NewAmsterdam Pharma Announces Commencement of $300 Million Public Offering of Ordinary Shares and Pre-Funded Warrants
NewAmsterdam Pharma Announces Commencement of $300 Million Public Offering of Ordinary Shares and Pre-Funded Warrants
NAARDEN, The Netherlands and MIAMI, Dec. 10, 2024 (GLOBE NEWSWIRE) -- NewAmsterdam Pharma Company N.V. (Nasdaq: NAMS; "NewAmsterdam" or the "Company"), a late-stage, clinical biopharmaceutical company developing oral, non-statin medicines for patients at risk of cardiovascular disease ("CVD") with elevated low-density lipoprotein cholesterol ("LDL-C"), for whom existing therapies are not sufficiently effective or well-tolerated, today announced the commencement of an underwritten public offering of $300.0 million of the Company's ordinary shares, nominal value €0.12 per share (the "Ordinary Shares"), and, to certain investors that so choose in lieu of Ordinary Shares, pre-funded warrants to purchase Ordinary Shares ("Pre-Funded Warrants," and such offering, the "Offering"). All Ordinary Shares and Pre-Funded Warrants to be sold in the proposed Offering will be sold by the Company. In addition, the Company expects to grant the underwriters a 30-day option to purchase up to an additional $45.0 million of Ordinary Shares, less underwriting discounts and commissions. The proposed Offering is subject to market and other conditions and there can be no assurance as to whether or when the proposed Offering may be completed, or as to the actual size or terms of the proposed Offering.
荷蘭納爾登和邁阿密,2024年12月10日(GLOBE NEWSWIRE) -- NewAmsterdam製藥公司N.V.(納斯達克:NAMS;"NewAmsterdam"或"公司"),是一家晚期臨床生物製藥公司,正在開發口服非他汀類藥物,以治療那些低密度脂蛋白膽固醇("LDL-C")升高、面臨心血管疾病("CVD")風險的患者,對於這些患者,現有療法的療效不足或耐受性差,今天宣佈啓動30000萬美元的公司普通股(每股名義價值€0.12,"普通股")的承銷公開發行,以及對於某些選擇以普通股代替的投資者,預先資金的購買普通股的權利證("預先資金的權利證",以及該發行稱爲"發行")。 所有將在提議的發行中出售的普通股和預先資金的權利證均由公司出售。此外,公司預計將向承銷商授予30天的期權,以購買最多額外4500萬美元的普通股,減去承銷折扣和佣金。提議的發行取決於市場和其他條件,無法保證提議的發行何時能夠完成,或者提議的發行的實際規模或條款。
Jefferies, Goldman Sachs & Co., Leerink Partners, TD Cowen, Guggenheim Securities and William Blair are acting as joint book-running managers for the proposed Offering.
Jefferies、高盛證券公司、Leerink Partners、TD Cowen、古根海姆證券和William Blair正在爲提議的發行擔任共同賬簿管理人。
The proposed Offering will be made pursuant to a registration statement on Form S-3, including a base prospectus, that was initially declared effective by the U.S. Securities and Exchange Commission (the "SEC") on July 12, 2024. The proposed Offering will be made only by means of a prospectus supplement and an accompanying prospectus, which will be filed with the SEC and will be available on the SEC's website located at www.sec.gov. A copy of the preliminary prospectus supplement and the accompanying prospectus, when available, may also be obtained from: Jefferies LLC, Attention: Equity Syndicate Prospectus Department, 520 Madison Avenue, New York, NY 10022, or by telephone at (877) 821-7388, or by email at Prospectus_Department@Jefferies.com; Goldman Sachs & Co. LLC, Attention: Prospectus Department, 200 West Street, New York, NY 10282, or by telephone at (866) 471-2526, or by email at Prospectus-ny@ny.email.gs.com; Leerink Partners LLC, Attention: Syndicate Department, 53 State Street, 40th Floor, Boston, MA 02109, or by telephone at (800) 808-7525, ext. 6105, or by email at syndicate@leerink.com; TD Securities (USA) LLC, 1 Vanderbilt Avenue, New York, NY 10017, or by telephone at (855) 495-9846, or by email at TD.ECM_Prospectus@tdsecurities.com; Guggenheim Securities, LLC, Attention: Equity Syndicate Department, 330 Madison Avenue, New York, NY 10017, or by telephone at (212) 518-9544, or by email at GSEquityProspectusDelivery@guggenheimpartners.com; or William Blair & Company, L.L.C., Attention: Prospectus Department, 150 North Riverside Plaza, Chicago, IL 60606, or by telephone at (800) 621-0687, or by email at prospectus@williamblair.com.
