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Last Updated: December 28, 2025

Profile for European Patent Office Patent: 2859886


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2859886

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Comprehensive Analysis of European Patent Office Drug Patent EP2859886: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent EP2859886, titled “Use of 2-Aryl-Substituted 4-Substituted-Piperidines as NYX-0195, NYX-0196, and NYX-0197 Inhibitors,” exemplifies recent innovations in pharmaceutical chemistry focused on novel inhibitors targeting specific biological pathways. This patent provides valuable insights into the scope of protection, claim structure, and the evolving patent landscape within the targeted pharmacological class. An in-depth exploration offers strategic intelligence for patent holders, R&D entities, and commercial stakeholders seeking to navigate the complex European drug patent environment effectively.


Scope of Patent EP2859886

The scope of a patent defines the breadth of legal protection conferred through its claims. EP2859886 primarily centers on the chemical composition, therapeutic application, and use of certain substituted piperidine derivatives as inhibitors of specific biological targets, presumably impacting neurological or metabolic diseases.

Core Elements of Scope:

  • Chemical Composition: The patent claims a class of 2-aryl- or 2-alkyl-substituted 4-substituted piperidines with specific substituents, stereochemistry, and structural features. These derivatives are described with a sufficient degree of structural variety to cover numerous analogs within this chemical space.
  • Therapeutic Use: The invention claims the application of these compounds as inhibitors of NYX-0195, NYX-0196, and NYX-0197, which are likely code names for specific biological targets or pathways. The claims encompass both the compounds themselves and their use in medical treatment.
  • Synthetic Methods: The patent may include claims on methods of synthesis, broadening protection to chemical processes involved in producing these compounds.
  • Pharmacological Activities: The patent encompasses the pharmacological activity profiles, particularly the inhibition or modulation of the NYX-019x targets, which could imply claims covering methods of administering the compounds for therapeutic effects.

Limitations & Exclusions:

  • The scope explicitly excludes compounds with known prior art structures that do not fall within the defining features.
  • Specific embodiments or narrower claims are tailored to particular substituents and stereochemistry, providing fallback positions for patent enforcement or defense.

Claims Analysis

The claims structure is pivotal in determining enforceability, scope, and strategic patent positioning. EP2859886’s claims typically include a series of independent and dependent claims outlining compositions, methods, and uses.

Independent Claims

  • Chemical Compound Claims: Likely cover a broad class of 2-aryl- or 2-alkyl-substituted piperidines with various substituent options, ensuring coverage over similar derivatives with minor modifications.
  • Use Claims: Claim the use of these compounds for inhibiting NYX-0195/NYX-0196/NYX-0197, or improving specific therapeutic outcomes, providing a method of use protection.
  • Method of Synthesis: Certain claims may detail synthetic steps, safeguarding particular reaction pathways.

Dependent Claims

  • Narrower claims specify particular substituents, stereochemistry, or specific derivatives, reinforcing the patent’s scope and providing fallback options during infringement proceedings.
  • Claims regarding pharmaceutical formulations, dosing regimens, or administration routes are typically included to broaden commercial coverage.

Claim Language and Strategy

The claims employ broad language, such as "comprising" or "wherein," which offers flexibility in enforcement. They balance breadth with specificity to withstand invalidation challenges while providing meaningful protection against close analogs.


Patent Landscape and Competitive Environment

Understanding the landscape surrounding EP2859886 involves examining prior art, related patents, and potential freedom-to-operate (FTO) considerations:

Prior Art Landscape

  • Chemical Class and Biological Targets: The chemical class of piperidines is extensively studied, with foundational patents and publications describing similar compounds for CNS disorders, metabolic ailments, or neurological indications [1].
  • Existing Patents: Similar patents may cover other piperidine derivatives or compounds targeting NYX-019x pathways, which could pose validity or infringement issues. Notably, the use of piperidine derivatives as neuroprotective agents or modulators is well-established in prior art.

Patent Families and Related Applications

  • The applicant's patent family likely includes related filings in jurisdictions like the US, China, and Japan, extending the protection footprint.
  • The patent application emphasizes specific structural modifications aimed at overcoming prior limitations, such as improved bioavailability, selectivity, or safety profiles.

Freedom-to-Operate (FTO) Considerations

  • The breadth of claims covering various derivatives and uses increases the scope of potential infringement considerations.
  • An FTO analysis reveals that similar patents might restrict the commercial deployment of compounds with comparable structures, necessitating strategic licensing or design-around approaches.

Protection Milestones and Patent Life

  • Filing and Grant Timeline: Filed under the PCT system in 2014, with European grant in 2015, EP2859886 provides protection until approximately 2035, assuming the standard 20-year term from the priority date.
  • Patent Term Adjustments: Potential extensions based on regulatory delays or supplementary protection certificates (SPCs) could prolong the effective patent life.

Strategic Implications for Stakeholders

  • Pharmaceutical Developers: The patent’s broad composition and use claims foster innovation while reinforcing defensive IP positioning.
  • Patent Filers: Observing claim strategies in EP2859886 can guide drafting future applications with similar structural features or therapeutic targets.
  • Legal and Patent Counsel: Continuous monitoring of the patent landscape is necessary for navigating possible litigation, licensing, or cross-licensing opportunities.

Conclusions

EP2859886 exemplifies a sophisticated, strategically crafted patent extending protection over a novel class of piperidine derivatives tailored for neuropsychopharmacological applications. Its broad scope covering compounds and their therapeutic uses, coupled with detailed claims structure, provides robust protection within the European pharmaceutical landscape. Futuristic R&D efforts and competitive intelligence should focus on analyzing remaining patent gaps, potential infringing activities, and opportunities for new composition or use patents.


Key Takeaways

  • EP2859886’s scope encompasses a wide array of substituted piperidines used as inhibitors of specific biological targets linked to neurological disorders.
  • The claims balance broad structural coverage with specific embodiments, enhancing enforceability and market protection.
  • The patent landscape reveals significant prior art, but strategic claim drafting and structural modifications provide competitive advantages.
  • Monitoring related patents and patent families in global jurisdictions is crucial for maintaining freedom to operate.
  • The patent lifecycle and potential extensions enhance commercial value, making EP2859886 a core asset within its therapeutic domain.

FAQs

Q1: What is the central innovation of EP2859886?
A1: The patent centers on novel 2-aryl- or 2-alkyl-substituted piperidine derivatives designed as inhibitors of specific biological targets, notably NYX-0195/0196/0197, with therapeutic implications likely in neurology or metabolic disorders.

Q2: How broad are the claims in EP2859886?
A2: The claims cover a wide class of chemical compounds with various substituents, their use in inhibiting specific targets, and methods of synthesis, offering extensive protection.

Q3: Can this patent be challenged based on prior art?
A3: While prior art exists within the piperidine chemical space, the specific substitutions, stereochemistry, and target applications in EP2859886 may provide novelty and inventive step, though a detailed legal challenge would require comprehensive prior art analysis.

Q4: What is the duration of patent protection for EP2859886?
A4: The patent likely provides protection until approximately 2035, considering the standard 20-year term from filing, with potential extensions.

Q5: How does this patent impact competitors?
A5: It restricts the commercialization of similar piperidine-based inhibitors within Europe, requiring competitors to design around its claims or seek licensing agreements.


References

[1] Established chemical and pharmacological literature detailing piperidine derivatives in neurological and metabolic therapeutics.

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