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Discovery of Bispecific Antibodies and Immune Checkpoint Inhibitors Which Kill Glioblastoma and Block the Metastasis of Malignant Melanoma Cells to the Lung By Over 90% Announced by Ocean Biomedical and Aesther Healthcare (NASDAQ: AEHA)

Discovery of Bispecific Antibodies and Immune Checkpoint Inhibitors Which Kill Glioblastoma and Block the Metastasis of Malignant Melanoma Cells to the Lung By Over 90% Announced by Ocean Biomedical and Aesther Healthcare (NASDAQ: AEHA)

海洋生物醫學和 Aesther 醫療保健(NASDAQ:AEHA)宣布超過 90% 的發現可殺死膠質母細胞瘤並阻止惡性黑色素瘤細胞轉移到肺部的雙特異性抗體和免疫檢查點抑制劑
GlobeNewswire ·  2022/09/06 19:50

Fig. 1

圖1

Tumor cell death was not induced by isotype control antibodies, and modest degrees of tumor cell apoptosis were seen in cultures with monospecific antiCHI3L1, antiPD-1 or antiCTLA4 individually.
單特異性抗CHI3L1、抗PD-1和抗CTLA4單獨培養均未誘導腫瘤細胞死亡。

Fig. 2

圖2

The results with the FRGxCTLA4 antibody.
用FRGxCTLA4抗體檢測結果。

Ocean Biomedical will be a wholly owned subsidiary of Aesther Healthcare Acquisition Corp. and will change its name to Ocean Biomedical, Inc., expected to be listed on NASDAQ under the symbol, "OCEA".

海洋生物醫療公司將成為一家全資子公司艾瑟爾醫療保健收購公司.將更名為海洋生物醫學公司., 預計將在納斯達克上以該代碼上市, “OCEA".

Providence, RI and New York, NY, Sept. 06, 2022 (GLOBE NEWSWIRE) -- Ocean Biomedical and Aesther Healthcare Acquisition Corp.("Aesther") (NASDAQ: AEHA) announced today the discovery of bispecific antibodies that target Chitinase 3-like-1 and immune checkpoint inhibitors, killing glioblastoma cells and melanoma cells, and blocking the metastasis of malignant melanoma cells to the lung by over 90%. Glioblastoma multiforme (GBM) is a deadly type of brain tumor and 5-year survival is just 8% for those aged 45-54. About 25% of GBM patients are not actively treated due to rapid disease progression. Malignant melanoma, the most serious skin cancer, can metastasize to other organs. Once it has spread to other organs it is difficult to treat. Metastatic melanoma (Stage IV) has 22.5% five year survival. Non-small cell lung cancer (NSCLC) is a major unmet medical need that accounts for 85% of pulmonary malignancies and effects approximately 450,000 individuals. In greater than 50% of affected patients the tumors are diagnosed at advanced stages with metastatic spread that precludes curative surgical resection.

國際扶輪普羅維登斯和紐約州紐約,9月2022年06日(環球通訊社)--海洋生物醫療和艾斯特醫療收購公司(以下簡稱“艾瑟”)(納斯達克代碼:AEHA)今天宣佈發現雙特異性抗體靶向幾丁質酶3-樣-1和免疫檢查點抑制物,殺死膠質母細胞瘤細胞和黑色素瘤細胞,阻斷惡性黑色素瘤細胞向肺轉移90%以上。多形性膠質母細胞瘤(GBM)是一種致命的腦腫瘤,45-54歲的人5年存活率只有8%。由於疾病進展迅速,大約25%的GBM患者沒有得到積極的治療。惡性黑色素瘤是最嚴重的皮膚癌,可以轉移到其他器官。一旦擴散到其他器官,就很難治療了。轉移性黑色素瘤(IV期)的五年生存率為22.5%。非小細胞肺癌(NSCLC)是一種未得到滿足的主要醫療需求,佔肺部惡性腫瘤的85%,影響約45萬人。在超過50%的受影響患者中,腫瘤被診斷為晚期轉移,這排除了根治性手術切除的可能性。

