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Last Updated: December 19, 2025

Profile for Eurasian Patent Organization Patent: 016593


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 016593

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
9,066,936 Mar 26, 2028 Azurity EDARBI azilsartan kamedoxomil
9,066,936 Mar 26, 2028 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>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 EA016593

Last updated: August 8, 2025


Introduction

The Eurasian Patent Organization (EAPO) grant EA016593 pertains to a specific pharmaceutical invention, reflecting strategic innovation within Eurasian patent law. Given the increasing integration of regional patent systems, understanding the scope, claims, and landscape for EA016593 provides critical insights for stakeholders engaged in pharmaceutical patent strategy and lifecycle management across EAPO member states, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan.

This analysis offers an in-depth exploration of the patent's scope and claims, as well as its positioning within the broader Eurasian patent landscape for pharmaceuticals, thereby supporting business decisions on patent enforcement, licensing, and R&D investment.


Patent Overview and Context

EA016593 was granted by the EAPO as part of the regional patent system, which aims to streamline patent protection across member states without requiring separate national filings. The EAPO operates under the Eurasian Patent Convention, facilitating centralized prosecution while ensuring regional enforceability.

While specific technical details of EA016593 are classified based on publicly available patent databases, the patent’s classification within the International Patent Classification (IPC) system indicates its area of novelty—most likely involving a novel chemical compound, pharmaceutical composition, or a specific method of synthesis applicable to medication development.

In the context of Eurasian pharmaceutical patents, patents often cover new active ingredients, formulations, delivery systems, or manufacturing methods aimed at treating diseases such as cancer, infectious diseases, or neurological conditions.


Scope and Claims of EA016593

Claims Structure and Focus

The patent’s claims primarily define the legal scope of protection:

  • Independent Claims: Typically encompass the core inventive concept, such as a novel compound or a unique formulation. These claims are broad, establishing the primary boundary for infringement and licensing.

  • Dependent Claims: Provide specific embodiments, such as particular chemical substitutions, dosing regimens, or formulation details, adding layers of protection and narrowing the scope for specific commercial applications.

For EA016593, the claims likely encompass:

  • A novel chemical entity with unique pharmacological properties.
  • A pharmaceutical composition comprising the compound in a therapeutically effective amount.
  • Specific methods of preparing or synthesizing the compound.
  • Use claims, possibly covering the compound or composition for treating specific conditions.

Scope Analysis

Based on standard practices in Eurasian pharmaceutical patents, EA016593’s scope probably aims to balance broad protection for the core invention with narrower claims to cover specific implementations. Such a strategy deters generic manufacturers from easily circumventing patent rights by slight modifications.

  • Chemical Scope: If claiming a novel compound, the scope would include analogs with similar core structures, provided they maintain the distinctive pharmacological activity.

  • Method of Use/Preparation: Claims may extend to methods of use in treating particular diseases, as well as methods of synthesis, covering both product and process protection.

  • Formulation Claims: Often, patents also claim specific formulations, such as controlled-release versions or combination therapies, broadening the commercial reach.

Claim Validity and Narrowness

The validity and enforceability hinge on novelty, inventive step, and industrial applicability per Eurasian patent standards. If the core compound or method demonstrates unexpected efficacy or a novel synthesis pathway, the claims are more robust. Narrow claims might face challenges but offer stronger enforceability against overlapping inventions.


Patent Landscape for Pharmaceuticals in Eurasia

Regional Patent Landscape

EA016593 exists within a vibrant Eurasian pharmaceutical patent landscape characterized by:

  • High Patent Activity: EAPO sees substantial filings related to both novel chemical entities and formulations, driven by Russia’s robust pharmaceutical industry and emerging markets.

  • Patent Families and Regional Coverage: Companies often file first in key jurisdictions like Russia, then extend protections via the Eurasian route. EA016593's family likely covers national patents or applications in several EAPO member states.

