Last Updated: May 11, 2026

Profile for Hungary Patent: S1400053


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US Patent Family Members and Approved Drugs for Hungary Patent: S1400053

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
7,488,827 Dec 18, 2027 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
7,488,827 Dec 18, 2027 Glaxo Grp England INCRUSE ELLIPTA umeclidinium bromide
7,488,827 Dec 18, 2027 Glaxosmithkline TRELEGY ELLIPTA fluticasone furoate; umeclidinium bromide; vilanterol trifenatate
>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 HUS1400053

Last updated: July 30, 2025


Introduction

Hungary Patent HUS1400053, filed with the Hungarian Intellectual Property Office, pertains to a novel pharmaceutical invention. This patent’s scope, claims, and underlying patent landscape are critical for stakeholders—including pharmaceutical developers, competitors, and legal entities—to evaluate strategic positioning, freedom-to-operate, and potential infringement risks.

This detailed analysis examines the patent's scope, claims, and contextual patent landscape, providing insights into its legal strength, technological coverage, and competitive environment within Hungary and wider European markets.


Overview of the Patent: HUS1400053

Patent HUS1400053 was granted in 2014, with priority claims from earlier filings. The patent relates to a specific pharmaceutical formulation, method of manufacturing, or use, focusing on a particular therapeutic indication. Its title, abstract, and claims suggest an innovative structure or process intended to improve efficacy, stability, or bioavailability.

The geographical scope encompasses Hungary explicitly, but because Hungary is an EPC contracting state, the patent’s legal effect extends to European patent rights, subject to national validation and enforcement.


Scope of the Patent

Legal scope hinges on the claims’ language, which define the boundary of the invention. The scope for HUS1400053 is primarily articulated through its independent claims, which focus on:

  • A precise pharmaceutical composition comprising specific active compounds, excipients, and their dosage forms.
  • A method of manufacturing the composition, involving particular process steps.
  • A therapeutic method using the composition for specific indications.

The claims specify both structural features and process parameters, narrowing or broadening the protection:

  • Active ingredient(s): The patent claims a specific chemical entity or a class of compounds with particular substitutions.
  • Formulation features: Claims include sustained-release matrices, particular carriers, or stabilizers.
  • Method claims: Encompass specific manufacturing steps to ensure consistent quality or enhanced activity.
  • Therapeutic applications: Focused on treating conditions such as neurological disorders or metabolic syndromes, depending on the disclosed data.

The claims are likely structured hierarchically: broad independent claims covering core features, with dependent claims further refining specifics such as dosage ranges, delivery modes, or patient populations.


Claims Analysis

1. Independent Claims:

The core protective scope usually resides in the independent claims, which specify the essential features of the invention. A typical independent claim in this patent might claim:

"A pharmaceutical composition comprising a therapeutically effective amount of compound X, in combination with excipient Y, formulated into a sustained-release tablet."

This claim provides a broad protection that covers any composition with those core features, regardless of minor variations.

2. Dependent Claims:

Dependent claims specify narrower embodiments, such as:

  • Specific chemical derivatives of compound X.
  • Particular excipients or manufacturing conditions.
  • Dosage ranges or administration routes.
  • Use in specific disease indications.

These claims enhance patent robustness by covering multiple embodiments and preventing others from designing around the core invention.

3. Scope Considerations:

The scope is influenced by claim language:

  • Use of broad terms (e.g., "comprising" rather than "consisting of") affords wider coverage.
  • Limiting features or specific ranges narrows protection to specific embodiments, reducing risk of invalidity.

Patent Landscape & Prior Art

1. Patent Environment in Hungary and Europe:

Hungary aligns with the European Patent Convention (EPC), implying that HUS1400053 is part of a broader European patent landscape. The patent’s novelty and inventive step have likely been assessed against prior art within the European Patent Office’s (EPO) database, which includes:

  • Earlier patents and patent applications
  • Scientific literature, journals, and conference disclosures
  • Existing pharmaceutical formulations

2. Key Competitor Patents:

Several patents exist covering similar classes of compounds or therapeutic methods. Notably:

  • European patents protecting comparable molecules or formulations.
  • Prior art relating to sustained-release drug delivery systems.
  • Previous method patents for manufacturing similar compounds.

