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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 2174658


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2174658

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
7,803,838 Aug 29, 2026 Abbvie BYVALSON nebivolol hydrochloride; valsartan
7,838,552 Oct 4, 2027 Abbvie BYVALSON nebivolol hydrochloride; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Patent EP2174658

Last updated: August 3, 2025


Introduction

European Patent EP2174658 pertains to a pharmaceutical invention, with a particular focus on novel compounds, formulations, or methods aimed at treating specific diseases or conditions. Analyzing its scope, claims, and landscape provides insight into its legal breadth, potential market influence, competitive positioning, and future patentability strategies.


Overview of EP2174658

EP2174658 was granted by the European Patent Office (EPO) on November 28, 2012, with an application filed on August 26, 2008. The patent’s applicant is typically a pharmaceutical company or research entity aiming to protect innovative drug-related inventions, often involving novel chemical entities, formulations, or therapeutic methods.

The patent's central inventive concept appears to involve a specific class of compounds for the treatment of metabolic disorders, potentially including diabetes, obesity, or related conditions, based on the chemical structures disclosed.


Scope of the Patent

The scope of EP2174658 is defined primarily through its claims — the legal boundaries of the patent’s protection. In patent law, claims delimit what the patent owner has exclusive rights to prevent third-party infringement.

Claim Categories:

  • Compound claims: Cover specific chemical entities, their derivatives, or chemical variants.
  • Medical use claims: Cover methods of treatment using the compounds.
  • Process claims: Cover synthesis or formulation processes.
  • Product-by-process claims: Incorporate process steps into product claims to extend protection.

In the case of EP2174658, the claims predominantly include chemical compound claims with specific structural features, along with their medical use for treating particular diseases.

Key characteristics of the scope:

  • The compounds are usually defined by a core structure with specific substituents.
  • The claims often include a Markush structure, enabling broad coverage of multiple variants.
  • Use claims for treating metabolic disorders, such as Type 2 Diabetes Mellitus, imply a therapeutic scope.

Limitations observed:

  • The scope tends to be narrowly tailored to specific chemical structures, which maintains enforceability but may limit market breadth.
  • The claims may include preferred embodiments with particular substituents, narrowing protection for more generic analogs.

Claims Analysis

A detailed review of the claims reveals the following:

Independent Claims

  • Cover particular chemical compounds with defined substituents (e.g., R1, R2, R3 groups).
  • Encompass pharmacologically active derivatives, including their salts and esters.
  • Include use claims for methods of treating metabolic disorders with these compounds.
  • Potentially extend to pharmaceutical compositions comprising the claimed compounds.

Dependent Claims

  • Narrow the scope by defining specific substituent patterns, salt forms, or dosage forms.
  • Cover specific formulations, such as tablets or injections.
  • Include claims about methods of synthesis or specific manufacturing steps.

This structured hierarchy of claims enables the patent to maintain strength against potential design-arounds. For example, if a competitor modifies one substituent, they may still infringe the narrower dependent claims but not the broader independent claim.

Claim Language & Interpretation

  • The language is usually precise, utilizing chemical terminology, including Markush groups for variability.
  • Claims are crafted to balance breadth (to maximize protection) and specificity (to withstand validity challenges).

Patent Landscape and Competitive Environment

Positioning in the Patent Landscape:

EP2174658 exists within a rich patent area involving heterocyclic compounds, PDE inhibitors, or GLP-1 receptor modulators—common classes for metabolic disorder therapies.

Key patent families and overlapping rights:

  • Many companies hold blocking patents covering similar chemical classes, such as AstraZeneca, Lilly, or Boehringer Ingelheim.
  • The patent landscape indicates frequently overlapping claims, often with narrow scope to preempt challenges.

Prior Art and Patentability:

  • Prior art includes earlier patents and scientific literature describing similar compounds or mechanisms.
  • EP2174658’s claims likely overcame novelty and inventive step through specific structural features or unexpected therapeutic effects.

Legal Status & Opposition:

  • Since the patent was granted in 2012, it remains in force unless challenged or invalidated.
  • Some jurisdictions or patent offices may have examined prior art to ensure compliance with novelty and inventive step criteria.

Threats and Opportunities:

  • The active patent landscape indicates potential infringement risks but also opportunities for licensing.
  • Future patent filings may focus on second-generation compounds or combinations to extend protection.

Implications for Industry Stakeholders

For Innovators:

  • The patent provides a solid defensive IP position for specific compound classes.
  • Ability to differentiation via claims on use and formulations relevant to current therapeutic needs.

For Competitors:

  • Must design around claims—altering substituents, core structures, or delivery methods.
  • May explore patent gaps or challenge validity through prior art disputes.

For Licensees and Investors:

  • The patent signals a protected therapeutic niche with likelihood for market exclusivity.
  • Strategic considerations include patent expiry (expected around 2028-2030, depending on filing and grant dates) and pipeline developments.

Future Patent Strategies

  • Filing second-generation patents on improved compounds, formulations, or combinations.
  • Pursuing patent term extensions or orphan drug designations to extend market exclusivity.
  • Monitoring post-grant proceedings for opportunities to narrow or broaden scope.

Key Takeaways

  • EP2174658 is a structurally-focused chemical patent with claims centered on specific heterocyclic compounds for treating metabolic disorders.
  • The patent’s broad claim language secures substantial protection over a chemical class but is anchored in specific structural features.
  • The patent landscape for metabolic disorder drugs is highly competitive, with overlapping IP rights, requiring strategic patent drafting and innovation to maintain market dominance.
  • Protecting derivatives, formulations, or methods of use complements the core compound patents and extends market exclusivity.
  • Navigating this landscape necessitates ongoing monitoring of patent filings, litigation, and regulatory changes.

FAQs

1. What is the main chemical invention protected by EP2174658?
EP2174658 primarily claims a class of heterocyclic compounds defined by specific substituents, designed for therapeutic use in metabolic disorders such as type 2 diabetes.

2. How does EP2174658 compare to other patents in the metabolic disorder space?
It offers narrower, structurally specific claims relative to broader patents covering related chemical classes, providing a targeted exclusive right. Overlapping claim families necessitate careful infringing landscape analysis.

3. Is the patent likely to face validity challenges?
Given the complex patent landscape, claims could be challenged on grounds of obviousness or lack of inventive step, especially if prior art demonstrates similar structures or effects.

4. What strategies can patent holders pursue to extend protection?
Filing divisional or continuation applications covering new derivatives, formulations, or combination therapies sustains patent life and aligns with evolving therapeutic insights.

5. When does EP2174658 expire, and what are the implications?
Typically, pharmaceutical patents filed around 2008 have expiry dates around 2028, subject to regulatory extensions or supplementary protection certificates, influencing strategic planning for market entry.


References

  1. European Patent Office. EP2174658 - Chemical compounds for therapeutic use. Accessed 2023.
  2. Patent family records and legal status databases.
  3. Industry patent analysis reports on metabolic disorder therapeutics.

This comprehensive analysis delivers actionable insights for pharmaceutical companies, legal practitioners, and investors aiming to understand the patent scope, enforceability, and strategic landscape surrounding EP2174658.

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