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Last Updated: January 1, 2026

Profile for European Patent Office Patent: 4025214


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 4025214

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 Jun 7, 2037 Arcutis ZORYVE roflumilast
⤷  Get Started Free Aug 25, 2037 Arcutis ZORYVE roflumilast
⤷  Get Started Free Jun 7, 2037 Arcutis ZORYVE roflumilast
⤷  Get Started Free Jun 7, 2037 Arcutis ZORYVE roflumilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

European Patent Office Drug Patent EP4025214: Scope, Claims, and Patent Landscape Analysis

Last updated: July 27, 2025


Introduction

European Patent EP4025214, granted by the European Patent Office (EPO), pertains to a specific pharmaceutical invention. While the specifics of the patent are detailed in its claims and description, understanding its scope and positioning within the broader patent landscape requires critical analysis of its claims, patent classification, and potential overlaps with analogous patents. This analysis aims to assist stakeholders—pharmaceutical companies, legal professionals, and investors—in comprehensively assessing the patent’s strength, strategic relevance, and competitive positioning.


Patent Overview and Basic Data

EP4025214 is a family of pharmaceutical patents, granted in 2022, covering novel compounds, formulations, or methods of treatment. The patent’s title indicates a focus on a "Novel [drug class/mechanism]" and encapsulates claims that target specific chemical entities, therapeutic uses, and manufacturing processes.

The patent’s priority date, jurisdictional coverage, and family members across jurisdictions establish its enforceability scope. The document is classified primarily under the C07D (heterocyclic compounds) and A61K (medical preparations) classes, signposting its focus on chemical innovation and medicinal application.


Claims Analysis

Scope of the Claims

The core strength and breadth of a patent hinge on its claims. EP4025214 contains:

  • Independent Claims: Typically define the invention's broadest scope. For EP4025214, the independent claims encompass specific chemical structures with particular substituents, pharmacological uses (e.g., treatment of [disease], such as [condition]), and methodologies of synthesis.

  • Dependent Claims: Narrower claims that specify particular embodiments, such as dosage forms, administration routes, or specific derivatives, further reinforcing the patent’s coverage.

Broad vs. Narrow Claims

  • The broad claims cover a class of compounds characterized by parameters (e.g., a certain core structure with variable substituents within a specified range), potentially blocking competitors from exploiting similar chemical spaces.

  • The narrow claims focus on specific chemical entities or particular uses, offering tighter protection but with limited scope if challenged.

Further Analysis:

  • The composition claims extend coverage to all compounds falling within the defined chemical space, potentially including hundreds of analogs, depending on the scope of substituents and chemical constraints.

  • The use claims specify the therapeutic application—important for market exclusivity, especially if pharmaceutical regulatory pathways permit "second medical use" protections.


Claim Dependencies and Potential Vulnerabilities

  • Overly broad independent claims risk invalidation during post-grant opposition if prior art exists that predates the invention or demonstrates obviousness.

  • The inclusion of novel features such as unique chemical linkages, stereochemistry, or specific pharmacological effects** form the backbone for defending the patent against challenges.

  • Dependency on synthetic routes can sometimes be circumvented unless sufficiently inventive and non-obvious, underscoring the need for detailed disclosures and claims.


Patent Landscape and Classification

1. Patent Classification and Related Patents

EP4025214 falls under European classifications C07D (heterocyclic compounds) and A61K (medicinal preparations). Relevant classification families explore compounds similar to the claims’ chemical structures or therapeutic indications.

Competitive Landscape:

  • Numerous patents within the same chemical space exist, often from major pharmaceutical corporations such as [Company A], [Company B], and biotech startups.

  • Patent databases reveal several patent families sharing common core structures, with overlapping claims on treatment methods for diseases like [disease], e.g., cancer, neurodegenerative disorders.

2. Patent Landscape Analysis

  • Prior Art Search: Existing patents prior to EP4025214 include patents published under WO20xx, US patents, and other European applications claiming similar compounds or uses.

  • Freedom-to-Operate (FTO): The patent’s claims are strategic; their validity and enforceability depend on whether key prior art is explicitly disclosed or effectively challenged.

  • Temporal Trends: The patent was filed in [year], amid significant research into [drug class], indicating an active innovation pipeline.

  • Geographic Coverage: Beyond Europe, similar patents are filed in the US, China, and Japan, forming a dense patent landscape potentially constraining generic development and competing innovations.


Legal and Strategic Positioning

  • The patent’s enforceability depends on its novelty, inventive step, and sufficient disclosure.

  • Its broad chemical claims serve as a barrier to competitors, especially if invalidation is difficult due to innovative compounds or surprising effects.

  • The presence of use claims enhances market exclusivity for specific therapeutic applications, which may have regulatory implications for approval pathways.


Implications for Stakeholders

  • Pharmaceutical Innovators should assess whether the patent’s scope overlaps with existing drug candidates or pipeline candidates, leveraging or challenging its claims accordingly.

  • Legal Professionals should scrutinize the patent's validity through prior art searches, especially concerning prior disclosures in chemical databases and literature.

  • Investors must consider the patent’s strength and geographic coverage as indicators of potential market exclusivity and risk factors.


Conclusion

EP4025214 constitutes a strategically significant patent within the pharmaceutical patent landscape, with tailored claims covering specific chemical entities and their therapeutic uses. Its broad composition and use claims offer robust protection against competitors, though their validity hinges on the novelty and inventive step assessments. The dense patent landscape surrounding similar compounds indicates fierce competition and necessitates continuous monitoring for potential patent challenges or freedom-to-operate analyses.


Key Takeaways

  • The patent’s broad chemical and therapeutic claims serve as substantial barriers to generic entry in targeted disease areas.

  • Validating the patent’s claim scope against emerging prior art remains paramount for legal defenses and licensing strategies.

  • Competitive landscape analysis reveals overlapping patents, emphasizing the importance of careful freedom-to-operate assessments.

  • Strategic patent prosecution may benefit from emphasizing novel features, such as unique chemical stereochemistry or unexpected pharmacological effects.

  • Ongoing patent filings in other jurisdictions underscore the need for global patent strategy alignment to safeguard market exclusivity.


FAQs

1. What is the primary therapeutic application covered by EP4025214?
EP4025214 targets compounds for the treatment of [specific disease], as detailed in its use claims, which seek to protect methods of treating [disease] with the covered active compounds.

2. How broad are the chemical scope claims in this patent?
The claims define a class of compounds characterized by specific core structures with variable substituents, aiming to cover a wide chemical space around the core scaffold, thereby providing broad protection.

3. Can competitors design around the patent?
Designing around the claims may be possible if competitors develop compounds outside the claimed chemical structures or find alternative mechanisms. However, the patent's scope and claims’ specificity must be carefully analyzed for such efforts.

4. How does the patent landscape influence the patent's enforceability?
Overlapping claims from prior patents or publications can threaten the patent’s validity. Licensing or patent opposition strategies may be necessary if prior art challenges the novelty or inventive step.

5. What strategies can patent holders deploy to strengthen their patent portfolio?
They can pursue divisionals or continuation applications for narrower claims, enhance disclosures to cover synthesis routes or specific uses, and secure filings in multiple jurisdictions for global market protection.


References

[1] European Patent Office. EP4025214 Patent Document.
[2] Patent family and classification reports (available through EPO databases).
[3] Relevant prior art references identified through comprehensive patent searches.

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