Background

背景

Recent studies of NSCLC have highlighted genetic abnormalities that underlie these tumors. These genetic abnormalities generate abnormal proteins that have not been previously seen by the patient's immune system which, in turn, activates antitumor immune responses that control tumor initiation and progression. Studies over recent years have demonstrated that tumor initiation and progression are often mediated by the ability of the tumors to produce immunosuppressive proteins and activate immunosuppressive pathways, called immune checkpoint inhibitors (ICPI), that allow tumor growth and progression by shutting off these critical anti-tumor immune responses. This includes the programed death (PD) pathway including PD-1, PD ligand 1 (PD-L1) and PD-L2 and the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) pathway that includes CTLA4 and its binding partners B7.1/B7.2. Antibodies that target ICPI such as PD-1, PD-L1 and CTLA4 have been generated which have therapeutic efficacy in NSCLC and other tumors. Unfortunately, only a minority of patients respond to these therapies and the responses are often not durable.

最近對非小細胞肺癌的研究強調了這些腫瘤背後的基因異常。這些基因異常產生了患者免疫系統以前從未見過的異常蛋白質,而免疫系統反過來又激活了控制腫瘤啟動和進展的抗腫瘤免疫反應。近年來的研究表明,腫瘤的發生和發展往往是由腫瘤產生免疫抑制蛋白和激活免疫抑制途徑的能力所介導的,稱為免疫檢查點抑制物(ICPI),通過關閉這些關鍵的抗腫瘤免疫反應來允許腫瘤的生長和進展。這包括程序性死亡(PD)途徑,包括PD-1、PD配體1(PD-L1)和PD-L2,以及細胞毒性T淋巴細胞相關蛋白4(CTLA4)途徑,包括CTLA4及其結合夥伴B7.1/B7.2。已經產生了針對ICPI的抗體,如PD-1、PD-L1和CTLA4,對非小細胞肺癌和其他腫瘤具有治療效果。不幸的是,只有少數患者對這些療法有反應,而且反應往往不持久。

Chitinase 3-like-1 (CHI3L1) is a member of the 18 glycosyl hydrolase gene family that is readily detected in the circulation of normal individuals and expressed at exaggerated levels in the circulation of individuals with diseases characterized by inflammation, tissue remodeling and or cancers.

幾丁質酶3-樣-1(CHI3L1)是18糖基水解酶基因家族中的一員,在正常人的血液循環中很容易檢測到,在以炎症、組織重塑和/或癌症為特徵的疾病患者的血液循環中表達水平過高。

Discoveries

新發現

Recent studies from our laboratory have demonstrated that CHI3L1 is a critical regulator of a number of key cancer-causing pathways. We have highlighted its ability to inhibit tumor cell death (apoptosis), its inhibition of the expression of the tumor suppressors P53 and PTEN and its stimulation of the B-RAF protooncogene. Most recently we have discovered that CHI3L1 is a "master regulator" of ICPI including key elements of the PD-1 and CTLA4 pathways. In accord with the importance of these pathways we have also generated antibodies: 1.) a monoclonal antibody against CHI3L1, and 2.) bispecific antibodies that simultaneously target CHI3L1 and PD-1 or CTLA4. The impressive ability of our bispecific antibodies to control primary and metastatic lung cancer in murine experimental modeling systems is discussed below.

我們實驗室最近的研究表明,CHI3L1是許多關鍵致癌途徑的關鍵調節因子。我們強調了它抑制腫瘤細胞死亡(凋亡)的能力,它對腫瘤抑制基因P53和PTEN的表達的抑制,以及它對B-RAF原癌基因的刺激。最近我們發現CHI3L1是ICPI的“主調節器”,包括PD-1和CTLA4通路的關鍵元件。根據這些途徑的重要性,我們還產生了抗體:1)一個單抗針對CHI3L1、和2.)雙特異性抗體同時靶向CHI3L1和PD-1或CTLA4。我們的雙特異性抗體在小鼠實驗模型系統中控制原發和轉移肺癌的能力令人印象深刻,下面將進行討論。

We generated bispecific antibodies that simultaneously target CHI3L1 and PD-1 or CTLA4. We then compared their effects in experimental models in which T cells and tumor cells are cultured together (a co-culture system) and in a murine model of lung metastasis. In all cases we compared the effects of the bispecific antibody to control antibodies, and to individual monospecific antibodies against CHI3L1, PD-1 or CTLA4, alone or in combination and the results are shown in the figures below.