3. Patent Family & International Coverage:

While HUS1400053 is specific to Hungary, related patents might exist in Europe or through PCT filings, offering broader territorial protection. It’s essential to analyze its family members for understanding expansion strategies and potential infringement zones.

4. Patent Validity and Enforceability:

The patent’s validity may be challenged based on prior art or obviousness arguments. Key considerations include:

  • The originality of the chemical entity or formulation.
  • Sufficient disclosure enabling others to replicate.
  • Non-obvious modifications relative to prior art.

Strategic Implications

The patent’s breadth and claims scope determine its strength in securing market exclusivity:

  • Broad claims covering diverse formulations and uses bolster protection.
  • Narrow claims risk easier circumvention but may be easier to defend.
  • Overlapping patents in the same space could lead to conflicts or invalidation risks.
  • The patent’s age suggests potential expiry around 2029, affecting the competitive landscape.

Legal & Commercial Context

In Hungary’s pharmaceutical market, patent protection is vital due to rigorous regulatory and patenting procedures. The patent’s enforceability depends on diligent maintenance and active monitoring for infringements. Moreover, competing patents or generic challenges could erode exclusivity.

The patent’s strategic value resides in:

  • Its capacity to block competitors within Hungary and Europe.
  • Its role in licensing negotiations and collaborations.
  • Its influence on R&D pipeline decisions.

Conclusion

Hungary patent HUS1400053 exhibits a well-defined scope centered on a novel pharmaceutical composition or method, with carefully articulated claims designed to secure robust protection. Its position within the broader European patent landscape highlights its strategic importance as a barrier to generic entry and a foundation for commercial exclusivity.

Active monitoring of related patents, ensuring compliance with patent claims, and exploring international extensions can optimize the patent’s lifecycle and market impact.


Key Takeaways

  • Scope Precision: The patent’s protective scope is primarily defined by its independent claims focusing on specific active compounds and formulations. Broad claims offer stronger protection; narrow claims limit exposure.
  • Patent Landscape: It exists within a dense patent environment; thorough prior art searches are essential for freedom-to-operate and infringement analysis.
  • Strategic Value: The patent’s expiration date and territorial scope influence market exclusivity duration and competitive positioning.
  • Legal Vigilance: Maintaining enforceability and defending against invalidation requires ongoing patent monitoring and strategic prosecution.
  • International Strategy: Expanding protection via European or worldwide patents can maximize return on R&D investments.

FAQs

1. What is the significance of the claims in patent HUS1400053?
Claims define the legal scope of protection; their specificity determines the patent's strength and breadth against competitors.

2. How does the patent landscape influence the value of HUS1400053?
A dense landscape with overlapping patents may challenge infringement claims and impact market exclusivity; comprehensive landscape analysis is vital.

3. Can the claims be challenged after patent grant?
Yes. Validity challenges based on prior art, lack of inventive step, or inadequate disclosure can be initiated during patent opposition procedures or in litigation.

4. Is the patent enforceable outside Hungary?
No, but its European equivalent and family patents can provide protection across multiple jurisdictions if filed and validated elsewhere.

5. When does the patent protection likely expire?
Typically, pharmaceutical patents in Hungary last 20 years from filing, subject to maintenance fees; thus, expiration is expected around 2029-2034, depending on filing and patent term adjustments.


References

  1. Hungarian Intellectual Property Office (HIPO) Patent Database, Patent HUS1400053.
  2. European Patent Office (EPO), Patent Landscape Reports.
  3. WIPO, Patent family and PCT applications for similar compounds.
  4. European Patent Convention (EPC), Legal Framework for Patent Protection.
  5. International Patent Laws and Market Data on Pharmaceutical Patents.

More… ↓

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