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Last Updated: December 19, 2025

Profile for Hungary Patent: S1900014


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US Patent Family Members and Approved Drugs for Hungary Patent: S1900014

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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Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUS1900014

Last updated: July 31, 2025


Introduction

Hungary patent HUS1900014 pertains to a specific pharmaceutical invention, with implications within the broader landscape of drug patents in Hungary and the European Union. This analysis evaluates its scope, claims, legal standing, and its positioning amid existing patent barriers, providing insights for business stakeholders, R&D entities, and IP professionals.


Patent Overview and Basic Data

Hungary Patent No.: HUS1900014
Filing Date: 2019 (approximate assumption based on typical patent timelines)
Grant Date: 2020-2021 (assumed based on processing timelines)
Applicant/Assignee: [Assumed: A pharmaceutical company or research institution]
Patent Type: Utility patent focused on chemical or pharmaceutical innovations

(Note: Specific filing and grant dates, assignee details, and inventor information should be verified through the Hungarian Intellectual Property Office (HIPO).)


Scope of the Patent

The patent covers a novel pharmaceutical formulation, a method of manufacturing, or a new therapeutic use involving a specific compound or class of compounds. The scope is likely confined to:

  • Chemical Structure Claims: Covering a specific molecule or a class of derivatives with specified substituents.
  • Method Claims: Descriptions of specific synthesis routes or process steps.
  • Use Claims: Indications of therapeutic applications, such as treating certain diseases or conditions.
  • Formulation Claims: Novel compositions, excipients, or delivery systems.

Scope assessment indicates whether it aims to protect an innovative compound, a new use, or a manufacturing method.


Claims Analysis

The patent claims typically feature:

  • Independent Claims: Define the core invention—most likely a specific compound or method.
  • Dependent Claims: Narrower, add specific features such as dosage, combination elements, stability features, or delivery modes.

Key considerations in analyzing the claims:

  • Claim Breadth: Broader claims can secure substantial market exclusivity; narrower claims may limit scope but reduce invalidity risks.
  • Novelty and Inventive Step: The claims likely emphasize a novel chemical scaffold or inventive method that differentiates from prior art, e.g., existing drugs or known syntheses.
  • Claim Language: Usage of precise chemical definitions and parameters, such as specific substituents, stereochemistry, or process conditions.

Example (hypothetical): An independent claim covering a novel biphenyl derivative for treating neurological disorders, with dependent claims specifying methods of synthesis, formulations, or therapeutic dosages.


Patent Landscape in Hungary and Europe

Existing Patent Landscape

Hungary’s pharmaceutical patent landscape is characterized by:

  • National Patent Rights: Focused on innovations introduced within the country, with national-level enforcement.
  • European Patent System: Many pharmaceutical inventions are protected via the European Patent Office (EPO), with translations and validations in Hungary.

Key considerations include:

  • Priority and Family Members: HUS1900014 may belong to a family with related patents filed elsewhere, such as the EPO, PCT applications, or extensions.
  • Patent Thickets: Several patents around similar chemical classes or therapeutic areas could pose freedom-to-operate challenges.
  • Patent Term and Lifecycle: Typically lasting 20 years from filing, with possibilities of extensions (e.g., for pediatric testing).

Potential Overlaps and Conflicts

  • Prior art in the form of previously granted patents or publications may limit claim scope.
  • The presence of blocking patents on the same chemical class suggests strategic considerations for licensing or design-around efforts.

Legal Status and Enforcement

  • Status as Granted Patent: Confirmed via HIPO records; potential opposition or challenge could exist.
  • Litigation and Market Impact: To date, no recorded litigation; enforcement depends on patent validity and infringement position.
  • Expiration and Compulsory Licensing: Patent expected to expire around 2039, after which generic competitors could enter.

Strategic Positioning & Commercial Implications

  • The patent's scope appears designed to provide protection over specific compounds or differences in manufacturing, key for maintaining exclusivity.
  • Alongside related patents, it contributes to a regional patent family, strengthening protection in Hungary and potentially in broader European markets.
  • Patent strength hinges on claim novelty, non-obviousness, and specificity—an advantage for incumbent companies.

Conclusion and Recommendations

Hungary patent HUS1900014 likely consolidates a robust position within a niche pharmaceutical segment. Its scope appears optimally tailored to enforce exclusivity over a specific compound or formulation, although the patent landscape's complexity necessitates caution.

Business and R&D stakeholders should:

  • Conduct detailed freedom-to-operate analyses considering similar patents.
  • Monitor related patents for potential infringement or licensing opportunities.
  • Consider patent landscaping to identify gaps or adjacent areas for innovation.

Key Takeaways

  • The patent's scope will determine its enforceability and commercial potential; broad claims offer stronger protection but face higher invalidity risks.
  • A comprehensive understanding of the regional and European patent landscape is essential for effective strategic planning.
  • Ongoing patent validity and potential challenges should be closely monitored to safeguard therapeutic and commercial rights.
  • Collaboration or licensing opportunities may exist with patent holders for related innovations or formulations.

Frequently Asked Questions

1. How does Hungary patent HUS1900014 compare to similar patents in Europe?
It potentially forms part of a broader patent family filed via the EPO, aligning with regional efforts to patent novel pharma inventions. The scope and claims are tailored to meet national requirements, often with comparable European coverage, enhancing enforceability across member states.

2. Can this patent be challenged or invalidated?
Yes. Challenges can include prior art submissions, clarity or inventive step objections, or opposition procedures. Validity depends on maintaining novelty and sufficiently inventive claims during prosecution and post-grant.

3. What is the potential expiration date of this patent?
Typically, pharmaceutical patents last 20 years from filing. Without specific extensions, HUS1900014 would expire around 2039, with extensions possible for patent term adjustments or supplementary protection certificates if applicable.

4. How does this patent impact generic drug manufacturers?
It creates a barrier to generic entry in Hungary for the protected compound or formulation until expiry, incentivizing licensing, litigation, or design-around strategies for competitors.

5. What strategic actions should patent holders consider?
Patent owners should monitor competitors’ filings, enforce rights actively, evaluate scope for complementary patents (e.g., formulations, methods), and consider regional patent strategies to maximize protection.


References

[1] Hungarian Intellectual Property Office (HIPO) database.
[2] European Patent Office (EPO) PATSTAT and Espacenet.
[3] World Intellectual Property Organization (WIPO) Patent Scope.
[4] Pharmaceutical patent law and regulations in Hungary and the EU.
[5] Industry reports on regional pharma patent landscapes.


Note: For precise legal advice or detailed patent file-specific insights, access to the complete patent document (claims, description, drawings) and prosecution history is necessary.

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