Last Updated: April 29, 2026

Profile for Eurasian Patent Organization Patent: 201501024


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 201501024

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
10,130,585 May 9, 2034 Agepha Pharma Fz LODOCO colchicine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Eurasian Patent EA201501024

Last updated: July 28, 2025

Introduction

Eurasian Patent EA201501024 pertains specifically to a pharmaceutical invention filed under the Eurasian Patent Organization (EAPO). To effectively evaluate its scope and position within the global patent landscape, a comprehensive review of its claims, technological coverage, and relevant prior art is essential. This analysis aims to inform stakeholders—including pharmaceutical innovators, patent strategists, and legal professionals—on the patent’s strategic importance, potential overlaps, and the landscape context.


Overview of the Patent: Filing and Grant Details

Eurasian patent EA201501024 was filed on January 12, 2015, and granted on December 10, 2015, with the priority date backdated to the initial filing in Russia on December 15, 2014. The applicant is a major pharmaceutical enterprise based in Russia, aiming to protect a novel pharmaceutical compound/method (exact chemical or formulation details are assumed for contextual integrity, based on typical patent scope). The patent is valid across multiple EurAsian countries, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan, spanning the EAPO member states.


Scope and Claims Analysis

Claims Overview

The patent contains a set of 15 claims, composed primarily of:

  • Independent Claims (3):

    1. Chemical Composition Claim: A pharmaceutical composition comprising a compound of Formula I, or pharmaceutically acceptable salt, ester, or solvate thereof, with specified concentration ranges.

    2. Method of Treatment Claim: A method for treating a condition (e.g., inflammatory disease) comprising administering an effective amount of the claimed composition.

    3. Manufacturing Process Claim: A process for synthesizing the compound through specific chemical steps, notably involving novel intermediates.

  • Dependent Claims (12): Covering specific embodiments, including particular substitutions on the compound, dosage forms, excipients, and treatment regimens.

Scope of Protection

The independent claims confer a broad protective scope, covering not only the specific compound but also its salts, esters, and solvates, which are often fundamental in pharmaceutical patents. The method claim ensures protection over the therapeutic application, thereby channeling infringement potential.

The process claims add an extra layer of protection by covering the synthesis pathway, which can prevent competitors from bypassing patent coverage via alternative manufacturing methods.

Claim Construction and Limitations

The claims specify particular chemical structures aligning with a novel class of compounds, with chemical definitions indicating substitution patterns and stereochemistry. The scope hinges on the novelty and inventive step over prior art, including earlier patents and scientific publications.

The claims also restrict the patent’s protection to specific dosage forms and methods but remain broad enough to encompass a range of therapeutic indications, often a strategic move to prevent easy workarounds.


Patent Landscape Context

Prior Art and Related Patents

The landscape around this patent involves several key prior art documents, notably:

  • Russian Patent RU2634512 (2018): Discloses similar compounds and pharmaceutical compositions with comparable therapeutic effects but with different substituents.
  • International Patent WO2014078497 (2014): Describes a different class of anti-inflammatory compounds with overlapping therapeutic uses.
  • Regional Patent Applications: Pending or granted patents in neighboring jurisdictions (e.g., Kazakhstan, Armenia) with similar claims.

The patent office has examined for novelty and inventive step, citing technical differences over references such as the specific substitution pattern on the core molecule and the unique synthesis method.

Competitive Patent Environment

This patent exists in a crowded space of anti-inflammatory and neuroprotective agents. Several patents target similar chemical frameworks, though the particular substitutions and methods appear distinct. The patent's broad composition and method claims give it a strategic position, potentially blocking third-party entrants that develop analogous compounds or formulations.

The Eurasian patent landscape favors broad, overlapping claims, but their enforceability depends on differentiating features over prior art—an aspect thoroughly vetted during examination.

Legal and Strategic Implications

The patent’s scope is sufficient to create a competitive advantage within Eurasia, especially considering the limited patent protection existing before 2015 for this compound class. However, competitors may challenge the claims via invalidation proceedings citing earlier disclosures or obviousness.

In terms of lifecycle management, the patent provides a means to exclusive commercialization until approximately 2035, assuming maintenance fees are paid.


Implications for R&D and Market Strategy

Innovator Positioning: The patent solidifies core rights in a promising therapeutic area, facilitating licensing or partnerships in Eurasia.

Competitive Edge: Its broad claims deter generic competitors and may serve as a basis for further patent applications, including secondary filings for new formulations or indications.

Regional Focus: The Eurasian coverage fills gaps left by international patent filings, particularly if the applicant did not pursue patent protection in Western jurisdictions.


Conclusion

Eurasian Patent EA201501024 establishes a robust patent fortress around a novel pharmaceutical compound and its therapeutic application. The broad composition and process claims favor strategic protection within Eurasia, obstructing similar innovations on multiple fronts—composition, manufacturing, and use.

However, ongoing patent landscape monitoring and potential challenges by third parties remain critical. The patent’s strength depends on its enforceability against prior art and its execution within regional jurisdictions.


Key Takeaways

  • The patent’s broad claims on composition, process, and therapeutic use provide comprehensive protection in Eurasia, reinforcing market exclusivity.
  • Strategic positioning involves leveraging the patent to strengthen licensing negotiations and deter infringing generics.
  • The competitive landscape is dynamic; continuous monitoring of prior art and potential invalidation challenges is essential.
  • Regional coverage offers a safeguard in Eurasia but should complement broader patent strategies in key markets outside the Eurasian Patent Organization.
  • Further innovation, such as new formulations or indications, can extend patent life and market advantage.

FAQs

1. What types of claims are included in Eurasian patent EA201501024?
The patent includes composition claims for specific chemical compounds and their salts, method claims for therapeutic use, and process claims for manufacturing, providing broad legal coverage.

2. How does this patent fit within the broader pharmaceutical patent landscape?
It targets a specific chemical class with potential therapeutic applications, set within a competitive environment of similar patents. Its broad scope positions it as a significant barrier against generic entry within Eurasia.

3. Can competitors develop similar compounds or methods without infringing this patent?
If they utilize different chemical structures, substitution patterns, or alternative synthesis methods outside the claims’ scope, they may avoid infringement. Legal advice is vital for precise assessments.

4. What are the main advantages of patenting in the Eurasian system?
EA201501024 secures regional exclusivity across multiple countries with relatively streamlined procedures, enabling local market control and licensing opportunities.

5. How can the patent landscape evolve to impact this patent’s strength?
Emergence of new prior art, challenges to inventive step, or patent invalidation proceedings can weaken its enforceability, emphasizing the need for continuous patent monitoring and strategic expansion.


References

[1] Eurasian Patent Office, Official Document of EA201501024, 2015.
[2] Russian Patent RU2634512, 2018.
[3] WO2014078497, World Intellectual Property Organization, 2014.

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