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Scinai Immunotherapeutics Regains Compliance With Nasdaq Minimum Bid Price Requirement; Continues to Work With the European Investment Bank to Convert Loan to Equity to Regain Compliance With Nasdaq Minimum Shareholders' Equity Requirement

Scinai Immunotherapeutics Regains Compliance With Nasdaq Minimum Bid Price Requirement; Continues to Work With the European Investment Bank to Convert Loan to Equity to Regain Compliance With Nasdaq Minimum Shareholders' Equity Requirement

Scinai免疫治療恢復符合Nasdaq最低買盤價格要求;繼續與歐洲投資銀行合作,將貸款轉爲股權以符合Nasdaq最低股東權益要求。
PR Newswire ·  06/07 19:00

JERUSALEM, June 7, 2024 /PRNewswire/ -- Scinai Immunotherapeutics Ltd. (Nasdaq: SCNI) (the "Company"), a biotechnology company focused on developing inflammation and immunology (I&I) biological products and on providing CDMO services through its Scinai Bioservices business unit, today announced that on June 5, 2024, it received formal notification from the Listing Qualification Department (the "Staff") of the Nasdaq Stock Market ("Nasdaq") that the Company has regained compliance with the minimum $1.00 bid price requirement set forth in Nasdaq Listing Rule 5550(a)(2) (the "Rule").

2024年6月7日,以色列耶路撒冷/PRNewswire/--Scinai免疫療法有限公司(納斯達克:SCNI)本公司是一家生物技術公司,專注於開發炎症和免疫(I&I)生物產品,並通過其Scinai Bioservices業務部門提供CDMO服務。2024年6月5日,本公司收到了納斯達克證券市場(“納斯達克”)上市資格部(“工作人員”)的正式通知,通知本公司已恢復其納斯達克上市規則5550(a)(2)(“規則”)規定的最低1.00美元的買盤價格要求的符合性。

The Company previously disclosed in a press release dated May 6, 2024, that it received a letter from the Staff notifying the Company of its noncompliance with the Rule by failing to maintain the required minimum bid price for the Company's American Depositary Shares ("ADSs"). The Company also disclosed in that press release that it had timely requested a hearing before an independent Nasdaq Hearings Panel (the "Hearings Panel") to present a plan to regain compliance and that its Board of Directors had already approved a ratio change of the ADSs to its non-traded ordinary shares, increasing the number of ordinary shares represented by each ADS from 400 to 4,000, effective May 21, 2024. Following the ratio change the closing bid price of the ADSs equaled or exceeded $1.00 per ADS for the following ten consecutive business days. As a result, the Company regained compliance with the Rule and the Staff issued the above-mentioned notification .

本公司先前曾在2024年5月6日發佈新聞稿披露,工作人員通知本公司其美國存託憑證("ADSs")的買盤價沒有保持所需的最低買盤價,因而不符合該規則,本公司在該新聞稿中還透露了本公司已及時在納斯達克獨立聽證會議上提出了恢復符合性的計劃,並且本公司董事會已經批准了ADSs與其非交易的普通股的比率變更,並將每個ADS代表的普通股數量從400增加到4,000,自2024年5月21日起生效。根據比率變更,ADSs的收盤買盤價在接下來的10個連續營業日內均等於或高於1.00美元。因此,本公司符合了規則,並且工作人員發佈了上述通知 。

On May 24, 2024, the Company announced the receipt of a Nasdaq Staff determination letter regarding noncompliance with the minimum shareholders' equity required for continued listing and that as part of the hearing previously requested with the Hearings Panel it would present a plan for the Company to regain compliance with this requirement (the "Plan"). The Company also announced that it was engaged in discussions with the European Investment Bank (the "EIB") regarding amending the finance contract with the EIB and the conversion of a significant portion of the loan owed by the Company to EIB into equity in the Company on terms the Company considers favorable to the Company and its shareholders. These discussions are advancing, and the Company believes it will be in a position to include the potential conversion as a key component of the Plan to be presented to the Hearings Panel on June 18, 2024. Any revised terms of the finance contract with the EIB are subject to obtaining formal approval from appropriate EIB governing bodies, negotiating and finalizing definitive agreements relating to the revised terms, and the fulfilment of any condition precedent, all to the EIB's satisfaction.

本公司於2024年5月24日宣佈收到納斯達克工作人員有關未達到繼續上市所需的最低股東權益的決定書,並作爲先前在聽證會議中請求的一部分,將提出本公司恢復符合性的計劃。本公司還宣佈,本公司已就修訂與歐洲投資銀行(“EIB”)的融資協議和轉換本公司拖欠給EIB的貸款的大部分款項爲本公司股本的條款進行討論,並認爲本公司將能夠將潛在轉換作爲將於2024年6月18日向聽證會議提交的計劃的關鍵組成部分。任何與EIB的融資協議修訂條款都需要獲得適當EIB管理機構的正式批准,並協商和最終確定與修訂條款相關的明確協議履行任何先決條件,以EIB的滿意。

In the notification provided by the Staff on June 5, 2024, the Staff stated that the Company remains non-compliant with the equity requirement in Listing Rule 5550(b)(1), or any of the alternative requirements under Listing Rule 5550(b), and accordingly the June 18, 2024, hearing will be held as scheduled.