提議的發行將根據美國證券交易委員會("SEC")於2024年7月12日初步宣佈生效的S-3表格註冊聲明進行,包括基礎招股說明書。提議的發行僅通過招股說明書補充和附帶招股說明書進行,這將提交給SEC,並將在SEC的官方網站www.sec.gov提供。當初步招股說明書補充和附帶招股說明書可用時,也可以從以下渠道獲得:Jefferies LLC,注意:股票承銷招股說明書部門,520 Madison Avenue, New York, NY 10022,或致電(877)821-7388,或發電子郵件至Prospectus_Department@Jefferies.com;高盛證券公司,注意:招股說明書部門,200 West Street, New York, NY 10282,或致電(866)471-2526,或發電子郵件至Prospectus-ny@ny.email.gs.com;Leerink Partners LLC,注意:承銷部門,53 State Street, 40th Floor, Boston, MA 02109,或致電(800)808-7525,轉6105,或發電子郵件至syndicate@leerink.com;TD Securities (USA) LLC,1 Vanderbilt Avenue, New York, NY 10017,或致電(855)495-9846,或發電子郵件至TD.ECM_Prospectus@tdsecurities.com;古根海姆證券公司,注意:股票承銷部門,330 Madison Avenue, New York, NY 10017,或致電(212)518-9544,或發電子郵件至GSEquityProspectusDelivery@guggenheimpartners.com;或William Blair & Company, L.L.C.,注意:招股說明書部門,150 North Riverside Plaza, Chicago, IL 60606,或致電(800)621-0687,或發電子郵件至prospectus@williamblair.com。
This press release shall not constitute an offer to sell or the solicitation of an offer to buy any securities, 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.
本新聞稿不構成出售任何證券的要約,也不構成購買任何證券要約的請求,亦不應在任何州或司法管轄區內銷售這些證券,在此類要約、請求或銷售在任何此類州或司法管轄區的證券法下未經註冊或資格審查而被認爲是非法的。
About NewAmsterdam
About NewAmsterdam
NewAmsterdam Pharma (Nasdaq: NAMS) is a late-stage biopharmaceutical company whose mission is to improve patient care in populations with metabolic diseases where currently approved therapies have not been adequate or well-tolerated. We seek to fill a significant unmet need for a safe, well-tolerated and convenient LDL-lowering therapy. In multiple phase 3 studies, NewAmsterdam is investigating obicetrapib, an oral, low-dose and once-daily CETP inhibitor, alone or as a fixed-dose combination with ezetimibe, as LDL-C lowering therapies to be used as an adjunct to statin therapy for patients at risk of CVD with elevated LDL-C, for whom existing therapies are not sufficiently effective or well-tolerated.
NewAmsterdam Pharma(納斯達克:NAMS)是一家晚期生物製藥公司,其使命是改善代謝疾病人群的患者護理,目前已批准的療法尚不夠充分或耐受良好。我們力求填補安全、耐受良好且方便的降低LDL的療法的重大未滿足需求。在多個三期研究中,NewAmsterdam正在研究obicetrapib,這是一種口服、低劑量、每日一次的CETP抑制劑,單獨使用或與ezetimibe固定劑量組合使用,作爲降低LDL-C的療法,用於治療心血管疾病(CVD)風險較高且LDL-C水平升高的患者,對於這些患者,現有療法的效果不足或耐受性不佳。
Forward-Looking Statements
前瞻性聲明
Certain statements included in this document that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements generally are accompanied by words such as "believe," "may," "will," "estimate," "continue," "anticipate," "intend," "expect," "should," "would," "plan," "predict," "potential," "seem," "seek," "future," "outlook" and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding the consummation of the proposed Offering as well as the timing and size of the proposed Offering and the grant to the underwriters of the option to purchase additional Ordinary Shares. These statements are based on various assumptions, whether or not identified in this document, and on the current expectations of the Company's management and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on as a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and may differ from assumptions. Many actual events and circumstances are beyond the control of the Company. These forward-looking statements are subject to a number of risks and uncertainties, including changes in domestic and foreign business, market, financial, political, and legal conditions; risks related to the approval of the Company's product candidate and the timing of expected regulatory and business milestones, including potential commercialization; ability to negotiate definitive contractual arrangements with potential customers; the impact of competitive product candidates; ability to obtain sufficient supply of materials; global economic and political conditions, including the Russia-Ukraine and Israel-Hamas conflicts; the effects of competition on the Company's future business; and those factors described in the Company's Annual Report on Form 10-K for the year ended December 31, 2023, as supplemented by other documents filed by the Company with the SEC. Additional risks related to the Company's business include, but are not limited to: uncertainty regarding outcomes of the Company's ongoing clinical trials, particularly as they relate to regulatory review and potential approval for its product candidate; risks associated with the Company's efforts to commercialize a product candidate; the Company's ability to negotiate and enter into definitive agreements on favorable terms, if at all; the impact of competing product candidates on the Company's business; intellectual property related claims; the Company's ability to attract and retain qualified personnel; and the Company's ability to continue to source the raw materials for its product candidate. If any of these risks materialize or the Company's assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. There may be additional risks that the Company does not presently know or that the Company currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. In addition, forward-looking statements reflect the Company's expectations, plans, or forecasts of future events and views as of the date of this document and are qualified in their entirety by reference to the cautionary statements herein. The Company anticipates that subsequent events and developments may cause the Company's assessments to change. These forward-looking statements should not be relied upon as representing the Company's assessment as of any date subsequent to the date of this communication. Accordingly, undue reliance should not be placed upon the forward-looking statements. Neither the Company nor any of its affiliates undertakes any obligation to update these forward-looking statements, except as may be required by law.
