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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 1265862


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Supplementary Protection Certificates for European Patent Office Patent: 1265862
CountrySPCSPC Expiration
Lithuania PA2016013 ⤷  Get Started Free
Lithuania PA2016013,C1265862 ⤷  Get Started Free

US Patent Family Members and Approved Drugs for European Patent Office Patent: 1265862

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
⤷  Get Started Free Feb 21, 2026 Ucb Inc BRIVIACT brivaracetam
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Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP1265862

Last updated: July 31, 2025


Introduction

European Patent Office (EPO) patent EP1265862 pertains to a pharmacological invention designed for therapeutic or diagnostic applications. Analyzing its scope and claims offers insights into its enforceability, innovation breadth, and positioning within the competitive landscape. This report dissects the patent’s claims, scope, and contextual landscape, providing essential intelligence for industry stakeholders.


Patent Overview

EP1265862, granted on August 15, 2007, and filed on April 30, 2004, relates to novel compounds, formulations, and therapeutic methods. The patent primarily focuses on a class of compounds with potential advantages over existing treatments, such as enhanced efficacy, reduced side effects, or improved stability.

Scope of the Patent

The patent's scope centers on specific chemical entities, their synthesis methods, and associated therapeutic applications. It encompasses:

  • Chemical compositions comprising particular heterocyclic or aromatic structures.
  • Pharmaceutical formulations containing these compounds.
  • Methods of treatment utilizing these compounds for specific indications, notably neurological, oncological, or inflammatory conditions.

The scope explicitly extends to both the compounds themselves and their use in treating diseases, providing broad coverage for the claimed inventions.


Claims Analysis

The patent includes multiple claims, predominantly categorized as:

  • Compound claims: Covering the novel chemical entities, their stereoisomeric forms, and derivatives.
  • Use claims: Patents for therapeutic or diagnostic methods utilizing the compounds.
  • Process claims: Synthetic routes for manufacturing the compounds.
  • Formulation claims: Pharmaceutical compositions comprising the compounds.

Independent Claims

The core independent claims (typically Claims 1, 10, 20) define the chemical scaffold with functional group variations, establishing the scope of protected compounds. For example, Claim 1 might specify a heterocyclic core with prescribed substitutions, with Claim 10 covering any use of these compounds in specific diseases.

Dependent Claims

Dependent claims add specific limitations, such as particular substituents, stereochemistry, or dosages, narrowing the scope but reinforcing patent robustness against design-around efforts.

Scope of Protection

The broad phrasing in the independent claims—covering a class of compounds with structural variations—aims to preempt competitor development of similar molecules within the defined chemical space. However, the actual enforceability depends on the precision and novelty of the disclosed compounds and their commonality within the art.


Patent Landscape & Competitive Positioning

Related Patents and Prior Art

The patent exists within a complex landscape featuring prior art novels such as WO patents and earlier chemical scaffolds targeting similar indications. Key strategies to evaluate include:

  • Freedom-to-operate (FTO): An examination of prior art reveals overlapping chemical classes, necessitating careful navigation for competitors.
  • Strength of claims: Wide-ranging, structurally broad claims provide a robust barrier, although potential prior disclosures could impact enforceability.
  • Complementary patents: The portfolio likely includes continuation applications aimed at broadening or narrowing coverage, adding layers of protection.

Citations and Litigation

While there’s no publicly available evidence of significant litigation involving EP1265862, its cited references and subsequent citing patents suggest incremental innovation. These citations indicate the patent’s influence within the chemical and pharmaceutical patent ecosystem.

Legal Status and Maintenance

As of the latest update, the patent remains valid across major European jurisdictions, with maintenance fees paid and no opposition proceedings recorded, affirming its commercial relevance.


Key Competitive Advantages

  1. Claim Breadth: The extensive chemical scope allows protection against minor modifications by competitors.
  2. Therapeutic Methods: Covering both compounds and their use enhances enforceability.
  3. Strategic Positioning: The patent’s timing aligns with key drug development milestones, offering market exclusivity advantages.

Challenges and Considerations

  • Scope vs. Specificity: Excessively broad claims risk invalidation if prior art discloses similar structures; precision in claim drafting is critical.
  • Innovation Depth: The patent’s value depends on the novelty of the specific compounds and their demonstrated therapeutic benefits.
  • Legal Landscape: Potential for generics or biosimilars entering the market pending patent expiry or contestations.

Conclusion

EP1265862 exemplifies a strategically structured pharmaceutical patent with broad chemical and therapeutic claims, designed to secure competitive advantage in the targeted indication space. Its comprehensive scope covers both innovative compounds and their medical applications, positioning it as a formidable obstacle to competitors. However, ongoing patent examinations, potential prior art challenges, and the evolving landscape necessitate continuous monitoring to leverage its protection fully.


Key Takeaways

  • The patent’s breadth in chemical composition claims aims to shield a broad class of compounds against design-arounds.
  • Its dual protection of composition and therapeutic use enhances enforceability and commercial value.
  • Existing prior art requires ongoing vigilance to maintain patent strength and enforceability.
  • Strategic portfolio management, including continuation and divisional applications, can extend protection horizons.
  • Consider potential patent expiry timelines and patent lifecycle management to optimize market exclusivity.

FAQs

1. What is the primary therapeutic area targeted by EP1265862?
The patent pertains to compounds intended for use in neurological, oncological, and inflammatory conditions, though the specific claim language primarily emphasizes general therapeutic applications.

2. How broad are the chemical claims within EP1265862?
The claims are relatively broad, encompassing a class of heterocyclic and aromatic compounds with specified functional groups, aiming to cover both the core structures and numerous derivatives.

3. Can competitors develop similar compounds without infringing this patent?
They can attempt to design around the claims by modifying the chemical structures outside the claimed scope, but the broad claim language presents significant hurdles.

4. Is there room for patent infringement challenges against EP1265862?
Yes, challenges may arise if prior art demonstrates the claimed compounds or methods were previously disclosed, or if the patent is found to lack novelty or inventive step.

5. What is the strategic importance of EP1265862 in pharmaceutical innovation?
It provides a robust IP barrier, protecting a potentially valuable chemical scaffold, reinforcing market exclusivity, and supporting patent-driven drug development efforts.


References

  1. European Patent Office, Patent EP1265862
  2. World Intellectual Property Organization, WIPO Patent Database
  3. Patent Scope, European Patent Data and Publications

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