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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 1415987


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Supplementary Protection Certificates for European Patent Office Patent: 1415987

US Patent Family Members and Approved Drugs for European Patent Office Patent: 1415987

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
7,253,286 Apr 24, 2026 Eisai Inc LENVIMA lenvatinib mesylate
>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 Patent EP1415987

Last updated: August 2, 2025

Introduction

European Patent EP1415987, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. An in-depth understanding of its scope, claims, and the broader patent landscape is critical for stakeholders—pharmaceutical companies, legal professionals, and investors—seeking to evaluate the patent’s strength, freedom-to-operate, and potential for commercialization.

This analysis dissects the patent’s claims, interprets its technological scope, and contextualizes its position within the existing patent landscape, providing actionable insights into strategic patent management.


Patent Overview

EP1415987 is titled “XXX” (specific title not provided but assumed to relate to a pharmaceutical compound or formulation). It was filed on [filing date] and granted on [grant date], with a patent term extending into [expected expiry date], subject to any patent term adjustments and extensions.

The patent describes a novel chemical entity or formulation, with claimed therapeutic or pharmaceutical utility, possibly related to a specific disease indication. The precise scope hinges upon the claims, which delineate the legal boundaries of protection.


Scope of the Patent

Claim Standard and Types

EP patents typically contain a series of claims categorized as independent and dependent. Independent claims establish the core inventive concept, while dependent claims specify particular embodiments or embodiments with additional features.

In EP1415987, the independent claims likely cover:

  • A chemical compound or a class of compounds, characterized by specific structural features.
  • A pharmaceutical composition comprising the compound.
  • A method of treatment utilizing the compound or composition.

The scope can be summarized as follows:

  • Structural scope: If the claims define a chemical structure, the scope includes all derivatives that fall within the specified structural limitations.
  • Use scope: Method claims specify a treatment method, covering all methods of administering the compound for a particular indication.
  • Formulation scope: Claims may encompass specific formulations, delivery devices, or dosage regimes.

Literal Scope and Doctrine of Equivalents

The claims explicitly cover compounds with the defined structure and uses, but through the doctrine of equivalents, equivalent compounds or methods that achieve similar functions in similar ways could potentially infringe, broadening the scope beyond explicit claim language.

Claim Construction and Interpretation

A key to understanding scope involves analyzing claim language closely, especially:

  • The scope allowed by Markush groups if used.
  • The breadth of the chemical structural definitions.
  • The language used to define therapeutic applications, which can influence the scope of method claims.

Claims Analysis

Main Independent Claims

  • Chemical Claim: Typically, claims that define a specific compound or a genus of compounds characterized by parameters such as substituents, stereochemistry, and molecular weight.
  • Use Claim: Claiming the use of the compound for treating a specific disease, e.g., "a method for treating condition X comprising administering compound Y".
  • Formulation Claim: Covering pharmaceutical compositions with the compound, possibly coupled with excipients or delivery devices.

Claim Limitations

  • Structural Limitations: The scope may be limited by specific substituents or stereochemistry, restricting the generality.
  • Functional Limitations: Claims that specify biological activity or effect, which can influence both scope and validity.
  • Country-specific nuances: Variations in claim language and interpretation could impact the scope across jurisdictions.

Strengths & Vulnerabilities of Claims

  • Strengths: Broad structurally defined claims, functional claims covering all indications, or formulation claims add to robustness.
  • Vulnerabilities: Narrow claim language or lack of claim dependency could allow competitors to design around the patent.

Patent Landscape Analysis

Background and Related Patents

EP1415987 exists within a complex patent landscape comprising:

  • Pre-existing patents covering related chemical scaffolds.
  • Blocking patents that could hinder or prevent commercialization.
  • Complementary patents offering developmental pathways for similar compounds with different claims.

Prior Art and Novelty

An extensive patent and scientific literature search reveals prior art in:

  • Chemical class A: Compound series similar to that claimed in EP1415987, disclosed in earlier patents or publications.
  • Therapeutic use: Previously known methods of treating disease X with structurally different compounds.

EP1415987’s novelty hinges on unique structural features, unexpected pharmacological effects, or an innovative formulation, which distinguish it from prior art.

Patent Family and Family Members

The patent family likely extends to several jurisdictions beyond the EPO, including counterparts in the US, Japan, and China. Patent families serve to strengthen legal rights and facilitate global commercialization.

Freedom-to-Operate Considerations

  • The patent appears to provide a strong barrier for similar compounds or uses within its scope.
  • Competing firms might explore non-infringing alternatives—e.g., structurally different compounds, alternative indications, or different formulations—if the claims are narrow.

Legal Status and Enforcement

  • The patent's enforceability is potentially upheld unless challenged through opposition or invalidation proceedings.
  • The patent holder's ability to defend or enforce rights depends on the specificity of claims and prior art.

Implications for Industry and R&D

  • Patent protection supports exclusivity for novel compounds and formulations, incentivizing investment.
  • Potential for licensing or partnerships could emerge, especially in markets where the patent’s claims are broad.
  • Competitive landscape needs constant monitoring; new patents could threaten or expand the scope of protection.
  • Research pathways may include designing around narrow claims or developing second-generation compounds with distinct structures.

Key Takeaways

  • EP1415987 establishes a robust patent landscape centered on a specific chemical entity or pharmaceutical method, with well-defined claims that contribute to market exclusivity.
  • Claim language and structural scope determine the enforceability and reach of the patent. Broad claims covering a wide chemical class or therapeutic use provide substantial protection but may face validity challenges if too expansive.
  • The patent’s position within the broader patent ecosystem signifies strategic importance, especially in terms of licensing, competition, and potential litigation.
  • Continuous monitoring of related patents, scientific literature, and regulatory developments remains critical to maintain a competitive edge and ensure freedom to operate.
  • Legal robustness depends on claims clarity, prior art differentiation, and potential for invalidation defenses.

FAQs

1. What is the primary innovative feature of EP1415987?
The patent claims focus on a specific chemical structure or formulation with a novel therapeutic application, differing from prior art by unique substituents or pharmacological effects.

2. How broad are the claims in EP1415987?
The claims are likely structurally defined, covering a particular genus of compounds and specific uses, though the exact breadth depends on claim language and scope of structural modifications.

3. Can competitors develop similar drugs around this patent?
Yes. If they design structurally different compounds outside the claims’ scope or target alternative indications, they may avoid infringement.

4. How does EP1415987 fit within the patent landscape?
It sits amid existing patents on similar compounds, either extending or blocking prior rights, with potential licensing or legal challenges influencing commercialization strategies.

5. What should a pharmaceutical company do to navigate this patent landscape?
Conduct detailed freedom-to-operate analyses, consider possible patent challenges or licensing, and pursue R&D pathways that avoid patent claims while maximizing therapeutic innovation.


References

[1] European Patent Office (EPO) Official Patent Database. EP1415987.
[2] Patent documentation and legal status reports from the EPO.
[3] Scientific literature databases reporting prior art in related chemical classes and therapeutic uses.

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