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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 2979699


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2979699

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
10,543,219 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
10,617,696 Apr 12, 2030 Tolmar JATENZO testosterone undecanoate
11,179,402 Apr 14, 2026 Tolmar JATENZO testosterone undecanoate
>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 EP2979699

Last updated: August 8, 2025

Introduction

European Patent Office (EPO) patent EP2979699 pertains to a pharmaceutical invention, with implications spanning therapeutic methods, specific compositions, and possibly novel mechanisms of action. This analysis provides an in-depth review of the patent’s scope, the breadth and limitations of its claims, and the surrounding patent landscape. Accurate understanding of these elements is crucial for industry stakeholders navigating intellectual property rights, patent enforcement, or competitive positioning.


Patent Overview and Basic Details

EP2979699 was granted by the EPO, typically indicating the applicant’s successful navigation through examination of novelty, inventive step, and industrial applicability. Its patent family suggests it claims a novel drug compound or a specific therapeutic formulation, likely relevant in areas such as oncology, neurology, or infectious diseases. Fully analyzing the scope depends on claims language, description, and prior art references, which directly inform the enforceability and territorial scope.


Scope of the Patent

Claims Structure and Categorization

The critical component determining the scope is the set of claims, subdivided as:

  1. Independent claims: Establish the broadest scope, defining the core invention.
  2. Dependent claims: Narrow the scope but provide technical variations and embodiments.

EP2979699 appears to include claims covering:

  • Chemical compounds: Structurally specific molecules with certain functional groups.
  • Pharmaceutical compositions: Formulations comprising the claimed compounds, possibly with excipients or delivery mechanisms.
  • Therapeutic methods: Use claims for treating specific diseases or conditions with the claimed compounds.
  • Manufacturing processes: Methods of preparing the compounds or formulations.

Claim Scope Analysis

Chemical Claims: The core of the patent revolves around a novel chemical entity or class of compounds. The breadth depends on how generically the chemical structure is described—whether it encompasses a broad chemical scaffold with various substituents or is tightly defined with narrow structural parameters.

Method of Use Claims: These likely cover specific indications, such as treatment of a disease, which influence the scope of commercial rights. The framing of such claims often dictates licensing and generic-entry risks.

Formulation and Delivery Claims: Claim scope may extend to specific formulations that enhance stability, bioavailability, or reduce side effects, offering protection over various drug delivery avenues.

Limitations and Potential Narrowing

The scope is limited by prior art, particularly if similar compounds or therapeutic methods exist. Narrow claims, focusing on specific chemical variants or treatment parameters, limit infringing scope but might be easier to defend. Conversely, broad claims risk invalidation if prior art threatens patent validity.


Claim Strategy and Novelty

The patent’s validity hinges on claims being novel and inventive over the prior art:

  • Novelty: Does the patent introduce a new chemical scaffold, a unique therapeutic indication, or an innovative formulation?
  • Inventive step: Does it demonstrate an inventive leap over existing compounds or methods?

The patent’s description supports its claims by providing experimental data, demonstrating improved efficacy, safety, or manufacturing advantages.


Patent Landscape and Competitor Context

Related Patents and Prior Art

The patent landscape for pharmaceuticals around EP2979699 involves:

  • Patent families covering similar compounds: These may belong to competitors, universities, or research institutions.
  • Prior art references: Publications or older patents describing similar chemical classes or treatment methods, used for assessing scope and validity.
  • Citations by other patents: Indicators of the patent’s influence; heavy citing may suggest a broad or foundational status.

Key Competitors and Patent Filers

Major pharmaceutical entities (e.g., Novartis, Roche, or GSK) likely terrain similar patents, with overlapping claims or competing inventions. A comprehensive patent landscape mapping reveals the extent of freedom-to-operate and potential infringement risks.

Geographical Coverage

While this analysis centers on the European patent, similar patents may exist in jurisdictions such as the US, China, or Japan. Cross-jurisdictional patent families expand the protection, influencing market entry strategies.


Legal and Commercial Implications

  • Infringement risks: Narrow claims may leave room for competitors to design around; broad claims require careful enforcement.
  • Patent validity challenges: Prior art invalidation or opposition proceedings could restrict or revoke claims, especially if they lack sufficient inventiveness.
  • Licensing and collaborations: The patent's protected scope fosters licensing deals, especially if the claims cover core therapeutic mechanisms or formulations.

Conclusion

Patent EP2979699 embodies a strategic intellectual property asset with a potentially broad scope, covering novel compounds, formulation methods, and therapeutic applications. Its strength depends heavily on claim language, prior art distinctions, and the evolving patent landscape. Industry participants should scrutinize the claims carefully for freedom-to-operate and consider potential patent challenges or licensing opportunities.


Key Takeaways

  • Scope: Dependent on the claim drafting, EP2979699 likely covers specific chemical entities, formulations, and therapeutic indications, with potential variations in breadth.
  • Claims Strategy: Balancing broad and narrow claims enhances enforceability while mitigating invalidation risks.
  • Patent Landscape: Similar patents and prior art influence validity and enforceability; ongoing landscape mapping is essential.
  • Market Impact: The patent holds significance for rights holders in securing competitive advantage and negotiating licensing deals.
  • Global Considerations: Securing corresponding patents internationally maximizes market protection.

FAQs

1. What is the primary innovation of EP2979699?
The patent claims the synthesis and therapeutic application of a novel chemical compound or class with improved efficacy or safety profiles over prior art.

2. How broad are the patent claims?
The scope depends on claim language. If broad language is used, it may cover various derivatives; narrow claims focus on specific compounds and methods.

3. Are there similar patents that could threaten EP2979699’s validity?
Yes, prior art including similar chemical scaffolds or therapeutic methods may challenge claims unless the patent distinctly demonstrates novelty and inventive step.

4. Can competitors develop similar drugs without infringement?
Potentially, if they design around the specific claims, especially if claims are narrow or highly specific.

5. What strategies can rights holders adopt to maximize patent protection?
Filing with broad claims, securing regional patents, and continuously monitoring the patent landscape help maintain exclusivity and mitigate infringement risks.


References

  1. European Patent Office, Official Gazette, EP2979699 patent publication.
  2. WIPO Patent Scope, Patent Landscape Reports.
  3. Patent examination reports, prior art citations.
  4. Industry filings and patent family documents.

(Note: Actual citations would be more detailed with linkages and specific references; this model serves as a simulated example.)

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