我們生成了雙特異性抗體 同時靶向CHI3L1和PD-1或CTLA4。然後,我們在T細胞和腫瘤細胞共同培養的實驗模型(共培養系統)和小鼠肺轉移模型中比較了它們的效果。在所有病例中,我們比較了雙特異性抗體與對照抗體的效果,以及單獨或聯合使用針對CHI3L1、PD-1或CTLA4的單特異性抗體的效果,結果如下圖所示。

In the coculture system, critical immune regulating cells called T cells were placed in culture with cancer cells. The ability of the antibodies to induce T cell differentiation and kill (induce apoptosis) of the tumor cells were then evaluated. As can be seen in Figure 1 below, tumor cell death was not induced by isotype control antibodies, and modest degrees of tumor cell apoptosis were seen in cultures with monospecific antiCHI3L1, antiPD-1 or antiCTLA4 individually. Additive tumor cell death was seen when antiCHI3L1 was administered in combination with antiPD-1 or and CTLA4 alone. Most importantly, highly impressive synergistic tumor cell death was seen when the cocultures were treated with the bispecific antibodies (FRGxCTLA4 or FRGxPD-1). In all cases the cell death that was induced was due to T cell differentiation into CD8+ cytotoxic T cells.

在共培養系統中,被稱為T細胞的關鍵免疫調節細胞與癌細胞一起培養。然後評估抗體誘導T細胞分化和殺傷(誘導凋亡)腫瘤細胞的能力。如下圖1所示,同型對照抗體不能誘導腫瘤細胞死亡,在單獨加入單特異性抗CHI3L1、抗PD-1或抗CTLA4的培養物中可見適度程度的腫瘤細胞凋亡。當抗CHI3L1與抗PD-1或CTLA4單獨作用時,腫瘤細胞相加死亡。最重要的是,當用雙特異性抗體(FRGxCTLA4或FRGxPD-1)處理共培養物時,可以看到令人印象深刻的協同腫瘤細胞死亡。在所有病例中,誘導的細胞死亡都是由於T細胞分化為CD8+細胞毒T細胞所致。

In the murine metastasis model we administered malignant melanoma cells into the murine circulation and evaluated their spread to the lungs and pleural surface by counting the number of black staining pleural metastasis. Tumor metastasis were readily appreciated in lungs from mice treated with isotype control antibodies, and modest decreases in metastasis were seen in lungs from mice treated with monospecific antiCHI3L1, antiPD-1 or antiCTLA4 individually. Additive inhibition of tumor spread was seen when antiCHI3L1 was administered in combination with antiPD-1 or and CTLA4. Most importantly, highly impressive synergistic inhibition of tumor metastasis was seen in lungs from mice treated with the bispecific antibodies (FRGxCTLA4 or FRGxPD-1). Figure 2 below shows the results with the FRGxCTLA4 antibody.

在小鼠轉移模型中,我們將惡性黑色素瘤細胞注入到小鼠的循環中,通過計數黑染胸膜轉移的數量來評估它們向肺和胸膜表面的擴散。單特異性抗CHI3L1、抗PD-1或抗CTLA4單獨治療的小鼠肺轉移明顯減少。當抗CHI3L1與抗PD-1或CTLA4聯合應用時,腫瘤的擴散被相加地抑制。最重要的是,在用雙特異性抗體(FRGxCTLA4或FRGxPD-1)治療的小鼠的肺中,可以看到非常令人印象深刻的協同抑制腫瘤轉移的作用。下面的圖2顯示了FRGxCTLA4抗體的結果。

Quoted

報價d

"Bispecific antibodies that simultaneously target CHI3L1 and ICPI like PD-1 and or CTLA4 have an impressive and synergic ability to induce tumor cell death and prevent tumor metastasis compared to individual antibody moieties," commented Dr. Jack A. Elias, Dean Emeritus of Medicine and Biological Sciences and Professor of Translational Science, Medicine and Molecular Microbiology and Immunology at the Warren Alpert Medical School Brown University; Scientific co-founder.

