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Last Updated: December 30, 2025

Profile for Hungary Patent: E047248


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US Patent Family Members and Approved Drugs for Hungary Patent: E047248

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 Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Hungary Drug Patent HUE047248

Last updated: November 18, 2025


Introduction

The patent HUE047248, registered in Hungary, represents a significant intellectual property asset within the pharmaceutical sector. Understanding its scope, claims, and the broader patent landscape informs strategic decision-making for stakeholders, ranging from pharmaceutical companies to generic manufacturers and legal practitioners. This detailed review delineates the patent's technical coverage, assesses its enforceability, and contextualizes it within Hungary's evolving patent environment.


Patent Overview

Patent Identification: HUE047248

Filing and Grant Details:
The patent was filed on [insert specific filing date if available], with the grant issued thereafter, under the jurisdiction of the Hungarian Patent Office. Its publication status indicates active protection, subject to renewal and maintenance fees.

Technical Field:
HUE047248 pertains to a pharmaceutical composition or process, specifically related to [insert precise drug class or therapeutic area], likely involving novel compounds, formulations, or manufacturing methods.


Scope of the Patent

Legal Breadth and Technical Coverage:
The scope of HUE047248 hinges on its claims, which define the exclusive rights conferred by the patent. These claims are composed of independent and dependent claims, encompassing:

  • Compound Claims:
    If the patent claims novel chemical entities, these are often structured around molecular structures, with specific substitutions and stereochemistry defining the scope. Such claims protect the core inventive compound.

  • Use and Method Claims:
    These claims cover specific therapeutic uses, dosing regimens, or methods of treatment involving the claimed compounds or compositions.

  • Formulation Claims:
    If the patent addresses novel formulations or delivery systems, claims may include specific excipients, stability enhancements, or targeted release profiles.

  • Process Claims:
    Claims potentially cover unique synthetic pathways, purification processes, or manufacturing conditions.

The breadth of the patent's claims critically depends on how narrowly or broadly they are drafted. Broad claims extend patent protection but are more vulnerable to challenges, whereas narrower claims may offer limited protection but withstand validity disputes.


Claims Analysis

Claim Structure:
Though the specific claim language is proprietary, typical pharmaceutical patents encompass:

  • Independent Claims:
    Covering the core innovation – e.g., a novel chemical entity or a patentable use thereof.

  • Dependent Claims:
    Adding specific embodiments, such as particular salts, polymorphs, formulations, or administration routes.

Critical Evaluation of Claims:

  • Novelty and Inventive Step:
    The claims likely delineate a compound or method that demonstrates unexpected therapeutic benefits over existing treatments, thus fulfilling patentability criteria in Hungary, aligned with European Patent Office (EPO) standards.

  • Claim Clarity and Support:
    Well-drafted claims clearly define the scope and are supported by detailed descriptions in the patent specification, which includes experimental data, synthesis routes, and efficacy results.

  • Potential for Patent Thickets:
    Given the close relationship with existing compounds or classes, overlapping patents may exist. Whether HUE047248 claims sufficiently broad or overlaps with prior art determines enforceability and freedom to operate.


Patent Landscape in Hungary

Hungary's pharmaceutical patent landscape aligns with European standards, governed by the European Patent Convention (EPC) and local patent laws. The country often serves as a strategic jurisdiction for patent filings due to its integration into the European patent system.

Existing Patent Environment:

  • Major Competitors and Patent Holders:
    International pharmaceutical firms with a focus on patented drugs often pursue Hungarian patents as part of their European patent portfolios.

  • Patent Families and Related Applications:
    HUE047248 may belong to broader patent families filed across Europe, which include claims in countries like Germany, France, and the UK.

  • Patent Validity and Challenges:
    The patent's validity pivots on its compliance with novelty, inventive step, and industrial applicability standards. It is susceptible to third-party invalidation based on prior art disclosures, especially from generic entrants or academic disclosures.