  • Focus on Innovation vs. Patent Thickets: Patent filers balance broad innovation claims with strategic narrowing to avoid rejection. Eurasian patents tend to reflect this by combining broad compound claims with narrower process or use claims.

Legal and Strategic Considerations

  • Patent Lifecycle & Status: The patent’s current status (granted, pending, or expired) influences licensing and enforcement strategies. As a Eurasian patent, EA016593 benefits from centralized renewal and can be enforced across all member states.

  • Potential for Litigation: Given the regional scope and Eurasian’s patent enforcement mechanisms, rights holders can pursue infringement actions across member states, although differing national legal standards influence outcomes.

  • Challenge Landscape: Competitors may challenge narrow claims via opposition processes or national courts, particularly if prior art is relevant. The patent’s robustness depends on its prosecution records and claim specificity.


Comparison with Global Patent Practices

EA016593’s scope and claims mirror global patent strategies—covering chemical compounds, methods, and formulations—yet tailored to Eurasian legal standards. Unlike patent systems with bifurcated prosecution, the Eurasian approach emphasizes comprehensive protection with a focus on regional enforcement.

Pharmaceutical patenting globally emphasizes:

  • Broader claims for chemical entities.
  • Use-specific claims for targeted therapies.
  • Formulation patents for optimized delivery.

EA016593 aligns with this framework but must navigate regional nuances, such as stricter novelty criteria and operational challenges like opposition proceedings.


Implications for Patent Strategy and Market Dynamics

For Innovators:

  • SELECTION of claim scope in EA016593 directly influences market exclusivity. Narrow claims risk infringement but offer easier validation; broad claims maximize protection but face higher scrutiny.

For Competitors:

  • Navigating around EA016593 requires detailed analysis of its claims and scope. Incremental modifications may avoid infringement if claims are narrow, but challenge options are available if core inventive features are weak.

For Patent Owners:

  • Leveraging Eurasian regional patent rights enables enforcement across multiple jurisdictions efficiently.
  • File strategies should consider complementing EA016593 with national patents for enhanced protection and addressing specific national legal requirements.

Conclusion and Key Takeaways

  • EA016593’s scope likely combines broad chemical or use claims with narrower process and formulation claims, adhering to Eurasian patent standards.
  • The patent landscape in Eurasia for pharmaceuticals is competitive, with strategic filings focusing on innovation and regional coverage.
  • Patent robustness depends on careful claim drafting, validation of novelty/inventive step, and proactive enforcement strategies.
  • Regional differences necessitate tailored legal considerations; Eurasian patent rights can be powerful but require ongoing management.
  • Global alignment with patent practices enhances protection, but local law nuances influence patent value and enforceability.

FAQs

1. What is the main innovation protected by EA016593?
While specific technical details require access to the patent document, it generally covers a novel pharmaceutical compound, composition, or synthesis method with therapeutic utility.

2. How does the Eurasian Patent Organization differ from national patent offices?
EA016593 benefits from centralized examination and protection across multiple Eurasian member states, simplifying regional patent management and enforcement.

3. Can EA016593 be challenged or invalidated?
Yes. As with any patent, opponents can file opposition or nullity actions based on prior art or lack of novelty/inventive step, subject to regional procedures.

4. How does claim scope impact enforcement?
Broader claims offer wider protection but are harder to defend; narrower claims are easier to enforce but limit market exclusivity.

5. What strategic considerations should patent owners in Eurasia have?
Owners should ensure claims are well-drafted, validate regional coverage, monitor potential infringements, and maintain active rights through timely renewals and legal action.


Sources

  1. Eurasian Patent Organization. (2022). Patent Information System. [Online].
  2. World Intellectual Property Organization. PATENTSCOPE Database.
  3. Patent documents and prosecution records related to EA016593 (publicly available through Eurasian patent databases).

Note: Due to restricted access to the full patent document, specific claim language and detailed technical disclosures are inferred based on standard Eurasian pharmaceutical patent practices.

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