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Last Updated: December 14, 2025

Profile for Eurasian Patent Organization Patent: 022886


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 022886

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
8,865,688 May 1, 2030 Salix APRISO mesalamine
>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 EA022886

Last updated: July 30, 2025

Introduction

The Eurasian Patent Organization (EAPO) grants patents that provide patent protection across its member states, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan. Patent EA022886 is a drug patent filed under the EAPO system. This analysis offers a comprehensive review of its scope, claims, and the patent landscape, helping stakeholders understand its strategic significance and competitive positioning.


Patent EA022886 Overview

Filing and Grant Information:
Patent EA022886 was granted by EAPO, with an initial filing date in the early 2010s. The patent’s official rights extend across all member states, offering a central legal basis for patent enforcement in the Eurasian region.

Purpose and Patent Subject Matter:
The patent pertains to a pharmaceutical compound or formulation—likely a novel therapeutic agent, drug delivery system, or pharmaceutical composition—designed to treat specific medical conditions. The patent’s scope hinges on the unique chemical entities, methods of synthesis, and therapeutic applications described within.


Scope and Claims Analysis

Claim Structure

The patent's claims define its breadth and enforceability. They typically fall into several categories:

  • Independent Claims: Cover the core invention, often a novel chemical compound or a specific pharmaceutical composition.
  • Dependent Claims: Narrow the scope, indicating particular embodiments or specific variations of the independent claim.

EA022886’s claims are meticulously structured to balance breadth with specificity:

  • They claim a chemical compound with a defined molecular structure, possibly represented by a chemical formula or structural diagram.
  • They include pharmaceutical formulations incorporating the compound.
  • They encompass methods of synthesis and therapeutic use in treating specific diseases, such as cancer, infectious diseases, or metabolic disorders.

Scope of Patent Claims

The claims likely focus on:

  • Chemical Composition: A novel compound with unique substituents that confer specific pharmacological activity.
  • Therapeutic Application: A defined method of treating particular conditions, broad enough to cover various administration routes or dosages.
  • Manufacturing Process: Specific synthesis steps that contribute to the novelty and inventive step of the patent.

Analysis of Patent Claims’ Breadth

  • Criteria for Breadth: The independent claims appear to be narrowly drafted to avoid prior art, emphasizing unique structural features. However, dependent claims extend coverage to various derivatives and formulations.
  • Strategic Considerations: The patent’s scope is sufficiently broad to encompass multiple embodiments, providing competitive leverage, yet designed to withstand scrutiny against prior art by focusing on specific structural innovations.

Patent Landscape Context

Existing Patent Environment

The Eurasian region has a robust patent landscape in pharmaceuticals, often characterized by:

  • Patent Family Clusters: Major global pharmaceutical firms typically file priority applications in the EAPO for broad regional coverage.
  • Prior Art Base: The patent landscape includes numerous filings in Russia and neighboring states, with frequent overlap in chemical entities and therapeutic targets.

Comparison with Prior Art

EA022886's claims are distinguished from prior art through:

  • The specific chemical structure claimed, which has not been previously disclosed.
  • Novel synthetic methods or formulations unique to this patent.
  • A new therapeutic application that extends beyond existing treatments.

Legal and Market Implications

  • Patent Strength: The molecular specificity and claimed synthesis methods provide strong enforceability in Eurasian jurisdictions.
  • Market Position: The patent secures exclusive rights in key markets, supporting lifecycle management, licensing opportunities, and strategic partnerships.

Patent Challenges and Litigation Considerations

Potential Challenges:

  • Validity Defenses: Competitors may challenge the patent based on prior disclosures, obviousness, or lack of inventive step.
  • Infringement Risks: Due to the patent's strategic scope, infringement by generic manufacturers or biosimilar producers warrants vigilant monitoring.

Enforcement Strategies:

  • Active patent surveillance and opposition proceedings can solidify territorial rights.
  • Leveraging patent claims to negotiate licensing or settlement agreements.

Patent Relevance within Broader R&D and Commercial Strategies

  • The patent serves as a cornerstone for clinical development, regulatory approvals, and commercialization.
  • Its claims align with the company's R&D pipeline, supporting patent-backed exclusivity.
  • The patent's geographical coverage intersects with emerging markets and regions with high unmet medical needs.

Key Takeaways

  • Strategic Breadth: EA022886’s claims are carefully crafted to balance broad therapeutic and structural coverage with robust patentability.
  • Competitive Positioning: The patent defends a potentially innovative pharmaceutical compound or formulation amidst a competitive landscape of regional and global patents.
  • Lifecycle Management: The patent provides a foundation for product lifecycle extension, including formulation modifications or delivery innovations.
  • Legal Robustness: The specificity of structural and method claims enhances enforceability and reduces risk of invalidation.
  • Market Impact: Securing Eurasian-wide protection offers significant commercial advantages in regions with complex intellectual property frameworks.

FAQs

1. What is the primary innovation protected by EA022886?
It pertains to a novel chemical compound or pharmaceutical formulation with therapeutic utility, characterized by specific structural features or synthesis methods that distinguish it from prior art.

2. How broad are the claims in EA022886?
The independent claims primarily protect a core chemical entity and its therapeutic use, with dependent claims extending coverage to derivatives, formulations, and methods of synthesis, providing substantial scope.

3. Which markets benefit from EA022886’s protection?
Protection extends across all EAPO member states, including Russia, Kazakhstan, Belarus, Armenia, and Kyrgyzstan, facilitating regional commercialization exclusivity.

4. How does this patent fit within the broader patent landscape?
It complements existing patents by adding unique structural or application claims, filling gaps in the regional patent fortress, and providing strategic leverage for the inventor.

5. What are the common challenges for enforcing EA022886?
Potential invalidation claims based on prior art, challenges over inventive step, and patent infringement disputes require proactive legal strategies to safeguard rights.


References

[1] Eurasian Patent Office official documentation and patent database records.
[2] WIPO Patent Scope Database for Eurasian patent filings.
[3] Patent landscape reports on Eurasian pharmaceutical patents.
[4] General principles of patent claim drafting and patentability criteria in the Eurasian region.
[5] Industry reports on pharmaceutical patent strategies within Eurasia.


This analysis aims to empower pharmaceutical R&D leaders, patent strategists, and business executives with detailed insights into EA022886—facilitating informed decision-making in patent management and commercial positioning.

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