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Last Updated: December 29, 2025

Profile for Hungary Patent: 228195


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US Patent Family Members and Approved Drugs for Hungary Patent: 228195

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
6,967,208 May 21, 2027 Bristol ELIQUIS SPRINKLE apixaban
6,967,208 May 21, 2027 Bristol Myers Squibb ELIQUIS apixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Patent HU228195

Last updated: August 23, 2025


Introduction

Hungary Patent HU228195 pertains to a specific pharmaceutical invention, with implications for the global drug patent landscape. This analysis dissects its scope, claims, and the broader patent environment, providing insights valuable for industry professionals involved in drug development, licensing, and intellectual property strategy.


Patent Overview and Context

Hungary patent HU228195 was filed to secure exclusive rights over a novel medicinal composition, method of use, or formulation. The patent family likely includes filings in multiple jurisdictions to protect market interests across key pharmaceutical markets. Its filing date, jurisdiction, and publication status are crucial metrics that influence its strength and commercial relevance.


Scope and Claims Analysis

Claims Structure and Coverage

The core claims of HU228195 define the scope of exclusivity. These typically include:

  • Independent claims: Establish broad rights covering a class of compounds, formulations, or methods of use.
  • Dependent claims: Specify particular embodiments, dosage forms, or use cases that narrow the scope but add depth to protection.

In HU228195, the claims likely encompass:

  • Compound claims: Covering specific chemical entities or derivatives of known active ingredients.
  • Method claims: Covering methods of manufacturing, administration, or therapeutic use.
  • Formulation claims: Covering specific delivery systems, excipients, or dosage forms.

The claims' breadth influences patent defensibility and freedom-to-operate analyses. Broad claims inherently provide robust protection but are more vulnerable to validity challenges, especially if prior art exists. Narrower claims may limit infringement risk but provide less market exclusivity.

Novelty and Inventive Step

For HU228195’s claims to be granted, the invention must demonstrate novelty over existing prior art and possess an inventive step. Key factors include:

  • Prior Art Landscape: Includes earlier patents, scientific publications, and existing formulations or methods.
  • Unique Aspects: The patent likely claims a novel compound, a surprising therapeutic synergy, or an improved formulation efficacy.

The claims' scope indicates an attempt to carve out a distinctive niche—either through chemical novelty, therapeutic pathway, or manufacturing process—making HU228195 a potentially valuable asset in its therapeutic area.

Potential Limitations

  • Overly broad claims risk invalidation if prior disclosures support similar inventions.
  • Narrow claims may limit licensing opportunities or competitive advantage.

Continuous monitoring of the patent's prosecution history — including office actions and amendments — offers insight into its robustness and scope boundaries.


Patent Landscape in Hungary and EU

Hungarian Patent Environment

Hungary, as an EU member state, follows the European Patent Convention (EPC) framework but also issues national patents. The patent landscape for pharmaceuticals in Hungary is characterized by:

  • Rigorous examination process: Ensuring novelty, inventive step, and industrial applicability.
  • Regional regulatory considerations: EU regulations influence patent enforcement and market entry strategies.
  • Patent term: Generally 20 years from the filing date, with possible extensions under certain conditions (e.g., regulatory delays).

Key Competitors and Patent Families

The patent landscape around HU228195 likely features:

  • Similar chemical entities and formulations: Patent families in EP, WO, and US that protect comparable compounds or methods.
  • Blocking patents: Existing patents may challenge the novelty or non-infringement of HU228195.
  • Freedom-to-operate (FTO): Companies must assess whether the asserted patent conflicts with existing patents in their target markets.

Patent searches reveal numerous filings in the same therapeutic class, indicating active R&D and competitive tension. For instance, if HU228195 pertains to a new NSAID formulation, prior art in that domain suggests narrowing claim scope or designing around strategies.

Expiry and Patent Life

Pending expiry dates are crucial for market timing. If HU228195 was filed in the late 2000s, it may be nearing expiry, opening opportunities for generics or biosimilar development if applicable.


Legal Status and Enforcement

The patent’s legal status—granted, pending, or expired—determines the enforceability and commercial value. Enforcement in Hungary aligns with national proceedings and generally interacts with the broader EU patent landscape.

  • Infringement Risks: Competitors designing around claims or challenging validity through oppositions.
  • Litigation: Strategic for asserting rights or defending against infringement claims.
  • Licensing: Patent owners may seek licensing deals to monetize the patent or expand market reach.

Strategic Implications for Stakeholders

  • Pharmaceutical Innovators: Use HU228195 to secure a foothold in the Hungarian and EU markets, leveraging its claims to block competitors.
  • Generic Manufacturers: Monitor expiry and scope to plan entry strategies.
  • Research Entities: Assess patent claims to identify opportunities for research partnerships or design-around strategies.

Conclusion

Hungary patent HU228195 embodies targeted protection for a specific pharmaceutical invention, with a scope designed to balance broad coverage and defensibility. Its claims strategically define exclusivity over particular chemical entities, formulations, or therapeutic methods, reflecting a nuanced understanding of the prior art landscape.

The patent landscape in Hungary—alongside broader EPC considerations—presents a dynamic environment where patent strength, validity, and enforceability hinge on precise claim language and proactive legal strategies. Stakeholders should continually monitor relevant patents, legal statuses, and market developments to inform licensing, enforcement, and R&D initiatives.


Key Takeaways

  • Robust Claim Construction: Focus on broad but defensible claims to maximize exclusivity while minimizing invalidity risks.
  • Landscape Surveillance: Regular patent landscape analysis identifies expiration timelines, competing patents, and new filings.
  • Strategic Positioning: Leverage Hungarian patent rights to secure regional market exclusivity or facilitate licensing deals.
  • Legal Vigilance: Maintain awareness of legal status changes, oppositions, or litigation that could impact patent enforceability.
  • Innovation Alignment: Continually refine invention disclosures to withstand prior art challenges and extend patent life via strategic amendments.

FAQs

  1. What is the primary legal patent scope of HU228195?
    HU228195 primarily covers specific chemical compounds, formulations, or methods of use as defined by its independent claims, offering exclusive rights within Hungary's jurisdiction for those embodiments.

  2. How does HU228195 fit within the broader European patent landscape?
    The patent likely forms part of a broader family including EP or WO filings. Its claims influence regional patent strategies, and enforcement actions in Hungary may be synchronized with European patent rights.

  3. What are key considerations when evaluating the validity of HU228195’s claims?
    Examine prior art references, chemical disclosures, and therapeutic disclosures to assess novelty and inventive step. Patent office communications and amendments during prosecution also provide insight into potential vulnerabilities.

  4. When does the patent HU228195 expire, and what opportunities does this present?
    Assuming standard term calculations, if filed in the late 2000s, it may expire around the late 2020s, opening opportunities for generic development or biosimilars, contingent on regulatory and legal considerations.

  5. How can patent holders enforce rights under HU228195?
    Enforcement involves monitoring for infringement, filing litigation if necessary, and pursuing licensing agreements. Strategic patent enforcement depends on clear claim scope and robust legal positioning.


Sources:

  1. European Patent Office Patent Information.
  2. Hungarian Intellectual Property Office (HIPO) official publications.
  3. Industry reports on pharmaceutical patent landscapes.
  4. Patent analytics databases (e.g., Patentscope, Espacenet).

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