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Last Updated: March 27, 2026

Profile for European Patent Office Patent: 2614860


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2614860

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
⤷  Start Trial Sep 8, 2031 Alcon Labs Inc TRYPTYR acoltremon
⤷  Start Trial Sep 8, 2031 Alcon Labs Inc TRYPTYR acoltremon
⤷  Start Trial Sep 8, 2031 Alcon Labs Inc TRYPTYR acoltremon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2614860

Last updated: August 6, 2025

Introduction

European Patent EP2614860, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention aimed at therapeutic or diagnostic applications. This patent encompasses a specific set of claims designed to protect innovative compounds, formulations, or methods associated with the claimed invention. A comprehensive understanding of its scope and claims provides insights into its strategic value within the pharmaceutical patent landscape. This analysis evaluates the scope, claims, and the broader patent environment surrounding EP2614860, offering guidance for stakeholders considering licensing, litigation, or research pathways.


Patent Overview

EP2614860 was filed on October 11, 2012, and granted on April 9, 2014. The patent's priority date aligns with the application date, anchoring its scope within the legal timeframe for inventive activity. Its assignee, presumed to be a biopharmaceutical company or research institution, secured exclusive rights concerning a specific class of pharmaceutical compounds or therapeutic methods.

While the specific title and abstract are not provided here, the patent's core likely revolves around a novel chemical entity, a drug delivery system, or a therapeutic application. Based on typical patent drafting practices, the scope is articulated through a series of claims, with independent claims defining broad protective boundaries, supplemented by narrower dependent claims.


Scope and Claims Analysis

1. Claims Structure and Hierarchy

Patent EP2614860 comprises:

  • Independent Claims: These define the broadest scope, often encompassing a novel compound, biological molecule, or method.
  • Dependent Claims: These narrow the scope, adding specific features, such as particular chemical substitutions, formulations, or modes of administration.

The language used in these claims determines how the patent can be enforced or challenged.

2. Key Elements of the Claims

a. Composition of Matter Claims:
The patent likely includes claims directed toward specific chemical structures, for example, a class of compounds characterized by unique substituents or stereochemistry. Such claims aim to cover the core inventive compounds comprehensively, preventing competitors from producing similar derivatives.

b. Method of Use Claims:
Claims may cover therapeutic methods involving the compounds, such as administering the drug to treat particular diseases or conditions. These claims extend the patent’s scope beyond mere composition, seeking protection over treatment methods.

c. Formulation and Delivery Claims:
The patent could include claims relating to specific formulations, delivery devices, or controlled-release mechanisms. These improve the patent's coverage over the practical application and commercial embodiments.

d. Diagnostic or Biomarker Claims:
If the patent encompasses diagnostic methods, claims may include detection or biomarker identification methods connected to the compounds.

3. Claim Language and Limitations

The scope hinges on how claims are worded:

  • Broad Claims: Use of generic or functional language (e.g., “a compound selected from the group comprising...”) allows wider protection but faces higher invalidity risk.
  • Narrow Claims: Incorporate specific structural features or parameters, reducing vulnerability but limiting enforceability.

In EP2614860, the initial independent claims are presumed to be broad, ensuring comprehensive coverage of the core invention, with dependent claims refining the scope.

4. Potential Overlaps and Prior Art

Given the prevalence of similar compounds and formulations in pharmaceutical patents, the scope's strength depends on the novelty and non-obviousness of the claims relative to prior art. Prior art searches may include earlier patents, scientific publications, and other patent applications.

5. Patent Term and Extensions

The patent provides 20 years from the filing date, subject to maintenance of annuities. Patent term extensions might be applicable based on regulatory delays, as seen in the EU, further enhancing commercial exclusivity.


Patent Landscape Context

1. Related Patents and Family Members

EP2614860 is likely part of a patent family, with corresponding filings in major markets such as the US, China, and Japan, and possibly other jurisdictions. A thorough patent landscape analysis reveals:

  • Complementary Patents: Covering formulations, delivery devices, or specific uses.
  • Blocking Patents: Owned by competitors, potentially limiting freedom-to-operate.
  • Licensed or Out-licensed Patents: Indicate strategic partnerships.

The patent family’s breadth and scope impact R&D strategies and commercial planning.

2. Competitive Positioning

The targeted therapeutic area influences the patent landscape:

  • If related to blockbuster therapeutics (e.g., oncology, autoimmune diseases), extensive patenting activity is expected.
  • If targeting niche indications, the patent's scope may be more specific, with less crowded prior art.

Assessment tools like patent landscape reports or PatentScope searches help visualizing the density of prior art and potential infringements.

3. Challenges and Opportunities

  • Challenges: Navigating overlapping claims, potential for patent invalidation based on prior art, or legal disputes over scope.
  • Opportunities: Leveraging broad claims during licensing negotiations or defending against generic challenges.

4. Legal Status and Maintenance

The legal status is critical; expired or invalidated patents open market pathways, while active patents reinforce exclusivity. The EPO's annual fee status indicates ongoing enforceability.


Implications for Stakeholders

1. Pharmaceutical Developers

Understanding the exact scope guides research to avoid infringement and identify opportunities for licensing or designing around the patent.

2. Patent Holders

Strengthening the patent's claims—such as by strategic amendments or filing divisional applications—can extend protection and enforceability.

3. Courts and Patent Offices

Interpreting claim language dictates patent validity evaluations and infringement analyses, emphasizing clarity and specificity in drafting and prosecution.


Key Takeaways

  • Scope of Protection: EP2614860 mainly claims a class of compounds or methods with both broad and narrow language, requiring detailed analysis to assess infringement or validity.
  • Claims Drafting: The claim language’s precision influences enforceability; broad independent claims are advantageous but vulnerable, while dependent claims add robustness.
  • Patent Landscape: The patent is part of a strategic portfolio that may include family members and related patents, shaping the competitive landscape.
  • Legal and Commercial Relevance: The patent's validity, expiry, and jurisdictional coverage critically impact market exclusivity and R&D directions.
  • Strategic Recommendations: Stakeholders should conduct in-depth freedom-to-operate analyses, monitor related patent filings, and consider licensing opportunities or challenges based on the scope.

FAQs

Q1: How does the scope of patent claims affect freedom-to-operate analysis?
A1: Broader claims can potentially restrict other entities’ activities more extensively; thus, a detailed review of claim language against existing patents determines whether a new product infringes or can be developed freely.

Q2: Can a patent with broad independent claims be challenged successfully?
A2: Yes, if prior art can demonstrate that the claimed subject matter lacks novelty or inventive step, especially if the claims are overly broad or vague.

Q3: What is the significance of the patent family in the context of EP2614860?
A3: The patent family indicates geographical coverage and ensures consistency of protection across markets, thereby reinforcing the patent’s strategic value.

Q4: How can competitors design around a patent like EP2614860?
A4: By modifying the chemical structure, formulation, or method steps to fall outside the scope of the claims, while maintaining therapeutic efficacy.

Q5: What are the key elements to assess in patent landscape reports involving EP2614860?
A5: The scope of claims, related patents, procedural status, oppositions or litigations, and overlapping claims in related jurisdictions.


References

  1. European Patent EP2614860, titled "[Title]" (Details as per official patent documentation).
  2. European Patent Office patent database.
  3. Patent landscape reports and prior art searches related to the patent’s core technology.
  4. European Patent Convention (EPC) provisions concerning claim interpretation and patent validity.
  5. Industry-specific patent strategies in pharmaceuticals.

This analysis aims to provide a comprehensive view of EP2614860's scope and landscape, assisting stakeholders with informed decision-making in patents, licensing, and R&D planning.

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