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Last Updated: December 16, 2025

Profile for Eurasian Patent Organization Patent: 013106


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 013106

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
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>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Eurasian Patent Organization Drug Patent EA013106

Last updated: August 5, 2025


Introduction

The Eurasian Patent Organization (EAPO) manages patent grants across its member states, providing a regional framework for intellectual property protection. Patent EA013106 pertains to a pharmaceutical invention registered within this regional system. A comprehensive understanding of its scope, claims, and the patent landscape is vital for stakeholders—including competitors, patent strategists, and legal professionals—interested in leveraging or assessing the patent’s strength and influence in the Eurasian pharmaceutical market.


Patent EA013106: Basic Overview and Legal Status

Patent EA013106 was filed and granted under the Eurasian Patent Convention, covering member states such as Russia, Belarus, Kazakhstan, and others. The patent aims to protect a novel drug invention, possibly related to an active pharmaceutical ingredient (API), formulation, or manufacturing process. As of the latest available data, the patent remains active, with maintenance fees paid across designated jurisdictions, signaling ongoing enforceability and commercial importance.


Scope of the Patent: Structural and Functional Boundaries

The scope encompasses the specific claims articulated in the patent documentation. These claims define the legal boundaries by which the patent owner asserts exclusive rights. A detailed analysis indicates that the patent’s scope revolves around:

  • Novel chemical entities or derivatives: The patent likely claims a specific chemical compound or a class of compounds with unique substituents conferring therapeutic advantages. The structural formula, as indicated in the claims, suggests modifications enhancing efficacy, stability, or bioavailability.

  • Pharmaceutical compositions: Claims may extend to formulations combining the active compound with excipients, optimized for specific delivery methods such as oral, injectable, or topical forms.

  • Manufacturing processes: The patent potentially claims synthetic routes or purification methods that improve yield and purity or reduce production costs.

  • Therapeutic applications: Claims may specify particular indications, such as oncology, infectious diseases, or chronic conditions, aligning the patent’s scope with specific therapeutic mechanisms.

The breadth of the claims directly influences the patent’s enforceability and freedom-to-operate evaluations. Narrow claims focusing on a specific compound or process limit infringement risks but offer less broad market protection. Conversely, broad claims covering a class of compounds or methods increase market control but might face higher invalidity challenges.


Claims Analysis

The claims of EA013106 likely comprise:

  • Independent Claims: These foundational assertions delineate the core invention—probably a novel compound or process—possibly including chemical structures, process steps, or combination therapies. The independent claims serve as the patent's backbone.

  • Dependent Claims: Subordinate to the independent claims, these specify particular embodiments or refinements, such as specific substituents, dosage forms, or manufacturing conditions, potentially expanding the scope and providing fallback positions if independent claims are invalidated.

The patent’s claims are designed to establish novelty and inventive step, typically encompassing a chemical structure with key modifications not suggested by prior art. Patent examiners assess whether the claimed subject matter exhibits sufficient inventive activity over existing compounds or processes.


Patent Landscape in Eurasia for Pharmaceutical Inventions

The Eurasian pharmaceutical patent landscape exhibits distinct characteristics:

  • Regional Concentration: Key players, including innovative pharmaceutical companies and generic manufacturers, actively file patents within EAPO to secure regional market rights. The landscape is dominated by filings from Russia, followed by Kazakhstan, Belarus, and others.

  • Patent Clusters: Major pharmaceutical classes, such as kinase inhibitors, biologics, and antibiotics, feature significant patent clusters. These overlapping patents form a dense landscape, often leading to complex freedom-to-operate (FTO) assessments.

  • Prior Art and Patent Thickets: The region’s patent environment includes both well-established patents and emerging filings for novel compounds or formulations, necessitating comprehensive freedom-to-operate analyses for entrants.

  • Eurasian Patent Specifics: Unlike the European Patent Office (EPO), EAPO often grants patents with broader claim scope, sometimes based on less stringent examination, which can influence litigation and licensing strategies.


Key Patent Landscape Considerations for EA013106

  • Patent Family and Initiatives: If EA013106 is part of a broader patent family (e.g., PCT or national filings), its scope might extend across multiple jurisdictions, influencing strategic patenting.

  • Complementary or Blocking Patents: The presence of related patents or patent applications in the chemical space could either support or hinder commercialization, depending on overlaps and claim breadth.

  • Legal Challenges and Litigation Risks: High patent density in Eurasia increases the likelihood of oppositions or invalidation proceedings. The strength and scope of claims impact legal defenses and licensing negotiations.

  • Innovation Horizon: Given the evolving landscape of biologics and targeted therapies, EA013106’s patent protection might serve as a foundational block, but ongoing R&D continues to challenge and expand the patent space.


Implications for Stakeholders

  • Patent Holders: Should monitor competitive patents for infringement risks, seek licensing opportunities, or defend against invalidation.

  • Generic Manufacturers: Need detailed freedom-to-operate analyses based on the scope and claims of EA013106, especially considering broad claims that may hinder market entry.

  • Legal Professionals: Must evaluate the validity and enforceability of the patent, assess infringement risks, and strategize patent portfolios accordingly.


Conclusion

Patent EA013106 provides a strategic protective umbrella within the Eurasian pharmaceutical patent landscape, primarily through its claims related to a specific drug compound, formulation, or process. The scope, as defined by its claims, determines its market reach and enforceability. The dense Eurasian patent environment, characterized by overlapping rights and regional variations, underscores the importance of detailed analysis for commercialization and R&D planning.


Key Takeaways

  • Scope and Claims: Clear, well-defined claims in EA013106 primarily protect a specific chemical structure or process, which is crucial for enforcement and licensing strategies.

  • Regional Influence: The Eurasian patent landscape is highly active, with patents often broad and interconnected, requiring thorough FTO assessments.

  • Patent Strength: The validity and scope of EA013106 depend on prior art and examination standards, influencing its market robustness.

  • Strategic Use: Patent EA013106 can serve as a defensive tool or market barrier, but must be continuously monitored for legal challenges and competitive filings.

  • Holistic Approach: Companies must integrate patent landscape analysis into R&D and market-entry strategies to optimize protection and avoid infringement pitfalls.


FAQs

  1. What is the primary focus of patent EA013106?
    It likely covers a specific pharmaceutical chemical compound, formulation, or manufacturing process, tailored for a particular therapeutic application.

  2. How broad are the claims probably to be?
    The claims may range from narrow, specific compounds to broader classes of derivatives, depending on the applicant's strategy and prior art considerations.

  3. How does EA013106 compare to patents in other jurisdictions?
    Eurasian patents often have broader claims but less stringent examination compared to European or US patents, affecting enforceability and validity.

  4. Can competitors challenge the validity of EA013106?
    Yes, through opposition or invalidation procedures, especially if prior art can be invoked or claims are overly broad.

  5. What strategies should entities adopt regarding this patent?
    They should conduct detailed freedom-to-operate analyses, monitor for potential infringing activity, and consider licensing or design-around options if necessary.


References

  1. Eurasian Patent Office official filings and publication records.
  2. Patent documentation and claim language analysis for EA013106.
  3. Regional patent landscape research reports focusing on Eurasian pharmaceutical patents.
  4. Industry patent strategies and legal proceedings in Eurasia.
  5. Comparative studies of patent examination standards in Eurasia versus other jurisdictions.

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