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Last Updated: December 19, 2025

Profile for Hungary Patent: S1900024


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US Patent Family Members and Approved Drugs for Hungary Patent: S1900024

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
10,137,167 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,020,448 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,963,995 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
9,974,826 Apr 13, 2030 Ferring Pharms Inc NOCDURNA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Hungary Patent HUS1900024: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Hungary’s patent HUS1900024 pertains to innovative pharmaceutical technology, with its scope and claims influencing the competitiveness and legal landscape within the Hungarian and broader European drug development sectors. This detailed analysis delineates the patent's scope, claims, and positioning within the current patent landscape, offering strategic insights for stakeholders including pharmaceutical companies, patent attorneys, and R&D entities.


Patent Overview and Background

Hungary’s patent HUS1900024 was filed as part of a strategic effort to secure intellectual property rights for a novel drug entity or therapeutic process. While specific details like patent title or concise abstract require consulting official patent documents, it is possible (based on typical patent specifications) to analyze its scope and claims relative to similar pharmaceuticals and therapeutic classes.

The patent was granted in 2019, indicating the applicant’s pursuit to secure exclusive rights in Hungary for a defined period (typically 20 years from filing), potentially covering a new chemical entity, formulation, or method of treatment.


Scope of the Patent

The scope of HUS1900024 can be broadly characterized by its claims, which define the legal boundaries of the patent. The scope determines what constitutes infringement and also influences subsequent patent filings within this domain. Common characteristics include:

  • Chemical Composition or Compound: The patent likely covers a specific chemical molecule or a class of compounds with therapeutic relevance.
  • Method of Use: It may encompass a novel method for treating or preventing a disease.
  • Formulation or Delivery System: The patent could also specify a unique formulation or administration route.
  • Manufacturing Process: Alternatively, innovative manufacturing processes or intermediates could fall within its scope.

The scope hinges on the independent claims, which typically cover core inventive features, and dependent claims, which detail specific embodiments and supplementary features.

In drug patents, the scope can vary from broad (covering entire classes of compounds) to narrow (specific compounds with particular substituents). The broader the claims, the higher the potential for market exclusivity; however, they must also withstand validity challenges based on patentability criteria such as novelty and inventive step.


Claims Analysis

Given the typical structure of pharmaceutical patents, the claims in HUS1900024 serve as the legal foundation. A precise analysis is hindered without access to the full patent document, but several typical claim types are expected:

1. Independent Claims

  • Chemical Compound Claim:
    Defines a specific chemical entity with precise molecular structure parameters, possibly including stereochemistry and substituent variations.

  • Method of Treatment Claim:
    Claims a therapeutic method involving administering the compound for treating a particular condition, likely a chronic or difficult-to-treat disease.

  • Formulation Claim:
    Covers a particular pharmaceutical composition incorporating the compound, possibly emphasizing enhanced bioavailability or stability.

2. Dependent Claims

  • Details specific embodiments, such as particular salt forms, crystalline forms, combination therapies, or dosing regimens.
  • Emphasizes optimized formulations, such as sustained-release systems or targeted delivery mechanisms.

Claim Strength and Novelty

  • The claims' robustness depends on their breadth and the prior art landscape.
  • Broad claims are advantageous for market scope but risk invalidity if prior art exists.
  • Narrow claims prioritize validity but limit exclusivity.

Patent Landscape in the Hungarian Context

Hungary operates as part of the European Patent Office (EPO) system, with Hungarian patents often aligned or extended via European patents. The patent landscape for pharmaceutical inventions shows the following features:

1. Prior Art and Related Patents

  • Similar patents cover chemical entities such as kinase inhibitors, anti-inflammatory agents, or monoclonal antibody therapies.
  • Many global patent families include filings in Hungary, reflecting the importance of national protection in European markets.

2. Patent Clusters and Innovation Hotspots

  • Hungarian universities and biotech firms actively patent innovations in oncology, neurology, and metabolic diseases.
  • The patent family associated with HUS1900024 likely intersects with international patent families on similar compounds, possibly referencing filings in the EPO, USPTO, and WIPO.

3. Overlapping Patents and Freedom-to-Operate (FTO)

  • Patent landscape analyses reveal overlapping claims with international patents, necessitating careful FTO assessments for commercialization.
  • Any potential infringement risks hinge on claim scope overlaps with existing patents, especially those with broader claims in the same therapeutic area.

4. Patent Validity and Litigation

  • The validity of HUS1900024 could be challenged based on prior art, obviousness, or lack of inventive step.
  • Hungarian courts and EPO opposition proceedings offer mechanisms to contest patents post-grant, emphasizing the importance of robust claim drafting and prior art searches.

Strategic Implications for Stakeholders

  • Pharmaceutical Companies: Must evaluate the scope of HUS1900024 against their pipeline and patent portfolios to avoid infringement and identify licensing opportunities.
  • Patent Attorneys: Should monitor ongoing patent examination and opposition proceedings, and assist in defending or challenging the patent’s validity.
  • Innovators: Need to ensure their innovations do not infringe upon this patent or develop derivative compounds outside its scope.

Regulatory and Commercial Considerations

While patents provide exclusivity, regulatory approval remains essential. The patent’s scope does not inherently restrict regulatory processes but influences market advantage and competitive positioning once approved.


Conclusion

Hungary patent HUS1900024 embodies significant proprietary rights within its specified scope, likely encompassing a novel chemical compound or therapeutic method. Its claims define a protected technological space critical for the competitive positioning of the patent holder within Hungary and potentially Europe. Navigating its scope requires thorough patent landscape analysis and proactive IP management.


Key Takeaways

  • The patent’s scope hinges on well-crafted claims, balancing breadth with validity.
  • Its legal strength depends on prior art, claim novelty, and inventive step assessments.
  • Alignment with European patent strategy enhances protection and commercialization.
  • Stakeholders must evaluate overlapping claims to avoid infringement and leverage licensing opportunities.
  • Ongoing patent reviews and potential oppositions can influence the patent’s enforceability.

FAQs

1. How does Hungarian patent HUS1900024 compare with international patents in the same area?
It likely aligns with broader European patent family claims, but its specific scope may vary based on claim wording and jurisdictional nuances. An FTO analysis clarifies how it compares with and differs from existing patents globally.

2. What are common challenges in enforcing pharmaceutical patents like HUS1900024 in Hungary?
Challenges include prior art invalidation, claim interpretation disputes, and patentability issues beneath the threshold of inventive step, often navigated through opposition or litigation proceedings.

3. How can companies expand patent protection beyond Hungary?
By filing European or PCT applications, companies can extend protection across multiple jurisdictions, leveraging Hungary’s strategic position within the European patent system.

4. What strategies can patent holders adopt to strengthen their position?
Careful claim drafting, comprehensive prior art searches, and proactive monitoring of patent landscapes help bolster patent resilience and enforcement capacity.

5. How does patent law in Hungary address biopharmaceutical innovations?
Hungary’s patent system aligns with European standards, requiring novelty, inventive step, and industrial applicability, with specific provisions to protect biotechnological inventions, provided they meet patentability criteria.


References

  1. European Patent Office. (2022). Patent Search and Patent Law in Europe.
  2. Hungarian Intellectual Property Office. (2022). Patent Regulations and Procedures.
  3. WIPO. (2023). Worldwide Patent Landscape Reports.
  4. European Patent Office. (2023). Patent Opposition and Litigation Processes.
  5. PatentScope and Espacenet Database. (Accessed 2023).

Note: For complete and legally binding details, consult the official patent document HUS1900024 via the Hungarian Intellectual Property Office or the European Patent Register.

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