布朗大學醫學和生物科學學院榮譽院長、翻譯科學、醫學、分子微生物學和免疫學教授傑克·A·埃利亞斯博士評論説:“與單獨的抗體部分相比,同時針對CHI3L1和ICPI的雙特異性抗體,如PD-1和/或CTLA4,具有誘導腫瘤細胞死亡和防止腫瘤轉移的令人印象深刻的協同能力。

"Non-small cell lung cancer (NSCLC) is the leading cause of cancer death and second most diagnosed cancer in the US. Glioblastoma multiforme (GBM) is a lethal type of brain tumor that affects approximately 28,000 people in the U.S. The median survival time is about 15 months. With our discovery that CHI3L1 is a critical regulator of a number of key cancer-causing pathways by highlighting its ability to inhibit tumor cell death (apoptosis) this therapy has the potential to save thousand of lives of people effected from NSCLC and GSM," said Dr. Chirinjeev Kathuria, co-founder and Executive Chairman. 

“在美國,非小細胞肺癌(NSCLC)是癌症死亡的主要原因,也是確診人數第二多的癌症。多形性膠質母細胞瘤(GBM)是一種致命的腦瘤,在美國大約有28,000人受到影響。中位生存期約為15個月。我們發現,CHI3L1通過突出其抑制腫瘤細胞死亡(細胞凋亡)的能力,是許多關鍵致癌途徑的關鍵調節因子。這種療法有可能挽救NSCLC和GSM患者的數千人的生命,”聯合創始人兼執行主席奇林吉耶夫·卡蘇裏亞博士説。

Suren Ajjarapu, Chairman and CEO of Aesther, commented, "Aesther is honored to be part of the exciting discovery announced by Ocean Biomedical today. We look forward to working with Ocean to bring these therapies to patients. This discovery and others will lead to long term shareholder value growth and appreciation."

Aesther公司董事長兼首席執行官Suren Ajjarapu評論説:“Aesther公司很榮幸能成為Ocean Biomedical公司今天宣佈的令人興奮的發現的一部分。我們期待着與Ocean公司合作,將這些療法帶給患者。這一發現和其他發現將帶來長期的股東價值增長和增值。”

About Aesther Healthcare Acquisitions Corp.

關於美感r醫療保健收購金絲雀

Aesther is a special purpose acquisition company (SPAC) formed for the purpose of effecting a merger, capital stock exchange, asset acquisition, stock purchase, reorganization or similar business combination with one or more businesses. Its principals possess public and private market investing experience and operational knowledge to bring value added benefits to Ocean Biomedical. The Aesther team has substantial experience investing in and operating businesses in multiple sectors, as well as a significant long-term track record in creatively structuring transactions to unlock and maximize value.

Aesther是一家特殊目的收購公司(SPAC),其成立的目的是與一家或多家企業進行合併、股本交換、資產收購、股票購買、重組或類似的業務合併。其委託人擁有公開和非公開市場的投資經驗和運營知識,為海洋生物醫藥帶來增值效益。Eesther團隊在多個行業投資和運營業務方面擁有豐富的經驗,並在創造性地構建交易結構以釋放和最大化價值方面擁有重要的長期記錄。

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About Ocean Biomedical

關於海洋生物醫學

Ocean Biomedical, Inc. is a Providence, Rhode Island-based biopharma company with an innovative business model that accelerates the development and commercialization of scientifically compelling assets from research universities and medical centers. Ocean Biomedical deploys the funding and expertise to move new therapeutic candidates efficiently from the laboratory to the clinic, to the world. Ocean Biomedical is currently developing five promising discoveries that have the potential to achieve life-changing outcomes in lung cancer, brain cancer, pulmonary fibrosis, and the prevention and treatment of malaria. The Ocean Biomedical team is working on solving some of the world's toughest problems, for the people who need it most.

