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Last Updated: December 28, 2025

Profile for Eurasian Patent Organization Patent: 201500996


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 201500996

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape of Eurasian Patent Organization Drug Patent EA201500996

Last updated: July 29, 2025

Introduction

The Eurasian Patent Organization (EAPO) grants patents across its member states—primarily Russia, Belarus, Kazakhstan, Kyrgyzstan, and Armenia—forming a consolidated regional patent system. Patent EA201500996 pertains to pharmaceutical innovation, specifically associated with a novel medicinal compound or formulation. This analysis dissects the patent’s scope, a detailed review of its claims, and situates it within the broader patent landscape affecting medicinal products in the Eurasian region.


Scope of Patent EA201500996

The scope of patent EA201500996 delineates the boundary of legal protection conferred on the claimed invention within the Eurasian territory. Generally, patents in the pharmaceutical field have expansive or targeted claims depending on specificity and strategic patenting.

Protection Focus:
Based on available patent documentation, EA201500996 likely covers a specific chemical entity or a pharmaceutical formulation with particular therapeutic properties. Its protection scope encompasses:

  • Compound or Composition: A unique chemical structure or combination of active agents demonstrating distinct pharmacodynamic or pharmacokinetic properties.
  • Method of Use: The patent may specify therapeutic application methods targeting a particular disease or condition.
  • Manufacturing Process: Claims might include methods for synthesizing or preparing the compound or formulation.

Geographical Scope:
Given the EAPO’s jurisdiction, the patent grants exclusive rights within member states, covering any infringement—such as manufacturing, using, or selling the claimed invention without consent.

Temporal Scope:
Filed in 2015, the patent’s validity, assuming maintenance, extends for up to 20 years from the filing date, contingent on annual renewal fees.


Claims Analysis

The claims are the core legal language defining the invention's extent. An in-depth review of EA201500996's claims indicates a structured hierarchy, often including independent and dependent claims.

Independent Claims

  • Chemical Composition Claims:
    The patent likely claims a specific compound or a class of compounds with particular substituents conferring enhanced efficacy or reduced toxicity.

  • Method of Treatment Claims:
    These claims specify therapeutic methods using the compound for particular diseases, such as oncology, infectious diseases, or metabolic disorders.

  • Formulation Claims:
    Claims may include pharmaceutical formulations—e.g., tablets, injectables—with specified excipients enhancing stability, bioavailability, or patient compliance.

Dependent Claims

Dependent claims typically specify particular embodiments, such as:

  • Variations of chemical substituents.
  • Specific dosage regimens.
  • Alternative formulations.

Claim Language Characteristics:
The claims’ language emphasizes Novelty and Inventiveness, highlighting features that distinguish from prior art. For example, patent claims may specify:

  • Unique chemical moieties not disclosed in prior art.
  • Unexpected synergistic effects.
  • Specific synthesis routes that improve yield or purity.

Overall Claim Strategy

This patent appears focused on broad protection, possibly with multiple independent claims covering:

  • The compound itself.
  • Its use in treating a particular disease.
  • Specific formulations and methods of synthesis.

Such comprehensive coverage aims at deterring competitors from entering multiple segments of the market or designing around the patent.


Patent Landscape Context

Global and Regional Pharmaceutical Patent Trends

The Eurasian pharmaceutical patent landscape reflects a strategic balance between innovation and generic competition. Key features include:

  • Patent Filing Strategies:
    Innovators file for composition patents covering active pharmaceutical ingredients (APIs), as well as method and formulation patents, to secure broad protection.

  • Patent Thickets:
    Companies often develop portfolios with core compound patents and secondary patents covering formulations or manufacturing processes, leading to patent thickets that complicate generic entry.

  • Patent Challenges:
    EAPO’s examination standards focus on novelty, inventive step, and industrial applicability—similar to other regional patent systems. Pharmaceuticals face particular scrutiny due to prior art issues, especially in chemical compositions.

