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Medicenna Therapeutics Announces Closing of CA$20 Million Investment From RA Capital Management

Medicenna Therapeutics Announces Closing of CA$20 Million Investment From RA Capital Management

Medicenna Therapeutics宣佈完成來自RA Capital Management的2000萬加元投資
GlobeNewswire ·  04/30 23:07

Not for distribution to United States news wire services or for dissemination in the United States

不得分發給美國新聞通訊社或在美國傳播

TORONTO and HOUSTON, April 30, 2024 (GLOBE NEWSWIRE) -- Medicenna Therapeutics Corp. ("Medicenna" or the "Company") (TSX: MDNA) (MDNAF: OTCQB), a clinical-stage immunotherapy company focused on the development of engineered cytokines, announced today the closing of its previously announced CA$20 million investment by RA Capital Management, a multi-stage investment manager based in Boston, MA, by way of a non-brokered private placement (the "Offering"). Medicenna intends to use the net proceeds from the Offering for further development of its MDNA11 program, advancement of its preclinical programs and general corporate purposes.

多倫多和休斯頓,2024年4月30日(環球新聞專線)——專注於工程細胞因子開發的臨床階段免疫療法公司Medicenna Therapeutics Corp.(“MDNA” 或 “公司”)(多倫多證券交易所股票代碼:MDNA)(MDNAF:OTCQB)今天宣佈,總部位於波士頓的多階段投資管理公司RA Capital Management先前宣佈的2000萬加元投資已結束。併購,通過非經紀私募配售(“發行”)。Medicenna打算將本次發行的淨收益用於進一步發展其 MDNA11 計劃、推進其臨床前項目和一般公司用途。

Pursuant to the terms of a subscription agreement entered into as of April 26, 2024 between the Company and RA Capital Healthcare Fund, L.P. ("RAHF"), a fund affiliated with RA Capital Management, RAHF subscribed for 5,141,388 common shares in the capital of the Company (the "Shares") at a price of CA$1.95 per share and, in lieu of common shares, pre-funded warrants to purchase 5,141,388 common shares (the "Pre-Funded Warrants") at a purchase price of CA$1.94 per pre-funded warrant, for total net proceeds to the Company of approximately CA$20 million.

根據截至2024年4月26日公司與隸屬於RA Capital Management的基金RA Capital Healthcare Fund, L.P.(“RAHF”)簽訂的認購協議的條款,RAHF以每股1.95加元的價格認購了公司資本中的5,14,388股普通股(“股份”),並以預先注資的認股權證代替普通股 1,388股普通股(“預融資認股權證”),每份預籌認股權證的收購價爲1.94加元,公司淨收益總額約爲2000萬加元。

The Shares and Pre-Funded Warrants have not been and will not be registered under the United States Securities Act of 1933, as amended (the "U.S. Securities Act"), or any U.S. state securities laws and may not be offered or sold within the "United States" or to "U.S. Persons" (as such terms are defined in Regulation S under the U.S. Securities Act) unless registered under the U.S. Securities Act and applicable state securities laws or pursuant to an applicable exemption from such registration is available.

股票和預先注資認股權證過去和將來都不會根據經修訂的1933年《美國證券法》(“美國證券法”)或任何美國州證券法進行註冊,除非根據美國證券法和適用的州證券法註冊,否則不得在 “美國” 或 “美國個人”(此類條款的定義見美國《證券法》S條例)或根據以下規定進行發行或出售此類登記可獲得適用的豁免。

This news release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

本新聞稿不構成出售要約或徵求購買這些證券的要約,在根據任何此類州或其他司法管轄區的證券法進行註冊或獲得資格認證之前,在任何州或其他司法管轄區出售此類證券是非法的,也不得在任何州或其他司法管轄區出售這些證券。

