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Atossa Therapeutics Appoints Heather Rees as Chief Financial Officer

Atossa Therapeutics Appoints Heather Rees as Chief Financial Officer

atossa therapeutics任命希瑟·里斯爲致富金融(臨時代碼)官員
Atossa Therapeutics ·  07/02 12:00

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,北美通報社(SEATTLE)——Atossa Therapeutics, Inc.(Nasdaq: ATOS)(簡稱“Atossa”或“該公司”)宣佈任命Heather Rees女士擔任該公司的新任首席財務官(CFO)。Rees女士最近擔任Atossa的高級副總裁兼財務主管。Atossa是一家臨床階段的生物製藥公司,致力於開發治療腫瘤領域重大未滿足醫學需求的創新藥物,重點關注乳腺癌。

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女士擔任CFO角色將帶來近30年的會計、商業和財務經驗。她在2017年加入該公司擔任控制器後,過去七年一直在Atossa工作。在加入Atossa之前,Rees女士領導了一項諮詢業務,向公司提供財務和會計服務,包括Getty Images Inc.、Flow International Corp和Avalara, Inc。早年的職業生涯中,她曾擔任Irdeto Inc.的美洲控制器。她的職業生涯始於Deloitte & Touche,在該公司的審計實踐中擔任高級經理。Rees女士於1996年被華盛頓州認證爲註冊會計師。

"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的合作和貢獻至關重要,是我們公司迄今取得成功的關鍵原因,這就是爲什麼她成爲我們新任首席財務官的明顯選擇,”Atossa的總裁兼首席執行官Steven Quay博士說道。 “這次任命證明了她在過去七年中的傑出表現以及她在行業和職能知識方面所擁有的深厚造詣。有了Rees女士擔任我們的首席財務官,多個數據里程碑即將在今年晚些時候到來,以及強大的資產負債表,爲我們提供了約三年的運營資金,我們有足夠的能力來完成我們的使命,從而爲我們的股東創造長期價值。”

"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."

“我很高興並自豪地被任命爲Atossa的新任首席財務官,” Rees女士說,“公司正處於發展的關鍵階段,我期待繼續與董事會和團隊密切合作,充分利用(Z)-endoxifen的價值,並在乳腺癌患者的生命中產生有意義的影響。”

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.

關於(Z)-Endoxifen
(Z)-endoxifen是最強效的選擇性雌激素受體調節劑(SERM),用於調節雌激素受體,同時導致雌激素受體的降解。它也已被證明在對其他激素治療方案產生耐藥的腫瘤患者中具有療效。除了其強效的抗雌激素作用外,(Z)-endoxifen已被證明能夠以臨床可達到的血濃度靶向PKCβ1,這是一種已知的致癌蛋白。最後,與標準治療(如他莫昔芬)相比,(Z)-endoxifen似乎具有相似甚至更大的骨促進作用,同時幾乎沒有子宮內膜增生作用。

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正在開發一種專有的口服(Z)-endoxifen配方,該配方不需要經過肝代謝即可達到治療濃度,並被密封以繞過胃部,因爲胃中的酸性條件會將(Z)-endoxifen轉化爲無活性的(E)-endoxifen。Atossa的(Z)-endoxifen已在1期和一小部分乳腺癌女性的2期試驗中證明安全。當前正在進行四項2期試驗:一項僅針對有測量乳房密度的健康女性,一項針對被診斷爲導管癌前病變的女性,另外還有兩項研究,其中包括針對ER+/HER2-乳腺癌女性的EVANGELINE研究。Atossa的(Z)-endoxifen由三項已頒發的美國專利和衆多不斷申請的專利保護。

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 .

關於Atossa Therapeutics
Atossa Therapeutics,Inc.是一家臨床階段的生物製藥公司,在腫瘤學領域開發使用(Z)-endoxifen預防和治療乳腺癌的創新藥物。欲知更多信息,請訪問網站。

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

聯繫方式:
Eric Van Zanten
投資者和公共關係副總裁
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.

前瞻性聲明
本新聞稿包含某些可能構成根據1995年《私人證券訴訟改革法案》的前瞻性聲明的信息。我們可能使用“期望”、“潛力”、“繼續”、“可能”、“將”、“應該”、“可以”、“願意”、“尋求”、“打算”、“計劃”、“估計”、“預計”、“相信”、“未來”或其他類似的詞語來辨別這些前瞻性聲明。本新聞稿中的前瞻性聲明受到風險和不確定性的影響,這些風險和不確定性可能導致實際結果、成果或實際結果或成果的時間安排(包括(Z)- 坦索芬計劃的數據時間安排,(Z)- 坦索芬作爲乳腺癌預防和治療劑的潛力以及(Z)- 坦索芬的潛在安全和耐受性特徵)與預期的不相符,包括與以下風險和不確定性有關的風險和不確定性:宏觀經濟狀況和不斷增加的地緣政治不穩定因素;發佈數據的預期時間;中間和最終臨床結果之間的任何變化;FDA和外國監管機構採取和不採取的行動;Atossa所需的監管批准的結果或時間安排,包括繼續計劃進行(Z)- 坦索芬試驗所需的批准;我們能否滿足監管要求;我們能否遵守納斯達克證券交易所的繼續上市要求;我們能否成功開發和商業化新療法;我們開發活動(包括(Z)- 坦索芬試驗)成功啓動或完成的成功、成本和時間安排;我們預期的患者入組速度;我們能否與第三方簽訂合同並能否充分履行;我們對潛在市場規模和特徵的估計;我們能否成功捍衛訴訟和其他類似投訴並建立和維護涵蓋我們產品的知識產權權利;我們能否成功完成面向乳腺組織密度X線攝影的婦女的口服(Z)- 坦索芬臨床試驗和我們針對乳腺癌婦女的(Z)- 坦索芬試驗,以及這些研究是否能夠達到其目標;我們對未來的財務表現、支出水平和資本來源的預期,包括我們籌集資金的能力;我們能否吸引和留住關鍵人員;我們預期的工作資本需求和現金儲備充足的預期;以及Atossa向證券交易委員會提交的文件中不時詳細列出的其他風險和不確定性。前瞻性聲明是根據本新聞稿發佈日期提供的。除法律規定外,我們無意更新任何前瞻性聲明,無論是因爲新信息、未來事件或情況還是其他原因。


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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