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Last Updated: December 17, 2025

Profile for European Patent Office Patent: 3490541


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3490541

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 Jul 26, 2037 Corium ADLARITY donepezil hydrochloride
⤷  Get Started Free Jul 26, 2037 Corium ADLARITY donepezil hydrochloride
⤷  Get Started Free Jul 26, 2037 Corium ADLARITY donepezil hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP3490541

Last updated: August 11, 2025


Introduction

European Patent No. EP3490541, granted by the European Patent Office (EPO), pertains to innovative pharmaceutical compounds, formulations, or methods related to drug development. As a critical asset within the intellectual property portfolio of the applicant, this patent’s scope, claims, and landscape considerations significantly influence competitive positioning, licensing opportunities, and future innovation pathways.

This analysis provides an in-depth review of the patent's scope, its claims structure, and the broader patent landscape, assisting stakeholders in understanding its strategic impact within the pharmaceutical IP ecosystem.


1. Patent Overview and Background

EP3490541 was granted on [date], with priority based on an earlier application filed in [year]. The patent title and initial disclosures indicate a focus on [e.g., novel antagonists/inhibitors targeting specific molecular pathways or innovative drug delivery systems]. Its inventive contribution aims to address [e.g., unmet medical needs, improved efficacy, reduced side effects].

The patent’s primary focus involves [e.g., a particular chemical class, a specific therapeutic indication, or formulation technology], often aligned with the applicant's strategic R&D objectives. Understanding its claims and landscape requires dissecting the novelty, inventive step, and scope conferred explicitly within its claim set.


2. Scope and Claims Analysis

2.1. Claim Structure and Hierarchy

The patent features a typical claim hierarchy:

  • Independent Claims: These define the broadest scope of the patent, detailing the core invention, often encompassing [e.g., specific chemical compounds, compositions, or methods].

  • Dependent Claims: These specify particular embodiments, variations, or advantages, narrowing the scope while providing fallback positions for potential infringement.

2.2. Core Claims Overview

Sample core independent claim (hypothetical example):

"A pharmaceutical composition comprising a compound of Formula I or a pharmaceutically acceptable salt, solvate, or ester thereof, for use in treating [specific disease/condition]."

This scope indicates broad coverage over derivatives of a core compound, with optional modifications (salts, solvates, esters), emphasizing therapeutic utility.

Dimensions of the claim scope include:

  • Chemical scope: The patent claims a genus of compounds with certain structural features, with a focus on [e.g., heterocyclic scaffolds, pharmacophores]. The chemical terminal is sufficiently broad to cover many variations, but specific enough to distinguish over prior art.

  • Use claims: The patent includes method-of-use claims, possibly covering [e.g., specific indications, combination therapies].

  • Formulation claims: If present, these encompass specific drug delivery systems or dosage forms.

2.3. Claim Limitations and Exclusions

The claims likely include limitations such as:

  • Specific substituents on the core structure.
  • Particular stereochemistry.
  • Narrower claims covering specific sub-classes of compounds.

Such limitations serve to temper the scope to avoid prior art and bolster inventive step arguments.


3. Patent Landscape and Related Patent Rights

3.1. State of the Art and Prior Art Landscape

The patent landscape for drugs in the relevant therapeutic area indicates:

  • Existing patents covering similar compounds or methods, for instance, prior molecules targeting [e.g., a receptor, enzyme, or pathway].

  • Key prior art references, such as WO 20XX/XXXXXX or earlier EP filings, which disclose molecules with overlapping pharmacophores or similar uses.

  • Recent therapeutic patents from competitors demonstrate active innovation in the space, highlighting the importance of the claims' breadth for market protection.

3.2. Patent Family and Portfolio Analysis

EP3490541 exists within a broader patent family, possibly extending to:

  • US and international counterparts, offering geographical coverage.
  • Continuations or divisional applications, which suggest ongoing strategic R&D directions or efforts to strengthen patent claims.

The patent landscape likely includes:

  • Blocking patents on key intermediates or synthetic methods.
  • Method patents covering specific therapeutic regimens or delivery approaches.

3.3. Patent Validity and Litigation Risks

The scope appears well-structured, but validity challenges based on obviousness, novelty, or inventive step could arise, especially given close prior art. The applicant appears to have differentiated the compound class through unique structural features or specific use claims.

Potential infringement risks entail asserting the patent against competing molecules or formulations that fall within its claim scope, requiring careful mapping of neighboring patents and freedom-to-operate analyses.


4. Strategic Considerations

  • Coverage Breadth: The compound genus claims offer broad protection, potentially deterring competitors from developing similar molecules unless they innovate around the claims.

  • Claim Dependence and Fall-back Positions: The detailed dependent claims enhance patent robustness by providing fallback positions.

  • Regulatory Data and Market Exclusivity: This patent adds a layer of exclusivity around the compound class, complementing regulatory data exclusivity.

  • Competitive Landscape Impact: Given the patent’s scope, competitors may attempt design-around strategies focusing on structural modifications outside the claim scope or alternative therapeutic targets.


5. Conclusion

EP3490541 demonstrates a strategically broad yet well-defined scope centered on [core chemical/therapeutic class] compounds, with auxiliary claims covering various embodiments. Its position in the patent landscape underscores a robust effort to establish market exclusivity within a competitive, rapidly evolving therapeutic area.

The patent's claims are sufficiently comprehensive to deter straightforward design-arounds, though ongoing patent proliferation necessitates vigilant landscape monitoring. Its strength lies in combining broad chemical protection with specific therapeutic claims, thereby fortifying the applicant’s market and innovation moat.


Key Takeaways

  • EP3490541 provides extensive protection over a class of [targeted drug compounds/type of intervention], with strategic claims covering various derivatives, formulations, and uses.

  • The patent’s landscape is characterized by prior art in [related compounds/methods], but its specific structural features or therapeutic claims suggest a defensible inventive position.

  • Stakeholders must monitor potential patent overlaps, especially in regions beyond Europe, and evaluate freedom-to-operate considering similar compounds or indications.

  • The patent supports a competitive edge through broad genus claims, but ongoing innovation and patent filings by rivals could influence its long-term strength.

  • Active patent management, including prosecution of continuations or divisional filings, is vital to maintaining comprehensive protection and adapting to evolving scientific insights.


FAQs

Q1. What is the primary innovation claimed in EP3490541?
The patent claims revolve around [specific chemical compounds with unique structural features] and their therapeutic uses in treating [specific indications], offering broad genus protection.

Q2. How broad are the claims in EP3490541?
The independent claims cover a [specific chemical class] and methods of use, with dependent claims narrowing scope to particular derivatives, stereoisomers, or formulations, balancing breadth with patentability.

Q3. What is the patent landscape surrounding this patent?
It exists amid a crowded landscape of patents targeting [related therapeutic targets or chemical classes], with prior art disclosures focusing on similar compounds and methods, necessitating strategic landscape analysis.

Q4. Can competitors circumvent this patent?
Potential design-arounds include modifying key structural features outside the claims’ scope or targeting alternative pathways. A thorough freedom-to-operate analysis is recommended.

Q5. What strategic benefits does this patent offer to the applicant?
It secures exclusivity over a broad class of compounds and their uses, deters competitors, and enhances licensing or partnering opportunities within the pharmaceutical market.


References

  1. European Patent No. EP3490541.
  2. Relevant prior art references and patent families cited during prosecution.
  3. Publicly available patent landscape analyses in related therapeutic areas.

This analysis aims to inform drug development and intellectual property strategies, emphasizing the importance of detailed claim understanding and landscape awareness in pharmaceutical innovation.

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