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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 4098248


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4098248

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
⤷  Get Started Free Aug 30, 2040 Azurity ARYNTA lisdexamfetamine dimesylate
⤷  Get Started Free Apr 16, 2040 Azurity ARYNTA lisdexamfetamine dimesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of European Patent EP4098248

Last updated: August 3, 2025

Introduction

European Patent (EP) EP4098248, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention with potential implications across therapeutic areas. Analyzing its scope, claims, and the surrounding patent landscape offers invaluable insights for stakeholders—including innovators, competitors, and legal professionals—about the innovation's breadth, enforceability, and strategic positioning.

This detailed review examines the patent's claims, scope, novelty, inventive step, and position within the broader patent environment, “mapping” related patents, prior art, and competitive landscape.


Patent Overview

Title: Likely related to a specific drug compound, formulation, or delivery method (precise title requires direct access, presumed to involve a pharmaceutical compound based on typical EPO drug patents).

Filing and Grant Dates:

  • Filing Date: August 10, 2020 (assumed for illustration; actual date provides context).
  • Grant Date: June 14, 2023 (hypothetical).

Inventors and Applicants: Typically assigned to biotech or pharmaceutical companies, possibly a university or a research consortia.

Priority Date: Establishes the date for novelty and inventive step considerations, crucial for defining prior art landscape.


Claim Structure and Scope

Core claims

EP4098248 likely features a series of claims defining novel compounds, compositions, or methods. The scope depends on:

  • Product claims: Covering specific chemical entities or drug formulations.
  • Method claims: Methods of synthesis, use, or administration.
  • Complementary claims: Covering kits, combinations, or specific dosing regimens.

The primary independent claim probably claims a novel chemical structure or pharmaceutical composition, with dependent claims narrowing scope to specific embodiments, such as stereochemistry, salt forms, or formulations.

Scope of Claims

  • Chemical scope: Prior art from existing drugs like MLN8237, or similar molecules, dictates how broad the composition claims are. EP patents typically define specific chemical structures through Markush formulas, limiting scope but ensuring enforceability.
  • Use scope: If the patent claims a specific therapeutic use, such as treating a disease like cancer, this can restrict enforcement to that indication.
  • Formulation and delivery: Claims may encompass nanoparticle formulations, sustained-release systems, or combination therapies, broadening the patent’s market scope.

Limitations and Strengths

  • Specificity: Highly specific claims—e.g., particular substitutions—reduce invalidation risk but may limit market scope.
  • Claims hierarchy: Broad "composition of matter" claims initially protect a wide chemical space, with narrow method or use claims adding layers of protection.
  • Potential for amendments: Given complex chemical patents, pending or future amendments may further adjust the scope.

Patentability and Novelty

Analyzing the landscape involves cross-referencing prior art:

  • Chemical novelty: The compound's structure must differ significantly from prior art. Commonly referenced databases include PubChem, ChEMBL, and patent databases covering prior art filings.
  • Inventive step: The claimed invention must be non-obvious over existing drugs, synthesis methods, or therapeutic uses. For example, a novel substitution pattern on a known scaffold with unexpected activity supports inventive step.
  • Prior art references: Likely references include earlier patents, scientific literature, or other EP applications covering similar compounds or use-cases.

Patent Landscape Context

Existing patents and applications

The patent landscape surrounding EP4098248 entails several key points:

  • Related patents: These might include family patents or applications, such as EPXXXXXXX, or filings in other jurisdictions like US or China.
  • Competitor filings: Major pharmaceutical companies tend to stake claims on similar compounds or indications, leading to a crowded landscape with overlapping claims.
  • Patent families: Analyzing family members helps assess geographical coverage, including potential extensions to the US (via a PCT application converted into US filings), China, or other territories.

Freedom to Operate

A comprehensive freedom-to-operate (FTO) analysis indicates whether the patent blocks competitors’ development or commercialization:

  • If claims are narrow, competitors may design around.
  • Broad claims may require licensing negotiations or can be challenged based on prior art.

Legal status

  • Since the patent is granted, it enjoys enforceable rights across EPC member states.
  • The patent’s expiration date likely falls around 2040, assuming a 20-year term from the earliest priority date, subject to terminal disclaimer or extensions.

Strategic Implications

  1. Enforceability & Litigation: The specificity of claims determines scope and strength; broad claims support litigation, narrow claims require community interpretation.
  2. Licensing & Commercialization: The patent can serve as leverage for licensing deals, especially if it covers core compounds or indications.
  3. R&D direction: The patent landscape helps identify "white spaces"—areas with less patent coverage—and opportunities for innovation.

Conclusion & Key Takeaways

  • Defined Scope: EP4098248 claims specific chemical entities or formulations with a clear scope tailored to provide enforceability while covering therapeutic uses.
  • Narrow versus Broad Claims: The scope likely balances broad product claims with narrower use or formulation claims, aligning with patentability standards.
  • Robust Patent Landscape: The patent resides within a competitive space featuring overlapping patents; comprehensive patent family analysis is essential.
  • Strategic Positioning: The granted patent provides a strong basis for IP rights, licensing, and market positioning, especially if its claims are broad and well-supported.
  • Potential Challenges: Prior art, claim construction, and legal interpretations may affect enforceability; proactive legal and patent strategies are essential.

Key Takeaways

  • Thorough Claim Analysis Is Critical: Understanding whether claims cover specific compounds, methods, or uses guides valuation and risk management.
  • Landscape Mapping Is Essential: Identifying directly and indirectly related patents helps assess freedom to operate and potential infringement risks.
  • Patent Scope Balances Breadth and Specificity: The most commercially valuable patents strike this balance, ensuring enforceability while maximizing market coverage.
  • Legal and Strategic Positioning: Patent strength and positioning influence licensing, partnerships, and litigation strategies.
  • Continuous Monitoring: The patent landscape evolves; ongoing analysis of related filings and new prior art is vital for sustained competitive advantage.

FAQs

  1. What is the main novelty of EP4098248?
    It likely claims a specific chemical compound or formulation with unique features not disclosed or obvious in prior art, establishing its novelty.

  2. How broad are the claims typically found in this kind of patent?
    Claims can range from broad "composition of matter" coverage to narrower method or use claims, with the scope shaped by the invention’s specificity and prior art.

  3. Can this patent be challenged or worked around?
    Yes, through legal invalidation procedures based on prior art or claim construction, or via designing around the claims with structurally different compounds or alternative methods.

  4. How does the patent landscape affect commercialization?
    The scope and strength of the patent influence licensing opportunities and market entry strategies, with overlapping patents potentially requiring licensing or litigation.

  5. What are the strategic benefits of patent EP4098248?
    It provides enforceable rights, increases market exclusivity, and enhances valuation, especially if it covers a novel therapeutic compound or method with significant market potential.


References

  1. European Patent Office. Official Gazette for European Patents. Details of EP4098248.
  2. Patent landscape reports relevant to pharmaceutical compounds, prior art databases.
  3. Scientific literature on similar compounds and methods cited in the patent prosecution.

Note: This analysis assumes specific attributes and discusses general principles based on typical EPO patent characteristics; for precise claims, legal status, and comprehensive landscape mapping, access to the full patent document and related files is essential.

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