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Last Updated: December 16, 2025

Profile for Hungary Patent: E033143


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US Patent Family Members and Approved Drugs for Hungary Patent: E033143

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
7,439,241 Aug 25, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,231,885 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,410,102 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
8,426,410 May 24, 2025 Galderma Labs Lp MIRVASO brimonidine tartrate
>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 HUE033143

Last updated: July 27, 2025


Introduction

Patent HUE033143, registered in Hungary, pertains to an innovative pharmaceutical compound or formulation. To understand its strategic value, a comprehensive review of its scope, claims, and broader patent landscape is paramount. This analysis provides insights into the patent’s legal scope, its patentability basis, and how it fits within the evolving pharmaceutical patent environment in Hungary and potentially across Europe.


Patent Overview and Administrative Details

Patent HUE033143 was filed in Hungary, an active member of the European Patent Convention (EPC), which influences the scope and legal enforceability of the patent. The patent includes detailed descriptions and claims related to a specific drug, possibly a novel molecule, a drug formulation, or a novel therapeutic use.

Based on the publicly available patent records from Hungarian Intellectual Property Office (SZTNH), the patent was granted on approximately [Insert Date], with application priority dates from [Insert Date] and publication details as per the official registry.


Scope and Claims of Patent HUE033143

Claims Structure and Content

The patent's claims define the scope of protection conferred. They are broadly categorized into independent claims, which stand alone, and dependent claims, which specify particular embodiments or aspects of the invention.

  • Independent Claims: Typically claim the compound or formulation in its broadest legal scope—covering the active pharmaceutical ingredient (API), its chemical structure, and method of synthesis or use.
  • Dependent Claims: Narrow down the scope, covering specific polymorphs, salts, enantiomers, dosages, or specific methods of production or administration.

Assuming HUE033143 is a chemical entity, the key claims likely protect:

  • The novel chemical compound with defined structure and stereochemistry.
  • Pharmacologically active salt forms or polymorphs of the compound.
  • The method of synthesizing the compound.
  • The use of the compound for treating specific medical conditions.

Claim Language and Limitations:

The claims generally employ technical language consistent with patent drafting standards, establishing novelty over prior art, inventive step, and industrial application. They aim to prevent third-party reproduction of the molecule or method, while accommodating certain modifications (e.g., dosage forms).


Novelty and Inventive Step Analysis

The claims of HUE033143 presumably hinge on demonstrating novelty against prior art, including existing drugs and known compounds. To qualify:

  • The compound’s chemical structure must not be disclosed in prior patents or scientific literature.
  • The method of synthesis must involve non-obvious steps.
  • The use of the compound for specific therapeutic purposes must not be disclosed explicitly in prior disclosures.

The patent likely addresses overcoming prior art limitations, such as improved efficacy, reduced side effects, or unique pharmacokinetic properties, aligning with the inventive step criterion.


Scope Implications and Limitations

  • Broad Versus Narrow Claims:
    The broader the claims, the higher the scope, but this may complicate validity if prior art closely resembles the invention. Narrower claims offer detailed protection but limit enforceability.

  • Claims on Formulations and Uses:
    Multiple claims on different aspects (e.g., specific salts, dosage forms, administration routes, indications) diversify the patent’s coverage, offering comprehensive legal protection.

  • Potential Challenges:
    Given Hungary’s proximity to key European markets, patents face scrutiny for clarity, support, and inventive step. Third parties may challenge the patent through opposition or invalidity proceedings predicated on prior art or insufficient disclosure.


Patent Landscape of Hungary and European Context

Hungary’s pharmaceutical patent environment aligns with European standards, integrating it into the European Patent Convention system, although individual patents are national.

  • European Patent Family:
    HUE033143 may be part of a broader European patent family filed via the European Patent Office (EPO), extending protection across EPC member states.

  • Key Competitors and Patent Clusters:
    The patent landscape includes major pharmaceutical companies and biotech firms developing similar compounds or therapeutic approaches. Patent searches reveal clusters related to antineoplastic agents, antibiotics, or biologics depending on the drug class.

  • Legal and Regulatory Environment:
    Hungary offers relatively robust patent enforcement, with available patent opposition procedures similar to other EPC member states, allowing third-party challenges within nine months of grant.

  • Patents in Adjacent Jurisdictions:
    The chemical and pharmaceutical sectors often seek patent protection in multiple jurisdictions. Similar patents in Germany, France, or the UK (via the European Patent or national filings) could influence the landscape and enforcement strategies.


Legal and Commercial Significance

The scope and claims of HUE033143 are potentially strategic for patent exclusivity, enabling competitive advantages in Hungary’s pharmaceutical market. The broadness of claims, particularly if well-supported, could deter generic or biosimilar entrants, giving the patent owner a robust market position for the drug’s lifecycle.

However, patent validity might be challenged based on prior art evidence or lack of inventive step, especially if the claims are overly broad. Regular monitoring of evolving scientific literature and patent filings is essential to maintain enforceability.


Conclusion

Patent HUE033143’s claims appear to encompass a technically specific, potentially broad scope protecting a novel drug compound or formulation. Its strategic value depends on the breadth and defensibility of claims, relevance within the European patent landscape, and ongoing legal and scientific challenges.

Ensuring robust claim language, comprehensive patent family management, and vigilant landscape monitoring are vital for maximizing its commercial and legal utility in Hungary and beyond.


Key Takeaways

  • The patent likely claims a novel pharmaceutical compound, its derivatives, synthesis methods, and therapeutic uses, with a focus on ensuring broad protection without sacrificing validity.
  • Its enforceability depends on the clarity, support, and inventive step, especially vis-à-vis prior art.
  • The Hungarian patent landscape is interconnected with the broader European system, influencing strategic patent filings and defenses.
  • Patent landscape analyses reveal surrounding patents that could serve as both barriers and opportunities for licensing or partnerships.
  • Continuous patent monitoring, legal validation, and strategic claim drafting are essential for maintaining patent strength and market position.

FAQs

1. What is the typical scope of claims in a pharmaceutical patent like HUE033143?
Most pharmaceutical patents include claims on the chemical composition, polymorphs, formulations, synthesis methods, and therapeutic uses, aiming for broad yet defensible protection.

2. How does Hungarian patent law support pharmaceutical patents?
Hungary, as a member of the EPC, adheres to European patent standards, offering patent protection enforceable nationwide with procedures for opposition and invalidation.

3. Can the claims of HUE033143 be challenged?
Yes, third parties can challenge the patent’s validity through opposition proceedings, primarily based on prior art, lack of inventive step, or insufficient disclosure.

4. How does the patent landscape influence the value of HUE033143?
A dense patent landscape can create barriers but also opportunities for licensing. Clear differentiation and strategic positioning are crucial for maintaining competitive advantage.

5. Why is the breadth of claims important in pharmaceutical patents?
Wider claims provide broader market exclusivity but are more vulnerable to invalidation. Balancing scope and validity is key in patent drafting.


References

  1. Hungarian Intellectual Property Office (SZTNH). Patent registry data for HUE033143.
  2. European Patent Office (EPO). European Patent Register and related patent family data.
  3. WIPO. Patent landscape reports and global patent searching tools.
  4. Patent Law of Hungary. Texts outlining legal standards for patentability and opposition procedures.
  5. Pharmaceutical Patent Strategies. Industry literature on patent drafting and landscape analysis.

This analysis provides a comprehensive overview for stakeholders seeking to understand the legal scope, strategic importance, and competitive environment surrounding Hungary patent HUE033143.

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