About Medicenna

關於 Medicenna

Medicenna is a clinical-stage immunotherapy company focused on developing novel, highly selective versions of IL-2, IL-4 and IL-13 Superkines and first-in-class empowered superkines. Medicenna's long-acting IL-2 Superkine, MDNA11, is a next-generation IL-2 with superior affinity toward CD122 (IL-2 receptor beta) and no CD25 (IL-2 receptor alpha) binding, thereby preferentially stimulating cancer-killing effector T cells and NK cells. Medicenna's IL-4 Empowered Superkine, bizaxofusp (formerly MDNA55), has been studied in 5 clinical trials enrolling over 130 patients, including a Phase 2b trial for recurrent GBM, the most common and uniformly fatal form of brain cancer. Bizaxofusp has obtained FastTrack and Orphan Drug status from the FDA and FDA/EMA, respectively. Medicenna's early-stage BiSKITs (Bifunctional SuperKine ImmunoTherapies) and the T-MASK (Targeted Metalloprotease Activated SuperKine) programs are designed to enhance the ability of Superkines to treat immunologically "cold" tumors.

Medicenna是一家臨床階段的免疫療法公司,專注於開發新型、高選擇性的IL-2、IL-4和 IL-13 Superkines以及同類首創的強化超因子。Medicenna 的長效 IL-2 Superkine MDNA11 是下一代白細胞介素-2,對 CD122(IL-2 受體 β)具有優異的親和力,並且沒有 CD25(IL-2 受體 α)結合,因此優先刺激殺癌效應 T 細胞和 NK 細胞。Medicenna的IL-4 Empowered Superkine bizaxofusp(前身爲 MDNA55)已在5項臨床試驗中進行了研究,招募了130多名患者,其中包括一項針對複發性GBM(最常見和最均勻致命的腦癌)的2b期試驗。Bizaxofusp已分別獲得美國食品藥品管理局和美國食品藥品管理局的FastTrack和Orphan Drug認證。Medicenna的早期BISKIT(雙功能SuperKine免疫療法)和T-MASK(靶向金屬蛋白酶活化SuperKine)計劃旨在增強Superkines治療免疫學 “冷” 腫瘤的能力。

For more information, please visit , and follow us on Twitter and LinkedIn.

欲了解更多信息,請訪問 Twitter 和 LinkedIn,並關注我們。

Forward-Looking Statements

前瞻性陳述

This news release contains forward-looking statements within the meaning of applicable securities laws. All statements in this news release, other than statements of historical facts, that address events or developments that the Company expects to occur are forward-looking statements, including, but are not limited to, statements relating to the Offering and the terms thereof, and the proposed use of proceeds from the Offering. Forward-looking statements also include express or implied statements regarding the future operations of the Company, estimates, plans, strategic ambitions, partnership activities and opportunities, objectives, expectations, opinions, forecasts, projections, guidance, outlook or other statements that are not historical facts, such as statements on the Company's cash runway, preclinical and clinical development activities, clinical trial designs, clinical potential, expectations and beliefs around safety profiles and upcoming milestones and data reporting, including with respect to MDNA11, the ABILITY study and its expansion, bizaxofusp (MDNA55), MDNA113 and MDNA223. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical studies may not be indicative of full results or results from later stage or larger scale clinical studies and do not ensure regulatory approval. You should not place undue reliance on these statements or the scientific data presented. Forward-looking statements are often identified by terms such as "will", "may", "should", "anticipate", "expect", "believe", "seek", "potentially" and similar expressions. Forward-looking statements are based on a number of assumptions believed by the Company to be reasonable at the date of this news release. Although the Company believes that the expectations reflected in such forward-looking statements are reasonable, there can be no assurance that such statements will prove to be accurate. These statements are subject to certain risks and uncertainties and may be based on assumptions that could cause actual results and future events to differ materially from those anticipated or implied in such statements. Important factors that could cause actual results to differ materially from the Company's expectations include the risks detailed in the latest Annual Report on Form 20-F of the Company and in other filings made by the Company with the applicable securities regulators from time to time in Canada.