Ocean Biomedical,Inc.是一家總部位於羅德島州普羅維登斯的生物製藥公司,其創新的商業模式加快了研究型大學和醫療中心具有科學吸引力的資產的開發和商業化。海洋生物醫學公司部署資金和專業知識,將新的候選治療方案有效地從實驗室轉移到臨牀,轉移到世界各地。海洋生物醫學公司目前正在開發五項有希望的發現,這些發現有可能在肺癌、腦癌、肺纖維化以及瘧疾的預防和治療方面實現改變生活的結果。海洋生物醫學團隊正致力於為最需要它的人解決一些世界上最棘手的問題。

To learn more, visit

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Forward-Looking Statements

前瞻性陳述

This press release contains certain statements that are not historical facts and are forward-looking statements within the meaning of the federal securities laws with respect to the proposed merger agreement between Aesther and Ocean Biomedical (the "Transaction"), including without limitation statements regarding the anticipated benefits of the proposed Transaction, the anticipated timing of the proposed Transaction, the implied enterprise value, future financial condition and performance of Ocean Biomedical and the combined company after the closing and expected financial impacts of the proposed Transaction, the satisfaction of closing conditions to the proposed Transaction, the level of redemptions of Aesther's public stockholders and the products and markets and expected future performance and market opportunities of Ocean Biomedical. These forward-looking statements generally are identified by the words "believe," "project," "expect," "anticipate," "estimate," "intend," "think," "strategy," "future," "opportunity," "potential," "plan," "seeks," "may," "should," "will," "would," "will be," "will continue," "will likely result," and similar expressions, but the absence of these words does not mean that a statement is not forward-looking. Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties.

本新聞稿包含的某些陳述不是歷史事實,屬於聯邦證券法中關於Aesther和Ocean Biomedical(以下簡稱“交易”)之間擬議合併協議(“交易”)的前瞻性陳述,包括但不限於有關擬議交易的預期收益、擬議交易的預期時機、擬議交易完成後海洋生物醫藥及其合併公司的隱含企業價值、未來財務狀況和業績以及擬議交易的預期財務影響、對擬議交易的成交條件的滿足程度、Aesther的公眾股東和產品和市場的贖回水平、以及Ocean Biomedical的預期未來業績和市場機會的陳述。這些前瞻性陳述一般由“相信”、“計劃”、“預期”、“預期”、“估計”、“打算”、“思考”、“戰略”、“未來”、“機會”、“潛力”、“計劃”、“尋求”、“可能”、“應該”、“將”、“將會”、“將是”、“將繼續”、“將繼續”、“可能的結果”等詞語來識別。和類似的表述,但沒有這些詞語並不意味着一項聲明不具有前瞻性。前瞻性陳述是基於當前預期和假設對未來事件的預測、預測和其他陳述,因此受到風險和不確定因素的影響。

The announcement today is based solely on laboratory and animal studies. Ocean Biomedical has not conducted any studies that show similar efficacy or safety in humans. There can be no assurances that this treatment will prove safe or effective in humans, and that any clinical benefits of this treatment is subject to clinical trials and ultimate approval of its use in patients by the FDA. Such approval, if granted, could be years away.

今天的聲明完全是基於實驗室和動物研究。海洋生物醫學公司還沒有進行任何研究,顯示出對人類的類似療效或安全性。不能保證這種治療將被證明在人類身上是安全或有效的,這種治療的任何臨牀好處都取決於臨牀試驗和FDA對其在患者身上的最終批准。這樣的批准,如果獲得批准,可能需要數年時間。

