Atossa Therapeutics Appoints Heather Rees as Chief Financial Officer
Atossa Therapeutics Appoints Heather Rees as Chief Financial Officer
SEATTLE, July 02, 2024 (GLOBE NEWSWIRE) -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) ("Atossa" or the "Company"), today announced the appointment of Heather Rees as the Company's new Chief Financial Officer (CFO). Ms. Rees most recently served as Atossa's Senior Vice President of Finance and Principal Accounting Officer. 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7月2日,北美通报社(SEATTLE)——Atossa Therapeutics, Inc.(Nasdaq: ATOS)(简称“Atossa”或“该公司”)宣布任命Heather Rees女士担任该公司的新任首席财务官(CFO)。Rees女士最近担任Atossa的高级副总裁兼财务主管。Atossa是一家临床阶段的生物制药公司,致力于开发治疗肿瘤领域重大未满足医学需求的创新药物,重点关注乳腺癌。
Ms. Rees brings almost 30-years of accounting, business and financial experience to the CFO role. She has spent the last seven years of her career at Atossa having joined the Company as Controller in 2017. Prior to joining Atossa, Ms. Rees led a consulting practice that delivered financial and accounting services to companies including Getty Images Inc., Flow International Corp, and Avalara, Inc. Earlier in her career she served as Controller of the Americas for Irdeto Inc. She began her career at Deloitte & Touche where she rose to the level of Sr. Manager in the firm's Audit practice. Ms. Rees was licensed as a Certified Public Accountant by the state of Washington in 1996.
Rees女士担任CFO角色将带来近30年的会计、商业和财务经验。她在2017年加入该公司担任控制器后,过去七年一直在Atossa工作。在加入Atossa之前,Rees女士领导了一项咨询业务,向公司提供财务和会计服务,包括Getty Images Inc.、Flow International Corp和Avalara, Inc。早年的职业生涯中,她曾担任Irdeto Inc.的美洲控制器。她的职业生涯始于Deloitte & Touche,在该公司的审计实践中担任高级经理。Rees女士于1996年被华盛顿州认证为注册会计师。
"Heather's partnership and contributions have been invaluable and key to the success of our Company to date, which is why she was the obvious choice to become our new Chief Financial Officer," said Steven Quay, M.D., Ph.D., Atossa's President and Chief Executive Officer. "This appointment is testament to her exemplary performance over the past seven years and the deep industry and functional knowledge she brings to the role. With Heather as our CFO, multiple data milestones coming later this year and a strong balance sheet that provides approximately three years of working capital, we are well positioned to deliver on our mission and to create long-term value for our shareholders."
“Heather的合作和贡献至关重要,是我们公司迄今取得成功的关键原因,这就是为什么她成为我们新任首席财务官的明显选择,”Atossa的总裁兼首席执行官Steven Quay博士说道。 “这次任命证明了她在过去七年中的杰出表现以及她在行业和职能知识方面所拥有的深厚造诣。有了Rees女士担任我们的首席财务官,多个数据里程碑即将在今年晚些时候到来,以及强大的资产负债表,为我们提供了约三年的运营资金,我们有足够的能力来完成我们的使命,从而为我们的股东创造长期价值。”
"I am excited and proud to be named Atossa's new Chief Financial Officer," said Ms. Rees. "The Company is at a critical stage of its development, and I look forward to continuing to work closely with the board and the team to fully capitalize on the value of (Z)-endoxifen and make a meaningful difference in the lives of patients with breast cancer."
“我很高兴并自豪地被任命为Atossa的新任首席财务官,” Rees女士说,“公司正处于发展的关键阶段,我期待继续与董事会和团队密切合作,充分利用(Z)-endoxifen的价值,并在乳腺癌患者的生命中产生有意义的影响。”
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 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 .
关于Atossa Therapeutics
Atossa Therapeutics,Inc.是一家临床阶段的生物制药公司,在肿瘤学领域开发使用(Z)-endoxifen预防和治疗乳腺癌的创新药物。欲知更多信息,请访问网站。
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。