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Scinai Immunotherapeutics Announces Receipt of Nasdaq Delisting Notification and Appeal

Scinai Immunotherapeutics Announces Receipt of Nasdaq Delisting Notification and Appeal

Scinai Immunotherapeutics宣布收到纳斯达克退市通知和上诉
PR Newswire ·  05/06 21:21

The Board has Approved a Ratio Change of the ADSs to Non-traded Ordinary Shares (equivalent to a reverse split) Designed to Regain Compliance

董事会已批准将ADS与非交易普通股的比率变更(相当于反向拆分),旨在恢复合规性

JERUSALEM, May 6, 2024 /PRNewswire/ -- Scinai Immunotherapeutics Ltd. (Nasdaq: SCNI), a biopharmaceutical 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 it had had received a staff determination letter (the "Letter") on April 30, 2024 from the Listing Qualifications Department (the "Staff") of The Nasdaq Stock Market LLC ("Nasdaq") notifying the Company that, due to the Company's non-compliance with the minimum $1.00 bid price requirement set forth in Nasdaq Listing Rule 5550(a)(2) (the "Rule"), the Company's American Depositary Shares ("ADSs") would be scheduled for delisting from The Nasdaq Capital Market and would be suspended for trading at the opening of business on May 7, 2024 unless the Company timely requests a hearing before an independent Nasdaq Hearings Panel (the "Panel").

耶路撒冷,2024 年 5 月 6 日 /PRNewswire/-- Scinai Immunotherapeutics Ltd. 专注于开发炎症和免疫学(I&I)生物产品以及通过其Scinai生物服务业务部门提供CDMO服务的生物制药公司(纳斯达克股票代码:SCNI)今天宣布,它已于2024年4月30日收到纳斯达克股票市场有限责任公司(“纳斯达克”)上市资格部门(“员工”)的员工决定函(“信函”),通知该公司到期对于公司未遵守《纳斯达克上市规则》5550 (a) (2)(“规则”)中规定的最低1.00美元投标价要求,除非公司及时要求独立的纳斯达克听证小组(“小组”)举行听证会,否则该公司的美国存托股票(“ADS”)将计划从纳斯达克资本市场退市,并将在2024年5月7日开盘时暂停交易。

As previously disclosed, on November 1, 2023, the Company received a letter from the Staff notifying the Company of its noncompliance with the Rule by failing to maintain a minimum bid price for the ADSs of at least $1.00 per share for the previous 33 consecutive business days. The Company was provided an initial 180-day grace period, or until April 29, 2024, to regain compliance with the Rule. To regain compliance with the Rule the closing bid price of the ADSs needed to be at least $1.00 per share for a minimum of ten consecutive business days during the compliance Period.

正如先前披露的那样,2023年11月1日,公司收到工作人员的来信,通知公司,由于未能在之前的连续33个工作日将ADS的最低出价维持在每股至少1.00美元,因此违反了该规则。公司最初获得了180天的宽限期,或直到2024年4月29日,以恢复对该规则的遵守。为了恢复对该规则的遵守,在合规期内至少连续十个工作日,ADS的收盘出价必须至少为每股1.00美元。

The Company has today appealed the delisting determination and requested a hearing before the Panel. Such a request automatically stays any suspension or delisting action pending the hearing and the expiration of any additional extension period granted by the Panel after the hearing.

该公司今天对除名决定提出上诉,并要求专家组举行听证会。在听证会和听证会后专家组批准的任何额外延长期限到期之前,此类请求将自动中止任何暂停或除名行动。

The Company also announces that its Board of Directors has 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, which is equivalent to a reverse split of 1 for 10. No action is required by the holders of the ADSs to affect the ratio change, and no fractional new ADSs will be issued in connection with the change in ADS ratio. Instead, fractional entitlements to new ADSs will be aggregated and the depositary bank will attempt to sell them with the net cash proceeds from the sale of the fractional ADS entitlements to be distributed to the applicable ADS holders by the depositary bank.

该公司还宣布,其董事会已批准将ADS与其非交易普通股的比率变动,将每股ADS所代表的普通股数量从400股增加到4,000股,相当于1比10的反向拆分。ADS的持有人无需采取任何行动来影响比率的变化,也不会发行与ADS比率变化相关的部分新ADS。取而代之的是,将汇总新存托凭证的部分权益,存托银行将尝试将其与出售部分ADS权益的净现金收益一起出售,由存托银行分配给适用的ADS持有人。

The anticipated effective date of the ratio change is May 21, 2024. The Company expects that the ratio change will correct the ADS trading price non-compliance issue, which in turn, because corrected prior to the hearing, would make the need for a hearing moot. If the ratio change does not correct the non-compliance prior to the hearing, the Company will request an extension of time sufficient to regain compliance vis-à-vis the referenced ratio change or, if necessary, a further ratio change. However, in such a case, there can be no assurance that the Company will obtain an extension period from the Panel to regain compliance, or, if the Panel grants such an extension period, that the Company will be able to evidence compliance with the Rule before the extension period expires.

