Essex Property Trust's Short Interest Rises 32.11%, Exceeds Industry Average
PorAinvest
miércoles, 20 de agosto de 2025, 6:42 pm ET1 min de lectura
ATOS--
Patient enrollment for the study is expected to begin in Q4 2025, following the Investigational New Drug (IND) filing. Topline data is anticipated in 2026. The selection of PSI underscores Atossa's commitment to advancing Z-endoxifen into its final steps before Phase 3 development [1].
PSI, known for its excellence in global oncology trial execution, has a proven track record of delivering regulatory-grade data and achieving on-time enrollment across diverse geographies. The company's proprietary machine-learning feasibility platform, VISIONAL™, has contributed to its success in moving swiftly from Phase 2 into Phase 3 trials [1].
Atossa believes Z-endoxifen has the potential to become a first-in-class therapy in the multi-billion-dollar market for metastatic breast cancer. The drug, a highly potent Selective Estrogen Receptor Modulator/Degrader (SERM/D), has demonstrated clinical activity even in tumors resistant to existing endocrine therapies [1].
The study is part of Atossa's broader pipeline, which includes additional Phase 2 studies in the ER+/HER2- neoadjuvant breast cancer setting and combination therapy with abemaciclib in women with early stage breast cancer at high risk of recurrence [1].
References:
[1] https://www.prnewswire.com/news-releases/atossa-therapeutics-selects-psi-as-contract-research-organization-for-pivotal-dose-ranging-study-of-z-endoxifen-in-metastatic-breast-cancer-302534234.html
Atossa Therapeutics has selected PSI as the contract research organization (CRO) to manage its planned Z-endoxifen monotherapy dose-ranging study in women with metastatic breast cancer. The study aims to evaluate safety, pharmacokinetics/pharmacodynamics, and preliminary anti-tumor activity. Patient enrollment is expected to begin in Q4 2025, with topline data anticipated in 2026.
Atossa Therapeutics, Inc. (Nasdaq: ATOS) has announced the selection of PSI as the contract research organization (CRO) to manage its planned Z-endoxifen monotherapy dose-ranging study in women with metastatic breast cancer (mBC). The study, designed with input from the U.S. Food and Drug Administration (FDA), aims to evaluate safety, pharmacokinetics/pharmacodynamics, and preliminary anti-tumor activity [1].Patient enrollment for the study is expected to begin in Q4 2025, following the Investigational New Drug (IND) filing. Topline data is anticipated in 2026. The selection of PSI underscores Atossa's commitment to advancing Z-endoxifen into its final steps before Phase 3 development [1].
PSI, known for its excellence in global oncology trial execution, has a proven track record of delivering regulatory-grade data and achieving on-time enrollment across diverse geographies. The company's proprietary machine-learning feasibility platform, VISIONAL™, has contributed to its success in moving swiftly from Phase 2 into Phase 3 trials [1].
Atossa believes Z-endoxifen has the potential to become a first-in-class therapy in the multi-billion-dollar market for metastatic breast cancer. The drug, a highly potent Selective Estrogen Receptor Modulator/Degrader (SERM/D), has demonstrated clinical activity even in tumors resistant to existing endocrine therapies [1].
The study is part of Atossa's broader pipeline, which includes additional Phase 2 studies in the ER+/HER2- neoadjuvant breast cancer setting and combination therapy with abemaciclib in women with early stage breast cancer at high risk of recurrence [1].
References:
[1] https://www.prnewswire.com/news-releases/atossa-therapeutics-selects-psi-as-contract-research-organization-for-pivotal-dose-ranging-study-of-z-endoxifen-in-metastatic-breast-cancer-302534234.html

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios