Barclays Inc., BTIG, LLC and Trian Partners Group LLC, as representatives of the Underwriters. |
| |
|
|
| 5.1 |
|
Opinion of Covington & Burling LLP. |
| |
|
|
| 23.1 |
|
Consent of Covington & Burling LLP (contained in Exhibit 5.1). |
| |
|
|
| 99.1 |
|
Press release, dated June 10, 2026. |
| |
|
|
| 99.2 |
|
Press release, dated June 10, 2026. |
| |
|
|
| 104 |
|
Cover Page Interactive Data File (embedded within the Inline XBRL document). |
SIGNATURE
Pursuant to the requirements of the Securities
Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| |
HUMACYTE,
INC. |
| |
|
|
| Date:
June 11, 2026 |
By: |
/s/
Dale A. Sander |
| |
|
Name: |
Dale
A. Sander |
| |
|
Title: |
Chief
Financial Officer, Chief Corporate Development Officer and Treasurer |
Exhibit 99.1
Humacyte, Inc. Announces Proposed Public Offering
of Common Stock
DURHAM, N.C., June 10, 2026 –
Humacyte, Inc. (Nasdaq: HUMA), a commercial-stage biotechnology platform company developing universally implantable, bioengineered
human tissues at commercial scale, today announced that it has commenced an underwritten public offering of its common stock. In
addition, Humacyte intends to grant the underwriters an option for a period of 30 days to purchase up to an additional 15% of the number
of shares of common stock sold in connection with the offering. All of the shares of common stock are being offered by Humacyte.
Barclays, BTIG and Titan Partners, a division of American Capital Partners,
are acting as joint book-running managers for the offering. The offering is subject to market conditions and there can be no assurance
as to whether or when the offering may be completed, or as to the actual size or terms of the offering.
Humacyte intends to use the net proceeds that it will receive from
the offering to fund the commercialization of Symvess®, the planned filing of a Biologics License Application supplement
in a hemodialysis indication and related activities, the development of the product candidates in its pipeline and for working capital
and general corporate purposes.
A shelf registration statement on Form S-3 (No. 333-290231) was previously
filed with the Securities and Exchange Commission (the “SEC”) on September 12, 2025 and declared effective by the SEC on September
22, 2025. The securities will be offered by means of a prospectus supplement and accompanying prospectus relating to the offering that
form a part of the registration statement. A preliminary prospectus supplement and the accompanying prospectus relating to and describing
the terms of the offering will be filed with the SEC and will be available on the SEC’s website at www.sec.gov. Copies of the preliminary
prospectus supplement, when available, and the accompanying prospectus relating to the offering may be obtained from Barclays Capital
Inc., c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, New York 11717, by telephone at (888) 603-5847, or by email
at barclaysprospectus@broadridge.com; BTIG, LLC, 65 East 55th Street, New York, New York 10022, by telephone at (212) 593-7555 or by email
at ProspectusDelivery@btig.com; or Titan Partners Group LLC, a division of American Capital Partners, LLC, 4 World Trade Center, 49th
Floor, New York, NY 10007, by phone at (929) 833-1246 or by email at prospectus@titanpartnersgrp.com.
This press release shall not constitute an offer to sell or the solicitation
of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or jurisdiction
in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such
state or jurisdiction.
About Humacyte
Humacyte, Inc. (Nasdaq: HUMA) is a commercial-stage biotechnology platform
company developing universally implantable, bioengineered human tissues at commercial scale, and in the first quarter of 2025 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. Humacyte 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 (“FDA”)
approval in the extremity vascular trauma indication, the acellular tissue engineered vessel (“ATEV”) is an investigational
product and has not been approved for sale by the FDA or any other regulatory agency.
