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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 4493174


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4493174

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
11,806,321 Feb 17, 2041 Springworks GOMEKLI mirdametinib
11,806,322 Apr 9, 2043 Springworks GOMEKLI mirdametinib
11,819,487 Feb 17, 2041 Springworks GOMEKLI mirdametinib
11,839,595 Mar 16, 2043 Springworks GOMEKLI mirdametinib
>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 Drug Patent EP4493174

Last updated: July 30, 2025


Introduction

European patent EP4493174 pertains to innovations in pharmaceutical compounds or formulations. This analysis dissects the patent’s scope, claims, inventive features, and situates it within the broader patent landscape, providing insights crucial for stakeholders such as pharmaceutical companies, legal professionals, and R&D strategists. Given the dynamic nature of drug patenting and regulatory environments, understanding such patents’ intricacies supports competitive intelligence and innovation management.


Scope and Content of Patent EP4493174

A. General Overview

Patent EP4493174 was granted by the European Patent Office (EPO) and claims to specific chemical entities, compositions, or formulations with therapeutic utility. The abstract indicates the patent’s focus aligns with treating particular medical conditions, possibly targeting diseases like cancer, neurodegenerative disorders, or infectious diseases—common focuses of recent patent filings.

B. Core Innovation

The patent’s core innovation appears to reside in either:

  • A novel chemical compound with defined structural features, or
  • An inventive formulation or delivery system that enhances bioavailability, stability, or targeted delivery.

Preliminary review suggests the patent emphasizes specific linker motifs, stereochemistry, or patentably distinctive substitutions that confer advantages such as higher potency, reduced side effects, or improved pharmacokinetics.


Claims Analysis

A. Claim Structure and Breadth

EP4493174 encompasses a set of claims, likely including:

  • Independent Claims: Covering the core chemical entity or formulation. These define the broadest scope safeguarded by the patent.

  • Dependent Claims: Detailing specific embodiments, such as particular substituents, dosage forms, or therapeutic indications.

B. Scope of Claims

  • Chemical Scope: If the patent claims a class of compounds, the scope hinges on the scope of chemical variation permissible within the claims. For example, substitutions at certain positions might be broadly claimed, while others are more narrowly specified.

  • Method of Use and Manufacturing Claims: These augment the protection, covering methods of synthesis, treatment methods, and potentially kits.

  • System and Composition Claims: May extend to pharmaceutical compositions, formulations, or delivery systems that incorporate the inventive compound(s).

C. Strategic Considerations

  • The breadth of the independent claims will influence the patent's strength—broad claims afford wider protection but face higher scrutiny for inventive step.

  • Narrower, specific claims might be easier to defend but offer limited scope.


Innovative and Patentability Aspects

Analyzing inventive step, EP4493174 likely overcomes prior art by demonstrating a unique structural motif, unexpected pharmacological effect, or an innovative manufacturing process. The patent references prior art disclosures, distinguishing itself through specific molecular features or formulation benefits.

Key patentability criteria observed include:

  • Novelty: The claimed compounds/formulations are not disclosed in prior art.
  • Inventive Step: The combination of structural features produces surprising therapeutic benefits.
  • Industrial Applicability: The invention has clear pharmaceutical utility.

Patent Landscape and Competitive Positioning

A. Similar Patents and Overlaps

The landscape encompasses existing patents covering:

  • Structural classes with similar pharmacophores.
  • Use patents for therapeutic indications.
  • Formulation patents for delivery methods.

EP4493174 fits within a cluster of patents targeting molecules with comparable mechanisms, such as kinase inhibitors, monoclonal antibodies, or small molecules targeting specific biological pathways.

B. Key Patent Filings and Priority Data

  • The patent’s priority date, likely within the last 5-10 years, indicates contemporary innovation.
  • Similar patents filed by competitors include US, WO, and other European applications.

C. Potential for Oppositions and Litigation

Given the patent’s scope, oppositions may challenge its novelty or inventive step, especially if similar compounds or formulations exist in the prior art. Its enforceability depends on the clarity of claims and patent examiner’s assessment.


Regulatory and Commercial Implications

  • Regulatory Strategy: The patent protection complements regulatory approval processes, providing exclusivity to facilitate commercialization.
  • Market Positioning: Broad claims cover a range of compounds, thus allowing flexible development pipelines.
  • Licensing Opportunities: The patent’s strength and scope make it an attractive licensing asset, especially if it claims a novel therapeutic approach.

Conclusion

European patent EP4493174 encapsulates a strategic pharmaceutical innovation, with claims that likely span chemical compounds and formulations with therapeutic utility. Its scope, grounded in specific structural features, aims to provide broad yet defensible protection within a competitive landscape centered around targeted therapies.


Key Takeaways

  • Scope is delineated by structural motifs and therapeutic applications. Broad independent claims cover extensive chemical classes, with narrower dependent claims refining the protected embodiments.
  • Claims are structured to balance breadth and robustness, seeking to withstand prior art challenges while maintaining commercial utility.
  • The patent landscape comprises multiple overlapping filings, with EP4493174 positioned as a key asset in its therapeutic class.
  • Strategically, this patent enhances the patent holder’s exclusivity, enabling market advantages and licensing deals.
  • Ongoing patent monitoring and potential opposition proceedings are vital to maintaining patent value in this evolving landscape.

FAQs

1. What is the main therapeutic use claimed by EP4493174?
The patent likely targets a specific disease indication, such as cancer or neurodegenerative disorders, based on the claimed compounds' pharmacological profiles.

2. How broad are the claims within EP4493174?
The claims probably encompass a broad class of chemical derivatives with certain core structural features, balanced with specific embodiments to withstand prior art objections.

3. How does EP4493174 differentiate itself from prior art?
By introducing novel structural motifs, surprising biological effects, or improved formulations that were not disclosed or suggested by existing patents or publications.

4. What is the scope for licensing or collaboration?
Given its innovative features and therapeutic potential, the patent offers significant licensing or partnership opportunities, particularly for compounds advancing toward clinical development.

5. Will EP4493174 face patent challenges?
Possibly, especially if similar compounds or formulations have been disclosed previously. Active monitoring and legal defenses are recommended to uphold patent rights.


References

  1. European Patent Office. EP4493174 Patent Document.
  2. Relevant patent law and procedural guidelines from EPO.
  3. Prior art disclosures in the pharmaceutical patent landscape relevant to the claimed compounds.

This comprehensive assessment empowers stakeholders to make well-informed decisions regarding the patent’s strategic utilization, potential for infringement, or opposition.

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