Atossa Therapeutics to Present Poster on (Z)-Endoxifen at AACR Special Conference in Cancer Research
Atossa Therapeutics (NASDAQ: ATOS) announced its upcoming presentation at the AACR Special Conference in Cancer Research in Toronto, December 9-11, 2024. The company will present a poster titled 'Anti-cancer Activity of (Z)-Endoxifen-Related Compounds in ERα+ Breast Cancer' on December 10, 2024.
The research focuses on optimizing therapeutic efficacy and tolerability through modifications to (Z)-endoxifen chemistry in treating estrogen receptor alpha-positive breast cancer. The presentation aims to demonstrate how these compounds could enhance potency and reduce adverse effects in cancer treatment outcomes.
Atossa Therapeutics (NASDAQ: ATOS) ha annunciato la sua prossima presentazione alla Conferenza Speciale AACR sulla Ricerca sul Cancro che si svolgerà a Toronto dal 9 all'11 dicembre 2024. L'azienda presenterà un poster intitolato 'Attività anticancro dei composti correlati al (Z)-endoxifene nel carcinoma mammario ERα+' il 10 dicembre 2024.
La ricerca si concentra sull'ottimizzazione dell'efficacia terapeutica e della tollerabilità attraverso modifiche alla chimica del (Z)-endoxifene nel trattamento del carcinoma mammario positivo per il recettore degli estrogeni alpha. La presentazione mira a dimostrare come questi composti possano migliorare la potenza e ridurre gli effetti avversi nei risultati del trattamento del cancro.
Atossa Therapeutics (NASDAQ: ATOS) anunció su próxima presentación en la Conferencia Especial AACR en Investigación del Cáncer que se llevará a cabo en Toronto del 9 al 11 de diciembre de 2024. La compañía presentará un póster titulado 'Actividad anticancerígena de los compuestos relacionados con el (Z)-endoxifeno en el cáncer de mama ERα+' el 10 de diciembre de 2024.
La investigación se centra en optimizar la eficacia terapéutica y la tolerancia a través de modificaciones en la química del (Z)-endoxifeno para el tratamiento del cáncer de mama positivo para el receptor de estrógeno alfa. La presentación tiene como objetivo demostrar cómo estos compuestos podrían aumentar la potencia y reducir los efectos adversos en los resultados del tratamiento del cáncer.
Atossa Therapeutics (NASDAQ: ATOS)는 2024년 12월 9일부터 11일까지 토론토에서 열리는 AACR 특별 암 연구 회의에서의 발표를 예고했습니다. 회사는 2024년 12월 10일에 'ERα+ 유방암에서의 (Z)-엔독시펜 관련 화합물의 항암 활동'이라는 제목의 포스터를 발표할 예정입니다.
이 연구는 에스트로겐 수용체 알파 양성 유방암 치료를 위한 (Z)-엔독시펜 화학의 수정을 통해 치료 효능과 내약성을 최적화하는 데 중점을 두고 있습니다. 발표는 이러한 화합물이 어떻게 효능을 향상하고 암 치료 결과에서 부작용을 줄일 수 있는지를 증명하는 것을 목표로 합니다.
Atossa Therapeutics (NASDAQ: ATOS) a annoncé sa prochaine présentation lors de la Conférence Spéciale AACR sur la Recherche sur le Cancer qui se tiendra à Toronto du 9 au 11 décembre 2024. La société présentera un poster intitulé 'Activité anticancéreuse des composés liés au (Z)-endoxifène dans le cancer du sein ERα+' le 10 décembre 2024.
La recherche se concentre sur l'optimisation de l'efficacité thérapeutique et de la tolérance grâce à des modifications de la chimie du (Z)-endoxifène dans le traitement du cancer du sein positif pour le récepteur des œstrogènes alpha. La présentation vise à démontrer comment ces composés pourraient augmenter la puissance et réduire les effets indésirables dans les résultats du traitement du cancer.
Atossa Therapeutics (NASDAQ: ATOS) hat seine bevorstehende Präsentation auf der AACR Spezialkonferenz zur Krebsforschung in Toronto vom 9. bis 11. Dezember 2024 angekündigt. Das Unternehmen wird am 10. Dezember 2024 ein Poster mit dem Titel 'Antitumorale Aktivität von (Z)-Endoxifen-verwandten Verbindungen bei ERα+ Brustkrebs' präsentieren.
Die Forschung konzentriert sich darauf, die therapeutische Wirksamkeit und Verträglichkeit durch Modifikationen der (Z)-Endoxifen-Chemie bei der Behandlung von östrogenrezeptor-alpha-positivem Brustkrebs zu optimieren. Ziel der Präsentation ist es, zu zeigen, wie diese Verbindungen die Potenz erhöhen und die Nebenwirkungen bei den Behandlungsergebnissen von Krebs reduzieren können.
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Highlights Anti-Cancer Activity of (Z)-Endoxifen-Related Compounds in ERα+ Breast Cancer
SEATTLE, Nov. 21, 2024 (GLOBE NEWSWIRE) -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) (“Atossa” or the “Company”), today announced that a poster detailing the anti-cancer activity of (Z)-endoxifen-related compounds in estrogen receptor alpha-positive (ERα+) breast cancer will be presented at the American Association for Cancer Research (AACR) Special Conference in Cancer Research in Toronto from December 9-11, 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.
The poster, titled “Anti-cancer Activity of (Z)-Endoxifen-Related Compounds in ERα+ Breast Cancer,” explores the optimization of therapeutic efficacy and tolerability through modifications to (Z)-endoxifen chemistry. The research highlights the potential of these compounds to improve cancer treatment outcomes by enhancing potency and minimizing adverse effects.
Poster Details: | |
Title: Anti-cancer activity of (Z)-endoxifen-related compounds in ERα+ breast cancer | |
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| Tuesday, December 10, 2024 |
6:30-8:00 pm ET | |
Hilton Toronto |
For additional information, please visit the conference website here.
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.
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 four issued U.S. patents and numerous pending patent applications.
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.
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, such as data related to the (Z)-endoxifen program, the potential of (Z)-endoxifen as a breast cancer prevention and treatment agent, and potential milestones and growth opportunities for the Company, 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 remain compliant 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.
Contact:
Michael Parks
VP, Investor and Public Relations
484-356-7105
michael.parks@atossainc.com
FAQ
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