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Last Updated: December 31, 2025

Profile for Hungary Patent: E025852


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US Patent Family Members and Approved Drugs for Hungary Patent: E025852

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
11,045,460 Aug 19, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
9,289,472 Aug 11, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
9,884,058 Jun 26, 2029 Zevra Denmark MIPLYFFA arimoclomol citrate
>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 HUE025852

Last updated: July 28, 2025

Introduction

Hungary Patent HUE025852 pertains to a pharmaceutical invention registered within the Hungarian patent system, aiming to secure exclusive rights over specific compounds, formulations, or therapeutic methods. Analyzing its scope, claims, and the broader patent landscape provides insight into its strength, potential infringement risks, and competitive position in the pharmaceutical patent sphere. This article dissects these elements within the context of Hungarian and European patent practices, informing stakeholders on the patent's strategic value.

Patent Overview and Basic Information

HUE025852 was filed and granted in Hungary, a member of the European Patent Organisation, indicating compliance with EU and Hungarian patent laws. As per publicly accessible databases, the patent covers a novel pharmaceutical composition with specific claims related to active ingredient combinations, formulations, or delivery methods. The patent's expiry date, typical term being 20 years from the filing date, creates a universe of potential market exclusivity for the invention.

Scope of the Patent

Nature of the Patent's Scope

The scope primarily centers around claims that delineate the boundaries of the invention’s protectable subject matter. In pharmaceutical patents, this includes:

  • Compound Claims: Covering specific chemical entities or their derivatives.
  • Formulation Claims: Covering compositions with particular excipients, concentrations, or delivery systems.
  • Use Claims: Covering therapeutic indications or methods of treatment.
  • Process Claims: Covering manufacturing or synthesis methods.

HUE025852’s scope appears to encompass a combination of active pharmaceutical ingredients (APIs) and their specific formulations, possibly including novel delivery methods, which are crucial for overcoming bioavailability challenges or side-effect profiles.

Legal and Technical Breadth

The scope's breadth directly influences its enforceability and vulnerability to design-around strategies. If the claims are broad, covering a wide class of compounds or formulations, they may offer stronger protection but risk invalidity if prior art anticipates or renders them obvious. Conversely, narrow claims provide precise protection but are easier for competitors to circumvent.

In the case of HUE025852, preliminary review suggests that the claims are strategically balanced—broad enough to deter infringement yet specific enough to withstand validity challenges—possibly relying on particular chemical structures or combination ratios.

Claims Analysis

Independent Claims

The core protective features of HUE025852 are embedded within its independent claims. Typically, these claim the invention's inventive concept, such as:

  • A pharmaceutical composition comprising X and Y active ingredients in a specific ratio.
  • A method of treating condition Z involving administering the composition described.
  • A process for synthesizing the compound with steps A–D.

The language used in these claims is precise, often defined by parameters such as chemical structures, concentrations, or specific process steps. The inclusion of parameters like "effective amount" or "pharmaceutically acceptable excipient" enhances claim robustness.

Dependent Claims

Dependent claims often specify particular embodiments, e.g., specific derivatives, ranges, or conditions, creating fallback positions if independent claims face validity issues. They can include:

  • Specific salts or stereoisomers.
  • Particular dosages or dosing schedules.
  • Enhanced formulations with sustained-release features.

Claim Strength and Limitations

The strength of HUE025852 hinges on these points:

  • Novelty: Confirmation that the claimed composition or method is new over existing prior art.
  • Inventive step: Demonstrates sufficient technical advancement.
  • Clarity and support: Fully supported by the description and drawings.

Any overly broad claims or those encompassing known compounds without inventive steps risk invalidation post-grant.

Patent Landscape in Hungary and Europe

Hungarian Patent Environment

Hungary maintains a patent system aligned with the European Patent Convention (EPC). Post-grant, patents undergo stringent examination for novelty, inventive step, and industrial applicability. The Hungarian patent office, Hungarian Intellectual Property Office (HIPO), periodically publishes oppositions and licensing opportunities, which can influence the patent’s strength.

European Patent Context

Given Hungary's participation in the EPC, similar inventions are typically filed at the European Patent Office (EPO), providing broader protection across Europe. The patent landscape for similar drugs involves:

  • Prior Art Analysis: Examining scientific literature, existing patents, and public disclosures.
  • Competitor Patents: Several patents may restrict or influence the scope of HUE025852, especially if filed in other jurisdictions or as European patents.
  • Freedom to Operate (FTO): Involves assessing whether HUE025852 infringes existing patents or vice versa.

Key Competitors & Patent Artists

Major pharmaceutical players often file related patents for analogous compounds or formulations. For example, if the invention relates to a novel antihypertensive agent, patents from companies like AstraZeneca or Novartis might overlap in claims or technology space, requiring careful fencing around the patent.

Filing Strategies and Litigation

The patent landscape suggests that inventors employ strategic filings—using broad initial claims and narrowing down during prosecution—to maximize coverage. Litigation or opposition in Hungary and Europe can challenge or defend the validity of HUE025852.

Enforceability and Commercial Relevance

The enforceability of HUE025852 depends on:

  • Claims validity: Rooted in a solid inventive step and novelty.
  • Clear claim language: Avoiding ambiguity.
  • Market presence: The patent’s geographical coverage and legal status influence licensing and enforcement strategies.

Given the legal complexities and active patenting in Hungary's pharmaceutical sector, a carefully prosecuted patent like HUE025852 can serve as a vital asset for commercial exclusivity, especially when combined with supplementary patents or regulatory data exclusivities.

Conclusion

HUE025852 demonstrates a carefully crafted patent with a balanced scope encompassing specific pharmaceutical compositions or methods. Its claims appear designed to withstand validation challenges while providing meaningful exclusivity in Hungary, with potential extensions across Europe. The patent landscape signals strong competition, necessitating vigilant monitoring and enforcement to retain market advantage. Strategic patent management, including comprehensive prior art searches and potential supplementary filings, will be essential for maximizing the patent’s value.


Key Takeaways

  • The scope of HUE025852 covers specific pharmaceutical compositions or methods, optimized for enforceability and market protection.
  • Its claims' strength relies on clear delineation of novel features supported by detailed description.
  • The Hungarian and European patent landscape is highly active, with overlapping patents potentially affecting claim validity and freedom to operate.
  • Ongoing patent life-cycle management, including opposition and licensing strategies, can enhance commercial leverage.
  • Monitoring competitive patents and continuously innovating beyond the patent’s scope remain critical for long-term success.

FAQs

1. Can HUE025852 be enforced against competitors in Hungary?
Yes. Provided the claims are valid and infringed, enforcement actions such as patent infringement litigation can be pursued within Hungarian courts.

2. How does European patent law affect the scope of HUE025852?
While HUE025852 is a Hungarian patent, similar or related inventions may be protected via European patents, influencing the scope and enforceability across multiple jurisdictions.

3. What strategies can weaken the patent's claims?
Prior art disclosures, obvious modifications, or misstatements during prosecution can challenge the claims’ validity, potentially weakening the patent.

4. Is it possible to extend protection beyond the original expiry?
In certain cases, supplementary protection certificates (SPCs) or regulatory data exclusivities can prolong market exclusivity beyond patent expiry.

5. How can companies avoid infringing HUE025852?
Competitors should perform detailed patent landscape analyses and design around the claims, for example, by modifying chemical structures or formulations to avoid overlap.


References

[1] Hungarian Intellectual Property Office (HIPO). Patent database.
[2] European Patent Office (EPO). Espacenet patent search.
[3] World Intellectual Property Organization (WIPO). PATENTSCOPE.

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