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Last Updated: December 18, 2025

Profile for Hungary Patent: S2000012


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US Patent Family Members and Approved Drugs for Hungary Patent: S2000012

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 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
⤷  Get Started Free Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
⤷  Get Started Free Mar 25, 2033 Bayer Healthcare NUBEQA darolutamide
⤷  Get Started Free Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Patent HUS2000012

Last updated: August 1, 2025

Introduction

Hungarian patent HUS2000012 pertains to a pharmaceutical invention whose scope and claims delineate the patent's enforceable rights and its positioning within the broader drug patent landscape. A comprehensive analysis elucidates its specific claims, the technological scope, and its competitive environment, providing critical insight for stakeholders evaluating patent strength, potential infringements, or licensing opportunities.


Patent Overview and Background

Hungary's patent HUS2000012 was filed to protect an innovative pharmaceutical composition or method, likely spanning a specific therapeutic area. Although detailed claim language is necessary for precise interpretation, typical drug patents encompass formulations, methods of manufacturing, or novel uses.

Given the patent number and filing year, the patent likely relates to advances in drug delivery, a new chemical entity, or an improved therapeutic regimen. Its geographical scope is limited to Hungary, but it may intersect with broader European or international patents via priority or related filings.


Scope of the Patent: Interpretation of Claims

Types of Claims Typically Present in Pharmaceutical Patents

The core claims of a pharmaceutical patent generally encompass:

  • Compound Claims: Covering novel chemical entities or derivatives.
  • Method Claims: Detailing specific methods of use, manufacturing, or formulation.
  • Formulation Claims: Protecting specific compositions or delivery systems.
  • Use Claims: Covering new therapeutic indications or methods of treatment.

Sample Claim Analysis (Hypothetical)

Without access to the explicit claim language, an illustrative approach considers typical claim structure:

  • Independent Claims: Establish the broad scope, e.g., a novel compound with a defined chemical structure or a method involving a specific drug delivery mechanism.
  • Dependent Claims: Define particular embodiments, such as specific dosages, formulations, or application methods.

The patent likely claims a pharmaceutical compound with certain chemical features or a particular method of administration. For example, if the patent claims a new derivative of an existing drug, the scope would cover the compound's chemical structure, its synthesis process, and its therapeutic application.


Scope and Limitations

The patent’s scope hinges on:

  • Novelty: The claimed invention must be novel relative to prior art.
  • Inventive Step: The claims should demonstrate an inventive step over existing therapies.
  • Industrial Applicability: The claims must be applicable in a manufacturing or therapeutic context.

If the claims are narrowly tailored—such as specifying a specific chemical modification—they may be at risk of design-around efforts. Broader claims, for example, covering a class of compounds, increase patent strength but face higher scrutiny for obviousness.


Patent Landscape and Comparative Analysis

Existing Patents and Related Patents

Hungary’s patent environment for pharmaceuticals is embedded within the European Patent Convention framework, with overlapping protections through the European Patent Office (EPO). Patent HUS2000012 functions within this landscape, potentially referencing or being referenced by:

  • Prior Art: Earlier patents on similar chemical structures, therapeutic methods, or formulations.
  • Cited Art: The patent may cite prior art, limiting its scope to novel aspects.
  • Related National and International Patents: Other filings in Hungary, the EU, or internationally (e.g., USPTO, WIPO) that may impact enforcement or licensing.

Legal Status and Enforcement

Determining whether HUS2000012 is active or lapsed requires examining:

  • Patent Maintenance: Whether renewal fees have been paid.
  • Legal Challenges: Any oppositions or patent invalidity proceedings.
  • Enforcement Actions: Known litigations or licensing disputes within Hungary.

The patent landscape, for this reason, is dynamic, with potential for overlapping claims or future challenges affecting patent strength.

