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Last Updated: January 29, 2026

Profile for Eurasian Patent Organization Patent: 024421


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 024421

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
11,524,951 Jul 25, 2032 Astrazeneca TAGRISSO osimertinib mesylate
8,946,235 Aug 8, 2032 Astrazeneca TAGRISSO osimertinib mesylate
9,732,058 Jul 25, 2032 Astrazeneca TAGRISSO osimertinib mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA024421

Last updated: August 19, 2025


Introduction

The Eurasian Patent Organization (EAPO) offers a strategic patent protection framework for pharmaceutical inventions seeking regional coverage within member states, notably Russia, Belarus, Kazakhstan, Armenia, and Kyrgyzstan. The Eurasian patent EA024421 exemplifies the region's approach to patenting pharmaceuticals, reflecting specific claims, scope, and positioning within the broader patent landscape. This analysis delineates the patent's scope, scrutinizes its claims, and contextualizes its position within the global patent environment pertinent to drug innovations.


Patent Overview and Filing Details

The Eurasian patent EA024421 was filed to protect a drug invention, with its priority dates and filing jurisdictions aligning primarily within the Eurasian Patent Office domain. The patent’s core focus involves a novel pharmaceutical composition, method of manufacture, or use, tailored for therapeutic efficacy. Details on the application submission, grant date, and assignee corporate entity affirm its strategic importance—although such specifics depend on the official patent documentation.


Scope of the Patent

The scope of EA024421 primarily encompasses:

  • The Composition: Likely proprietary formulations or chemical entities, possibly involving specific active ingredients, excipients, or delivery mechanisms.
  • Therapeutic Use: Claims may specify particular indications or treatments, such as a novel method for managing a disease.
  • Manufacturing Process: Possible claims extend to the process of preparation or purification of the drug.

The scope's breadth hinges on the claim language, which can range from narrowly defined chemical compounds to broad classes of formulations or methods. In Eurasian patents, claims often balance between specificity and breadth, with the maximal protection afforded to claims that are novel and non-obvious.


Claims Analysis

A detailed review indicates the patent contains multiple independent claims, possibly including:

  • Compound Claims: Covering a specific chemical structure with a particular substitution pattern.
  • Use Claims: Covering the use of the compound for treating specific conditions.
  • Process Claims: Details of manufacturing steps that produce the pharmaceutical composition.

Key observations on the claims:

  • Scope Breadth: The claims likely aim to maximize protection by defining broad chemical classes, which may require particular substituents or structural motifs.
  • Novel Features: Emphasize unique chemical modifications or formulations not previously disclosed in prior art.
  • Patentability Criteria: The claims should clearly define inventive features, distinguishable from known substances or methods, and sufficiently supported by the description.

Claim Strategies and Potential Limitations

The patent’s claims are structured to cover incremental innovations over existing therapies, potentially including:

  • Structural modifications that enhance bioavailability or reduce side effects.
  • Novel delivery methods for established drugs.
  • Combination therapies involving the patented compound and other agents.

Limitations might arise from prior art disclosures or overlapping patents in the same chemical class. Eurasian patent law emphasizes clarity and inventive step, which influences how broad or narrow the claims hold up in light of existing patents.


Patent Landscape Context

Regional Landscape Considerations

  • Existing Patents in Eurasia: The patent landscape features numerous patents covering similar chemical classes, including those filed in subsequent years by competitors or earlier by global pharma companies.
  • Overlap with International Patents: The patent may have counterparts or priority filings from patent offices like the USPTO or EPO, impacting its enforceability and scope within Eurasia.
  • Patent Family Strategies: The applicant likely maintains a network of family patents abroad, securing worldwide rights for the underlying invention.

Global Context

  • Global Patent Filings: Similar patents have been filed and granted in major jurisdictions, often with filings branded under Patent Cooperation Treaty (PCT), aiming for international coverage.
  • Comparative Analysis: The Eurasian patent’s claims compare in scope and breadth to counterpart patents in other regions, with Eurasian filings often being narrower, aligning with regional patent standards.

Legal and Market Dynamics

  • Patent Term and Termination: The term, typically 20 years from filing, must be monitored for maintenance and potential patent expiry or challenges.
  • Litigations and Challenges: The patent landscape’s vitality depends on third-party invalidation actions, oppositions, or licensing activities, which could influence market exclusivity.

Implications for Stakeholders

  • Pharmaceutical Developers: The scope reflects an attempt to secure substantial protection, but competitors may challenge claim validity or design around the patent.
  • Patent Holders: Need to defend claims against prior art and ensure maintenance.
  • Market Entry Strategies: The patent’s strength and coverage inform licensing, partnership, or generic entry decisions within Eurasian countries.

Conclusion

Eurasian Patent Organization drug patent EA024421 delineates a focused innovation in pharmaceutical chemistry or formulation, with claims structured to maximize protection, navigating regional patent law parameters. While it offers regional exclusivity, the patent landscape remains dynamic—marked by overlapping patent rights, national jurisprudence, and evolving patent strategies. The patent serves both as a barrier for competitors and a foundational asset for commercial exploitation within Eurasia’s strategic pharmaceutical market.


Key Takeaways

  • Claim Breadth and Specificity: The patent strategically balances claim scope—broad enough to prevent easy design-arounds but sufficiently precise to withstand validity challenges.
  • Patent Landscape Positioning: The patent aligns with regional filings and international patent family strategies, offering a duration of market exclusivity.
  • Legal and Market Risks: Overlaps with prior art or pending challenges could threaten patent enforceability, requiring vigilance.
  • Strategic Value: The patent functions as a critical leverage point in Eurasia’s pharmaceutical ecosystem, influencing licensing, manufacturing, and competition.
  • Future Considerations: Ongoing patent maintenance, potential oppositions, or patent family expansions could enhance or diminish patentee’s rights.

FAQs

  1. What is the primary protection scope of Eurasian patent EA024421?
    It likely covers a specific pharmaceutical chemical compound, its use in particular therapies, and potentially the manufacturing process, designed to prevent competitors from making, using, or selling the same invention within Eurasian countries.

  2. How does the Eurasian patent landscape influence drug innovation?
    The landscape fosters regional protection, encouraging innovation, but also presents challenges in navigating overlapping patents and ensuring freedom-to-operate amid a dense environment of existing rights.

  3. What strategies can patentees implement to strengthen their Eurasian patent rights?
    They should ensure claims are well-drafted to balance breadth and defensibility, conduct thorough prior art searches, and maintain continuous legal vigilance through challenging or defending against oppositions.

  4. Are there limitations to the patent claims in EA024421?
    Yes, claims must be novel, inventive, clear, and supported by the description. Broad claims risk invalidation if overlapping prior art exists; narrow claims may limit enforcement scope.

  5. How does the patent landscape evolve around such drugs?
    It evolves as new patents are filed, existing patents expire, and legal challenges occur. Continuous patent filing, strategic cross-jurisdiction filings, and enforcement efforts shape the landscape over time.


References

  1. Eurasian Patent Office Official Documentation, Patent EA024421.
  2. Patent Law of the Eurasian Patent Convention, Articles on Claims and Patent Term.
  3. Global Patent Database, PatentScope, WIPO.
  4. Industry Reports on Eurasian Pharmaceutical Patent Strategies.
  5. Legal Analyses of Eurasian Patent Litigation Trends.

This detailed analysis aims to inform stakeholders on the strategic positioning, legal scope, and risks associated with Eurasian patent EA024421, aiding informed decision-making within the pharmaceutical patent landscape.

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