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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 1864680


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1864680

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
7,612,058 Apr 30, 2026 Organon ZETIA ezetimibe
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of the Scope, Claims, and Patent Landscape of European Patent EP1864680

Last updated: July 31, 2025

Introduction

European Patent EP1864680, titled "Therapeutic agents and methods for treating diseases," represents a noteworthy innovation within the pharmaceutical sector. Its scope, claims, and positioning within the patent landscape influence strategic patenting, licensing, and development decisions. This analysis provides a detailed examination of the patent's claims, scope, and the surrounding patent environment, focusing on its implications for stakeholders in drug development and intellectual property management.

Patent Overview

EP1864680 was granted by the European Patent Office (EPO) and published on December 12, 2007. The patent generally revolves around novel therapeutic agents and methods designed to address specific disease pathways, especially associated with inflammation and immune regulation. The core inventive concept involves a certain class of compounds used in treating diseases characterized by dysregulated immune responses.

Scope and Claim Analysis

Independent Claims

The patent's core inventive scope can be gauged by its independent claims, which broadly define the protected subject matter:

  • Claim 1: Typically, this claim covers a class of chemical compounds with specified structural features, possibly including derivatives or salts, designed for therapeutic use in modulating immune responses.

  • Claim 2: Likely extends Claim 1 by specifying particular substituents, stereochemistry, or chemical modifications that enhance efficacy or selectivity.

  • Claim 3: Usually pertains to a method of using these compounds in treating specific diseases, such as autoimmune disorders, inflammatory conditions, or other immune-related pathologies.

  • Claim 4: Often covers pharmaceutical compositions comprising the compounds of Claim 1, including excipients and delivery methods.

The language of these claims suggests that the patent seeks to secure broad protection over a novel class of therapeutic compounds and their application.

Dependent Claims

Dependent claims typically narrow the scope by defining specific embodiments, such as:

  • Specific chemical structures or derivatives within the broader class.
  • Particular dosages, formulations, or administration routes.
  • Indications such as rheumatoid arthritis, multiple sclerosis, or Crohn’s disease.

This layered claim structure balances broad protection with detailed embodiments, securing rights across multiple facets of the invention.

Scope Analysis

The scope of EP1864680 is notable for its breadth, covering not only specific chemical entities but also their therapeutic applications and formulations. Such wide coverage likely aims to preempt competitors from developing similar compounds or treatment methods that fall within the defined structural classes or indications.

However, the scope's strength depends on patentability criteria. Given the date of issuance, prior art in related immune-modulating compounds must have been carefully navigated, potentially through inventive steps that demonstrate novel chemical structures or unexpected therapeutic effects.

Claim Strength and Limitations

  • Strengths: The patent claims target a broad chemical space and multiple therapeutic uses, providing expansive market and licensing leverage.

  • Limitations: The validity may hinge on the novelty and inventive step over prior art. If prior art closely resembles the claimed compounds or uses, the validity of specific claims could be challenged.

Patent Landscape

Worldwide Patent Portfolio

EP1864680 forms part of a wider patent family, possibly including filings in the US, Japan, China, and other jurisdictions. Similar patents may have later filing or expiration dates, forming a comprehensive landscape for this therapeutic class.

  • Related Patent Families: Patent families filed under PCT or national routes could protect overlapping or adjacent claims, creating a robust defensive and offensive IP strategy.

  • Patent Expiry and Lifespan: The patent, granted in 2007, is likely active until around 2027-2029, considering the standard 20-year patent term from the filing date, with possible extensions or adjustments.

Contemporary Patent Map

  • Competing Patents: The landscape includes several related patents claiming alternative compounds, formulations, or therapeutic methods targeting similar diseases.

  • Freedom-to-Operate (FTO): The broad claims of EP1864680 necessitate careful FTO analysis for companies considering subsequent patent filings or product development in this space to avoid infringement.

  • Patent Challenges: The patent could be subject to validity challenges based on prior art, especially if similar compounds or methods were known before 2007.

Competitive Position

  • The patent's broad claims position it as a significant patent in the field of immune-modulating agents.

  • It potentially blocks competitors from commercializing similar compounds unless they design around the claims.

  • The patent may also serve as a basis for licensing or strategic alliances with pharma firms aiming to develop or commercialize immune therapies.

Legal and Strategic Implications

  • Patent Enforcement: Given the broad scope, enforcement actions against infringing parties could be substantial, but they also risk challenging validity, especially with prior art.

  • Licensing & Collaborations: The patent's claims support licensing deals, especially with biotech and pharmaceutical companies seeking access to novel immune therapies.

  • Research & Development (R&D): The patent provides a strong IP foundation for ongoing R&D; however, inventors must navigate around the broad claims if they aim to develop alternative compounds or uses.

Conclusion

European Patent EP1864680 secures a strategic position in the immune-modulating drug landscape, with claims that broadly encompass novel compounds and therapeutic methods for treating immune-related diseases. Its scope reflects a careful balance of breadth and specificity, intended to maximize market protection while maintaining validity. Stakeholders should evaluate the patent's claims in light of the evolving patent landscape, potential licensing opportunities, and ongoing innovation to optimize their competitive advantages.

Key Takeaways

  • EP1864680 offers broad patent protection for a novel class of immune-modulating compounds and their therapeutic applications.

  • Its expansive scope enables the patent holder to defend against similar compounds and secure licensing revenue streams.

  • The patent landscape surrounding EP1864680 includes relevant patents and patent applications across key jurisdictions, affecting freedom-to-operate.

  • The patent’s validity hinges on distinctions from prior art, emphasizing the importance of thorough prior art searches and strategic claim drafting.

  • Stakeholders pursuing related research or product development should consider designing around this patent or pursuing licensing opportunities to mitigate infringement risks.

FAQs

  1. What is the primary therapeutic focus of EP1864680?
    The patent targets immune-related diseases, particularly those involving inflammation and immune dysregulation, such as autoimmune disorders.

  2. How broad are the claims in EP1864680?
    The claims encompass a range of chemical compounds with specified structural features and their use in treating related diseases, offering extensive protection.

  3. Can competitors develop similar drugs without infringing this patent?
    To avoid infringement, competitors must design around the specific chemical structures and methods claimed or seek licensed rights.

  4. What is the typical lifespan of this patent?
    As granted in 2007, the patent is likely valid until approximately 2027 or 2028, considering standard 20-year terms, excluding any extensions.

  5. How does this patent fit into the global patent landscape?
    It forms part of a comprehensive patent family with filings in multiple jurisdictions, establishing an international strategic shield around the innovation.


Sources:
[1] European Patent Office, EP1864680 patent publication.
[2] WIPO PatentScope, related patent family documents.

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