该比率变更的预计生效日期为2024年5月21日。该公司预计,该比率的变化将纠正ADS交易价格违规问题,这反过来又由于在听证会之前得到纠正,因此听证会变得毫无意义。如果比率变更未能纠正听证会前的违规行为,则公司将要求延长足够的时间以恢复对参考比率变更的合规性,或在必要时进一步更改比率。但是,在这种情况下,无法保证公司将获得专家组的延长期限以恢复合规,也无法保证如果专家小组批准了延长期限,公司将能够在延长期到期之前证明遵守了该规则。

During the period before the hearing, if any, the ADSs shares will continue to trade on Nasdaq.

在听证会之前的时期(如果有),ADS的股票将继续在纳斯达克交易。

About Scinai Immunotherapeutics

关于 Scinai 免疫疗法

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 GMP manufacturing, and pre-clinical and clinical trial design and execution services to early stage biotech companies. Company website: .

Scinai Immunotherapeutics Ltd.(纳斯达克股票代码:SCNI)是一家生物制药公司,拥有两个互补的业务部门,一个专注于炎症和免疫学(I&I)生物治疗产品的内部开发,首先是针对医疗需求未得到满足的疾病的创新、去风险的纳米VHH抗体(nanoABS)产品线,另一个是提供生物药物开发、分析方法开发的精品CDMO GMP 制造、临床前和临床试验的设计和执行服务,直至早期阶段生物技术公司。公司网站:.

Company Contacts

公司联系人

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

投资者关系 | +972 8 930 2529 | [email protected]
业务发展 | +972 8 930 2529 | [email protected]

Forward-Looking Statements

前瞻性陈述

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 price of our ADSs will not increase proportionally as a result of the change in ADS ratio or sufficiently to cure the Nasdaq non-compliance, the risk of delisting of the ADSs from listing on Nasdaq, 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 maintain its listing on Nasdaq; 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 10-K filed with the Securities and Exchange Commission ("SEC") on April 17, 2023, and the Company's subsequent filings with the SEC. Scinai undertakes no obligation to revise or update any forward-looking statement for any reason.

本新闻稿包含1995年《私人诉讼改革法》所指的前瞻性陈述。诸如 “期望”、“相信”、“打算”、“计划”、“继续”、“可能”、“将”、“预期” 等词语以及类似的表述旨在识别前瞻性陈述。除历史事实陈述外,所有陈述均为前瞻性陈述。此类陈述的示例包括但不限于ADS的未来价格。这些前瞻性陈述反映了管理层当前对某些当前和未来事件的看法,并受各种风险、不确定性和假设的影响,这些风险和假设可能导致结果与管理层的预期存在重大差异 Scinai 免疫疗法有限公司风险和不确定性包括但不限于 我们的ADS价格不会因ADS比率的变化而成比例上涨或不足以纠正纳斯达克违规行为的风险, 美国证券交易所从纳斯达克上市的风险、延迟上市的风险、Scinai无法开展其研发活动或其研发活动未取得成果,包括所设想的活动 体内研究和临床试验; Scinai无法继续在纳斯达克上市的风险;Scinai无法成功扩大其在纳斯达克上市的风险 CDMO 业务或许可其他 nanoABS;风险 Scinai可能无法以有吸引力的条件获得额外资本;nanoABS的治疗和商业潜力无法得到满足或Scinai无法成功将nanoABS推向商业化的风险;nanoABS的临床前和临床试验数据延迟的风险(如果有);我们的业务战略可能不成功的风险;欧洲投资银行(EIB)的风险根据与Scinai的融资合同,可能会加快融资速度;Scinai获得以下权利的能力其他产品机会;Scinai按照Scinai可以接受的条件或完全可以接受的条件进行合作的能力;Scinai在耶路撒冷的制造工厂获得监管部门批准的时间(如果有的话);制造设施无法用于各种应用和其他疫苗和治疗技术的风险;以及药物开发涉及漫长而昂贵的过程且结果不确定的风险。有关影响公司的风险和不确定性的更多详细信息载于公司于2023年4月17日向美国证券交易委员会(“SEC”)提交的10-K表年度报告以及公司随后向美国证券交易委员会提交的文件中的 “风险因素” 标题下。Scinai没有义务出于任何原因修改或更新任何前瞻性陈述。

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SOURCE Scinai Immunotherapeutics Ltd.

来源 Scinai Immuntherapeutics Ltd.

译文内容由第三方软件翻译。


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