本文件中包含的某些聲明並非歷史事實,而是1995年美國私人證券訴訟改革法案下安全港條款所指的前瞻性聲明。前瞻性聲明通常伴隨着諸如「相信」、「可能」、「將會」、「估計」、「繼續」、「預期」、「打算」、「期待」、「應該」、「會」、「計劃」、「預測」、「潛在」、「看起來」、「尋求」、「未來」、「展望」及類似表達,預測或指示未來事件或趨勢,或者它們並非歷史事項的陳述。這些前瞻性聲明包括但不限於有關擬議發行的完成以及擬議發行的時間和規模以及授予承銷商購買額外普通股的選擇權的聲明。這些陳述基於各種假設,無論在本文件中是否被識別,基於公司管理層的當前預期,並非對實際表現的預測。這些前瞻性聲明僅爲說明目的提供,並不意味着要作爲也不得被依賴作爲擔保、保證、預測或確定的事實或可能性的聲明。實際事件和情況難以預測,可能與假設有所不同。許多實際事件和情況超出了公司的控制。這些前瞻性聲明受多種風險和不確定性的影響,包括國內外業務、市場、金融、政治和法律條件的變化;與公司產品候選者的批准及預期監管和業務里程碑(包括潛在商業化)相關的風險;與潛在客戶談判確定合同安排的能力;競爭性產品候選者的影響;獲得足夠原材料供應的能力;全球經濟和政治情況,包括俄羅斯-烏克蘭和以色列-哈馬斯衝突的影響;競爭對公司未來業務的影響;以及公司在截止至2023年12月31日的10-K表格年度報告中描述的那些因素,及公司向SEC提交的其他文件所補充的因素。與公司業務相關的其他風險包括但不限於:關於公司正在進行的臨床試驗結果的不確定性,特別是涉及監管審查和潛在批准的部分;與公司努力使產品候選者商業化相關的風險;公司在有利條款上談判並簽署確定協議的能力(如果能夠的話);競爭性產品候選者對公司業務的影響;與知識產權相關的索賠;公司吸引和留住合格人員的能力;以及公司繼續爲其產品候選者採購原材料的能力。如果這些風險中的任何一個顯現或公司的假設證明不正確,實際結果可能會與這些前瞻性聲明所暗示的結果有重大不同。可能還有其他公司當前未知道或目前認爲不重要的風險,也可能導致實際結果與前瞻性聲明中的結果不同。此外,前瞻性聲明反映了公司截至本文件日期的預期、計劃或未來事件的預測,完全受有限的警告性聲明約束。公司預期後續事件和進展可能導致公司的評估發生變化。這些前瞻性聲明不應被視爲代表公司在此通信日期之後的任何日期的評估。因此,不應對前瞻性聲明過度依賴。公司及其任何關聯公司不承擔更新這些前瞻性聲明的義務,除非法律要求。
Company Contact
Matthew Philippe
P: 1-917-882-7512
matthew.philippe@newamsterdampharma.com
公司聯繫人
馬修·菲利普
P: 1-917-882-7512
matthew.philippe@newamsterdampharma.com
Media Contact
Spectrum Science on behalf of NewAmsterdam Pharma
Jaryd Leady
P:1-856-803-7855
jleady@spectrumscience.com
媒體聯繫
Spectrum Science代表NewAmsterdam Pharma
賈瑞德·利迪
電話:1-856-803-7855
jleady@spectrumscience.com
Investor Contact
Precision AQ on behalf of NewAmsterdam
Austin Murtagh
P: 1-212-698-8696
austin.murtagh@precisionaq.com
投資者聯繫
Precision AQ代表NewAmsterdam
奧斯汀·穆爾塔
電話:1-212-698-8696
austin.murtagh@precisionaq.com
譯文內容由第三人軟體翻譯。