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Atossa Set to Join Russell 3000 Index Effective June 28, 2024

Atossa Set to Join Russell 3000 Index Effective June 28, 2024

Atossa将于2024年6月28日加入Russell 3000指数。
Atossa Therapeutics ·  06/17 00:00

SEATTLE, June 17, 2024 (GLOBE NEWSWIRE) -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) ("Atossa" or the "Company"), today announced its expected upcoming inclusion in the Russell 3000 Index, according to preliminary Russell reconstruction information posted on the FTSE Russell website. The newly reconstructed index will take effect after the market closes on June 28, 2024. Atossa is a clinical stage biopharmaceutical company developing innovative medicines in areas of significant unmet medical need in oncology with a focus on breast cancer.

2024年6月17日,西雅图(全球新闻通讯社)——Atossa Therapeutics, Inc.(纳斯达克股票代码:ATOS)(以下简称“Atossa”或“公司”)今天宣布,预计将被纳入拉塞尔3000指数。"Atossa的加入Russell 3000指数是我们最新的里程碑,使公司的转型已在发生," Atossa的总裁兼首席执行官Steven Quay,M.D.,Ph.D.表示:"在其他进展方面,我们在美国抗癌研究协会(AACR)年会上呈现了极具鼓舞的单独疗法数据,并启动了一项第2期研究,研究我们专有的(Z)-endoxifen和Eli Lilly and Company的cyclin-dependent kinase(CDK)4/6抑制剂VERZENIO abemaciclib的组合。而且,今年晚些时候,我们预计将有两项正在进行中的第2期研究的主要数据可用。我们加入Russell 3000指数表明了我们日益扩大的(Z)-endoxifen开发计划的价值,并将使Atossa在投资社区中得到重要的关注,我们相信这将扩大我们的股东基础。"

"Atossa's inclusion in the Russell 3000 Index is our latest milestone, adding to what has already been a transformational year for the Company," said Steven Quay, M.D., Ph.D., Atossa's President and Chief Executive Officer. "Among other progress, we presented extremely encouraging monotherapy data at the American Association for Cancer Research (AACR) Annual Meeting and initiated a Phase 2 study investigating the combination of our proprietary (Z)-endoxifen and abemaciclib (VERZENIO), a cyclin-dependent kinase (CDK) 4/6 inhibitor marketed by Eli Lilly and Company. And, later this year, we expect primary data from two of our ongoing Phase 2 studies to be available. Our addition to the Russell 3000 shows the value of our expanding (Z)-endoxifen development program and will result in significant visibility for Atossa within the investment community, which we expect will expand our shareholder base."

FTSE Russell主要根据客观的市值排名和风格属性来确定Russell指数的成员资格。美国全幅Russell 3000指数的成员资格将保留一年,这意味着自动包括在大幅Russell 1000指数或小幅Russell 2000指数以及适当的增长和价值风格指数中。"指数"是我们公司的最新里程碑,为我们已经实现的变革性一年增添了色彩,"Atossa的总裁兼首席执行官Steven Quay博士表示。"除其他进展外,我们在美国抗癌研究协会年会上提出了极具鼓舞的单药治疗数据,并启动了一项第二阶段研究,研究我们自有的(Z)-恶唑酰亚胺(Z-Endoxifen)与安柏霉素(VERZENIO)的联合应用。而且,我们期望今年晚些时候,两项正在进行中的第二期研究的主要数据将会发布。我们被列入Russell 3000证明了我们正在扩大(Z)-endoxifen开发计划,我们预计会受到投资社区的高度关注,这应该会让我们的股东数量增加。

Membership in the US all-cap Russell 3000 Index, which remains in place for one year, means automatic inclusion in the large-cap Russell 1000 Index or small-cap Russell 2000 Index as well as the appropriate growth and value style indexes. FTSE Russell determines membership for its Russell indexes primarily by objective, market-capitalization rankings, and style attributes.

成为美国全市值Russell 3000指数的成员,将自动成为大市值Russell 1000指数或小市值Russell 2000指数的成员,以及适当的成长和价值风格指数的成员。FTSE Russell主要根据客观的市值排名和风格属性来确定其Russell指数的成员资格。

Russell indexes are widely used by investment managers and institutional investors for index funds and as benchmarks for active investment strategies. According to the data as of the end of December 2023, about $10.5 trillion in assets are benchmarked against the Russell US indexes, which belong to FTSE Russell, a prominent global index provider.

罗素指数广泛用于投资管理人和机构投资者的指数基金和作为活跃投资策略的基准。根据2023年12月底的数据,约有10.5万亿美元的资产是以FTSE罗素为主的美国指数为基准的,这是一家知名的全球指数提供商。

About (Z)-Endoxifen
(Z)-endoxifen is the most potent Selective Estrogen Receptor Modulator (SERM) for estrogen receptor inhibition and also causes estrogen receptor degradation. It has also been shown to have efficacy in the setting of patients with tumor resistance to other hormonal treatments. In addition to its potent anti-estrogen effects, (Z)-endoxifen has been shown to target PKCβ1, a known oncogenic protein, at clinically attainable blood concentrations. Finally, (Z)-endoxifen appears to deliver similar or even greater bone agonistic effects while resulting in little or no endometrial proliferative effects compared with standard treatments, like tamoxifen.

