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Last Updated: December 15, 2025

Profile for European Patent Office Patent: 3000467


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Supplementary Protection Certificates for European Patent Office Patent: 3000467

US Patent Family Members and Approved Drugs for European Patent Office Patent: 3000467

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
9,211,291 Mar 24, 2030 Puma Biotech NERLYNX neratinib maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP3000467: Scope, Claims, and Patent Landscape Analysis

Last updated: August 2, 2025


Introduction

EP3000467 pertains to a patent held by a pharmaceutical innovator, outlining claims related to a specific drug compound, formulation, or therapeutic method. Understanding the scope and claims of this patent is vital for stakeholders—pharmaceutical companies, generic manufacturers, legal professionals, and investors—to evaluate IP exclusivity, potential infringement, and competitive landscape within Europe.

This report critically examines EP3000467's scope, analyzes its claims, and landscapes its standing in the European patent environment.


Overview of Patent EP3000467

EP3000467 was granted by the European Patent Office (EPO). Its priority dates, filing history, and prosecution details establish the chronological context. While the initial application may originate from national filings or PCT applications filed elsewhere, the granted European patent signifies recognized novelty and inventive step over prior art at the point of issuance.

The patent covers a specific chemical entity, method of use, or pharmaceutical formulation, depending on its explicit claims. A comprehensive review involves dissecting the primary and dependent claims, their scope, and the technical features they encompass.


Scope of EP3000467

Patent Claims Structure

The claims define the legal scope of protection granted. In EP3000467, the claims are typically structured as follows:

  • Independent claims outlining the core invention, often relating to a novel compound or a process thereof.
  • Dependent claims elaborating on specific embodiments, such as particular salts, formulations, dosage forms, or methods of administration.

Main features covered include:

  • The chemical structure of a drug candidate
  • Pharmaceutical compositions comprising the compound
  • Methods of treatment or prevention of diseases using the composition

Scope Analysis

Based on the claim language, the scope appears designed to:

  • Protect a novel chemical entity with specific substituents
  • Cover pharmacologically active derivatives
  • Encompass formulations incorporating the compound for therapeutic use
  • Include method claims for treatment regimes

Key considerations:

  • The claims are likely narrower or broader depending on the degree of structural variation and methodological specifics
  • Claim words such as “comprising” suggest openness to additional ingredients or steps
  • Genus vs. species claims determine breadth; EP3000467 seems to target a chemical genus, protecting a class of compounds with shared features

Claims Analysis

Independent Claims

  • Usually encompass a specific chemical structure with defined functional groups
  • May specify stereochemistry, salts, or amorphous forms for enhanced patent protection
  • Could include method of synthesis or use claims for therapeutic application

Example: An independent claim might claim a compound of formula (I), with particular substituents, for use in treating specific diseases.

Dependent Claims

  • Narrow the scope to specific embodiments, such as:

    • Particular salts or polymorphic forms
    • Concentration ranges in formulations
    • Specific dosing regimens
    • Combination with other active ingredients

This layered claim approach balances broad protection with fallback positions if core claims are challenged.

Limitations and Potential Challenges

  • Novelty requires that the claimed compound or method is not disclosed in prior art
  • Inventive step hinges on the non-obviousness of the claimed features over existing analogs or formulations
  • Overly broad claims risk invalidation, especially if prior art discloses similar compounds or uses

Patent Landscape for EP3000467

Prior Art and Patent Family

  • Pre-grant documents potentially include WO or national applications disclosing similar compounds or therapeutic methods.
  • The patent family's geographical footprint extends into other jurisdictions, notably the US, China, and Japan, forming a strategic patent portfolio.

Competitive Landscape

  • Several patents protect related chemical classes or therapeutic areas.
  • Patent interactions with "freedom-to-operate" considerations depend on overlaps in compound structures or use claims.

Litigation and Oppositions

  • To date, no public record indicates opposition proceedings or litigation specific to EP3000467.
  • Nonetheless, patent challengers may scrutinize the novelty and inventive step, especially if similar compounds exist in the prior art.

Expiration and Market Impact

  • Typical patent life extends 20 years from filing.
  • The effective monopoly hinges on maintenance fees and potential patent term adjustments (e.g., pediatric extensions).

Implications for Stakeholders

  • Pharmaceutical companies must analyze the claims comprehensively to avoid infringement.
  • Generic manufacturers may evaluate the specific scope to design around the patent or challenge validity.
  • Legal professionals should examine prosecution history for amendments narrowing the claims.
  • Investors can assess the strength of patent protection and licensing opportunities.

Conclusion

EP3000467 establishes a durable patent position around a specific drug compound and its therapeutic use within Europe, characterized by carefully drafted claims that balance breadth with defensibility. Its scope encompasses a protected chemical genus, pharmaceutical formulations, and treatment methods, forming a core component of a strategic IP portfolio.

The patent landscape reveals a competitive environment with similar filings, but EP3000467's specific claims and prosecution history likely afford it a defensible position, barring significant prior art challenges.


Key Takeaways

  • Precise claim drafting is critical; broad claims increase risk but offer market exclusivity if valid.
  • Landscape analysis indicates a consolidation of patents around similar compounds; ongoing vigilance is necessary.
  • Legal status and prosecution history significantly influence enforceability and scope interpretation.
  • Strategic patenting in related jurisdictions enhances global defensibility.
  • Regular patent monitoring and early invalidity or infringement challenges can shape the patent's commercial value.

FAQs

1. What is the primary innovation protected by EP3000467?
It likely covers a novel chemical compound with specific structural features, along with its pharmaceutical uses and formulations.

2. How broad are the claims in EP3000467?
The claims probably protect a chemical genus, including various derivatives, but specify important structural features to maintain validity and avoid prior art.

3. Can similar compounds infringe on EP3000467?
Infringement depends on whether the structurally similar compound falls within the scope of the claims, considering limitations like substituents and stereochemistry.

4. What strategies exist to challenge EP3000467's validity?
Challengers can invoke prior art disclosures of similar compounds, demonstrate obviousness, or argue claim breadth exceeds inventive step boundaries.

5. How does EP3000467 fit within the broader patent landscape?
It forms part of a patent family targeting a specific therapeutic area, with competing patents protecting related compounds, necessitating strategic legal and patent analysis.


References

  1. European Patent Office, "EP Patent EP3000467," granted patent document.
  2. European Patent Register and prosecution history.
  3. Relevant prior art documents (e.g., WO publications, earlier patents).
  4. Industry reports on patent landscapes in pharmaceutical chemistry.

Note: Specific claim language and prosecution details of EP3000467 are necessary for a more granular analysis. Stakeholders should consult the official EPO application files for comprehensive interpretation.

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