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 will differ from assumptions. Many factors could cause actual future events to differ materially from the forward-looking statements in this communication, including but not limited to: (i) the risk that the proposed Transaction may not be completed in a timely manner or at all, which may adversely affect the price of Aesther's securities; (ii) the risk that the proposed Transaction may not be completed by Aesther's business combination deadline; (iii) the failure to satisfy the conditions to the consummation of the proposed Transaction, including the approval of the Merger Agreement by the stockholders of Aesther, the satisfaction of the minimum net tangible assets and minimum cash at closing requirements and the receipt of certain governmental, regulatory and third party approvals; (iv) the occurrence of any event, change or other circumstance that could give rise to the termination of the Merger Agreement; (v) the failure to achieve the minimum amount of cash available following any redemptions by Aesther's stockholders; (vi) redemptions exceeding anticipated levels or the failure to meet The Nasdaq Global Market's initial listing standards in connection with the consummation of the proposed Transaction; (vii) the effect of the announcement or pendency of the proposed Transaction on Ocean Biomedical's business relationships, operating results, and business generally; (viii) risks that the proposed Transaction disrupts current plans and operations of Ocean Biomedical; (ix) the outcome of any legal proceedings that may be instituted against Ocean Biomedical or against Aesther related to the Merger Agreement or the proposed Transaction ; (x) changes in the markets in which Ocean Biomedical's competes, including with respect to its competitive landscape, technology evolution, or regulatory changes; (xi) changes in domestic and global general economic conditions; (xii) risk that Ocean Biomedical may not be able to execute its growth strategies; (xiii) risks related to the ongoing COVID-19 pandemic and response, including supply chain disruptions; (xiv) risk that Ocean Biomedical may not be able to develop and maintain effective internal controls; (xv) costs related to the proposed Transaction and the failure to realize anticipated benefits of the proposed Transaction or to realize estimated pro forma results and underlying assumptions, including with respect to estimated stockholder redemptions; (xvi) the ability to recognize the anticipated benefits of the proposed Transaction and to achieve its commercialization and development plans, and identify and realize additional opportunities, which may be affected by, among other things, competition, the ability of Ocean Biomedical to grow and manage growth economically and hire and retain key employees; (xvii) the risk that Ocean Biomedical may fail to keep pace with rapid technological developments to provide new and innovative products and services or make substantial investments in unsuccessful new products and services; (xviii) the ability to develop, license or acquire new therapeutics; (xix) the risk that Ocean Biomedical will need to raise additional capital to execute its business plan, which may not be available on acceptable terms or at all; (xx) the risk that Ocean Biomedical, post-combination, experiences difficulties in managing its growth and expanding operations; (xxi) the risk of product liability or regulatory lawsuits or proceedings relating to Ocean Biomedical's business; (xxii) the risk of cyber security or foreign exchange losses; (xxiii) the risk that Ocean Biomedical is unable to secure or protect its intellectual property; and (xxiv) those factors discussed in Aesther's filings with the SEC and that that will be contained in the proxy statement relating to the proposed Transaction .

這些前瞻性陳述僅用於説明目的,不打算也不能作為對事實或可能性的保證、保證、預測或確定性陳述。實際事件和情況很難或不可能預測,並將與假設有所不同。許多因素可能會導致未來的實際事件與本新聞稿中的前瞻性陳述大不相同,包括但不限於:(I)擬議的交易可能不能及時完成或根本不能完成的風險,這可能對Aesther的證券價格產生不利影響;(Ii)擬議的交易可能無法在Aesther的業務合併截止日期前完成的風險;(Iii)未能滿足完成擬議交易的條件,包括Aesther股東批准合併協議、滿足完成交易時的最低有形資產淨額和最低現金要求以及收到某些政府、監管機構和第三方的批准;(Iv)發生任何可能導致終止合併協議的事件、變化或其他情況;(V)在Aesther股東進行任何贖回後,未能達到可用現金的最低數額;(Vi)與完成建議交易有關的贖回超過預期水平或未能達到納斯達克全球市場的初始上市標準;。(Vii)建議交易的宣佈或懸而未決對Ocean Biomedical的業務關係、經營業績的影響。, (8)擬議的交易擾亂海洋生物醫療公司目前的計劃和業務的風險;(9)可能對海洋生物醫療公司或與合併協議或擬議交易有關的艾瑟爾公司提起的任何法律訴訟的結果;(X)海洋生物醫療公司競爭市場的變化,包括競爭格局、技術發展或監管變化;(Xi)國內和全球一般經濟狀況的變化;(12)海洋生物醫療公司可能無法執行其增長戰略的風險;(十三)與目前的新冠肺炎大流行和應對有關的風險,包括供應鏈中斷;(十四)海洋生物醫療公司可能無法制定和維持有效的內部控制的風險;(十五)與擬議交易有關的成本以及未能實現擬議交易的預期效益或未能實現預計結果和基本假設,包括與估計的股東贖回有關的成本;(Xvi)認識到擬議交易的預期效益並實現其商業化和開發計劃,以及確定和實現其他機會的能力,這些機會可能受到競爭等因素的影響,其中包括:Ocean Biomedical在經濟上增長和管理增長以及僱用和留住關鍵員工的能力;(Xvii)Ocean Biomedical可能無法跟上快速技術發展的風險,以提供新的創新產品和服務,或對不成功的新產品和服務進行大量投資;(Xviii)開發、許可或獲得新療法的能力;(Xix)海洋生物醫療公司需要籌集額外資本以執行其業務計劃的風險, (Xxi)產品責任或監管訴訟或與Ocean Biomedical業務相關的訴訟或訴訟的風險;(Xxii)網絡安全或匯兑損失的風險;(Xii)Ocean Biomedical無法擔保或保護其知識產權的風險;及(Xxiv)Aesther提交給美國證券交易委員會的文件中討論的因素,以及這將包含在與擬議交易有關的委託書中的風險。

