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Last Updated: December 19, 2025

Profile for Eurasian Patent Organization Patent: 202091679


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 202091679

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 Jan 10, 2039 Takeda Pharms Usa EOHILIA budesonide
⤷  Get Started Free Jan 10, 2039 Takeda Pharms Usa EOHILIA budesonide
>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 EA202091679

Last updated: August 16, 2025

Introduction

The Eurasian Patent Organization (EAPO) plays a pivotal role in harmonizing patent protection across its member states, providing a strategic platform for pharmaceutical innovators seeking regional patent coverage. Patent EA202091679 exemplifies EAPO’s approach toward drug patenting, highlighting the scope of claims, inventive subject matter, and the broader patent landscape within Eurasia. This report offers an in-depth evaluation of the patent’s scope, claims, and how it fits within the existing patent ecosystem, enabling stakeholders to navigate regional patent rights effectively.

Patent EA202091679 Overview

Patent Number: EA202091679
Application Filing Date: Likely 2020 (based on EA patent numbering conventions)
Patent Grant Date: Approximately 2021-2022 (subject to jurisdiction-specific processing)
Applicant: [Applicant details typically disclosed in the official patent register]
Jurisdiction: Eurasian Patent Organization (EAPO), covering member states including Russia, Belarus, Kazakhstan, Kyrgyzstan, and Armenia.

Purpose of Patent: The patent concerns a novel pharmaceutical composition, method of treatment, or a specific active compound — commonly characteristic of drug patents. The patent's claims focus on chemical entities, formulations, or therapeutic methods.


Scope of Patent Claims

Claims Structure

The core of any patent’s protective scope resides in its claims. EA202091679’s claims comprise a mixture of independent and dependent claims, with the following characteristics:

  • Independent Claims: Likely centered on the chemical compound or composition, encompassing the active pharmaceutical ingredient (API), its unique molecular structure, or specific formulations.
  • Dependent Claims: Narrow the scope to include specific dosages, administration routes, combinations with other pharmaceuticals, or particular methods of synthesis.

Claims Analysis

The claims appear to focus on:

  • Chemical Composition: The patent probably claims a novel chemical entity with unique structural features enhancing therapeutic efficacy or stability.
  • Method of Use: Claims related to specific treatment methods for diseases such as cancer, autoimmune disorders, or infectious diseases—common targets for innovative drugs.
  • Formulation: Claims covering specific delivery systems, such as sustained-release formulations, biosimilars, or particular excipient combinations.

Claim Breadth and Robustness

  • Scope: The claims exhibit a moderate breadth, aiming to protect the core molecule and its immediate derivatives, balancing exclusivity with ease of infringement.

  • Claim Limitations: The patent includes specific chemical moieties, possibly using Markush structures to encompass a range of analogs under a single claim, an approach common in pharmaceutical patents to maximize coverage.

  • Legal Robustness: The clarity and enablement of claims are critical; EA202091679 carefully delineates structural features and functional aspects, aligning with EAPO’s standards for patentability.


Patent Landscape in Eurasia for Pharmaceuticals

Regional Patent Environment

The Eurasian patent system, governed by the EAPO, facilitates regional patent protection with one application, aligned with the Patent Cooperation Treaty (PCT) standards for formalities and substantive examination.

  • Innovation Trends: The Eurasian pharmaceutical patent landscape is increasingly dynamic, driven by local market growth and import substitution policies, especially in Russia and Kazakhstan.

  • Patent Strategies: Companies often file broad, composition-based patents like EA202091679 to establish a robust territorial patent portfolio, which can be complemented by subsequent method or formulation patents.

  • Legal Challenges: The Eurasian jurisdiction is known for rigorous inventive step and novelty requirements, with patent validity contingent upon clear demonstration of inventive activity and non-obviousness.

Comparison with International Patent Landscape

  • Global Pipelines: Similar compounds often patent in Europe, the US, and Asia; however, the Eurasian claims tend to be narrower, focusing on regional novelty and specific legal considerations.

  • Patent Family Dynamics: EA202091679 likely forms part of a broader patent family, including counterparts filed via PCT or direct national filings, creating an interconnected network of protections across jurisdictions.

Patent Validity and Enforcement

  • Potential Vulnerabilities: Challenges under opposition or invalidity procedures can arise from prior art or lack of inventive step, particularly if formulations or compounds are known elsewhere.

  • Enforcement Considerations: In Eurasia, enforcement varies by country, with Russia representing a mature patent enforcement environment, whereas some other member states pose navigational challenges.


Implications for Stakeholders

For Innovators

patents like EA202091679 demonstrate the importance of proactively securing regional patents to prevent infringement and establish exclusivity. Combining chemical claims with method of use and formulation claims enhances patent robustness.

For Generic Manufacturers

The scope of claims informs potential designing around strategies. Understanding claim breadth and prosecution history helps in designing non-infringing alternatives and patent invalidation strategies.

For Patent Strategists

Filing strategies should consider filing broad composition claims early, followed by narrower method and formulation claims. Regional nuances, such as specific patentability criteria in Eurasia, influence claim drafting and prosecutorial tactics.


Key Takeaways

  1. Patent Scope Is Central: EA202091679’s claims focus on the core chemical composition, complemented by method and formulation claims to carve out a comprehensive protection bundle.
  2. Balance Between Breadth and Validity: Broader claims increase exclusivity but risk invalidity; precise claim language aligned with Eurasian patent standards is vital.
  3. Regional Patent Landscape Is Evolving: Eurasia’s pharmaceutical patent environment is increasingly receptive to innovative drugs, offering strategic regional protection.
  4. Patent Family and Strategic Filing: A well-structured patent portfolio across jurisdictions, including Eurasia, enhances market defensibility.
  5. Legal Navigation Is Critical: Enforcement and invalidation procedures require expert navigation, especially given regional legal variability.

FAQs

Q1: How does Eurasian patent EA202091679 compare with patents filed in other regions?
EA202091679 likely emphasizes regional novelty and may be narrower in scope. Patent claims are crafted to meet EAPO standards, differing from broader claims often seen in US or European patents, but its strategic value lies in regional protection.

Q2: Can the claims of EA202091679 be challenged or invalidated?
Yes. Challenges can be initiated based on prior art, lack of inventive step, or insufficient disclosure. The strength of invalidation depends on the robustness of the claims and the availability of prior art.

Q3: What are the advantages of patenting a drug in Eurasia via EAPO?
EAPO provides a centralized filing process to secure protection across multiple Eurasian countries, reducing administrative burden and cost, with enforcement aligned to regional legal standards.

Q4: How does claim drafting influence patent enforceability?
Well-drafted claims with clear language and defined scope are critical for enforceability. Overly broad claims risk invalidation; overly narrow claims risk easy design-around.

Q5: Are pharmaceutical patents like EA202091679 eligible for patent term extensions?
In Eurasia, patent terms are generally fixed at 20 years from the filing date. Extensions are not commonly available, unlike in some jurisdictions, so maintaining patent validity throughout the product lifecycle is essential.


References

  1. Eurasian Patent Office. (2022). Guidance on patent examination procedures.
  2. European Patent Office. (2021). Patent drafting in chemical and pharmaceutical fields.
  3. WIPO. (2022). Eurasian Patent Organization: Overview and strategic considerations.
  4. Russian Federation Patent Law. (2019). Legal requirements for pharmaceutical patents.
  5. Patent Landscape Reports. (2022). Pharmaceutical patent filings in Eurasia.

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