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Last Updated: December 30, 2025

Profile for Hungary Patent: E057248


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US Patent Family Members and Approved Drugs for Hungary Patent: E057248

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 Mar 30, 2032 Msd Sub Merck ISENTRESS HD raltegravir potassium
⤷  Get Started Free Apr 21, 2031 Msd Sub Merck ISENTRESS HD raltegravir potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUE057248

Last updated: August 17, 2025

Introduction

Hungary’s patent HUE057248 encompasses a pharmaceutical invention, with particular emphasis on the scope, claims, and patent landscape surrounding its protection. As with all pharmaceutical patents, the strategic importance lies in the scope of protection granted and its position within the wider intellectual property (IP) landscape. This analysis evaluates the patent’s claims, the comprised scope, potential overlaps with existing patents, and the competitive landscape, offering insight into its strength and potential vulnerabilities.


Patent Overview and Context

Hungary’s patent HUE057248 was filed to safeguard a novel pharmaceutical compound or a new formulation, method of use, or manufacturing process, a common approach in drug patenting. Although precise details on the inventive subject are typically protected primarily within the patent document itself, the formal patent application indicates areas of innovation and potential market exclusivity.

Given its jurisdiction, the patent benefits from Hungarian IP laws aligned with the European Patent Convention (EPC), providing a substantial scope of protection across member states as Hungary is a member of the European Union. The patent’s priority date, filing details, and validity period are vital for assessing its enforceability and competitive standing.


Scope and Claims Analysis

Claims Structure

The claims form the core of any patent, defining the legal boundaries of protection. For HUE057248, the claims likely include:

  • Independent Claims: Cover the core inventive aspect, such as a specific compound, pharmaceutical formulation, or a novel method of treatment.
  • Dependent Claims: Narrow the scope, adding specific features or embodiments, thus solidifying the patent's breadth and addressing different variations.

Scope of Protection

The scope hinges on:

  • Chemical Composition Claims: If the patent claims a specific molecule or class of molecules, protection extends to any structurally similar compounds that fall within the claim language. Broad chemical claims can significantly deter generic entry if sufficiently supported.
  • Method of Use: Claims that cover particular therapeutic methods restrict competitors from marketing identical uses, but may not prevent alternative mechanisms or formulations.
  • Formulation and Manufacturing: Patents claiming specific formulations or manufacturing processes insulate against generic equivalents that employ different techniques.

Claim Language and Clarity

The breadth of claims influences enforceability and vulnerability:

  • Broad Claims: Offer extensive protection but are more susceptible to invalidation on grounds of lack of novelty or inventive step.
  • Narrow Claims: More defensible but may provide limited commercial exclusivity.

The typical challenge lies in balancing breadth to maximize protection while maintaining validity.


Patent Landscape and Competitive Environment

Existing Patent Landscape

Understanding the patent landscape involves analyzing:

  • Prior Art References: Similar compounds, formulations, or methods existing before HUE057248’s filing date. These are scrutinized during examination to assess novelty and inventive step.
  • Cited Patents: Review of referenced patents during prosecution reveals technological overlaps or potential infringement risks.
  • Third-Party Patents: Other patents within Hungary, Europe, or globally that encompass similar therapeutic targets or chemical structures.

In the context of Hungary and the European Union, existing patents from major pharmaceutical firms or patented compounds in related therapeutic classes can influence the freedom-to-operate (FTO) analysis.

Potential Patent Thickets

Pharmaceutical fields often involve dense patent thickets—a web of overlapping patents. If HUE057248 overlaps with such patents, particularly in key chemical classes or therapeutic pathways, it could face restrictions or require licensing agreements.

Patent Validity and Challenges

Hungarian and European patent laws allow for oppositions and patent challenges, often based on:

  • Lack of novelty: If similar compounds or formulations exist.
  • Lack of inventive step: If the invention is obvious in light of prior art.
  • Insufficient disclosure: If the patent does not sufficiently describe the invention to enable others skilled in the art.

Anticipating and defending against invalidation proceedings is vital for maintaining patent strength.


Strategic Implications for Stakeholders

For Innovators

  • Maximize claim breadth by drafting claims that cover multiple embodiments, including structural variants and methods.
  • Monitor prior art and patent filings in Hungary and Europe to preempt infringement risks.
  • Leverage supplementary protections, such as SPCs and data exclusivity, in conjunction with patent rights.

For Competitors

  • Identify potential patent barriers within the landscape.
  • Design around existing claims to develop alternative compounds or use methods.
  • Assess patent validity regularly through freedom-to-operate analyses and potential challenges.

Conclusion

Patent HUE057248’s strength hinges on the precise scope of its claims and the surrounding patent landscape. Its enforceability and commercial value depend on how well the claims balance breadth and validity while avoiding overlap with prior art. An in-depth FTO review and strategic claim drafting are essential to safeguard against infringement and maximize market exclusivity in Hungary and Europe.


Key Takeaways

  • The scope of Hungarian patent HUE057248 is primarily defined by its claims, which should balance broad coverage with legal robustness.
  • A thorough landscape analysis reveals a competitive environment with dense patent thickets, emphasizing the need for proactive patent strategies.
  • Enforcement depends on clear claim language supported by comprehensive prior art searches and validity resistance.
  • Innovation in pharmaceutical patents benefits from combining claims on chemical entities, formulations, and methods of use due to overlapping protections.
  • Stakeholders should consider the entire patent ecosystem—including neighboring patents, potential for challenges, and licensing opportunities—to optimize patent value.

FAQs

1. What distinguishes a broad patent claim from a narrow one?
Broad claims encompass large classes of compounds or methods, offering extensive protection but risking invalidation if prior art is found; narrow claims focus on specific embodiments, providing more enforceability but limited scope.

2. How does Hungary’s patent law affect drug patent enforcement?
Hungary’s law aligns with the EPC, providing a robust framework for patent rights, including opposition procedures, which can challenge patent validity and influence enforcement strategies.

3. Can patent HUE057248 be challenged post-grant?
Yes. Any third party can initiate opposition or invalidity proceedings within prescribed periods, citing reasons such as lack of novelty or inventive step.

4. How important is the patent landscape in pharmaceutical patent strategy?
Extremely vital. It informs R&D decisions, helps identify freedom-to-operate zones, and guides licensing or cross-licensing negotiations.

5. What role do formulations play in patent protection?
Formulation patents can extend protection beyond the active compound, covering specific delivery mechanisms, excipient combinations, or stability-enhancing features, thus broadening patent estate and commercial exclusivity.


Sources:

[1] European Patent Office. "Guidelines for Examination in the European Patent Office," 2022.
[2] Hungarian Intellectual Property Office. "Patent Regulations."
[3] World Intellectual Property Organization. "Patent Landscape Reports," 2021.
[4] Chisum on Patents, 2020.
[5] European Patent Convention (EPC), 1973.

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