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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3470400


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3470400

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent EP3470400

Last updated: August 9, 2025

Introduction

European Patent EP3470400, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention with potential implications across therapeutic areas. This analysis aims to elucidate the scope of the patent claims, their breadth, and situate the patent within the broader landscape of related drug patents, thereby informing strategic decision-making for stakeholders including pharmaceutical companies, IP professionals, and investors.

Patent Overview

EP3470400 was granted on [date], with original application filed on [filing date]. The patent aims to protect specific compounds, formulations, or methods associated with a defined therapeutic purpose. It likely targets a specific molecular structure or a novel use of a known compound, aligned with common practices in drug patenting.

The patent's claims delineate its legal scope, determining the rights conferred upon the patent holder and shaping the competitive landscape.

Scope of the Claims

1. Independent Claims

The core of EP3470400 comprises independent claims that articulate the inventive subject matter. Typically, such claims encompass:

  • Chemical compounds: Specific molecular entities with well-defined chemical structures, often represented with Markush groups allowing structural variability.
  • Pharmaceutical formulations: Particular compositions, excipients, or delivery methods involving the core compounds.
  • Method of use: Therapeutic applications, such as treating a particular disease or condition, often with precise parameters (dosage, administration route, or treatment regimen).

Key feature of the scope: The claims tend to be narrowly tailored to specific compounds or methods, providing robust protection if successfully granted, but potentially vulnerable to design-around strategies by competitors.

2. Dependent Claims

Dependent claims elaborate on the independent claims, adding features such as:

  • Specific substituents or chemical modifications.
  • Particular dosages, formulations, or delivery methods.
  • Use in specific patient populations or for targeted indications.

These serve to reinforce protection over narrower but commercially valuable embodiments.

3. Claim Breadth and Limitations

The claims' scope largely hinges on:

  • Structural specificity: The degree of chemical definition influences scope—broader claims encompass a wider array of compounds but may face obstacles in patentability.
  • Therapeutic claims: Often, claims directed toward methods of use are narrower, constrained by existing prior art.
  • Process claims: If present, may cover synthetic routes or manufacturing steps.

Legal considerations: European patent law mandates clarity, novelty, and inventive step, constraining overly broad claims. The scope must balance exclusivity with legal robustness.

Patent Landscape Analysis

1. Existing Patent Families and Prior Art

A detailed landscape indicates a landscape packed with patents related to the core chemical classes or therapeutic areas. Relevant prior art includes:

  • Earlier patents on molecular classes: The patent may build upon or carve out distinctions from previous compounds disclosed in prior art (e.g., WO patents, national patent documents).
  • Use-specific patents: Competing patents might focus on alternative uses or delivery methods for similar compounds, influencing the scope of EP3470400's enforceability.
  • Process patents: Inventive manufacturing routes could intersect with EP3470400, particularly if the synthesis or formulation methods are novel.

2. Key Competitors and Patent Holders

Major pharmaceutical entities active in this domain often pursue overlapping claims, creating a crowded patent environment. Notable patent holders could include:

  • Established pharmaceutical companies with substantial R&D footprints.
  • Academic institutions contributing novel compounds or methods.
  • Patent aggregators harvesting fragmented IP rights for strategic licensing or litigation.

3. Patent Term and Legal Lifecycle

  • The patent's expiry is typically 20 years from the priority date, with potential extensions (e.g., Supplementary Protection Certificates in Europe).
  • Ongoing patent prosecution or oppositions could alter scope or enforceability.
  • Patent families related to EP3470400, such as divisional or continuation applications, may expand the overall patent estate for the invention.

4. Cross-Referenced Patents and Published Applications

The landscape includes numerous patents citing or citing EP3470400, revealing networks of technological advancement and potential licensing opportunities or legal challenges.

Implications for the Industry

The scope of EP3470400, combined with the existing patent environment, influences:

  • Freedom to operate (FTO): Parties must navigate overlapping rights, especially in highly crowded therapeutic classes.
  • Litigation landscape: Broad claims can lead to infringement suits, while narrow claims may necessitate careful interpretation.
  • Research and development: The patent's scope may either shield innovations or stimulate efforts to design around protected compounds or methods.

Strategic Considerations

  • Developers should analyze the specific molecular claims to assess potential for designing alternative compounds.
  • License negotiations may target specific claims or the broader patent family.
  • Monitoring patent filings and legal events related to EP3470400 is essential for risk management.

Key Takeaways

  • EP3470400 claims are likely centered on particular chemical entities, formulations, or therapeutic methods, with scope influenced by molecular and use-specific limitations.
  • The patent landscape surrounding the patent is dense, featuring active competitors, prior art, and ongoing patent filings.
  • Thorough landscape analysis underscores the importance of precise claim drafting, vigilant monitoring, and strategic IP management for all stakeholders involved.

FAQs

1. What are the main features protected by EP3470400?
EP3470400 likely protects specific chemical compounds, formulations, or therapeutic methods, with claims tailored to particular structures, uses, or delivery methods.

2. How broad are the claims in EP3470400?
The breadth depends on the claim drafting—chemical claims are often specific to particular structures, while use or formulation claims may be broader but constrained by prior art.

3. What is the significance of the patent landscape surrounding EP3470400?
The landscape reveals competing patents, potential freedom to operate issues, and opportunities for licensing or collaboration within overlapping therapeutic and chemical classes.

4. How does the patent landscape influence drug development efforts?
A crowded environment may limit development options or necessitate designing around existing patents, while a clear space may streamline commercialization efforts.

5. What strategic steps should IP professionals consider regarding EP3470400?
Professionals should analyze claim scope, monitor legal status, evaluate potential infringement risks, and explore licensing or strategic patent filings aligned with the patent's scope.


References

[1] European Patent Office patent database. EP3470400.
[2] World Intellectual Property Organization. Patent Landscape Reports.
[3] European Patent Convention and Guidelines for Examination.
[4] Industry reports on patent strategies in pharmaceuticals.
[5] Prior art databases and patent filings in the relevant therapeutic areas.

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