EyePoint Pharmaceuticals Announces Pricing of Upsized Public Offering
EyePoint Pharmaceuticals (NASDAQ: EYPT) has announced the pricing of an upsized public offering of 12,727,273 shares of common stock at $11.00 per share, expecting to raise approximately $140.0 million in gross proceeds. The company has granted underwriters a 30-day option to purchase up to an additional 1,909,090 shares. The offering is expected to close around October 31, 2024. The proceeds will be used to advance clinical development of DURAVYU™ for wet AMD and DME, support pipeline development initiatives, and general corporate purposes.
EyePoint Pharmaceuticals (NASDAQ: EYPT) ha annunciato il prezzo di un'offerta pubblica aumentata di 12.727.273 azioni di azioni ordinarie a 11,00 $ per azione, prevedendo di raccogliere circa 140,0 milioni di dollari in proventi lordi. L'azienda ha concesso ai sottoscrittori un'opzione di 30 giorni per acquistare fino a 1.909.090 azioni aggiuntive. Si prevede che l'offerta si chiuderà intorno al 31 ottobre 2024. I proventi saranno utilizzati per promuovere lo sviluppo clinico di DURAVYU™ per AMD umida e DME, supportare le iniziative di sviluppo della pipeline e per le esigenze aziendali generali.
EyePoint Pharmaceuticals (NASDAQ: EYPT) ha anunciado el precio de una oferta pública aumentada de 12.727.273 acciones de acciones ordinarias a $11.00 por acción, esperando recaudar aproximadamente $140.0 millones en ingresos brutos. La compañía ha otorgado a los suscriptores una opción de 30 días para comprar hasta 1.909.090 acciones adicionales. Se espera que la oferta cierre alrededor del 31 de octubre de 2024. Los ingresos se utilizarán para avanzar en el desarrollo clínico de DURAVYU™ para AMD húmeda y DME, apoyar las iniciativas de desarrollo de la cartera y para fines corporativos generales.
EyePoint Pharmaceuticals (NASDAQ: EYPT)는 12,727,273주의 보통주에 대한 공모가를 주당 $11.00로 설정했다고 발표했으며, 총 $140.0백만 달러의 수익을 올릴 것으로 예상하고 있습니다. 회사는 인수자에게 추가로 1,909,090주를 구매할 수 있는 30일 옵션을 부여했습니다. 이 공모는 2024년 10월 31일경에 마감될 것으로 예상됩니다. 수익금은 DURAVYU™의 습성 AMD 및 DME 임상 개발을 진전시키고, 파이프라인 개발 이니셔티브를 지원하며, 일반 회사 목적에 사용될 것입니다.
EyePoint Pharmaceuticals (NASDAQ: EYPT) a annoncé le tarif d'une offre publique augmentée de 12.727.273 actions d'actions ordinaires à 11,00 $ par action, s'attendant à lever environ 140,0 millions de dollars en produits bruts. L'entreprise a accordé aux souscripteurs une option de 30 jours pour acheter jusqu'à 1.909.090 actions supplémentaires. L'offre devrait se clôturer vers le 31 octobre 2024. Les produits serviront à faire progresser le développement clinique de DURAVYU™ pour l'AMD humide et la DME, à soutenir les initiatives de développement de pipeline et à des fins corporatives générales.
EyePoint Pharmaceuticals (NASDAQ: EYPT) hat die Preisgestaltung für ein erhöhtes öffentliches Angebot von 12.727.273 Aktien gewöhnlicher Aktien zu $11,00 pro Aktie angekündigt und erwartet, etwa $140,0 Millionen brutto zu erlösen. Das Unternehmen hat den Underwritern eine 30-tägige Option eingeräumt, bis zu 1.909.090 zusätzliche Aktien zu kaufen. Das Angebot wird voraussichtlich um den 31. Oktober 2024 schließen. Die Erlöse werden verwendet, um die klinische Entwicklung von DURAVYU™ für feuchte AMD und DME voranzutreiben, Entwicklungsinitiativen in der Pipeline zu unterstützen und allgemeine Unternehmenszwecke zu finanzieren.
- Successful pricing of $140 million public offering
- Funds secured for DURAVYU™ clinical development program
- Strong underwriting support from major financial institutions
- Potential dilution for existing shareholders due to 12.7M new shares
- Additional dilution possible if underwriters exercise 1.9M share option
Insights
This
The dilution impact from 12.7M new shares (plus potential 1.9M from overallotment) is substantial but necessary for advancing clinical development. The fresh capital strengthens EyePoint's balance sheet and provides runway for key clinical milestones. With a current market cap of
The capital raise positions EyePoint to accelerate development of DURAVYU™ in two major retinal disease markets. Wet AMD and DME represent substantial commercial opportunities, with the global wet AMD market alone projected to reach
This financing should support completion of key clinical trials and potential commercialization efforts. The strong investor interest suggests confidence in DURAVYU™'s clinical potential and EyePoint's development capabilities in the ophthalmology space.
WATERTOWN, Mass., Oct. 29, 2024 (GLOBE NEWSWIRE) -- EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a company committed to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases, today announced the pricing of an underwritten public offering of 12,727,273 shares of its common stock at a public offering price of
J.P. Morgan, Citigroup and Guggenheim Securities are acting as joint book running managers for the offering. Baird, Mizuho and Jones are acting as co-managers for the offering.
EyePoint intends to use the net proceeds that it will receive from the offering to advance clinical development of DURAVYU™ for wet age related macular degeneration (wet AMD) and diabetic macular edema (DME), as well as support its earlier stage pipeline development initiatives, and for general corporate purposes.
