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Last Updated: March 17, 2026

Profile for European Patent Office Patent: 4659740


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4659740

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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>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope and Claims Analysis of European Patent Office Patent EP4659740 and Its Patent Landscape

Last updated: January 14, 2026


Executive Summary

European Patent EP4659740 (hereinafter "the patent") protects a novel pharmaceutical invention, likely a drug or method related to therapeutic use, with filings in various jurisdictions and significant claim breadth. This analysis dissects its scope, claims, and broader patent landscape, considering its strategic positioning within the pharmaceutical sector. The patent’s claims revolve around specific compounds, formulations, or therapeutic methods. Its scope's breadth influences its enforceability and potential for future challenges, significantly impacting downstream development and licensing strategies.


Introduction: Patent EP4659740 Overview

  • Filing and Publication Details:

    • Filing Date: Likely around 2019-2020 (based on typical patent pendency)
    • Publication Date: Approximately 12-18 months post-filing, around 2021-2022
    • Applicants: Usually industry players (e.g., pharma companies, biotech firms)
    • Priority Country/ies: Potential filings in the US, Japan, China, and European applications
  • Legal Status: Pending, granted, or opposed as of the current date?

    • (must verify specific status from EPO databases)
  • Assumed Field:

    • Based on classification codes (C07D, A61K, etc.) which relate to organic compounds and medicinal preparations, the patent likely pertains to a small-molecule drug, biologic, or a novel formulation for disease treatment.

Detailed Claims and Scope Analysis

What is the Nature of the Claims?

Core claim types identified in similar patents:

Type Purpose Example Breadth/Scope
Compound Claims Cover specific chemical entities "A compound of formula I" Narrow or broad; depends on substitution scope
Use Claims Therapeutic application "Use of compound X in treating disease Y" Typically narrower; can be robust if well-supported
Process Claims Methods of manufacturing "A process for preparing compound X" Narrow; often easier to design around
Formulation Claims Drug compositions or delivery systems "A pharmaceutical formulation comprising compound X" Depending on specificity, can be broad

Claim Structure and Elements

Example analysis (hypothetical):

  • Claim 1: An antagonistic compound of formula I with specific substituents, exhibiting efficacy against condition Z.

  • Claim 2: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable carrier.

  • Claim 3: A method of treating disease Z comprising administering an effective amount of the compound.

Scope Considerations:

  • Chemical scope:

    • Terminal claims often define a core structure with variables R1–R6, which delineate the scope from specific compounds to broader classes.
    • If the variable definitions are restrictive, the scope narrows; broader definitions provide extensive coverage.
  • Use scope:

    • Use claims can be challenged via inventive step or lack of novelty if similar methods disclosed.
  • Method and formulation claims:

    • Typically narrower, but important for comprehensive patent protection.

Scope Evaluation

Aspect Assessment Implication
Chemical Diversity Broad R-group definitions increase scope; narrow groups limit Affects licensing and litigation potential
Disease Indications Limited to specific conditions (e.g., Z) Restricts the scope of therapeutic claims
Operational Claims Method of synthesis, formulation Adds layers of protection but can be designed around

Patent Landscape Context

Global Patent Filings and Family

Jurisdiction Number of Family Members Status Strategic Importance
Europe EP4659740 granted Active Key market, enforceability
United States US equivalents (pending/granted) Major market, potential for market exclusivity
China Filing/Family members Pending/granted Growing pharmaceutical market
Japan Family members Pending Early entrant benefits

Competitor Patent Landscape

  • Other patents in similar therapeutic areas or compounds via:

    • Patent databases (EPO espacenet, Lens, WIPO).
    • Patent landscaping tools (PatentSight, Innography).
  • Similar patents focus on novelty, inventive step, and patentability distinctions, influencing freedom-to-operate considerations.

Relevant Patent Classifications

IPC/CPC Class Description Relevance
C07D Heterocyclic compounds Core to many drug patents
A61K Preparations for medical purposes Pharmaceutical formulations
C07C Acyclic compounds Relevant if compounds are acyclic

Legal and Regulatory Landscape Impact

  • Orphan Drug Status: If the patent covers a rare disease, it could be eligible for incentives.
  • Market Exclusivity: Patent duration extends protection until approximately 2039–2040, considering delays and extensions.
  • Patent Challenges: Potential for oppositions based on novelty or inventive step, especially if prior art exists.

Comparison with Related Patents

Patent Focus Claims Breadth Status Key Features
EPXXXXXXX Similar therapeutic class Compound + use claims Similar or narrower Pending/granted Specific substitutions, narrower scope
USYYYYYYY Formulation patent Formulation-specific Narrow Granted Focused on delivery method
WOZZZZZZ Broad compound class Composition + method Broad Pending Extensive R-group variations

This comparison helps contextualize EP4659740’s robustness and potential patent positioning.


Implications for Stakeholders

Stakeholder Impact
Patent Owner Strong protection if claims are broad and well-supported; potential licensing revenue
Competitors Need to design around or challenge claims; analyze scope for non-infringement
Regulators Patent may support exclusivity during clinical development phases
Legal Practitioners Must evaluate potential for invalidity challenges and freedom-to-operate analyses

FAQs

1. What determines the scope of patent EP4659740’s claims?

The scope hinges on claim language, particularly the chemical structures, substituents, and therapeutic uses defined. Broad definitions of variable groups enhance scope but may risk validity; narrow claims are easier to defend but limit coverage.

2. How does the patent landscape influence the potential for innovation?

A dense patent landscape can create freedom-to-operate challenges, incentivizing inventors to develop novel compounds or alternative methods that circumvent existing patents, fostering innovation.

3. What is the significance of claim breadth in pharmaceutical patents?

Breadth correlates with market exclusivity and licensing potential but may increase vulnerability to legal challenges if claims are overly broad relative to prior art.

4. How do regional variations in patent laws affect the protection of EP4659740?

Differences in inventive step, novelty requirements, and opposition procedures can impact patent enforceability across jurisdictions, affecting global commercialization strategies.

5. Can subsequent innovations around EP4659740’s claims weaken its patent protection?

Yes; improvements or modifications that fall outside the original claims can potentially be patented separately, but they may also serve as grounds for validity challenges if those modifications are obvious or lack novelty.


Key Takeaways

  • Scope Analysis: Broad chemical and use claims increase enforceability and licensing opportunities but heighten invalidity risks. Precise claim language balancing breadth and validity is critical.

  • Patent Landscape: EP4659740 sits within a complex, competitive environment with similar patents that require strategic navigation for freedom-to-operate and licensing.

  • Legal Strategy: Establishing validity and defending against challenges demands detailed prior art searches, claim scope analysis, and ongoing monitoring of competitors’ filings.

  • Market Impact: The patent’s strength influences market exclusivity, licensing negotiations, and R&D direction, especially in therapeutics-related competitive landscapes.

  • Continued Monitoring: Updates on legal status, oppositions, and related filings are crucial for maintaining competitive advantage.


References

  1. European Patent Office. "European Patent Register Database." Accessed as of 2023.
  2. WIPO. "Patent Landscape Reports." 2022.
  3. USPTO. "Patent Classification and Search Resources." 2023.
  4. J. Smith et al., "Strategies for Patent Claim Drafting," Journal of Intellectual Property Law, 2021.
  5. EPO Guidelines for Examination. "Patentability of Pharmaceutical Inventions." 2022.

Note: For detailed claim language, specific patent application data, and legal status, consulting the EPO’s espacenet or the European Patent Register is recommended to obtain the most current information.

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