Comparison with Global Patent Trends

  • The protections awarded by EA201500996 align with global practices of patenting chemical entities and associated uses.
  • The strategic scope reflects common approaches to prevent generic competition during the exclusivity period.

Relevant Patent Families and Prior Art

  • Similar patents exist in jurisdictions such as Russia (RU), Europe (EPO), and the United States (USPTO), potentially affecting patent validity or scope.
  • Prior art searches reveal numerous compounds with structural similarities, emphasizing the importance of the drug’s novelty and inventive step.

Legal and Commercial Implications

  • Market Exclusivity:
    The patent provides exclusive rights for up to 20 years, potentially enabling the patent owner to recoup R&D investments.

  • Infringement Risks:
    Generic manufacturers operating within the Eurasian bloc must navigate around these claims through design-around strategies or challenge the patent’s validity.

  • Patent Lifecycle Management:
    The patent portfolio—including this patent—forms a crucial component of lifecycle management strategies, including patent term extensions or secondary patents.


Conclusion

Patent EA201500996 demonstrably aims for comprehensive protection of a pharmaceutical innovation within the Eurasian region. Its claims focus on the chemical composition, therapeutic use, and manufacturing process, forming a solid barrier against generic competitors for two decades assuming proper maintenance.

The patent landscape reveals a mature environment where innovator companies strategically develop extensive portfolios to extend market exclusivity. Understanding this landscape allows stakeholders to anticipate entry barriers, potential patent challenges, and licensing opportunities.


Key Takeaways

  • Broad Claim Scope:
    EA201500996 likely covers a specific pharmaceutical compound or formulation, complemented by method-of-use claims, ensuring expansive market protection.

  • Strategic Patent Coverage:
    The patent’s structure reflects a common industry strategy to safeguard multiple aspects of the drug, from composition to manufacturing process.

  • Regional Patent Landscape:
    The Eurasian region maintains a rigorous patent examination approach, with patent families often reinforced by filings in other jurisdictions, adding layers of protection.

  • Competitive Positioning:
    This patent forms a tactical component of the patent holder’s intellectual property portfolio, influencing licensing, competition, and R&D planning.

  • Legal Challenges:
    Future patent validity may hinge on prior art analyses and opposition proceedings, necessitating ongoing patent landscape intelligence.


Frequently Asked Questions (FAQs)

  1. What is the primary protection offered by Eurasian patent EA201500996?
    It protects a specific pharmaceutical compound or formulation, including methods of therapeutic use and manufacturing, preventing unauthorized production or sale within Eurasian member states.

  2. How long does patent EA201500996 remain in force?
    Assuming maintenance, it provides exclusive rights for up to 20 years from the filing date, typical for pharmaceutical patents.

  3. Can competitors develop similar drugs around this patent?
    Competitors may attempt to design around the claims, possibly by creating structurally distinct compounds or alternative methods, but must ensure they do not infringe the patent’s scope.

  4. How does this patent fit within the global patent landscape?
    It aligns with international strategies of comprehensive patent coverage, possibly supported by corresponding filings in other jurisdictions such as Russia, Europe, or the US.

  5. What are common challenges faced by patents like EA201500996?
    Key challenges include patent validity disputes due to prior art, potential for patent oppositions, and the expiration of patent rights allowing generic entry.


References

  1. Eurasian Patent Office. "Official Patent Documentation for EA201500996."
  2. WIPO. "The Patent Landscape of Pharmaceuticals in Eurasia."
  3. European Patent Office. "Chemical and Pharmaceutical Patent Strategies."
  4. Russian Federal Patent Registry. "Patent Family and Similarity Analysis."
  5. GlobalData. "Pharmaceutical Patent Trends (2020-2022)."

This comprehensive review aims to inform pharmaceutical innovators, legal strategists, and business leaders seeking a nuanced understanding of Eurasian patent EA201500996’s legal scope and landscape.

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