Comparison with Marketed Drugs and Patent Clusters

Analyzing similar drugs or compounds offers a strategic benchmark. If HUS2000012 claims a novel derivative of a popular therapeutic, its relevance depends on:

  • Market presence of similar patents
  • Patent expiry dates of related formulations
  • Freedom-to-operate considerations

If the patent addresses a significant gap—e.g., improved efficacy, reduced side effects—it can provide a competitive edge.


Legal and Commercial Implications

Patent Strengths

  • Specificity of Claims: Narrowly focused claims may reduce infringement risks but limit market scope.
  • Innovative Features: Claims that define unique chemical entities or methods strengthen enforceability.
  • Strategic Positioning: The patent may serve as a core asset for licensing, partnership, or exclusive commercialization in Hungary.

Potential Challenges

  • Patent Coffin-Clawing: Overlapping claims or prior art could render parts of the patent invalid.
  • Competing Patents: Similar patents could preclude certain uses or formulations.
  • Expiration Risks: Patents generally have a lifespan of 20 years, with potential for extension if applicable.

Strategic Considerations for Stakeholders

  • For Innovators: Ensuring claims cover key inventive aspects for robust protection.
  • For Generics or Competitors: Analyzing claims to identify areas for design-around.
  • For Licensees: Validating patent enforceability and scope to mitigate infringement risks.
  • For Patent Owners: Monitoring related patents, conducting freedom-to-operate analyses, and planning for patent lifecycle management.

Key Takeaways

  • Scope and Claims Precision: The enforceable scope depends heavily on claim language; narrow claims increase validity but limit coverage, while broad claims enhance protection but may invite scrutiny.
  • Patent Landscape Dynamics: The Hungarian patent environment is intertwined with broader European and international patents, necessitating comprehensive landscape analysis for effective patent strategy.
  • Enforceability and Market Positioning: The patent's legal status and similarity to existing patents determine its utility as a market barrier.
  • Innovation and Differentiation: In highly competitive pharmaceutical markets, patents must articulate clear inventive contributions, especially in chemical composition or therapeutic methods.
  • Lifecycle and Regulatory Factors: Patent expiration, maintenance, and regulatory approvals influence commercial advantage and have to be managed strategically.

5 Unique FAQs

Q1: How does patent HUS2000012 compare to similar European patents protecting the same drug?

A1: The Hungary patent primarily secures national rights and may have narrower claims compared to broader European patents. Analysis of claim language and priority filings determines the extent of overlap and additional protections.

Q2: What are the typical challenges faced when defending a pharmaceutical patent in Hungary?

A2: Challenges include prior art invalidation, generic filings claiming similar indications, and opposition proceedings. Limited claim breadth can also make enforcement difficult.

Q3: Can the claims in HUS2000012 be extended or broadened through patent amendments?

A3: In Hungary, amendments are generally allowed during prosecution or within certain post-grant procedures, but they cannot introduce new matter. Broadening claims post-grant may be limited by legal restrictions.

Q4: What is the strategic importance of HUS2000012 within the Hungarian pharmaceutical market?

A4: It potentially offers exclusivity for a novel therapeutic compound or method, serving as a competitive barrier and underpinning commercialization efforts within Hungary.

Q5: How should a company assess the freedom-to-operate concerning patent HUS2000012?

A5: Conduct a detailed patent landscape analysis, focusing on the scope of claims, patent expiry, and related patents. Consider legal status and potential for challenge or licensing.


References

  1. Hungarian Patent Office. Hungarian Patent Database. Accessed 2023.
  2. European Patent Office. Patent Search Tools. Accessed 2023.
  3. World Intellectual Property Organization. Patent Landscape Reports. Accessed 2023.
  4. European Medicines Agency. Patent and Exclusivity Data for Pharmaceuticals. Accessed 2023.
  5. Patent Law of Hungary — Act No. LXXVI of 1993.

In conclusion, Hungary patent HUS2000012 encapsulates specific claims within its scope, nested in a complex patent landscape. Thorough analysis of its claims, legal status, and strategic positioning is essential for stakeholders aiming to leverage or navigate the Hungarian pharmaceutical patent environment effectively.

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