本新聞稿包含適用證券法所指的前瞻性陳述。除歷史事實陳述外,本新聞稿中所有涉及公司預計將發生的事件或事態發展的陳述均爲前瞻性陳述,包括但不限於與本次發行及其條款以及本次發行所得收益的擬議用途有關的陳述。前瞻性陳述還包括有關公司未來運營、估計、計劃、戰略抱負、合作活動和機會、目標、預期、觀點、預測、指導、展望或其他非歷史事實的陳述的明示或暗示陳述,例如關於公司現金流的陳述、臨床前和臨床開發活動、臨床試驗設計、臨床潛力、對安全概況以及即將到來的里程碑和數據報告的期望和信念,包括 MDNA11、ABILITY 研究及其擴展、bizaxofusp (MDNA55)、MDNA113 和 MDNA223。藥物開發和商業化涉及高風險,只有少數研發計劃導致產品的商業化。早期臨床研究的結果可能並不表示全部結果或後期或更大規模臨床研究的結果,也不能確保監管部門的批准。你不應過分依賴這些陳述或提供的科學數據。前瞻性陳述通常用 “將”、“可能”、“應該”、“預期”、“期望”、“相信”、“尋求”、“可能” 等術語和類似的表述來識別。前瞻性陳述基於公司在本新聞發佈之日認爲合理的許多假設。儘管公司認爲此類前瞻性陳述中反映的預期是合理的,但無法保證此類陳述會被證明是準確的。這些陳述存在某些風險和不確定性,可能基於的假設可能導致實際結果和未來事件與此類陳述中的預期或暗示存在重大差異。可能導致實際業績與公司預期存在重大差異的重要因素包括公司最新的20-F表年度報告以及公司不時向加拿大相關證券監管機構提交的其他文件中詳述的風險。

The reader is cautioned that assumptions used in the preparation of any forward-looking information may prove to be incorrect. Events or circumstances may cause actual results to differ materially from those predicted, as a result of numerous known and unknown risks, uncertainties, and other factors, many of which are beyond the control of the Company. The reader is cautioned not to place undue reliance on any forward-looking information. Such information, although considered reasonable by management, may prove to be incorrect and actual results may differ materially from those anticipated or implied in forward-looking statements. Forward-looking statements contained in this news release are expressly qualified by this cautionary statement. The forward-looking statements contained in this news release are made as of the date hereof and except as required by law, we do not intend and do not assume any obligation to update or revise publicly any of the included forward-looking statements.

提醒讀者,在準備任何前瞻性信息時使用的假設都可能被證明是不正確的。由於許多已知和未知的風險、不確定性和其他因素,其中許多是公司無法控制的,事件或情況可能導致實際業績與預測存在重大差異。提醒讀者不要過分依賴任何前瞻性信息。儘管管理層認爲此類信息是合理的,但可能被證明是不正確的,實際結果可能與前瞻性陳述中的預期或暗示結果存在重大差異。本新聞稿中包含的前瞻性陳述受本警示聲明的明確限制。本新聞稿中包含的前瞻性陳述自發布之日起作出,除非法律要求,否則我們無意也不承擔任何義務公開更新或修改所包含的任何前瞻性陳述。

This news release contains hyperlinks to information that is not deemed to be incorporated by reference in this news release.

本新聞稿包含指向本新聞稿中未以引用方式納入的信息的超鏈接。

Investor and Media Contact:

投資者和媒體聯繫人:

Christina Cameron
Investor Relations, Medicenna Therapeutics
ir@medicenna.com
(647) 953-0673

克里斯蒂娜卡梅隆
投資者關係,Medicenna Therapeutics
ir@medicenna.com
(647) 953-0673


譯文內容由第三人軟體翻譯。


以上內容僅用作資訊或教育之目的,不構成與富途相關的任何投資建議。富途竭力但無法保證上述全部內容的真實性、準確性和原創性。
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