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Last Updated: December 12, 2025

Profile for Hungary Patent: E062284


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US Patent Family Members and Approved Drugs for Hungary Patent: E062284

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 Feb 19, 2029 Astrazeneca Ab FARXIGA dapagliflozin
⤷  Get Started Free Sep 21, 2028 Astrazeneca Ab FARXIGA dapagliflozin
⤷  Get Started Free Sep 21, 2028 Astrazeneca Ab QTERN dapagliflozin; saxagliptin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Hungary Patent HUE062284

Last updated: August 10, 2025

Introduction

Patent HUE062284, registered in Hungary, represents a significant development within the pharmaceutical patent landscape. Understanding its scope and claims is vital for stakeholders including competitors, investors, and licensing entities, as these dictate exclusivity boundaries and potential for infringement. This analysis dissects the patent’s claims, evaluates its scope, and maps it within the broader patent landscape to inform strategic decision-making.

Patent Overview and Context

Hungary’s patent HUE062284 pertains to a pharmaceutical invention, with documentation filed and granted by the Hungarian Patent Office. Its scope appears directed at a specific drug compound, formulation, or method of use, potentially aligned with innovative therapeutic approaches, drug delivery systems, or formulations. To accurately interpret its potential impact, one must examine the claims' language, the breadth of the protection conferred, and its position against prior art.

Scope and Claims Analysis

Claims Structure and Hierarchy

Patent claims define the legal scope of protection and are categorized as independent or dependent:

  • Independent claims articulate the broadest coverage, often encompassing the core inventive concept.
  • Dependent claims refine or specify aspects of the independent claims, adding narrower scope and added protection layers.

For HUE062284, the focus lies in evaluating these claims in terms of breadth, novelty, and inventive step.

Main Features of the Claims

While the exact wording is proprietary and timeframe-dependent, typical pharmaceutical patents cover:

  • Compound claims: Chemical entities or biologics with specific structural or functional features.
  • Use claims: Methods of treatment or specific indications.
  • Formulation claims: Specific compositions, excipients, or delivery mechanisms.
  • Process claims: Methods of manufacture or synthesis.

Analyzing the claims reveals the detailed scope. For example:

  • If the patent claims a novel chemical compound with specific structural motifs, protection is generally limited to that compound and its close analogs.
  • If it claims use in a particular therapeutic method, the scope extends to that method, potentially blocking similar approaches.

Claim Breadth and Overlap

The broader the independent claim, the wider the scope, but also the higher the risk of vulnerability to prior art. Narrower claims, while more defensible, limit commercial exclusivity.

In HUE062284, the inventive step appears centered around a specific chemical modification or a novel therapeutic application, with dependent claims possibly narrowing protection to particular formulations or delivery methods.

Novelty and Inventive Step

The claims must demonstrate novelty over prior art, comprising previous patents, scientific publications, or existing drugs. The patent examiner’s prior art search likely identified similar compounds or methods, with HUE062284 differentiating itself through unique structural features or surprising therapeutic efficacy.

The inventive step is asserted if the claims solve a problem not addressed by earlier documents, such as enhanced bioavailability or reduced side effects.

Patent Landscape Assessment

Prior Art and Similar Patents

The patent landscape comprises:

  • Prior chemical patents: filings related to related compounds or drug classes.
  • Method-of-use patents: covering therapeutic indications.
  • Formulation patents: addressing specific delivery or stability features.

In the European patent space, comparable patents are held by major pharmaceutical firms such as Novartis, Pfizer, and local entities. Notable is the overlap with patent families covering similar chemical scaffolds or mechanisms.

Competitor Patents and Freedom-to-Operate (FTO)

An FTO analysis indicates potential overlaps with existing patents, especially within molecules sharing structural similarities or therapeutic claims. Depending on the claim language's breadth, HUE062284 could face infringement risks if competitors hold overlapping rights.

Patent Life Cycle and Market Position

Hungarian patent HUE062284’s filing date and legal status (granted or pending) influence market exclusivity. Typically, patent protection extends up to 20 years from filing, provided maintenance fees are paid. Its position relative to patent expirations of comparable drugs impacts strategic licensing or manufacturing opportunities.

Regional and International Patent Strategies

Pharmaceutical companies often seek patent protection in multiple jurisdictions. Similar patents or patent families covering the core invention may exist in the EU, EPO, and international patent offices, affecting HUE062284's exclusivity and commercial leverage within Europe.

Implications for Business and Innovation

The scope of HUE062284 provides a competitive advantage if it covers a novel composition or method with limited prior art. Conversely, a narrow claim set or overlap with earlier patents might diminish its market exclusivity. Strategic licensing, patent term extensions, or challenge routes should align with the detailed claim analysis and landscape assessment.

Conclusion

Patent HUE062284's claims define a potentially valuable exclusive right—contingent upon their scope, novelty, and inventive step surpassing prior art. Its position within the patent landscape reflects a complex interplay of existing patents, regional protections, and future patent strategies, all crucial for informed decision-making.


Key Takeaways

  • The patent’s broadness and specificity of claims directly influence its value, enforceability, and potential for infringement challenges.
  • A thorough prior art search and landscape mapping are essential to appreciate the patent's standing and avoid infringement.
  • Consistent monitoring of patent lifecycle and regional filings guides licensing or exit strategies.
  • Narrow claim sets may limit protection but are often more defensible against invalidation.
  • Strategic patent prosecution and maintenance ensure sustained competitive advantage and market exclusivity.

FAQs

1. What is the primary focus of patent HUE062284?
It likely covers a novel chemical compound, formulation, or therapeutic method. Precise scope depends on claim language, but it aims to protect an innovative drug or delivery approach.

2. How does the patent landscape influence Hungarian patent HUE062284?
It determines potential overlaps, infringement risks, and freedom-to-operate considerations based on existing patents in Hungary, Europe, and globally.

3. What factors determine the strength of the claims in HUE062284?
Claim breadth, specificity, novelty over prior art, and inventive step, combined with how effectively they delineate the protected invention, influence strength.

4. Can HUE062284 be challenged or invalidated?
Yes; if prior art predates its filing date or demonstrates obviousness, third parties can file for patent invalidation through legal proceedings.

5. How does regional patent law impact protection in Hungary?
Hungarian patent law aligns with EU standards, requiring whether the claims meet novelty and inventive step criteria, with enforcement rights limited to Hungary unless extended via European or international filings.


Sources

[1] European Patent Office Patent Database, Hungarian Patent Office records, relevant patent literature on pharmaceutical patents.

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