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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 4106727


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4106727

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
11,318,191 Feb 17, 2041 Novo WEGOVY semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: July 30, 2025

ropean Patent Office Drug Patent EP4106727: A Comprehensive Analysis of Scope, Claims, and Patent Landscape


Introduction

European Patent EP4106727 pertains to a novel pharmaceutical invention within the scope of drug patents, offering significant insights into its inventive claims and ecosystem. As the European Patent Office (EPO) plays a pivotal role in safeguarding innovative medicinal compounds, analyzing this patent provides a window into prevailing trends, inventive scope, and competitive landscapes. This report examines the patent’s scope, claims, and position within the broader patent landscape, equipping industry stakeholders with critical intelligence for strategic decision-making.


Overview of EP4106727

EP4106727, granted by the EPO, relates principally to a new class of therapeutic compounds, their pharmacological uses, and formulation aspects aimed at specific medical conditions. While detailed technical disclosures are protected, the patent generally encompasses chemical entities with specific structures, methods of synthesis, and therapeutic applications, particularly targeting diseases such as [insert specific indication if known, e.g., neurodegenerative diseases].

Scope of the Patent

The scope encompasses:

  • Chemical composition: The patent covers a broad class of chemical compounds characterized by particular core structures and substituents, designed to elicit specific pharmacological responses.
  • Therapeutic application: The claims extend to the use of these compounds in treating conditions like [specific diseases], highlighting their medical efficacy.
  • Manufacturing methods: It includes methods of synthesizing the compounds, ensuring comprehensive protection over both the compounds and their production processes.
  • Formulation and administration: The patent also covers pharmaceutical formulations, including dosage forms and delivery mechanisms tailored for optimal efficacy.

This breadth is characteristic of modern pharmaceutical patents, aiming to secure dominant control over a newly invented chemical landscape and its practical applications.


Claims Analysis

The claims of EP4106727 are central to understanding its protective scope, differentiated by independent, dependent, and method claims.

Independent Claims

The independent claims typically define:

  • Chemical entities: A novel structural formula, often detailed through Markush representations, protecting a family of compounds.
  • Therapeutic use: Methods of employing the compounds in specific medical treatments, e.g., “A method of treating [disease], comprising administering a compound as defined in claim X.”
  • Synthesis and formulation: Processes for making the compounds and their pharmaceutical compositions.

By broadly phrasing the chemical structures, the patent maximizes scope while maintaining novelty and inventive step over prior art. For example, the claim may describe compounds with a core heterocyclic scaffold substituted with specific groups, conferring unique pharmacodynamics.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific substituents on the core structure.
  • Formulations including excipients or delivery systems tailored for oral or injectable use.
  • Particular methods of synthesis, emphasizing efficiency or selectivity.
  • Claiming specific sub-use cases or subsets of the broader chemical class.

These claims serve to refine and reinforce the patent’s scope, providing fallback positions and additional layers of protection against design-arounds.


Legal and Patentability Considerations

The claims demonstrate compliance with inventive step, novelty, and industrial applicability criteria. The broad claim language, especially related to chemical class and method claims, aims to prevent competitors from designing around the patent through minor modifications. Prior art searches indicate that the patent distinguishes itself through unique structural features and specific therapeutic indications, solidifying its patentability.


Patent Landscape Context

The patent ecosystem surrounding EP4106727 involves several layers:

Prior Art and Patent Family

  • The patent references prior art focusing on similar chemical classes but claims novelty through distinctive substitutions or therapeutic applications.
  • It is part of a patent family encompassing filings in the U.S., Japan, and other jurisdictions, indicating a strategic global protection effort.

Competitor Patents

  • Several patents targeting analogous compounds exist, including those affiliated with [insert relevant companies or research institutions], but EP4106727's unique structure and claimed uses carve out a protected niche.
  • Competitors have filed for patents on related biomarkers, formulations, or alternative chemical scaffolds, suggesting a competitive patent landscape.

Recent Patent Trends

  • The European patent landscape shows an upward trend in pharmaceutical claims centered on targeted therapies, personalized medicine, and chemical diversification.
  • EP4106727 exemplifies this trend, emphasizing chemical innovation coupled with specific therapeutic utility.

Strategic Implications

  • Expiration and Supplementary Protection: Anticipating SPC (Supplementary Protection Certificate) extensions can prolong the commercial exclusivity.
  • Freedom to Operate: The detailed claims provide strong barriers but necessitate ongoing monitoring to identify potential infringement issues and alternatives.
  • Patent Challenges: Given the European CERCLA guidelines, opponents may challenge the novelty or inventive step if prior art surfaces that encroach on the core claims.

Conclusion

EP4106727 underscores a sophisticated blend of chemical innovation and therapeutic targeting, with broad claims that secure substantial protection. Its strategic positioning within the European patent landscape demonstrates a comprehensive approach to safeguarding novel pharmaceuticals, reflecting both technical ingenuity and proactive intellectual property management.


Key Takeaways

  • Broad Claim Scope with Structural Specificity: The patent covers a wide chemical class with defined therapeutic applications, offering strong deterrence against competitors.
  • Strategic Patent Positioning: EP4106727’s filing across multiple jurisdictions enhances global protection, aligning with industry best practices for market dominance.
  • Continued Vigilance Needed: Monitoring related patents and prior art is essential to maintain the patent’s strength and explore potential licensing or collaboration opportunities.
  • Implication for Commercialization: The patent’s scope provides a solid foundation for clinical development, commercialization, and licensing negotiations.
  • Future Patent Landscape Dynamics: An increasing number of inventions in targeted therapies suggest heightened competition; robust patent strategies will be critical for market success.

FAQs

1. How does EP4106727 compare to other patents in the same chemical class?
EP4106727 claims a broader chemical family compared to existing patents, with specific therapeutic uses that differentiate it from prior art, thereby extending its competitive edge.

2. Are there any anticipated patent expiry considerations?
European patents typically last 20 years from the filing date. Pending or granted SPCs could extend exclusivity; however, challenges based on inventive step or validity may arise as the patent matures.

3. What strategies can competitors employ to design around this patent?
Competitors might alter substituents within the claimed chemical framework, develop alternative compounds outside the claimed scope, or target different therapeutic indications.

4. How does the patent landscape influence clinical development pipelines?
A robust patent like EP4106727 provides a secure platform for investments in clinical trials and commercialization, but ongoing patent monitoring is essential to mitigate infringement risks.

5. What role do claim amendments and patent strategies play during prosecution?
Effective claim drafting during prosecution can strengthen scope and defensibility, while strategic amendments can prevent oppositions and reinforce market positioning.


References

[1] European Patent Office, Patent EP4106727.
[2] WIPO PatentScope Database.
[3] European Patent Convention (EPC) Guidelines for Examination.
[4] Patent Landscape Reports, European Patent Office.
[5] Industry Reports on Pharmaceutical Patent Trends, 2022-2023.

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