工作人員在2024年6月5日提供的通知中表示,公司仍不符合上市規則5550(b)(1)中的權益要求,或者不符合上市規則5550(b)中的任何備選要求,因此將如期於2024年6月18日舉行聽證會。

About Scinai Immunotherapeutics

關於Scinai免疫療法

Scinai Immunotherapeutics Ltd. (Nasdaq: SCNI) is a biopharmaceutical company with two complementary business units, one focused on in-house development of inflammation and immunology (I&I) biological therapeutic products beginning with an innovative, de-risked pipeline of nanosized VHH antibodies (NanoAbs) targeting diseases with large unmet medical needs, and the other a boutique CDMO providing biological drug development, analytical methods development, clinical cGMP manufacturing, and pre-clinical and clinical trial design and execution services to early stage biotech drug development programs. Company website: .

Scinai免疫療法有限公司(納斯達克:SCNI)是一家擁有兩個互補的業務部門的生物製藥公司,一個業務部門專注於內部開發以納米尺寸的VHH抗體(NanoAbs)爲開始的炎症和免疫(I&I)生物治療產品,針對具有巨大醫學需求的疾病,另一家專注於提供生物藥物開發,分析方法開發,臨床cGMP製造以及早期生物技術藥物開發項目的臨床試驗設計和執行服務的精品CDMO。公司網站:.

Company Contacts

公司聯繫方式

Investor Relations | +972 8 930 2529 | [email protected]
Business Development | +972 8 930 2529 | [email protected]

投資者關係 | +972 8 930 2529 | [email protected]
業務發展 | +972 8 930 2529 | [email protected]

Forward-Looking Statements

前瞻性聲明

This press release contains forward-looking statements within the meaning of the Private Litigation Reform Act of 1995. Words such as "expect," "believe," "intend," "plan," "continue," "may," "will," "anticipate," and similar expressions are intended to identify forward-looking statements. All statements, other than statements of historical facts, are forward-looking statements. Examples of such statements include, but are not limited to, the future price of the ADSs. These forward-looking statements reflect management's current views with respect to certain current and future events and are subject to various risks, uncertainties and assumptions that could cause the results to differ materially from those expected by the management of Scinai Immunotherapeutics Ltd. Risks and uncertainties include, but are not limited to, the risk that the Company will be unable to meet the continued listing requirements of Nasdaq, including the risk that the consummation of the conversion of the EIB loan to equity would not resolve the recent deficiency notice from NASDAQ with respect to the Stockholders' Equity Requirement; the risk of delay in, Scinai's inability to conduct, or the unsuccessful results of, its research and development activities, including the contemplated in-vivo studies and a clinical trial; the risk that Scinai will not be successful in expanding its CDMO business or in-license other NanoAbs; the risk that Scinai may not be able to secure additional capital on attractive terms, if at all; the risk that the therapeutic and commercial potential of NanoAbs will not be met or that Scinai will not be successful in bringing the NanoAbs towards commercialization; the risk of a delay in the preclinical and clinical trials data for NanoAbs, if any; the risk that our business strategy may not be successful; the risk that the European Investment Bank (EIB) may accelerate the financial facility under its finance contract with Scinai; Scinai's ability to acquire rights to additional product opportunities; Scinai's ability to enter into collaborations on terms acceptable to Scinai or at all; timing of receipt of regulatory approval of Scinai's manufacturing facility in Jerusalem, if at all or when required; the risk that the manufacturing facility will not be able to be used for a wide variety of applications and other vaccine and treatment technologies; and the risk that drug development involves a lengthy and expensive process with uncertain outcomes. More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors" in the Company's Annual Report on Form 20-F filed with the Securities and Exchange Commission ("SEC") on May 15, 2024, and the Company's subsequent filings with the SEC. Scinai undertakes no obligation to revise or update any forward-looking statement for any reason.

本新聞稿包含根據1995年《私人訴訟改革法》發佈的前瞻性陳述。例如,“預計”,“相信”,“打算”,“計劃”,“繼續”,“可能”,“將”,“預計”的詞語和類似表達式旨在識別前瞻性陳述。所有陳述,除非是歷史事實的陳述,否則都是前瞻性陳述。這些前瞻性陳述反映了Scinai免疫療法有限公司管理層對於某些當前和未來事件的當前視角,且可能受到各種風險,不確定因素和假設的影響,這可能導致Scinai免疫療法有限公司的結果與管理層的預期不同。風險和不確定因素包括但不限於:本公司不能滿足納斯達克的持續上市要求的風險,包括EIB貸款轉換爲股東權益的達成將不能解決納斯達克就股東權益要求發出的最近不合格通知的風險;Scinai的研究和開發活動,包括擬議中的體內研究和臨床試驗的延遲、無法進行或失敗的風險;Scinai將不成功地擴大其CDMO業務或授權其他NanoAbs的風險;Scinai可能無法以有吸引力的條件獲得額外資本,如果有的話;NanoAbs的治療和商業潛力可能無法得到滿足,或Scinai將無法成功將NanoAbs推向商業化;如果有的話,NanoAbs的臨床前和臨床試驗數據的延遲的風險;本公司的業務戰略可能不成功的風險;瑞典投資銀行(EIB)可能加速其與Scinai的融資活動;Scinai獲取其他產品機會的能力;Scinai能否接受或參與合作的風險;是時候或需要時,Scinai能否獲得監管機構批准其在耶路撒冷的製造設施的時間;製造設施將能否用於廣泛的應用和其他疫苗和治療技術的風險;以及藥物開發涉及漫長而昂貴的不確定結果的過程的風險。有關影響公司的風險和不確定因素的更詳細信息,請參閱本公司於2024年5月15日向證券交易委員會提交的年度報告20-F中的“風險因素”標題以及本公司隨後向SEC提交的文件。Scinai免疫療法有限公司不承擔修訂或更新任何前瞻性陳述的義務,無論出於何種原因。

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SOURCE Scinai Immunotherapeutics Ltd.

來源:Scinai免疫療法有限公司

譯文內容由第三人軟體翻譯。


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