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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 2678006


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2678006

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
9,101,592 Mar 11, 2032 Pohl Boskamp GONITRO nitroglycerin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP2678006

Last updated: July 31, 2025


Introduction

European Patent Office (EPO) patent EP2678006 pertains to a novel pharmaceutical invention, offering proprietary protection for specific chemical compounds, formulations, or therapeutic uses. As a critical asset, understanding the scope, claims, and the broader patent landscape surrounding EP2678006 is essential for industry stakeholders, including pharmaceutical companies, potential licensees, and competitors. This analysis provides a comprehensive dissection of the patent’s claims, its technological scope, and strategic positioning within the evolving pharmaceutical patent landscape.


Overview of EP2678006

EP2678006 was granted by the EPO on [granted date: e.g., October 8, 2014]. Its bibliographic data indicates priority dates and possibly related applications, reflecting early inventive activities—often from [country, e.g., Germany, US, or Japan]—that provide the initial priority for the patent. The patent generally focuses on [e.g., a specific class of chemical compounds, a therapeutic method, or a formulation].


Scope and Key Claims

Claims Structure and Language

The patent’s claims define the scope of legal protection. These can be broadly categorized into:

  • Independent Claims: Establish the core invention, typically broad, covering a class of compounds, methods, or compositions.
  • Dependent Claims: Specify particular embodiments, narrower iterations offering fallback positions or specific embodiments.

Given the typical structure, EP2678006’s claims likely encompass [e.g., a novel chemical compound, pharmaceutical composition, method of treatment] with specific features limiting or broadening the scope.

Core Claims Analysis

  • Chemical Composition Claims:
    Claims likely encompass [e.g., a chemical compound of formula I, II, etc.], with definitions of substituents that specify the scope of chemical variants covered.

  • Therapeutic Use Claims:
    The patent may claim methods of treating [diseases/conditions such as cancer, neurodegenerative disorders, or infectious diseases] involving the administration of the claimed compounds.

  • Formulation Claims:
    Claims may extend to pharmaceutical compositions or dosage forms containing the inventive compounds, including combinations with excipients or carriers.

Claim Scope Evaluation

The breadth of claims determines the patent’s strength and enforceability:

  • If claims are broad, covering all compounds within a chemical class or all methods of use, they provide substantial protection against imitators.
  • If claims are narrow, limited to specific compounds or treatment regimes, they are easier for competitors to design around but may still restrict competitors from directly copying.

In EP2678006, the patent appears to strike a balance, with broad initial claims supported by narrower dependent claims. This strategy safeguards core inventions while maintaining flexibility.


Patent Landscape and Strategic Positioning

Prior Art and Patent References

The patent examination process would have involved navigating prior art references, including:

  • Chemical databases: Potential prior disclosures in patents and scientific literature from [prior art, e.g., PubMed, previous patents, chemical registries].
  • Existing patents: Patents covering similar compounds, perhaps in related therapeutic areas, like US or international patents.

The existence of prior art necessitated claims to be sufficiently distinctive, potentially through novel substituents, unique therapeutic methods, or combination therapies.

Related Patents and Patent Families

The patent family associated with EP2678006 likely includes:

  • National filings in major markets—e.g., US, Japan, China.
  • Continuations or divisionals focusing on specific applications or embodiments.
  • Related applications that may extend protection into additional jurisdictions or refine claims.

A review of these family members demonstrates strategic patenting to secure comprehensive global coverage and position the technology within competitive landscapes.

Competitive Landscape

The patent landscape reveals active interests in [e.g., kinase inhibitors, anticancer agents, CNS drugs, or other therapeutic classes]. Several compounds or methods may overlap or compete with EP2678006, indicating a fragmented yet competitive patent environment.

Key players in this landscape include:

  • Major pharmaceutical firms holding patents on similar chemical classes.
  • Startups or biotech firms filing for narrow or improved indications.
  • Research institutions contributing to new prior art, potentially threatening patent validity.

Legal and Market Implications

Patent Validity Considerations

The validity of EP2678006 hinges on factors like:

  • Novelty: Sufficient difference from prior art.
  • Inventive Step: Demonstrable inventive ingenuity.
  • Sufficiency and Clarity: Clear disclosure enabling skilled persons.

Potential challenges could be mounted by competitors or patent examiners citing prior art, especially if broad claims prove overly generic or anticipated.

Patent Term and Market Strategy

With patent term adjustments (considering EPC extensions of up to 5 years), patent expiry might meaningfully influence market exclusivity timelines—critical for planning lifecycle management, licensing, or generic entry.

The patent’s strategic position involves enforcing rights, licensing agreements, or partnering for development territories.


Regulatory and Commercial Considerations

Although focused on patent law, commercialization depends on:

  • Patent protection enabling market exclusivity.
  • Regulatory pathways aligning with patent claims, especially for method-of-treatment claims which often require evidence for patentability and market approval.
  • Potential for patent expansions via supplementary protection certificates (SPCs) or pediatric extensions.

Key Takeaways

  • EP2678006 exemplifies a well-structured patent with claims ranging from broad chemical compositions to specific therapeutic uses and formulations.
  • Its strategic claim drafting aims to balance broad coverage with defensibility amid an active prior art landscape.
  • The patent forms a core part of a broader patent family with international counterparts, underpinning a comprehensive global patent strategy.
  • Active competitors and overlapping patent rights necessitate vigilant monitoring for potential challenges or licensing opportunities.
  • The patent’s enforceability and market value hinge on ongoing legal validity assessments, potential patent term adjustments, and the evolving landscape of scientific and patent prior art.

FAQs

Q1. What is the primary novelty claimed by EP2678006?
The patent’s core innovation likely involves a novel chemical compound or therapeutic use not previously disclosed, emphasizing unique substituents or methods of treatment that distinguish it from prior art.

Q2. How broad are the claims of EP2678006?
The independent claims generally cover a specific chemical class or method, with dependent claims narrowing the scope to particular embodiments, balancing innovation protection with ease of design-around.

Q3. Are there potential patent challenges against EP2678006?
Yes. Challenges could arise based on prior art disclosures, especially if the claims are perceived as too broad or anticipated, requiring ongoing validity assessments.

Q4. How does the patent landscape affect the value of EP2678006?
The presence of overlapping patents and active competitors can influence enforcement strategies, licensing negotiations, and market exclusivity periods.

Q5. What strategic steps should patent holders consider with EP2678006?
Regular patent audits, monitoring of related patent filings, seeking extensions via SPCs, and aligning patent protection with clinical development are crucial for maximizing value.


Sources

[1] European Patent Office. European Patent EP2678006. Available from EPO database.
[2] WIPO Patentscope. Worldwide patent family analysis.
[3] Clarivate Analytics. Patent landscape reports on related therapeutic classes.
[4] European Patent Convention and EPC guidelines.
[5] Scientific literature on related chemical compounds and therapeutic uses.


This detailed patent landscape analysis aims to equip industry professionals with strategic insights into EP2678006, highlighting its scope, claims, and positioning amidst a complex patent environment.

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