Forward-Looking Statements
This press release contains forward-looking statements that are based
on beliefs and assumptions and on information currently available. In some cases, you can identify forward-looking statements by the following
words: “may,” “will,” “could,” “would,” “should,” “expect,” “intend,”
“plan,” “anticipate,” “believe,” “estimate,” “predict,” “project,”
“potential,” “continue,” “ongoing” or the negative of these terms or other comparable terminology,
although not all forward-looking statements contain these words. These statements involve risks, uncertainties, and other factors that
may cause actual results, levels of activity, performance, or achievements to be materially different from the information expressed or
implied by these forward-looking statements. Although Humacyte believes that it has a reasonable basis for each forward-looking statement
contained in this press release, Humacyte cautions you that these statements are based on a combination of facts and factors currently
known by it and its projections of the future, about which Humacyte cannot be certain. Forward-looking statements in this press release
include, but are not limited to, statements regarding the timing and success of the proposed offering; whether Humacyte will be able to
raise capital through the sale of shares of common stock in the offering and the anticipated use of proceeds from the proposed offering.
Humacyte cannot assure you that the forward-looking statements in this press release will prove to be accurate. These forward-looking
statements are subject to a number of significant risks and uncertainties that could cause actual results to differ materially from expected
results, including, among others, changes in applicable laws or regulations, the possibility that Humacyte may be adversely affected by
other economic, business, and/or competitive factors, and other risks and uncertainties, including those described under the header “Risk
Factors” in Humacyte’s Annual Report on Form 10-K for the year ended December 31, 2025 and in Humacyte’s Quarterly Report
on Form 10-Q for the quarter ended March 31, 2026, each filed by Humacyte with the SEC, and in future SEC filings. Most of these factors
are outside of Humacyte’s control and are difficult to predict. Furthermore, if the forward-looking statements prove to be inaccurate,
the inaccuracy may be material. In light of the significant uncertainties in these forward-looking statements, you should not regard these
statements as a representation or warranty by Humacyte or any other person that Humacyte will achieve its objectives and plans in any
specified time frame, or at all. Except as required by law, Humacyte has no current intention of updating any of the forward-looking statements
in this press release. You should, therefore, not rely on these forward-looking statements as representing Humacyte’s views as of
any date subsequent to the date of this press release.
Humacyte Investor Contact:
Joyce Allaire
LifeSci Advisors LLC
+1-617-435-6602
jallaire@lifesciadvisors.com
investors@humacyte.com
Humacyte Media Contact:
Rich Luchette
Precision Strategies
+1-202-845-3924
rich@precisionstrategies.com
media@humacyte.com
Exhibit 99.2
Humacyte, Inc. Announces Pricing of Public Offering
of Common Stock
DURHAM, N.C., June 10, 2026 –
Humacyte, Inc. (Nasdaq: HUMA), a commercial-stage biotechnology platform company developing universally implantable, bioengineered
human tissues at commercial scale, today announced the pricing of an underwritten public offering of 47,619,048
shares of its common stock at a public offering price of $1.05 per share. The aggregate gross
proceeds from this offering are expected to be $50 million, before deducting underwriting
discounts and commissions and other offering expenses payable by Humacyte. The closing of the offering is expected to occur on or about
June 12, 2026, subject to the satisfaction of customary closing conditions. In addition,
Humacyte has granted the underwriters an option for a period of 30 days to purchase up to an additional 7,142,857
shares of Humacyte’s common stock at the public offering price, less underwriting discounts and commissions. All of the shares of
common stock are being sold by Humacyte.
Barclays, BTIG and Titan Partners, a division of American Capital Partners,
are acting as joint book-running managers for the offering.
Humacyte intends to use the net proceeds that it will receive from
the offering to fund the commercialization of Symvess®, the planned filing of a Biologics License Application supplement
in a hemodialysis indication and related activities, the development of the product candidates in its pipeline and for working capital
and general corporate purposes.