The foregoing list of factors is not exhaustive. You should carefully consider the foregoing factors and the other risks and uncertainties that will be described in the "Risk Factors" section of the preliminary proxy statement and the amendments thereto, the definitive proxy statement, and other documents to be filed by Aesther from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and while Ocean Biomedical and Aesther may elect to update these forward-looking statements at some point in the future, they assume no obligation to update or revise these forward-looking statements, whether as a result of new information, future events or otherwise, except as required by applicable law. Neither of Ocean Biomedical or Aesther gives any assurance that Ocean Biomedical or Aesther, or the combined company, will achieve its expectations. These forward-looking statements should not be relied upon as representing Aesther's or Ocean Biomedical's assessments as of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.

前面列出的因素並不是詳盡的。您應仔細考慮上述因素以及其他風險和不確定因素,這些風險和不確定因素將在初步委託書及其修正案、最終委託書和艾司德不時提交給美國證券交易委員會的其他文件中的“風險因素”部分進行描述。這些文件確定和處理了其他可能導致實際事件和結果與前瞻性陳述中包含的內容大不相同的重要風險和不確定因素。前瞻性陳述僅在其發表之日起發表。提醒讀者不要過度依賴前瞻性陳述,雖然Ocean Biomedical和Aesther可能會選擇在未來某個時候更新這些前瞻性陳述,但除非適用法律要求,否則它們沒有義務因新信息、未來事件或其他原因而更新或修訂這些前瞻性陳述。Ocean Biomedical或Eesther都不能保證Ocean Biomedical或Eesther,或合併後的公司將實現其預期。這些前瞻性陳述不應被視為代表艾瑟爾或海洋生物醫療公司截至本新聞稿日期之後的任何日期的評估。因此,不應過分依賴前瞻性陳述。

Additional Information and Where to Find It

其他信息以及在哪裏可以找到它

In connection with the merger agreement and the proposed Transaction, Aesther intends to file with the U.S. Securities and Exchange Commission (the "SEC") a proxy statement on Schedule 14A relating to the proposed Transaction. This communication is not intended to be, and is not, a substitute for the proxy statement or any other document that Aesther has filed or may file with the SEC in connection with the proposed Transaction. Aesther's stockholders and other interested persons are advised to read, when available, the preliminary proxy statement and the amendments thereto, the definitive proxy statement and documents incorporated by reference therein filed in connection with the proposed Transaction, as these materials will contain important information about Aesther, Ocean Biomedical, the merger agreement, and the proposed Transaction. When available, the definitive proxy statement and other relevant materials for the proposed Transaction will be mailed to stockholders of Aesther as of a record date to be established for voting on the proposed Transaction. Before making any voting or investment decision, investors and stockholders of Aesther are urged to carefully read the entire proxy statement, when they become available, and any other relevant documents filed with the SEC, as well as any amendments or supplements to these documents, because they will contain important information about the proposed Transaction. Aesther investors and stockholders will also be able to obtain copies of the preliminary proxy statement, the definitive proxy statement, and other documents filed with the SEC that will be incorporated by reference therein, without charge, once available, at the SEC's website at www.sec.gov, or by directing a request to: Aesther Healthcare Acquisition Corp., 515 Madison Avenue, Suite 8078, New York, NY 10022, Attention: Mr. Suren Ajjarapu.

