Humacyte Announces Pricing of $15.0 Million Registered Direct Offering
Humacyte (Nasdaq: HUMA) has announced a $15.0 million registered direct offering of common stock and warrants. The company will sell 2,808,988 shares of common stock and warrants to purchase an equal number of shares at $5.34 per share. Half of the warrants will expire in 180 days, while the other half will expire in four and a half years from issuance. The offering is expected to close around November 15, 2024. The proceeds will be approximately $15.0 million before expenses.
Humacyte (Nasdaq: HUMA) ha annunciato un'offerta diretta registrata di azioni ordinarie e warrant del valore di 15,0 milioni di dollari. L'azienda venderà 2.808.988 azioni di azioni ordinarie e warrant per acquistare un numero equivalente di azioni a 5,34 dollari per azione. La metà dei warrant scadrà in 180 giorni, mentre l'altra metà scadrà quattro anni e mezzo dopo l'emissione. Si prevede che l'offerta si chiuda intorno al 15 novembre 2024. I proventi saranno di circa 15,0 milioni di dollari prima delle spese.
Humacyte (Nasdaq: HUMA) ha anunciado una oferta directa registrada de acciones ordinarias y warrants por un valor de 15,0 millones de dólares. La compañía venderá 2.808.988 acciones de acciones ordinarias y warrants para adquirir un número igual de acciones a 5,34 dólares por acción. La mitad de los warrants vencerán en 180 días, mientras que la otra mitad vencerá en cuatro años y medio a partir de la emisión. Se espera que la oferta cierre alrededor del 15 de noviembre de 2024. Los ingresos serán de aproximadamente 15,0 millones de dólares antes de gastos.
휴마사이트 (Nasdaq: HUMA)는 1,500만 달러 규모의 보통주 및 워런트의 등록된 직접 공모를 발표했습니다. 이 회사는 2,808,988주의 보통주와 동일한 수의 주식을 구매할 수 있는 워런트를 주당 5.34달러에 판매할 것입니다. 워런트의 절반은 180일 후에 만료되고, 나머지 절반은 발행일로부터 4년 반 후에 만료됩니다. 이 공모는 2024년 11월 15일경에 마감될 것으로 예상됩니다. 수익은 비용을 제외하고 약 1,500만 달러에 이를 것입니다.
Humacyte (Nasdaq: HUMA) a annoncé une offre directe enregistrée d'actions ordinaires et de bons de souscription d'une valeur de 15,0 millions de dollars. La société va vendre 2.808.988 actions ordinaires et des bons de souscription pour acquérir un nombre égal d'actions au prix de 5,34 dollars par action. La moitié des bons de souscription expirera dans 180 jours, tandis que l'autre moitié expirera quatre ans et demi après leur émission. L'offre devrait se clôturer autour du 15 novembre 2024. Les recettes seront d'environ 15,0 millions de dollars avant les frais.
Humacyte (Nasdaq: HUMA) hat ein registriertes Direct Offering von Stammaktien und Warrants im Wert von 15,0 Millionen Dollar angekündigt. Das Unternehmen wird 2.808.988 Aktien von Stammaktien und Warrants zum Kauf einer gleichen Anzahl von Aktien zu einem Preis von 5,34 Dollar pro Aktie verkaufen. Die Hälfte der Warrants läuft in 180 Tagen ab, während die andere Hälfte viereinhalb Jahre nach der Ausgabe verfällt. Es wird erwartet, dass das Angebot etwa am 15. November 2024 abgeschlossen wird. Die Einnahmen werden voraussichtlich etwa 15,0 Millionen Dollar vor Ausgaben betragen.
- Secured immediate funding of $15.0 million through registered direct offering
- Potential dilution of existing shareholders through issuance of 2,808,988 new shares
- Additional dilution risk from 2,808,988 warrant shares if exercised
- Relatively short-term financing solution indicating possible cash needs
Insights
This registered direct offering signals a significant capital raise but comes with notable dilution implications. The deal structure at
The total potential dilution could reach
DURHAM, N.C., Nov. 14, 2024 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable, bioengineered human tissue at commercial scale, today announced that it entered into a securities purchase agreement with an institutional investor to purchase approximately
Under the terms of the securities purchase agreement, the Company has agreed to sell 2,808,988 shares of its common stock and warrants to purchase up to 2,808,988 shares of common stock. 1,404,494 warrants will be exercisable immediately, have an exercise price of
The gross proceeds to the Company from the registered direct offering are estimated to be approximately
The proposed offering of the common stock and warrants described above is being offered by the Company pursuant to a “shelf” registration statement on Form S-3 (File No. 333-267225) filed with the Securities and Exchange Commission (SEC) and declared effective by the SEC on September 9, 2022, and the accompanying prospectus contained therein.
The offering is being made only by means of a prospectus supplement and accompanying prospectus. A prospectus supplement describing the terms of the public offering will be filed with the SEC and will form a part of the effective registration statement.
Copies of the prospectus supplement and the accompanying prospectus relating to this offering may be obtained, when available, on the SEC’s website at http://www.sec.gov.
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 developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. The Company develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s initial product candidates, a portfolio of ATEVs, are currently in late-stage clinical trials targeting multiple vascular applications, including vascular trauma repair, arteriovenous (AV) access for hemodialysis, and peripheral artery disease. A Biologics License Application for the ATEV in the vascular trauma indication is currently under review by the FDA and was granted Priority Review. Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery, treatment of type 1 diabetes, and multiple novel cell and tissue applications. Humacyte’s 6mm ATEV for AV access in hemodialysis was the first product candidate to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation and has also received FDA Fast Track designation. Humacyte’s 6mm ATEV for urgent arterial repair following extremity vascular trauma and for advanced PAD also have received an RMAT designations. The ATEV received priority designation for the treatment of vascular trauma by the U.S. Secretary of Defense. The ATEV is an investigational product and has not been approved for sale by the Food and Drug Administration or any international 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 we believe that we have a reasonable basis for each forward-looking statement contained in this press release, we caution you that these statements are based on a combination of facts and factors currently known by us and our projections of the future, about which we cannot be certain. Forward-looking statements in this press release include, but are not limited to, the statements regarding the anticipated closing of the offering; the anticipated use of proceeds from the offering; the outcome of the FDA’s review of our BLA seeking approval of the ATEV in the vascular trauma indication; the initiation, timing, progress, and results of our preclinical and clinical trials; the anticipated characteristics and performance of our ATEV; our ability to successfully complete preclinical and clinical trials for our ATEVs; the anticipated benefits of our ATEV relative to existing alternatives; the anticipated commercialization of our ATEVs and our ability to manufacture at commercial scale; the implementation of our business model and strategic plans for our business; and the timing or likelihood of regulatory filings, acceptances, and approvals. We 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 our Annual Report on Form 10-K for the year ended December 31, 2023, in our Quarterly Report on Form 10-Q for the quarter ended September 30, 2024, 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 us or any other person that we will achieve our objectives and plans in any specified time frame, or at all. Except as required by law, we have 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 our 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
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