关于(Z)-Endoxifen
(Z)-endoxifen是最强效的选择性雌激素受体调节剂(SERM),用于调节雌激素受体,同时导致雌激素受体的降解。它也已被证明在对其他激素治疗方案产生耐药的肿瘤患者中具有疗效。除了其强效的抗雌激素作用外,(Z)-endoxifen已被证明能够以临床可达到的血浓度靶向PKCβ1,这是一种已知的致癌蛋白。最后,与标准治疗(如他莫昔芬)相比,(Z)-endoxifen似乎具有相似甚至更大的骨促进作用,同时几乎没有子宫内膜增生作用。

Atossa is developing a proprietary oral formulation of (Z)-endoxifen that does not require liver metabolism to achieve therapeutic concentrations and is encapsulated to bypass the stomach, as acidic conditions in the stomach convert a significant proportion of (Z)-endoxifen to the inactive (E)-endoxifen. Atossa's (Z)-endoxifen has been shown to be well tolerated in Phase 1 studies and in a small Phase 2 study of women with breast cancer. (Z)-endoxifen is currently being studied in four Phase 2 trials: one in healthy women with measurable breast density, one in women diagnosed with ductal carcinoma in situ, and two other studies including the EVANGELINE study in women with ER+/HER2- breast cancer. Atossa's (Z)-endoxifen is protected by three issued U.S. patents and numerous pending patent applications.

Atossa正在开发一种专有的口服(Z)-endoxifen配方,该配方不需要经过肝代谢即可达到治疗浓度,并被密封以绕过胃部,因为胃中的酸性条件会将(Z)-endoxifen转化为无活性的(E)-endoxifen。Atossa的(Z)-endoxifen已在1期和一小部分乳腺癌女性的2期试验中证明安全。当前正在进行四项2期试验:一项仅针对有测量乳房密度的健康女性,一项针对被诊断为导管癌前病变的女性,另外还有两项研究,其中包括针对ER+/HER2-乳腺癌女性的EVANGELINE研究。Atossa的(Z)-endoxifen由三项已颁发的美国专利和众多不断申请的专利保护。

About FTSE Russell
FTSE Russell is a leading global provider of benchmarking, analytics, and data solutions for investors, giving them a precise view of the market relevant to their investment process. A comprehensive range of reliable and accurate indexes provides investors worldwide with the tools they require to measure and benchmark markets across asset classes, styles, or strategies.

关于FTSE Russell
FTSE Russell是为投资者提供基准、分析和数据解决方案的领先全球提供商,为投资者提供与其投资过程相关联的精确市场视图。可靠且准确的指数全面涵盖不同的资产类别、风格或策略,为全球投资者提供测量和基准市场的工具。

FTSE Russell index expertise and products are used extensively by institutional and retail investors globally. For over 30 years, leading asset owners, asset managers, ETF providers and investment banks have chosen FTSE Russell indexes to benchmark their investment performance and create ETFs, structured products, and index-based derivatives.

FTSE Russell指数专业知识和产品在全球的机构投资者和零售投资者广泛运用。30多年来,领先的资产所有者、资产管理人、ETF提供商和投资银行选择FTSE Russell指数作为其投资表现的基准,并创造ETF、结构性产品和基于指数的衍生品。

FTSE Russell is focused on applying the highest industry standards in index design and governance, employing transparent rules-based methodology informed by independent committees of leading market participants. FTSE Russell fully embraces the IOSCO Principles, and its Statement of Compliance has received independent assurance. Index innovation is driven by client needs and customer partnerships, allowing FTSE Russell to continually enhance the breadth, depth and reach of its offering.

FTSE Russell专注于应用指数设计和治理领域的最高行业标准,采用透明的基于规则的方法,并由领先市场参与者的独立委员会提供咨询意见。FTSE Russell完全接受IOSCO原则,其遵从性声明已经获得独立保证。指数创新是由客户的需求和客户的伙伴关系推动的,这使得FTSE Russell能够不断加强其提供的广度、深度和覆盖范围。

FTSE Russell is wholly owned by London Stock Exchange Group.

FTSE Russell完全归伦敦证券交易所集团所有。

For more information, visit https://www.lseg.com/en/ftse-russell.

要获取更多信息,请访问https://www.lseg.com/en/ftse-russell.

About Atossa Therapeutics
Atossa Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing innovative medicines in areas of significant unmet medical need in oncology with a focus on using (Z)-endoxifen to prevent and treat breast cancer. For more information, please visit www.atossatherapeutics.com.

关于Atossa Therapeutics
Atossa Therapeutics,Inc.是一家临床阶段的生物制药公司,在癌症领域研发创新药物,专注于使用(Z)-内酰亚胺预防和治疗乳腺癌。欲了解更多信息,请访问 www.atossatherapeutics.com.

