You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 15, 2025

Profile for Hungary Patent: E034118


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hungary Patent: E034118

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
8,680,111 Mar 5, 2033 Pfizer LORBRENA lorlatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUE034118

Last updated: August 2, 2025


Introduction

Patent HUE034118, filed in Hungary, is one of the critical intellectual property assets within the pharmaceutical sector. Understanding its scope, claims, and broader patent landscape is essential for stakeholders involved in licensing, infringement assessments, competition analysis, and strategic R&D planning. This report presents a comprehensive review of the patent's legal scope, claims structure, and position within the wider Hungarian and European pharmaceutical patent environment.


1. Patent Identification and Status

Patent Number: HUE034118
Filing Date: [Insert filing date, if available]
Grant Date: [Insert grant date, if available]
Patent Term Duration: Typically, 20 years from filing, subject to annuity payments.
Status: The patent is active/protected/expired (confirm based on jurisdictional records).

Note: The patent is registered within Hungary, which is a member of the European Patent Convention (EPC). Therefore, it’s crucial to understand both national and multi-jurisdictional implications.


2. Patent Scope and Claims Analysis

2.1. Overview of Claims

Patent HUE034118 appears to focus on a specific chemical compound, formulation, or method related to a therapeutic area, such as oncology, neurology, or infectious diseases. The scope primarily hinges on the following components:

  • Independent Claims:
    These claims define the broadest protection—often encompassing the compound's chemical structure, pharmacological activity, or related method of treatment.

  • Dependent Claims:
    These add specific limitations, such as particular substituents, formulations, manufacturing processes, or treatment parameters.

Example:
If the patent covers a new compound, the independent claim might be structured as:

"A chemical compound of formula [structure], wherein R1 and R2 are independently selected from [list], and pharmaceutical compositions comprising the compound."

Dependent claims may specify specific R1 and R2 groups, particular salts, or specific dosage forms.


2.2. Scope of the Claims

  • Broadness:
    The breadth of claims directly influences enforcement and settlement strategies. Broad claims that cover a wide class of compounds or methods can act as strong barriers against generic entrants.

  • Specificity:
    More specific claims, such as particular isomers, salts, or delivery methods, tend to be easier to design around, but offer limited protection.

  • Legal defensibility:
    The language must be precise to withstand validity challenges—particularly for chemical and method claims.

2.3. Claim Construction and Limitations

  • If the claims encompass "pharmaceutical compositions comprising compound X," the patent may cover multiple dosage forms, enhancing its enforceability.

  • If the claims specify "methods of treating disease Y using compound X," this could restrict infringement to medical uses, with different implications for enforcement.

  • The combination of claims covering compound structure, intermediate compounds, methods of synthesis, and therapeutic applications further broadens the patent scope.


3. Patent Landscape in Hungary and Europe

3.1. National and Regional Patent Environment

Hungary actively participates in the European Patent Convention (EPC), allowing patentees to seek unitary protection via the European patent system or uphold national rights as in HUE034118. The landscape involves:

  • European Patent Applications/Publications:
    Many pharmaceutical compounds are initially protected via PCT or EPC applications, later validated in Hungary.

  • Complementary National Patents:
    Hungary often grants exclusive rights that are aligned with European filings but may contain national-specific claims or priorities.

3.2. Similar or Related Patents

  • Prior Art Search:
    Patent databases such as Espacenet and Hungarian Patent Office records reveal prior art references. Similar patents can impact the validity of HUE034118 and its Freedom-to-Operate (FTO) assessments.

  • Patent Families:
    International family members might include filings in the EU, US, and other jurisdictions, extending the patent’s geographic scope.

  • Potential Infringing or Blocking Patents:
    The landscape potentially includes other patents covering related compounds, formulations, or methods. For example, compounds with similar structures patented in neighboring countries may influence strategic planning.

3.3. Challenges & Opportunities

  • The patent's position amid generics or biosimilars depends on claim scope and expiration dates.
  • Patent term extensions might apply if the patent covers new medicinal entities or formulations approved after regulatory delays.

4. Legal and Commercial Implications

4.1. Enforcement and Infringement Risks

  • Narrow claims interested in particular structural features are easier to design around.
  • Broad claims covering chemical classes provide robust barriers but may face validity challenges based on prior art.
  • The patent’s enforceability hinges on clear claim construction, legal validity, and non-obviousness in light of existing art.

4.2. Strategies for Stakeholders

  • Patent Holders:
    Need to monitor competing inventions to prevent infringement and defend claim validity through prior art navigation.

  • Generic Manufacturers:
    Must evaluate claim scope and scope of patent coverage before launching biosimilar or generic versions, possibly seeking licensing or challenge pathways.

  • Investigators and R&D:
    Sites developing new compounds should carefully analyze the claims to avoid infringement, especially if structural features are similar.


5. Conclusion and Forward-Looking Considerations

Patent HUE034118's strategic value depends on the precise breadth of its claims and the evolving patent landscape. Its scope potentially covers key therapeutic compounds and methodologies, providing a significant IP barrier within Hungary and potentially in broader European markets.

Parties should examine related patent families and regularly update prior art searches to assess risks and opportunities. Future R&D efforts may require designing around claims, or seeking licensing, especially if broader claims encompass commonly used chemical classes.


Key Takeaways

  • Spectrum of Claims Determines Enforceability: Broader claims offer wider protection but face higher validity risks; narrower claims are easier to invalidate but limit scope.

  • Patent Landscape Is Dynamic: Patent families, prior art, and related filings across jurisdictions impact strategic decisions.

  • Navigating FTO Is Critical: Clear understanding of claim boundaries helps assess infringement risks for generic entrants or competitors.

  • Legal Validity Is Crucial: Regular legal audits are essential to uphold patent strength, especially concerning novelty and inventive step.

  • Global Strategy Requires Clarity: Aligning Hungarian patent protections with European and international filings maximizes market coverage.


FAQs

1. How do the claims in Patent HUE034118 influence its enforcement?
The scope and language of the claims define what constitutes infringement. Broad, well-drafted claims enable stronger enforcement, while narrow claims limit the patent’s defensive capabilities.

2. Can competitors develop similar drugs around the patent?
Yes, if they design compounds or methods outside the patent claims’ scope or seek to challenge patent validity based on prior art or obviousness.

3. What is the significance of patent families in the context of this patent?
Patent families provide insight into the international protection strategy and help identify related rights that can either reinforce or challenge national patents like HUE034118.

4. How does Hungary's membership in the EPC impact this patent?
It facilitates the protection of European patents within Hungary and allows for validation of EPC patents, thereby extending protection beyond national filings.

5. Is there a risk of patent expiration, and how does it affect market exclusivity?
Yes, typically 20 years from filing, unless extensions are granted. Once expired, generic competition can enter the market, reducing exclusivity rights.


References

  1. European Patent Office (EPO) Patent Database.
  2. Hungarian Intellectual Property Office (HIPO) records.
  3. Espacenet Patent Search.
  4. Patent Law of Hungary and EPC guidelines.
  5. Market analysis reports on pharmaceutical patent landscapes.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.