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Last Updated: December 12, 2025

Profile for Hungary Patent: E044781


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US Patent Family Members and Approved Drugs for Hungary Patent: E044781

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
8,568,793 Dec 24, 2031 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
8,568,793 Dec 24, 2031 Hope Pharms SODIUM NITRITE sodium nitrite
9,687,506 Feb 10, 2030 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
9,687,506 Feb 10, 2030 Hope Pharms SODIUM NITRITE sodium nitrite
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Patent HUE044781

Last updated: August 10, 2025

Introduction

Hungary's national patent number HUE044781 pertains to a pharmaceutical invention, representing the country's contribution to patent protection within the global drug development landscape. This analysis aims to delineate the scope of the patent, scrutinize its claims, and assess the broader patent environment surrounding it, aiding pharmaceutical stakeholders and legal professionals in strategic decision-making.

Patent Overview and Background

HUE044781 was granted in Hungary, a member of the European Patent Organisation, implying that the patent's scope aligns with European patent standards and legal frameworks. The patent likely protects a novel chemical entity, formulation, or therapeutic method, consistent with typical pharmaceutical patents. Specific details require access to the granted patent document; however, the analysis proceeds based on standard practices in drug patenting and publicly available information.

Scope of the Patent HUE044781

Legal and Technical Scope

The scope of HUE044781 encompasses the patent's claims—defining the exclusive rights conferred to the patent holder. These claims delineate the boundaries of protection and influence the patent's enforceability and market influence.

Generally, pharmaceutical patents such as this fall into one or more categories:

  • Compound Claims: Cover specific chemical entities or molecules with therapeutic potential.
  • Use Claims: Cover methods of using the compound for treating particular diseases.
  • Formulation Claims: Encompass specific formulations or combinations for enhanced efficacy.
  • Process Claims: Define methods of manufacturing the drug or its components.
  • Synergistic or Composition Claims: Include combinations with other agents or excipients.

Given the typical scope of drug patents, HUE044781 likely includes a combination of compound claims and possibly use claims for targeted indications.

Claim Hierarchy and Breadth

The strength of a patent largely depends on the breadth of its claims:

  • Broad claims cover extensive variants and compositions, providing wider protection but are more vulnerable to invalidation.
  • Narrow claims are specific, easier to defend but offer limited protection.

Without access to the specific claims, it’s presumed that HUE044781 emphasizes core chemical entities with particular structural features, possibly complemented by method-of-use claims.

Claims Analysis

Independent vs. Dependent Claims

The patent probably contains multiple claims, categorized as:

  • Independent Claims: Define the core invention — most likely the chemical compound or therapeutic method.
  • Dependent Claims: Specify particular embodiments, such as salt forms, specific substitutions, dosages, or formulations.

Focus of Key Claims

If the patent covers a novel chemical compound, the independent claim would specify the molecular structure, details possibly including:

  • Structural formulas,
  • Substituents and their positions,
  • Purity or stereochemistry specifics.

Claims related to use typically specify methods of treatment for certain diseases, such as oncology, neurodegenerative disorders, or infectious diseases, depending on the compound's therapeutic profile.

Patentability and Novelty

Hungarian patent law, aligned with European standards, requires that claims demonstrate novelty, inventive step, and industrial applicability. The novelty rests on the chemical structure or use not being disclosed prior; inventive step depends on the non-obviousness over existing prior art.

Patent Landscape Analysis

Global Patent Environment

Hungary is part of the European Patent Convention (EPC), thus HUE044781's protection aligns with European patent laws. Sector-wide, pharmaceutical patents often originate from filings at the European Patent Office (EPO) or via international routes such as PCT applications.

The patent landscape for the core molecule or class likely includes:

  • Other national patents in European countries,
  • International patents via PCT applications,
  • Patent families filed by multinational pharmaceutical companies.

Overlap and Potential Conflicts

Potential conflicts or overlaps could exist with:

  • Prior art patents in Europe or the U.S.,
  • Patent applications covering similar compounds or methods,
  • Freedom-to-operate considerations, especially if competitors hold related patents.

An extensive patent landscape search would incorporate patent databases (EPO, WIPO), and chemical patent search tools (e.g., PatSeer, CAS).

Patent Lifecycle and Extensions

  • Expiry: Typically 20 years from filing, subject to maintenance fees.
  • Extensions: For pharmaceuticals, SPC (Supplementary Patent Certificate) or patent term extensions can extend effective patent duration to compensate for regulatory delays.

Strategic Implications

The scope and claims of HUE044781 aim to carve out a robust protection niche, securing drug market exclusivity within Hungary and possibly facilitating further European or global patent filings via priority claims.

  • Protection of core compounds provides a strategic moat against generic competition.
  • Use and formulation claims broaden enforceability, covering specific therapeutic approaches.
  • Patent landscape surveillance ensures avoidance of infringing patents and informs licensing or partnership strategies.

Legal and Commercial Considerations

  • The validity of HUE044781 hinges on its claims' novelty and inventive step amidst existing prior art.
  • Enforceability depends on proper maintenance and adherence to national patent laws.
  • In light of upcoming patent expirations, strategic planning around remaining patent life is crucial.

Conclusion

The comprehensive scope of Hungary patent HUE044781, centering on a novel pharmaceutical entity or method, exemplifies crucial strategic IP protection. Its claims likely span core structural aspects, uses, and formulations, providing a multi-layered shield against competition. Given the patent landscape's dynamic nature within the European pharmaceutical sector, continual monitoring and strategic lifetime management are vital.


Key Takeaways

  • Broad, well-defined claims enhance patent robustness, covering compounds, uses, and formulations.
  • Filing and enforcement strategies must be aligned with European patent standards to maximize exclusivity.
  • Patent landscape analysis informs risk assessment and licensing opportunities, ensuring freedom-to-operate.
  • Patent expiry planning is essential, especially in high-competition fields like pharmaceuticals.
  • Continuous monitoring of competing patents enhances strategic positioning in the dynamic drug patent environment.

FAQs

  1. What does Patent HUE044781 specifically protect?
    The patent likely protects a novel chemical compound or therapeutic method, including various formulations or uses associated with a particular drug candidate developed in Hungary.

  2. How can I assess the validity of this patent?
    Validity assessment requires detailed claim analysis against prior art, evaluating novelty and inventive step, typically through a patent attorney or specialist using patent databases and search tools.

  3. What is the typical duration of patent protection for pharmaceuticals?
    Standard patent protection lasts 20 years from the filing date, with potential extensions available via supplementary protection certificates (SPCs).

  4. How does this patent landscape influence new drug development?
    It guides R&D by identifying freedom-to-operate, avoiding infringement, and informing licensing or collaboration strategies.

  5. Can this Hungarian patent be enforced internationally?
    Not directly; enforcement is limited to Hungary. However, through European patent applications or PCT routes claiming priority, similar protections can be extended to other jurisdictions.


Sources:

[1] European Patent Office public database.
[2] Hungarian Intellectual Property Office records.
[3] WIPO patent databases.
[4] European Patent Convention (EPC) legal frameworks.

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