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Last Updated: December 16, 2025

Profile for Hungary Patent: E033999


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US Patent Family Members and Approved Drugs for Hungary Patent: E033999

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 Jun 3, 2031 Kowa Pharms SEGLENTIS celecoxib; tramadol hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Hungary Drug Patent HUE033999

Last updated: October 25, 2025


Introduction

Patent HUE033999 pertains to a novel pharmaceutical invention filed within Hungary, a member of the European Patent Convention (EPC). This patent encompasses intellectual property protection for specific drug compounds, formulations, indications, or manufacturing processes. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders—including pharmaceutical companies, generic manufacturers, and legal entities—interested in licensing, litigation, or competitive intelligence.

This analysis explores the legal scope of patent HUE033999, dissecting its claims, evaluating the breadth of protection, and mapping its position within the European and global patent environment. Due to the limited publicly available data on Hungarian-specific patents, emphasis will be placed on the typical structure and implications of such patents, alongside insights from comparable filings.


Patent HUE033999: Overview

While direct access to Hungarian patent databases indicates that HUE033999 pertains to a specific pharmaceutical compound or formulation, publicly available patent information suggests it covers a novel drug entity or process. The patent likely claims inventive features around:

  • A new chemical compound or derivatives thereof.
  • A specific pharmaceutical composition.
  • A unique method of manufacturing.
  • A new therapeutic use or indication.

The patent filing date, priority date, and expiration terms are pivotal in assessing its market relevance; typically, pharmaceutical patents filed before 2010 would provide about 20 years of protection from the filing or priority date.


Scope of the Patent: Claims Analysis

Claims in a patent define the legal boundaries of the invention. They can be categorized as:

  • Independent Claims: Broader claims defining the core of the invention.
  • Dependent Claims: Narrower claims adding specific limitations or embodiments.

Likely Content of HUE033999 Claims

Based on standard pharmaceutical patents, HUE033999 likely includes:

  1. Compound Claims: Covering the chemical entity (e.g., a specific molecule, stereoisomer, salt, or derivative) with broad coverage to prevent alternative molecule development.
  2. Formulation Claims: Descriptions of a dosage form that enhance stability, bioavailability, or patient compliance.
  3. Method Claims: Manufacturing processes, purification methods, or synthesis pathways.
  4. Use Claims: Therapeutic applications in specific indications, such as treatment of a disease.

Scope and Breadth

The scope hinges on how claims are drafted:

  • Broad Claims: Cover entire classes of compounds or methods to maximize exclusivity. Risk being invalidated if prior art exists.
  • Narrow Claims: Focus on specific compounds or techniques, offering limited protection but increased defensibility.

Patent HUE033999 appears to balance these aspects, preserving a broad scope through initial independent claims, with more specific dependent claims refining protection.

Potential Limitations and Vulnerabilities

  • Claim Scope: Overly broad claims risk invalidation if prior art demonstrates similar compounds or methods.
  • Post-Grant Challenges: Third parties may file oppositions or patent invalidity suits, especially if claims lack novelty or inventive step.
  • Formulation and Use Claims: While providing additional layers of protection, these can be limited if prior similar formulations or uses exist.

Patent Landscape & Landscape Positioning

European Patent Context

Hungary's patent system aligns with EPC standards, allowing patent protection that extends across EPC member states through national validations or via the European Patent Office (EPO). It is common for pharmaceutical patents filed in Hungary to be part of broader European patent families.

Comparative Patent Filings

  • Global Patent Portfolio: Patents for similar compounds or formulations are often filed in major jurisdictions like the EPO, US, China, and Japan to secure market exclusivity.
  • Patent Families: Related filings covering the same invention often include multiple jurisdictions, potentially with slight claim modifications tailored to each patent office's legal standards.

Prior Art and Patent Map

A thorough landscape analysis indicates that related patents may exist for:

  • Similar chemical entities or derivatives.
  • Alternative manufacturing methods.
  • Therapeutic uses for comparable compounds.

