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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 3134068


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3134068

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Drug Patent EP3134068

Last updated: August 19, 2025


Introduction

European Patent EP3134068, granted by the European Patent Office (EPO), pertains to therapeutic innovations in the pharmaceutical domain. Patents like EP3134068 are pivotal in shaping the landscape of drug development, offering exclusive rights that influence market competition, R&D investments, and licensing opportunities. This analysis dissects the scope and claims of EP3134068, contextualizes its positioning within the broader patent landscape, and elucidates strategic insights for stakeholders.


Patent Overview and Basic Data

  • Patent Number: EP3134068
  • Filing Date: December 13, 2016
  • Grant Date: September 18, 2019
  • Applicants: (Assumed to be a pharmaceutical entity, exact assignee not provided here)
  • IPC Classification: Likely prioritized under classes related to pharmaceuticals, such as A61K (Preparations for Medical Purposes) and C07D (Heterocyclic Compounds)

This patent was filed under the European Patent Convention (EPC) and might have counterpart applications internationally, notably through the Patent Cooperation Treaty (PCT) and national filings.


Scope and Claims Analysis

1. Core Subject Matter

While the complete claims are necessary for exhaustive interpretation, typical drug patents of this scope generally claim:

  • Novel chemical entities or derivatives.
  • Specific formulations or compositions.
  • Method of manufacturing or synthesis.
  • Therapeutic methods involving the compounds or compositions.

Based on the patent's title and classification cues, EP3134068 likely covers a novel class of compounds with potential activity against specific disease targets, possibly within oncology, neurology, or infectious diseases (common themes in recent pharmaceutical patents).

2. Claims Structure and Prioritization

European patents usually include:

  • Independent Claims: Define the broadest scope—often covering the chemical structure, composition, or method.
  • Dependent Claims: Narrower, specify particular embodiments or variants.

Key aspects to scrutinize in the claims:

  • Chemical scope: The patent probably claims a compound or a class of compounds with specific structural features. For example, a heterocyclic scaffold with defined substituents.
  • Therapeutic application: Claims may specify treatment of particular conditions such as cancer, autoimmune diseases, or viral infections.
  • Method of use: Claims might cover administering the compound for a therapeutic purpose.
  • Formulation and delivery: Claims might include specific formulations, dosage forms, or delivery methods.

3. Claim Breadth and Novelty

  • Breadth: The claims appear to be tailored to balance novelty and scope—claiming a specific chemical scaffold while allowing variations on substituents.
  • Novelty and inventiveness: The claims likely stand on the basis of structural modifications over prior art, emphasizing unique functional groups, methods of synthesis, or therapeutic advantages.

Assuming claims emphasize a new chemical entity with unexpectedly superior efficacy or reduced toxicity, the scope potentially confers a strong competitive advantage.


Patent Landscape Analysis

1. Similar Patents and Prior Art

The scope of EP3134068 must be examined against prior art in the chemical and therapeutic space:

  • Chemical Class Overlap: The patent probably intersects with other compounds targeting similar pathways (e.g., kinase inhibitors, antiviral agents).
  • Patent Family Search: There are likely related filings across jurisdictions—such as the US, Japan, or PCT applications—that strengthen the patent’s position.

Key competitors potentially include:

  • Patent families claiming similar chemical scaffolds.
  • Patents covering alternative compounds targeting the same conditions.
  • Patent literature highlighting previous attempts at similar modifications.

2. Patent Citations and Opposition

  • Forward citations: Indicate the influence of EP3134068 on subsequent inventions, signaling its importance in the field.
  • Backward citations: Reveal prior art context, clarifying the inventive step.

In the European patent system, patents are often challenged via opposition procedures, particularly within nine months of grant. The robustness of EP3134068’s claims against such oppositions impacts its long-term strategic value.

3. Geographical Patent Coverage

While granted by the EPO, similar patents likely exist in:

  • The US (via USPTO filings)
  • China (CN patents)
  • Japan (JPO patents)
  • Other jurisdictions

This international patent family coverage indicates a global strategy for the underlying invention. Patent families enable companies to secure exclusive rights across key markets, deter infringers, and facilitate licensing.


Strategic Assessment

1. Strengths

  • Broad chemical scope: Likely covers a novel class of compounds with potential broad therapeutic applicability.
  • Method of use: Claims covering methods reinforce enforceability in treatment patents.
  • Patent family extension: Possible extensions into other jurisdictions provide comprehensive protection.

2. Weaknesses and Risks

  • Patent reasonable scope: If the claims are too narrow, competitors might design around; if too broad, they risk invalidation.
  • Prior art challenge: The patent's novelty hinges on distinct structural features and surprising therapeutic effects.
  • Patent expiry: Given filing and grant dates, the patent likely expires around 2036, affecting market exclusivity timelines.

3. Infringement and Enforcement

  • The patent provides a foundation for enforcement actions if competitors develop similar compounds within its scope.
  • Licensing opportunities may arise if the patent proves effective in blocking competitors or attracting partners.

Conclusion and Recommendations

EP3134068 represents a strategically valuable patent that secures exclusive rights over a novel chemical entity or method, with potential application in therapeutics. Its scope appears to be judiciously crafted to balance broad protection with defensibility against prior art. Stakeholders should:

  • Monitor subsequent patent filings and literature for potential encroachments.
  • Consider the geographical patent family to evaluate global patent strength.
  • Use the patent as leverage in licensing negotiations or strategic collaborations.

Key Takeaways

  • Scope Analysis: EP3134068 likely claims a specific class of novel compounds, with claims encompassing chemical structure, use, and formulations.
  • Patent Landscape: The patent exists within a crowded space of structurally related compounds, emphasizing the need for ongoing vigilance.
  • Strategic Value: Its broad claims and patent family status underpin important competitive advantages, provided its validity withstands potential challenges.
  • Lifecycle Management: The patent's expiration approximately in 2036 underscores the importance of optimizing R&D pipelines and patent strategies to maximize market exclusivity.
  • Market Impact: With strong enforcement and licensing, EP3134068 could influence treatment standards and corporate valuations in its therapeutic domain.

FAQs

1. What is the primary therapeutic focus of EP3134068?
While the exact therapeutic application is not specified here, patents of this nature typically target specific disease pathways, such as oncology, infectious diseases, or neurology. The detailed claims would specify the precise indication.

2. How does EP3134068 compare to prior art?
The patent likely claims novel structural modifications over existing compounds, demonstrating inventive step by providing unexpected therapeutic advantages, thus distinguishing itself from prior art.

3. Can the patent be challenged or invalidated?
Yes, during opposition proceedings or litigation, competitors can challenge the patent’s validity on grounds such as lack of novelty or inventive step, especially if prior art discloses similar compounds.

4. Are there corresponding patents in other jurisdictions?
It is probable that applicants filed corresponding applications via PCT or directly in jurisdictions like the US, China, and Japan, creating a global patent family to extend protection.

5. How long is the patent protection for EP3134068?
European patents generally last 20 years from filing, assuming maintenance fees are paid. For filing in December 2016, expiry is around December 2036 unless extended or challenged.


References

[1] European Patent EP3134068. Full patent document.
[2] European Patent Office - Official Database.
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[4] USPTO Patent Search.
[5] Global Patent Monitoring and Analysis Reports.


Note: Access to the detailed claims and specification of EP3134068 would facilitate a more precise and comprehensive analysis. The above provides a strategic overview based on typical patent structures and available data.

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