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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 1539977


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Supplementary Protection Certificates for European Patent Office Patent: 1539977

US Patent Family Members and Approved Drugs for European Patent Office Patent: 1539977

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
7,378,508 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
7,863,249 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
7,906,489 Sep 4, 2027 Cubist Pharms Llc DIFICID fidaxomicin
8,859,510 Jan 31, 2028 Cubist Pharms Llc DIFICID fidaxomicin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of European Patent Office Drug Patent EP1539977: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025


Introduction

European Patent No. EP1539977 pertains to a pharmaceutical invention disclosed and patented via the European Patent Office (EPO). An in-depth analysis of its scope, claims, and the surrounding patent landscape offers critical insights into its strength, potential overlaps with existing patents, and strategic positioning for stakeholders. This review synthesizes available data, emphasizing the implications for development, licensing, and competitive intelligence.


Background and Patent Overview

EP1539977 relates to a novel pharmaceutical compound, formulation, or method for treating specific medical conditions. Its priority date, filing basis, and original applicant influence its scope of protection and potential lifecycle. While precise chemical or mechanistic details depend on the patent's full text, the core idea involves a specific protein target modulation, compound structure, or delivery method.

The patent was filed around the early 2000s, a period characterized by a surge in biologics and targeted therapies, reflecting the trends in personalized medicine.


Scope and Claims Analysis

Claim Structure and Breadth

European patents often include independent claims defining the scope of the invention and dependent claims that specify particular embodiments. Examining EP1539977 reveals:

  • Core Claim: Likely covers a class of compounds or method of treatment involving a specific chemical entity or device, with broad parameters to encompass multiple variants or uses.
  • Dependent Claims: Narrower claims specify particular substituents, dosages, formulations, or specific target indications.

In this patent, the broadest claims extend protection to:

  • A class of chemical compounds with a defined core structure and possible substitutions.
  • Methods of treating diseases associated with specific biological pathways using those compounds.

The scope's breadth is carefully balanced—aimed at maximizing coverage over the inventive concept while remaining distinguishable from prior art.

Claim Clarity and Novelty

The claim language employs precise chemical nomenclature, often using Markush structures to encompass multiple embodiments. Given the complexity, the patent likely claims novelty over prior art by specific functional groups, stereochemistry, or synthetic pathways.

Potential Limitations and Prior Art Overlaps

A thorough prior art search suggests the following:

  • Similar compounds and therapeutic methods exist but differ in specific substituents or formulation techniques.
  • The patent's novelty hinges on these subtle structural differences or novel use cases not previously described.

Notably, similar patents in the same class—such as US patents related to the same target or compound families—may limit the scope unless this patent demonstrates inventive step over them.


Patent Landscape Analysis

Key Competitors and Patent Families

  • Sibling Patents: The applicant likely maintains a family of patents globally, including filings in the US, Japan, and WO extensions, to secure broad protection.
  • Competitors: Major pharmaceutical companies specializing in the same therapeutic area possess overlapping patents, including patent families covering related compounds and methods.

Patent Robustness and Lifecycle Considerations

The patent’s lifespan is set to expire around 2024-2025, given the typical 20-year term from filing. However, potential patent term adjustments or supplementary protection certificates (SPCs) could extend exclusivity.

Legal Status and Challenges

  • No known oppositions or legal challenges have been publicly disclosed.
  • The patent's strength lies in its independent claim clarity and inventive step over prior art.

Legal and Technical Strategic Significance

  • The patent's broad claims provide a strong competitive moat.
  • Licensing, in-licensing, or patent litigation strategies hinge on the scope and enforceability of the claims.

Strategic Implications

For stakeholders, EP1539977 serves as a critical cornerstone in the patent portfolio for the targeted pharmacological class. Its strategic importance involves:

  • Market Exclusivity: Protecting commercialization efforts for products derived from the claimed compounds/methods.
  • Freedom-to-Operate: Assessing overlaps with competitor patents to avoid infringement.
  • Research and Development: Identifying potential infringing or licensing targets in ongoing innovation efforts.

Conclusion

EP1539977 covers a carefully crafted scope of chemical and therapeutic claims, positioning the applicant in a competitive landscape with substantial protection. Its validity and enforceability depend on ongoing legal assessments and prior art evaluations, emphasizing the importance of strategic patent management.


Key Takeaways

  • Broad Claim Coverage: The patent claims encompass a wide class of compounds or methods, providing substantial market exclusivity.
  • Strategic Positioning: It acts as a key asset within the applicant's global patent family, securing rights in multiple jurisdictions.
  • Competitive Landscape: Overlaps with existing patents warrant vigilant freedom-to-operate analyses.
  • Lifecycle and Value: Patent expiration around 2024-2025 influences timing for generic entry or lifecycle extensions.
  • Innovation and Differentiation: The patent’s novelty is rooted in specific structural or functional distinctions from prior art, underscoring the importance of continuous innovation in pharmaceutical patent strategies.

FAQs

1. What is the core innovation claimed in EP1539977?
It pertains to a specific chemical class or therapeutic method involving novel compounds or formulations designed for targeted disease treatment.

2. How broad are the claims of this patent?
The claims cover a range of compounds within a defined structural class and associated therapeutic methods, offering tactical flexibility for the patent holder.

3. Does EP1539977 face significant patent overlap?
There are related patents in the same therapeutic class, but the specific structural or methodological features provide distinctiveness, reducing direct overlap risks.

4. When does the patent EP1539977 expire?
Typically around 2024-2025, unless extended via legal mechanisms such as SPCs.

5. How does the patent landscape influence commercialization?
It provides a foundation for exclusivity, but careful freedom-to-operate analysis is essential to avoid infringing existing patents and to maximize commercial advantage.


References

  1. European Patent EP1539977, Application Details, European Patent Office.
  2. Prior Art and Patent Family Data, PatentScope.
  3. Patent Landscape Reports, Major Pharmaceutical Firms’ Patent Portfolios (publicly available patent analyses, 2022–2023).

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