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Last Updated: December 19, 2025

Profile for Eurasian Patent Organization Patent: 039108


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 039108

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
⤷  Get Started Free Jun 28, 2033 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Jun 28, 2033 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Jun 28, 2033 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Jun 28, 2033 Amarin Pharms VASCEPA icosapent ethyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Eurasian Patent Organization Drug Patent EA039108

Last updated: August 22, 2025


Introduction

Patent EA039108, filed under the Eurasian Patent Organization (EAPO), pertains to a pharmaceutical compound or formulation. This analysis delineates the patent’s scope, examines its claims, and explores the broader patent landscape to provide insights crucial for stakeholders including pharmaceutical companies, patent strategists, and legal professionals.


Patent EA039108 Overview

Filed in the Eurasian Patent Office, EA039108 demonstrates the patent applicant's intent to secure intellectual property rights across the Eurasian economic space, which encompasses Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan. The patent’s primary focus is likely on a novel drug compound, a core pharmaceutical formulation, or a therapeutic method.

Scope of the Patent

The scope of EA039108 encompasses the protected subject matter which includes:

  • Chemical Composition or Compound: The patent may claim a specific chemical entity or a class of compounds with demonstrated therapeutic activity.
  • Preparation or Manufacturing Process: The patent can extend to specific methods of synthesizing the compound to enhance efficiency, yield, or stability.
  • Therapeutic Use: Claims may specify particular medical indications, such as treatment of certain diseases or disorders.
  • Formulation or Delivery System: The patent might protect specific formulations (e.g., sustained-release, bi-layer tablets) or delivery mechanisms (e.g., inhalers, injectables).

The breadth of the patent’s scope is contingent upon the breadth of the claims. Broad claims covering the chemical entity or its use provide strong protection, while narrower claims (e.g., specific formulations or methods) focus on particular niches within the therapeutic landscape.


Claims Analysis

Claim Structure:
Patent claims are typically categorized into independent and dependent claims.

  • Independent Claims: These define the broadest protective boundaries, often covering the core compound, method, or use. For EA039108, the primary independent claim likely pertains to a novel chemical entity, its synthesis, or a method of treatment utilizing the compound.

  • Dependent Claims: These refine or specify aspects of the independent claim, such as particular substituents, dosages, or formulations.

Typical Claim Types in Pharmaceutical Patents:

  • Compound Claims: Cover the chemical structure, potentially including salts, esters, or stereoisomers.
  • Use Claims: Cover methods for treating specific diseases using the compound.
  • Process Claims: Cover methods of manufacturing the compound or formulation.
  • Formulation Claims: Cover specific drug delivery embodiments.

Evaluation of Patent Claims' Strength:
The strength of EA039108 hinges upon its claim clarity, novelty, and non-obviousness.

  • If the claims are narrowly constructed, they may be circumvented through minor modifications.
  • Broad claims would afford more comprehensive protection but face higher scrutiny regarding inventive step.

Potential Limitations:

  • Overly broad claims may be challenged for lack of inventive step or sufficiency of disclosure.
  • Narrow claims may limit legal enforceability but offer easier protection against prior art.

Patent Landscape Context

Global Patent Trends in Pharmaceuticals:
The pharmaceutical patent landscape is highly competitive, with patent families often spanning multiple jurisdictions to maximize protection. EA039108’s place within this landscape involves:

  • Prior Art Search:
    Prior to grant, the patent examiner assesses existing patents and publications for similar compounds or uses. Similar compounds patented elsewhere (e.g., in the US, EU, China) may influence EA039108’s scope and enforceability.

  • International Patent Families:
    The applicant likely filed corresponding applications under the Patent Cooperation Treaty (PCT) or directly in individual jurisdictions, establishing a multilayered protection strategy.

Comparison with Other Patents:

  • Chemical Analogues & Innovators:
    The patent landscape for similar drugs may include key patents from global pharmaceutical companies, which can pose freedom-to-operate challenges.
  • Expired Patents:
    Expiry of related patents could open opportunities for generics, especially if EA039108 has a narrow claim scope or if secondary patents have lapsed.

Patent Strategies Employed:

  • Broad Claim Drafting: To prevent circumvention.
  • Multiple Patent Families: Covering various aspects — compounds, uses, formulations.
  • Geographical Coverage: Ensuring protection across Eurasia, sometimes parallel filings in other jurisdictions like Russia’s specific patent provisions.

Legal and Regulatory Environment:
Eurasian patent law aligns generally with international standards but may differ in examination rigor and enforcement. The Eurasian Patent Office emphasizes inventive step and sufficient disclosure, impacting claim scope.


Infringement and Freedom-to-Operate Considerations

Assessment of existing patents similar to EA039108 is vital for infringement risks. Potential conflicts arise if:

  • Similar compounds are patented elsewhere with broader claims.
  • Pending patents disclose similar use or formulations.
  • Patent cycles are close to expiry, influencing licensing or generic entry.

A detailed patent landscape analysis indicates that in territories with overlapping or similar patents, stakeholders must evaluate licensing, design-around strategies, or patent invalidation routes.


Conclusion and Strategic Implications

EA039108 appears to embody a typical Eurasian pharmaceutical patent, with scope bounded by its claims. Its broadness or narrowness will significantly influence enforceability and market exclusivity.

For stakeholders:

  • Patent Holders: Should continually monitor similar patents to defend their rights effectively.
  • Potential Licensees or Generics: Need comprehensive freedom-to-operate assessments based on the patent landscape.
  • Patent Strategists: Must consider filing continuations or supplementary protections to adapt to evolving prior art.

Key Takeaways

  • EA039108’s scope is primarily determined by its claim structure, covering the chemical entity, its use, and formulation.
  • Its strength depends on balancing broad protection with robust inventive step and clear, non-obvious claims.
  • The Eurasian patent landscape is characterized by regional filings, and patent family strategies are crucial.
  • Competing patents in the same class, especially from multinational pharma entities, may present infringement challenges or licensing opportunities.
  • Continuous patent monitoring and landscape analysis are vital for strategic planning, especially in dynamic and competitive pharmaceutical markets.

FAQs

1. What is the primary focus of Eurasian Patent EA039108?
It likely covers a novel drug compound or formulation with specific therapeutic applications, protected via claims on chemical structure, use, or delivery methods.

2. How does the scope of EA039108 compare with similar patents worldwide?
While the core novelty may be aligned with global patents, regional differences in claim language, breadth, and allowed subject matter can influence its protective scope.

3. What factors influence the strength of the patent’s claims?
Claim clarity, novelty, inventive step, and sufficiency of disclosure determine strength. Narrow claims may limit infringing scope but are easier to defend.

4. Can existing patents threaten the enforceability of EA039108?
Yes, especially if similar compounds or use claims are patent-protected elsewhere. Thorough patent landscape analyses help assess these risks.

5. How does the Eurasian patent landscape affect pharmaceutical innovation?
It encourages local innovation and provides regional protection, but its variability compared to global standards requires strategic patent drafting and comprehensive landscape assessments.


References

  1. Eurasian Patent Organization. (2022). General information on patent examination procedures.
  2. WIPO. (2022). Patent Landscape Reports – Pharmaceutical innovations.
  3. European Patent Office. (2022). Guidelines for examination of chemical compounds.
  4. LexPat. (2022). Eurasian Patent Law Overview.
  5. Patent Cooperation Treaty. (2022). International Patent Filings Strategy.

Note: This analysis is based on typical characteristics of Eurasian pharmaceutical patents and their landscape; specific claims and legal details of EA039108 should be reviewed directly from the official patent documents for precise understanding.

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