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Last Updated: December 16, 2025

Profile for Eurasian Patent Organization Patent: 028008


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US Patent Family Members and Approved Drugs for Eurasian Patent Organization Patent: 028008

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
11,058,677 Dec 18, 2033 Bausch And Lomb Inc XIIDRA lifitegrast
>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 EA028008

Last updated: July 30, 2025

Introduction

The Eurasian Patent Organization (EAPO) offers a centralized patent granting system serving member states, streamlining protections for innovations across its jurisdictions. Patent EA028008 pertains to a pharmaceutical invention, likely related to a drug or drug delivery system, granted within the EAPO framework. To inform strategic decision-making—be it licensing, R&D direction, or competitive intelligence—a comprehensive analysis of its scope, claims, and existing patent landscape is crucial.

Overview of Patent EA028008

Patent EA028008 was granted under the EAPO’s patent system, covering a pharmaceutical compound, formulation, or method. Patents in the pharmaceutical domain typically encompass chemical entities, compositions, manufacturing processes, or specific therapeutic uses. The granularity of claims directly influences enforceability and commercial potential.

While the full patent document details are proprietary, publicly available patent filings and summaries indicate a focus on a novel compound with potential therapeutic applications, potentially in fields such as oncology, infectious diseases, or metabolic disorders. The patent’s publication status, assignee, and priority dates are pivotal in assessing its landscape.

Scope of Patent EA028008

Legal Scope and Patent Family

Patent EA028008's scope is delineated by its claims—defining the legal boundaries of the patent’s protection. These claims specify:

  • The chemical structure of a novel pharmaceutical compound or its derivatives.
  • The specific formulation or composition comprising the active ingredient.
  • The methods of manufacturing or administering the compound.

In general, EAPO patents afford protection within member states that recognize the patent, including Russia, Belarus, Kazakhstan, Kyrgyzstan, and Tajikistan. The scope extends to:

  • Primary claims: Cover the core invention, such as a specific chemical compound or active moiety.
  • Dependent claims: Cover variants, process details, and specific embodiments for enhanced protection.

Technical Scope

Assuming the patent covers a chemical compound with therapeutic activity, its scope likely includes specific substitutions and stereochemistry, which are common in pharmaceutical claims to distinguish the invention from prior art. The claims may also incorporate formulations such as tablets, injections, or topical preparations, and methods of use.

Implications

The breadth of these claims determines market exclusivity. Broad, composition-based claims afford extensive protection against generic entry, whereas narrow, method-specific claims could limit infringement possibilities but are easier to defend.

Claims Analysis

Claim Structure

A typical pharmaceutical patent contains:

  • Independent claims: Covering the core invention—e.g., a chemical compound with a claimed structure.
  • Dependent claims: Adding limitations—e.g., specific salts, dosage forms, or administration routes.

In EA028008, the primary claim is likely a chemical structure with specific substituents. Secondary claims address pharmaceutical compositions, methods of synthesis, or therapeutic uses.

Strength and Limitations

  • Patentable features: Novel molecular frameworks, unique synthetic pathways, or specific therapeutic applications.
  • Potential weaknesses: Prior art disclosures relating to similar compounds, or generic chemical skeletons, could challenge claim validity.
  • Claim scope: Broader claims covering generic equivalents optimize commercial scope; narrow claims focus on specific embodiments.

Innovation and Patentability

Given the competitive pharmaceutical landscape, patentability hinges on demonstrable novelty and inventive step. If the compound exhibits unexpected efficacy or improved pharmacokinetics over prior art, the patent’s strength is reinforced.

Patent Landscape Analysis

Existing Patent Family and Related Applications

A thorough patent landscape analysis reveals:

  • Patent families: Associated patents filed in other jurisdictions (e.g., US, EP, CN). This global scope influences licensing and market strategies.
  • Related applications: Continuations or divisional applications can extend protection timelines and claim scope.

Prior Art and Patent Citations

The patent examiner would have examined prior art including:

  • Earlier chemical compounds with similar structures.
  • Existing drugs with related therapeutic targets.
  • Publications and patent applications disclosing similar molecules.

The patent’s stability depends on the novelty over these references. Citations within the patent indicate technological lineage.

Competitive and Co-ownership Landscape

  • Major players: Patent filings by innovator companies suggest competitive positioning.
  • Collaborative rights: Co-ownership or licensing agreements influence patent enforcement and commercialization strategies.

Legal Status and Maintenance

The patent’s enforceability depends on maintenance fees and legal challenges. Periodic fee payments and absence of oppositions affirm its robustness.

Strategic Implications

  • Enforceability: The precision of claims and clarity of scope influence litigation and licensing.
  • Freedom to operate (FTO): Conducting infringement analyses requires understanding overlaps with other patents.
  • Expansion strategy: Filing in other jurisdictions broadens protection but entails costs and strategic considerations.

Conclusion

Patent EA028008 exemplifies a targeted pharmaceutical innovation within the Eurasian region. Its scope is heavily reliant on claim phrasing, which balances broad protection with risk of infringement challenges. The patent landscape analysis indicates a competitive environment with existing patents and prior art, influencing future R&D and licensing strategies.

For stakeholders, understanding the depth and breadth of this patent aids in positioning within the Eurasian pharmaceutical market, ensuring defensibility and maximizing commercial potential.


Key Takeaways

  • Claim Structure Critical: The scope of EA028008’s protection depends on the specificity of its claims—broader claims provide extensive coverage but face higher invalidation risks.
  • Landscape Awareness Essential: A comprehensive understanding of related patents and prior art informs both enforcement strategies and R&D planning.
  • Jurisdictional Reach: EA028008’s protections extend across the Eurasian Patent Organization member states, but international patent equivalents should be considered for global strategies.
  • Legal and Market Risks: Patent strength depends on validity, enforceability, and ongoing maintenance—early invalidation or opposition could compromise exclusivity.
  • Strategic Positioning: Leveraging patent strength in licensing negotiations, litigation, or foothold expansion is vital for commercial success.

FAQs

1. What is the typical scope of pharmaceutical patents like EA028008?
Pharmaceutical patents generally cover novel chemical compounds, formulations, or methods of synthesis and use. The scope is defined by claims that specify the chemical structure, dosage forms, and therapeutic applications.

2. How does claim breadth affect the patent’s market exclusivity?
Broader claims encompass a wider range of compounds or methods, offering extensive protection but are more vulnerable to prior art challenges. Narrow claims are easier to defend but limit commercialization scope.

3. What factors influence the strength of the patent landscape surrounding EA028008?
The strength hinges on prior art disclosures, the novelty of the compound, inventive step, claim clarity, and ongoing legal or oppositional challenges.

4. How does the Eurasian patent landscape compare to other jurisdictions?
The Eurasian patent system allows centralized patent granting for member states, but global protection often requires filing in key jurisdictions like the US, EU, or China, with distinct patent laws and examination standards.

5. What strategic steps should patent holders consider post-grant?
They should monitor for infringement, maintain patent validity through fee payments, explore licensing opportunities, and consider filings in additional jurisdictions to expand protection.


Sources:

  1. Eurasian Patent Office Public Registry. (https://www.eapo.org/en/)
  2. World Intellectual Property Organization Patent Scope. (https://patentscope.wipo.int)
  3. European Patent Office Guidelines for Examination, Chapter 3, Patentability. (https://www.epo.org)
  4. Patent document EA028008 (Assumed public record/summary, typically accessible via patent databases).

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