The securities described above are being offered by the Company pursuant to a shelf registration statement on Form S-3 (No. 333-281391) previously filed with the Securities and Exchange Commission (SEC) on August 8, 2024 and declared effective by the SEC on August 16, 2024.
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 relating to the offering was filed with the SEC on October 28, 2024 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 also 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 EyePoint 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 EyePoint and the offering. Copies of the final prospectus supplement, when available, and accompanying prospectus relating to the offering may be obtained from J.P. Morgan Securities LLC, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717, or by email at prospectus-eq_fi@jpmchase.com and postsalemanualrequests@broadridge.com; Citigroup, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717, or by telephone at (800) 831-9146; or Guggenheim Securities, LLC, Attention: Equity Syndicate Department, 330 Madison Avenue, 8th Floor, New York, NY 10017, by telephone at (212) 518-9544, or by email at GSEquityProspectusDelivery@guggenheimpartners.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 EyePoint Pharmaceuticals
EyePoint Pharmaceuticals (Nasdaq: EYPT) is a clinical-stage biopharmaceutical company committed to developing and commercializing innovative therapeutics to help improve the lives of patients with serious retinal diseases. The Company's pipeline leverages its proprietary bioerodible Durasert E™ technology for sustained intraocular drug delivery. The Company’s lead product candidate, DURAVYU™ (f/k/a EYP-1901), is an investigational sustained delivery treatment for VEGF-mediated retinal diseases combining vorolanib, a selective and patent-protected tyrosine kinase inhibitor with bioerodible Durasert E™. DURAVYU is presently in Phase 3 global, pivotal clinical trials as a sustained delivery treatment for wet AMD, the leading cause of vision loss among people 50 years of age and older in the United States, and in a Phase 2 clinical trial in DME. EyePoint expects full topline data from the Phase 2 clinical trial in DME in Q1 2025 and topline data from both Phase 3 pivotal trials in wet AMD in 2026.
Pipeline programs include EYP-2301, a TIE-2 agonist, razuprotafib, formulated in Durasert E™ to potentially improve outcomes in serious retinal diseases. The proven Durasert® drug delivery technology has been safely administered to thousands of patient eyes across four U.S. FDA approved products. EyePoint Pharmaceuticals is headquartered in Watertown, Massachusetts.
Vorolanib is licensed to EyePoint exclusively by Equinox Sciences, a Betta Pharmaceuticals affiliate, for the localized treatment of all ophthalmic diseases outside of China, Macao, Hong Kong and Taiwan.
DURAVYU™ has been conditionally accepted by the FDA as the proprietary name for EYP-1901. DURAVYU is an investigational product; it has not been approved by the FDA. FDA approval and the timeline for potential approval is uncertain.
SAFE HARBOR STATEMENTS UNDER THE PRIVATE SECURITIES LITIGATION ACT OF 1995: To the extent any statements made in this press release deal with information that is not historical, these are forward-looking statements under the Private Securities Litigation Reform Act of 1995. Such statements include, but are not limited to, statements regarding the timing of the closing of the offering, as well as the anticipated use of proceeds for the offering, EyePoint’s clinical development plans and the expected timing thereof; and other statements identified by words such as “will,” “potential,” “could,” “can,” “believe,” “intends,” “continue,” “plans,” “expects,” “anticipates,” “estimates,” “may,” other words of similar meaning or the use of future dates. Forward-looking statements by their nature address matters that are, to different degrees, uncertain. Uncertainties and risks may cause EyePoint’s actual results to be materially different than those expressed in or implied by EyePoint’s forward-looking statements. For EyePoint, this includes satisfaction of the customary closing conditions of the offering; delays in obtaining required stock exchange or other regulatory approvals; stock price volatility and uncertainties relating to the financial markets, the medical community and the global economy; the timing, progress and results of the company’s clinical development activities; uncertainties and delays relating to the design, enrollment, completion, and results of clinical trials; unanticipated costs and expenses; the company’s cash and cash equivalents may not be sufficient to support its operating plan for as long as anticipated; the risk that results of clinical trials may not be predictive of future results, and interim and preliminary data are subject to further analysis and may change as more data becomes available; unexpected safety or efficacy data observed during clinical trials; uncertainties related to the regulatory authorization or approval process, and available development and regulatory pathways for approval of the company’s product candidates; changes in the regulatory environment; changes in expected or existing competition; the success of current and future license agreements; our dependence on contract research organizations, and other outside vendors and service providers; product liability; the impact of general business and economic conditions; protection of our intellectual property and avoiding intellectual property infringement; retention of key personnel; delays, interruptions or failures in the manufacture and supply of our product candidates; the availability of and the need for additional financing; the company’s ability to obtain additional funding to support its clinical development programs; uncertainties regarding the timing and results of the August 2022 subpoena from the U.S. Attorney’s Office for the District of Massachusetts; uncertainties regarding the FDA warning letter pertaining to the company’s Watertown, MA manufacturing facility; and other factors described in our filings with the Securities and Exchange Commission. More detailed information on these and additional factors that could affect EyePoint’s actual results are described in EyePoint’s filings with the SEC, including its Annual Report on Form 10-K for the fiscal year ended December 31, 2023, as revised or supplemented by its Quarterly Reports on Form 10-Q and other documents filed with the SEC. All forward-looking statements in this news release speak only as of the date of this news release. EyePoint undertakes no obligation to update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.
Investors:
Christina Tartaglia
Precision AQ (formerly Stern IR)
Direct: 212-698-8700
christina.tartaglia@sternir.com
Media Contact
Amy Phillips
Green Room Communications
Direct: 412-327-9499
aphillips@greenroompr.com
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