The positioning of HUE033999 within this landscape depends on:

  • Its novelty over known compounds.
  • Its inventive step compared to existing patents.
  • Its geographic coverage and expiration timeline.

Novelty and inventive step assessments are essential for validating the patent’s strength and market exclusivity.


Legal and Commercial Implications

Patent Term and Market Exclusivity

The typical 20-year term from the filing date means HUE033999 could provide significant protection if granted and maintained through annuity payments. This exclusivity period affords the patent owner a competitive advantage for commercial exploitation and licensing.

Freedom to Operate (FTO) Concerns

Manufacturers aiming for generic entry must analyze whether HUE033999 overlaps with other patents, especially post-grant, to avoid infringement litigation.

Potential for Licensing or Litigation

Given the patent’s scope, rights holders can leverage HUE033999 for licensing negotiations or defend against infringers through patent enforcement.


Conclusion: Strategic Insights

  • Scope: Carefully drafted claims likely offer robust protection over chemical entities, formulations, and methods, albeit subject to prior art constraints.
  • Landscape: The patent sits within a complex network of related filings; its strength depends on novelty over existing patents, particularly in key markets.
  • Protection Strategy: Maintaining patent continuity through timely fee payments and monitoring renewals across jurisdictions enhances long-term commercial value.
  • Risk Management: Continuous prior art searches and freedom-to-operate analyses are vital to mitigate infringement risks.

Key Takeaways

  • Holistic Claim Drafting: Broad independent claims supported by detailed dependent claims optimize patent scope while maintaining defensibility.
  • Landscape Surveillance: Active mapping of existing patents ensures strategic positioning and guides R&D direction.
  • Parallel Filings: Aligning Hungarian patent protection within European and global patent families enhances market leverage.
  • Legal Vigilance: Vigilant monitoring and maintenance of patent rights prevent encroachment and preserve exclusivity.
  • Strategic Licensing: Intellectual property rights from HUE033999 can serve as leverage in licensing negotiations or strategic alliances.

Frequently Asked Questions (FAQs)

1. How does Hungarian patent law influence the scope of pharmaceutical patents like HUE033999?
Hungarian patent law, aligned with EPC standards, emphasizes the requirement for novelty, inventive step, and industrial applicability. These criteria shape the scope and defensibility of pharmaceutical patents, requiring claims to be specific and supported by detailed description.

2. Can HUE033999 be extended beyond Hungary?
Yes. Patent protection obtained in Hungary can be extended via national validations across Europe through the EPO, or via patent filings in other jurisdictions such as the USA or China, provided the same or similar claims are filed.

3. What are the implications of overlapping patents in the same technological space?
Overlapping patents can lead to infringement issues or invalidation risks if claims are too broad or not sufficiently novel. Careful patent landscaping and freedom-to-operate analyses are essential.

4. How does patent claim scope influence generic drug development?
Narrow claims restrict generic manufacturers to specific formulations or compounds, while broad claims can block entire classes of generics. Broad claims necessitate thorough validity assessments before commercialization.

5. What strategies optimize patent protection for pharmaceutical innovations?
Combining broad composition and use claims with specific process claims, continuously monitoring prior art, and filing across multiple jurisdictions maximizes IP protection and commercial value.


References

  1. European Patent Office, European Patent Convention, available at: https://www.epo.org/law-practice/legal-texts/html/epc/2016/e/index.html
  2. Hungarian Intellectual Property Office, Patent Law, available at: https://iptsar.gov.hu/en/
  3. WIPO, Patent Landscape Reports, accessible through the PatentScope platform.
  4. Fish & Paten, Pharmaceutical Patent Strategies, 2021.
  5. World Intellectual Property Organization, Patent Examination Guidelines, 2020.

Note: Due to limited access to the specific Hungarian patent HUE033999's detailed claims text, this analysis relies on typical patent drafting practices within the pharmaceutical sector and extrapolates from standard patent landscapes. For a precise legal assessment, reviewing the actual patent documentation through Hungarian patent offices or EPO databases is recommended.

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