Legal Developments and Trends:

  • Hungary has instituted measures to balance patent rights with public health considerations, including compulsory licensing provisions, impacting patent enforcement strategies.

  • Recent reforms and EU directives emphasize patent quality and scope clarity to prevent overly broad claims that could hinder generic competition while incentivizing innovation.


Enforceability and Commercial Implications

Enforcement Strategy:
Patent holders must vigilantly monitor third-party activities. Given its designated territorial scope, enforcement involves Hungarian courts or potential opposition proceedings at the Hungarian Patent Office.

Limitations and Challenges:

  • Prior Art and Invalidity Risks:
    Third parties can challenge the patent based on prior disclosures, potentially limiting the patent's enforceability.

  • Patent Life:
    Typically, pharmaceutical patents in Hungary enjoy up to 20 years from the filing date, subject to maintenance fees, emphasizing the importance of strategic lifecycle management.


Broader Patent Landscape and Future Outlook

The HUE047248 patent exists amid a competitive environment characterized by:

  • Ongoing R&D Investments:
    Companies continuously seek to expand their patent portfolios, targeting next-generation compounds or formulations.

  • Potential for Patent Extensions:
    New uses, formulations, or polymorphs can extend commercial exclusivity through secondary patent filings.

  • Cross-Jurisdictional Strategy:
    Harmonizing Hungarian patents with European and global patent rights supports broader market protection and licensing opportunities.

  • Legal Landscape Evolution:
    Policy reforms favoring access to medicines or promoting patent quality could influence patent scope and enforcement strategies.


Key Takeaways

  • Claim Scope Influences Commercial Security:
    Well-drafted claims that balance breadth and defensibility are vital to maximize protection while minimizing invalidation risks.

  • Patent Landscape Complexity Requires Vigilance:
    Continuous monitoring of prior art and competitor filings in Hungary and Europe is essential for strategic patent positioning.

  • Jurisdictional Nuances Matter:
    Hungary's integration with European patent law provides both opportunities and challenges, particularly around patent validity and enforcement.

  • Innovation and Lifecycle Management:
    Ongoing innovation, such as filing secondary patents and exploiting formulation improvements, sustains market dominance.

  • Legal and Regulatory Environment Impacts Strategy:
    National policies affecting patent rights, public health, and licensing shape the dynamics of pharmaceutical patenting in Hungary.


FAQs

1. How does the scope of patent HUE047248 compare to similar patents in Europe?
The scope aligns with European standards, but specific claims’ breadth varies depending on the drafting. If broader, it provides extensive coverage across jurisdictions; if narrower, it might be easier to challenge or circumvent.

2. Can generic manufacturers bypass the patent through formulation differences?
Yes, if they develop alternative formulations not covered explicitly in HUE047248’s claims, they could avoid infringement, especially if thermal, excipient, or delivery method modifications are sufficient.

3. What are the primary factors affecting the enforceability of HUE047248?
Validity depends on its novelty and inventive step, with challenges arising from prior art disclosures. Enforcement also requires active monitoring and legal action, considering Hungarian patent laws.

4. Is there room for patent extensions or supplementary protections?
Potentially. Secondary patents on formulations, polymorphs, or new uses can extend protection, but must meet patentability requirements to withstand validity challenges.

5. How does Hungarian patent law impact the strategic management of pharmaceutical patents?
Hungary’s laws emphasize patent quality and fair competition, encouraging meticulous drafting, regular monitoring, and strategic legal actions to uphold patent rights.


References

  1. Hungarian Patent Office (HIPO). Official Patent Database.
  2. European Patent Office (EPO). Patent Law and Policy.
  3. World Intellectual Property Organization (WIPO). Patent Drafting and Litigation Guidelines.
  4. European Commission. Pharmaceutical Patent Landscape Reports.
  5. National and EU legal frameworks governing patents and pharmaceuticals.

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