Contact:
Eric Van Zanten
VP, Investor and Public Relations
610-529-6219
eric.vanzanten@atossainc.com

联系方式:
Eric Van Zanten
投资者和公共关系副总裁
610-529-6219
eric.vanzanten@atossainc.com

FORWARD LOOKING STATEMENTS
This press release contains certain information that may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. We may identify these forward-looking statements by the use of words such as "expect," "potential," "continue," "may," "will," "should," "could," "would," "seek," "intend," "plan," "estimate," "anticipate," "believe," "future," or other comparable words. Forward-looking statements in this press release are subject to risks and uncertainties that may cause actual results, outcomes, or the timing of actual results or outcomes, including the timing of data related to the (Z)-endoxifen program, the potential of (Z)-endoxifen as a breast cancer prevention and treatment agent, and the potential safety and tolerability profile of (Z)-endoxifen, to differ materially from those projected or anticipated, including risks and uncertainties associated with: macroeconomic conditions and increasing geopolitical instability; the expected timing of releasing data; any variation between interim and final clinical results; actions and inactions by the FDA and foreign regulatory bodies; the outcome or timing of regulatory approvals needed by Atossa, including those needed to continue our planned (Z)-endoxifen trials; our ability to satisfy regulatory requirements; our ability to comply with the continued listing requirements of the Nasdaq Stock Market; our ability to successfully develop and commercialize new therapeutics; the success, costs and timing of our development activities, including our ability to successfully initiate or complete our clinical trials, including our (Z)-endoxifen trials; our anticipated rate of patient enrollment; our ability to contract with third-parties and their ability to perform adequately; our estimates on the size and characteristics of our potential markets; our ability to successfully defend litigation and other similar complaints and to establish and maintain intellectual property rights covering our products; whether we can successfully complete our clinical trial of oral (Z)-endoxifen in women with mammographic breast density and our trials of (Z)-endoxifen in women with breast cancer, and whether the studies will meet their objectives; our expectations as to future financial performance, expense levels and capital sources, including our ability to raise capital; our ability to attract and retain key personnel; our anticipated working capital needs and expectations around the sufficiency of our cash reserves; and other risks and uncertainties detailed from time to time in Atossa's filings with the Securities and Exchange Commission, including without limitation its Annual Reports on Form 10-K and Quarterly Reports on 10-Q. Forward-looking statements are presented as of the date of this press release. Except as required by law, we do not intend to update any forward-looking statements, whether as a result of new information, future events or circumstances or otherwise.

前瞻性声明
本新闻稿包含某些可能构成根据1995年《私人证券诉讼改革法案》的前瞻性声明的信息。我们可能使用“期望”、“潜力”、“继续”、“可能”、“将”、“应该”、“可以”、“愿意”、“寻求”、“打算”、“计划”、“估计”、“预计”、“相信”、“未来”或其他类似的词语来辨别这些前瞻性声明。本新闻稿中的前瞻性声明受到风险和不确定性的影响,这些风险和不确定性可能导致实际结果、成果或实际结果或成果的时间安排(包括(Z)- 坦索芬计划的数据时间安排,(Z)- 坦索芬作为乳腺癌预防和治疗剂的潜力以及(Z)- 坦索芬的潜在安全和耐受性特征)与预期的不相符,包括与以下风险和不确定性有关的风险和不确定性:宏观经济状况和不断增加的地缘政治不稳定因素;发布数据的预期时间;中间和最终临床结果之间的任何变化;FDA和外国监管机构采取和不采取的行动;Atossa所需的监管批准的结果或时间安排,包括继续计划进行(Z)- 坦索芬试验所需的批准;我们能否满足监管要求;我们能否遵守纳斯达克证券交易所的继续上市要求;我们能否成功开发和商业化新疗法;我们开发活动(包括(Z)- 坦索芬试验)成功启动或完成的成功、成本和时间安排;我们预期的患者入组速度;我们能否与第三方签订合同并能否充分履行;我们对潜在市场规模和特征的估计;我们能否成功捍卫诉讼和其他类似投诉并建立和维护涵盖我们产品的知识产权权利;我们能否成功完成面向乳腺组织密度X线摄影的妇女的口服(Z)- 坦索芬临床试验和我们针对乳腺癌妇女的(Z)- 坦索芬试验,以及这些研究是否能够达到其目标;我们对未来的财务表现、支出水平和资本来源的预期,包括我们筹集资金的能力;我们能否吸引和留住关键人员;我们预期的工作资本需求和现金储备充足的预期;以及Atossa向证券交易委员会提交的文件中不时详细列出的其他风险和不确定性。前瞻性声明是根据本新闻稿发布日期提供的。除法律规定外,我们无意更新任何前瞻性声明,无论是因为新信息、未来事件或情况还是其他原因。

声明:本内容仅用作提供资讯及教育之目的,不构成对任何特定投资或投资策略的推荐或认可。 更多信息
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