A shelf registration statement on Form S-3 (No. 333-290231) was previously
filed with the Securities and Exchange Commission (the “SEC”) on September 12, 2025 and declared effective by the SEC on September
22, 2025. The securities are being offered by means of a prospectus supplement and accompanying prospectus relating to the offering that
form a part of the registration statement. A preliminary prospectus supplement and the accompanying prospectus relating to and describing
the terms of the offering was filed with the SEC on June 10, 2026 and is available on the
SEC’s website at www.sec.gov. The final prospectus supplement relating to and describing the terms of the offering will be filed
with the SEC and will be available on the SEC’s website at www.sec.gov. Before investing in the offering, you should read each of
the prospectus supplement and the accompanying prospectus relating to the offering in their entirety as well as the other documents that
Humacyte has filed with the SEC that are incorporated by reference in the prospectus supplement and the accompanying prospectus relating
to the offering, which provide more information about Humacyte and the offering. Copies of the final prospectus supplement, when available,
and accompanying prospectus relating to the offering may be obtained from Barclays Capital Inc., c/o Broadridge Financial Solutions, 1155
Long Island Avenue, Edgewood, New York 11717, by telephone at (888) 603-5847, or by email at barclaysprospectus@broadridge.com; BTIG,
LLC, 65 East 55th Street, New York, New York 10022, by telephone at (212) 593-7555 or by email at ProspectusDelivery@btig.com; or Titan
Partners Group LLC, a division of American Capital Partners, LLC, 4 World Trade Center, 49th Floor, New York, NY 10007, by phone at (929)
833-1246 or by email at prospectus@titanpartnersgrp.com.
This press release shall not constitute an offer to sell or the solicitation
of an offer to buy any of the securities described herein, nor shall there be any sale of these securities in any state or jurisdiction
in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such
state or jurisdiction.
About Humacyte
Humacyte, Inc. (Nasdaq: HUMA) is a commercial-stage biotechnology platform
company developing universally implantable, bioengineered human tissues at commercial scale, and in the first quarter of 2025 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. Humacyte 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 (“FDA”)
approval in the extremity vascular trauma indication, the acellular tissue engineered vessel (“ATEV”) is an investigational
product and has not been approved for sale by the FDA or any other regulatory agency.
Forward-Looking Statements
This press release contains forward-looking statements that are based
on beliefs and assumptions and on information currently available. In some cases, you can identify forward-looking statements by the following
words: “may,” “will,” “could,” “would,” “should,” “expect,” “intend,”
“plan,” “anticipate,” “believe,” “estimate,” “predict,” “project,”
“potential,” “continue,” “ongoing” or the negative of these terms or other comparable terminology,
although not all forward-looking statements contain these words. These statements involve risks, uncertainties, and other factors that
may cause actual results, levels of activity, performance, or achievements to be materially different from the information expressed or
implied by these forward-looking statements. Although Humacyte believes that it has a reasonable basis for each forward-looking statement
contained in this press release, Humacyte cautions you that these statements are based on a combination of facts and factors currently
known by it and its projections of the future, about which Humacyte cannot be certain. Forward-looking statements in this press release
include, but are not limited to, statements regarding the timing and satisfaction of customary closing conditions of the offering and
the anticipated use of proceeds from the offering. Humacyte cannot assure you that the forward-looking statements in this press release
will prove to be accurate. These forward-looking statements are subject to a number of significant risks and uncertainties that could
cause actual results to differ materially from expected results, including, among others, changes in applicable laws or regulations, the
possibility that Humacyte may be adversely affected by other economic, business, and/or competitive factors, and other risks and uncertainties,
including those described under the header “Risk Factors” in Humacyte’s Annual Report on Form 10-K for the year ended
December 31, 2025 and in Humacyte’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, each filed by Humacyte with
the SEC, and in future SEC filings. Most of these factors are outside of Humacyte’s control and are difficult to predict. Furthermore,
if the forward-looking statements prove to be inaccurate, the inaccuracy may be material. In light of the significant uncertainties in
these forward-looking statements, you should not regard these statements as a representation or warranty by Humacyte or any other person
that Humacyte will achieve its objectives and plans in any specified time frame, or at all. Except as required by law, Humacyte has no
current intention of updating any of the forward-looking statements in this press release. You should, therefore, not rely on these forward-looking
statements as representing Humacyte’s views as of any date subsequent to the date of this press release.
Humacyte Investor Contact:
Joyce Allaire
LifeSci Advisors LLC
+1-617-435-6602
jallaire@lifesciadvisors.com
investors@humacyte.com
Humacyte Media Contact:
Rich Luchette
Precision Strategies
+1-202-845-3924
rich@precisionstrategies.com
media@humacyte.com