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Atossa Advances Global Patent Strategy for Z-Endoxifen with New Protection in Israel and Ongoing Renewals

Key Takeaway: Atossa Therapeutics has announced significant progress in its global patent strategy for Z-endoxifen, including the issuance of a patent in Israel. The patent, which covers high-purity enteric formulations and manufacturing methods, is part of Atossa's strategy to support its clinical and commercial plans. Additionally, Atossa received a Certificate of Patent Renewal for the Israeli patent, reinforcing its commitment to managing its intellectual property effectively. The company aims to harness these protections to deliver Z-endoxifen to patients and enhance shareholder value.

Market Sentiment Analysis

POSITIVE FACTORS

  • Atossa has secured a new patent for Z-endoxifen in Israel, bolstering its intellectual property.
  • The patent covers high-purity formulations and manufacturing methods, indicating a strong quality control approach.
  • The CEO emphasized the importance of strong patents for long-term value creation.

Full Press Release Details

Portfolio covers high-purity Z-endoxifen enteric formulations, performance characteristics, and manufacturing methods, part of Atossa's multi-jurisdiction IP strategy to support clinical and commercial plans
SEATTLE, Oct. 13, 2025 /PRNewswire/ -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) ("Atossa" or the "Company"), a clinical-stage biopharmaceutical company developing new approaches in breast cancer treatment and prevention, announces key progress in its global intellectual-property strategy for Z-endoxifen, including the issuance of an Israeli patent and continued renewals that reinforce protection for the Company's lead program across major jurisdictions. The Israeli patent (No. 304863), titled, "Methods for Making and Using Endoxifen," was granted on July 2, 2025, with priority to multiple U.S. provisional applications filed in 2017–2018.
The allowed claims in Israel include oral, delayed-release (enteric) dosage forms comprising at least 90% by weight Z-endoxifen, with optional impurity limits (<2%), defined release characteristics in gastric and intestinal media, dose strengths (e.g., 1–4 mg and 8 mg), and pharmacokinetic performance targets (e.g., plasma exposures and steady-state levels). The claims also cover manufacturing methods that enrich the Z-isomer via stepwise crystallization and solvent control. These protections align with Atossa's quality-by-design approach to deliver a consistent, high-purity Z-endoxifen product.
In parallel, Atossa received a Certificate of Patent Renewal from the Israel Patent Office confirming fee payment and renewal status for Patent No. 304863, further supporting the life-cycle management of Z-endoxifen IP in this jurisdiction.
"Strong, durable patents are foundational to our Z-endoxifen strategy," said Steven Quay, M.D., Ph.D., Atossa Therapeutics Chairman and CEO. "This new protection in Israel, together with our broader global filings, covers what we believe are the critical elements of product quality, performance, and manufacturing needed to bring Z-endoxifen to patients and to create long-term value for shareholders."
About the Patent Scope in Israel
The granted patent includes: (i) enteric oral formulations with ≥90% Z-endoxifen; (ii) optional impurity and residual-solvent limits; (iii) stability and delayed-release attributes (acid resistance and intestinal release); (iv) dose ranges including 1–4 mg and 8 mg; (v) PK targets such as steady-state plasma levels and exposure ranges; and (vi) a multi-step crystallization process to enrich the Z-isomer. Collectively, these claims support Atossa's global protection for Z-endoxifen composition, performance, and process.
About Atossa Therapeutics
Atossa Therapeutics, Inc. (Nasdaq: ATOS) is a clinical-stage biopharmaceutical company developing innovative therapies for significant unmet needs in breast cancer. Atossa's strategy emphasizes disciplined capital allocation, focusing resources on programs and data packages that can enable future regulatory submissions and potential commercialization. For more information, visit www.atossatherapeutics.com and refer to Atossa's filings with the U.S. Securities and Exchange Commission (SEC).
Forward-Looking Statements
This press release contains forward-looking statements, including statements regarding Atossa's commercial readiness, financing strategy, operational plans, and the development and potential commercialization of (Z)-endoxifen. These statements are subject to risks and uncertainties that could cause actual results to differ materially, including market conditions, regulatory outcomes, clinical results, manufacturing and supply, intellectual-property challenges, and the Company's ability to secure sufficient funding on acceptable terms. For a discussion of risks and uncertainties, please refer to Atossa's filings with the U.S. Securities and Exchange Commission. Atossa undertakes no obligation to update forward-looking statements, except as required by law.
Source Documents (Israel)
Certificate of Patent—No. 304863; Title: Methods for Making and Using Endoxifen; Filing 2018-09-10; Grant 2025-07-02; Priority to U.S. provisionals.
Certificate of Patent Renewal—No. 304863 (Israel Patent Office).
Allowed claims, including high-purity Z-endoxifen enteric formulations, release/PK attributes, and manufacturing steps.
SOURCE Atossa Therapeutics Inc

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Frequently Asked Questions

What is Z-endoxifen used for?

Z-endoxifen is developed for breast cancer treatment and prevention.

What recent patent did Atossa secure?

Atossa received a patent in Israel for methods related to Z-endoxifen.

What are the key features of the Israeli patent?

It covers high-purity enteric formulations and specific pharmacokinetic targets.

How does Atossa ensure product quality?

Through a validated manufacturing method that enriches the Z-isomer.

What is Atossa's strategy for Z-endoxifen?

Atossa focuses on strong patents to enhance product quality and shareholder value.

Last updated: Oct 13, 2025