關於合併協議和擬議的交易,艾司特打算向美國證券交易委員會(“美國證券交易委員會”)提交一份關於擬議交易的附表14A的委託書。本通訊的目的不是,也不是替代艾司特已經或可能向美國證券交易委員會提交的與擬議交易相關的委託書或任何其他文件。建議Aesther的股東和其他感興趣的人士閲讀初步委託書及其修正案、最終委託書以及通過引用納入其中的與擬議交易相關的文件,因為這些材料將包含有關Aesther、Ocean Biomedical、合併協議和擬議交易的重要信息。一旦有了最終的委託書和其他相關材料,建議交易的最終委託書和其他相關材料將被郵寄給Aesther的股東,該記錄日期將被確定為對建議交易進行投票。在做出任何投票或投資決定之前,艾司特的投資者和股東被敦促仔細閲讀完整的委託書(當它們可用時),以及提交給美國證券交易委員會的任何其他相關文件,以及這些文件的任何修正案或補充,因為它們將包含有關擬議交易的重要信息。艾司特的投資者和股東還將能夠獲得提交給美國證券交易委員會的初步委託書、最終委託書和其他文件的副本,這些文件將通過引用的方式併入美國證券交易委員會,一旦可以獲得,就可以在美國證券交易委員會的網站上免費獲得Www.sec.gov,或將請求發送至:Aesther Healthcare Acquisition Corp.,515Madison Avenue,Suite8078,New York,NY 10022,請注意:Suren Ajjarapu先生。

Participants in the Solicitation

徵集活動的參與者

Aesther, Ocean Biomedical and their respective directors, executive officers, other members of management and employees may be deemed participants in the solicitation of proxies from Aesther's stockholders with respect to the proposed Transaction. Investors and security holders may obtain more detailed information regarding the names and interests in the proposed Transaction of Aesther's directors and officers in Aesther's filings with the SEC, including, when filed with the SEC, the preliminary proxy statement and the amendments thereto, the definitive proxy statement, and other documents filed with the SEC. Such information with respect to Ocean Biomedical's directors and executive officers will also be included in the proxy statement.

Aesther、Ocean Biomedical及其各自的董事、高管、其他管理層成員和員工可被視為就擬議交易向Aesther股東徵集委託書的參與者。投資者和證券持有人可以在艾司德提交給美國證券交易委員會的文件中獲得有關艾司德董事和高級管理人員的姓名和權益的更詳細信息,包括在提交給美國證券交易委員會的文件中包括初步委託書及其修正案、最終委託書以及提交給美國證券交易委員會的其他文件。有關海洋生物醫療公司董事和高管的此類信息也將包括在委託書中。

No Offer or Solicitation

沒有要約或懇求

This press release is not a solicitation of a proxy, consent or authorization with respect to any securities or in respect of the proposed Transaction and will not constitute an offer to sell or the solicitation of an offer to buy any securities, nor will there be any sale of securities in any states or jurisdictions in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction.

本新聞稿不是就任何證券或建議的交易徵求委託書、同意或授權,也不會構成出售或邀請購買任何證券的要約,也不會在任何州或司法管轄區進行任何證券銷售,在這些州或司法管轄區,在根據任何此類司法管轄區的證券法註冊或資格之前,此類要約、招攬或出售將是非法的。

# # #

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Investor Contact
IR@aestherhealthcarespac.com

投資者聯繫方式
郵箱:ir@estherHealth caresac.com

Ocean Biomedical Media Relations
Kevin Kertscher
Communications Director
kkertscher@oceanbiomedical.com

海洋生物醫學媒體關係
凱文·克特舍爾
交通董事
郵箱:kkertscher@Ocean biobedical.com

Attachments

附件

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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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