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Last Updated: December 28, 2025

Profile for Hungary Patent: E043732


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US Patent Family Members and Approved Drugs for Hungary Patent: E043732

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
10,016,429 Dec 12, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
10,610,530 Dec 12, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
8,722,693 Dec 12, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
8,722,693 Dec 12, 2028 Incyte Corp JAKAFI ruxolitinib phosphate
8,822,481 Dec 12, 2028 Incyte Corp OPZELURA ruxolitinib phosphate
>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 HUE043732

Last updated: July 30, 2025


Introduction

Patent HUE043732, filed and granted in Hungary, encapsulates intellectual property rights surrounding a specific pharmaceutical invention. This analysis dissects the scope of the patent, its claims, and situates it within the broader patent landscape. Understanding the patent’s coverage informs stakeholders about its enforceability, potential for infringement, infringement risks, and opportunities for licensing or design-around strategies.


Patent Overview and Basic Details

Patent HUE043732 originated from a national or regional application process, providing exclusive rights within Hungary. The patent’s filing date, grant date, and expiration are critical markers; typically, pharmaceutical patents have a 20-year term from the earliest filing date, possibly adjusted for national phases or patent term extensions.

Although specific details such as applicant, inventor, or filing date are not provided here, the patent’s scope involves a drug or pharmaceutical process, and its claims define the boundaries of the invention.


Scope of the Patent

The scope of HUE043732 hinges on its claims—the legal boundaries defining what the patent legally protects. Pharmaceutical patents generally protect either:

  • The compound or active pharmaceutical ingredient (API);
  • The process for synthesizing the compound;
  • The formulation or dosage form;
  • The therapeutic use or method of treatment.

In Hungary, as in the broader European and global context, the scope can be both product-specific and process-specific.

Key considerations:

  • Product Claims: If the patent claims a novel API or a specific salt, ester, or derivative, the scope is limited to that compound’s structure, purity, and possibly its method of manufacturing.
  • Method Claims: Encompass proprietary processes for synthesizing the API, which are patentable if sufficiently inventive.
  • Use Claims: Cover therapeutic or prophylactic indications, especially if the invention relates to a novel medical use or new treatment method.
  • Formulation Claims: Cover specific formulations or delivery systems that enhance bioavailability or stability.

The breadth of the claims directly impacts the patent’s enforceability and the scope of potential infringement.


Claims Analysis

Without the exact claim language, a typical pharmaceutical patent might include:

  • Independent Claims: Core claims defining the primary invention — for instance, a new chemical compound with specified structural features or a novel process for its synthesis.
  • Dependent Claims: Narrower claims that specify particular embodiments or methods, such as specific salts, polymorphs, or combination therapies.

Example (hypothetical): If HUE043732 claims a novel compound, the independent claim might describe the chemical structure broadly, while dependent claims specify particular substituents, stereochemistry, or salts.

Patentability and Validity Considerations:

  • Novelty: The invention must be new; prior art in the form of existing drugs, publications, or patents can challenge this.
  • Inventive Step: The invention must not be obvious; especially relevant if similar compounds or processes exist.
  • Industrial Applicability: The invention must be capable of commercial production and use.

Claim language precision determines enforcement. Overly broad claims can be vulnerable to invalidation, while narrow claims may provide limited protection.


Patent Landscape in Hungary and International Context

Hungary’s position within the European patent regime offers insight into the patent landscape:

  • European Patent System: Hungary is part of the European Patent Convention (EPC), allowing patent holders to validate patents across member states. However, since HUE043732 appears to be a national patent, direct extension or harmonization pathways are limited unless a European patent is involved.

  • Overlap with European Patents: Competitors may challenge or seek to design around the patent through existing European patents, particularly if the patent claims are narrow.

  • Patent Family and Global Status: To assess the global patent landscape, one must investigate if similar patents exist internationally, e.g., via the World Intellectual Property Organization (WIPO), European Patent Office (EPO), or national filings in major markets (US, China, Japan).

  • Freedom-to-Operate (FTO): Determining whether the patent hinders or permits commercial activities in Hungary and neighboring countries necessitates detailed prior art searches and patent mapping.

  • Patent Litigation and Opposition: In Hungary, patent validity can be challenged via opposition procedures or invalidity suits, impacting the patent’s enforceability.


Patent Landscape and Competitive Positioning

The patent’s landscape context hinges on:

  • Existence of similar patents: The pharmaceutical field often involves multiple patents covering different aspects (composition, process, use, formulation). Overlapping patents can cause freedom-to-operate (FTO) challenges, or provide avenues for licensing and collaboration.

  • Innovation Status: If HUE043732 protects a novel compound or process, patent expiration dates and previous art influence strategic decisions. The emergence of biosimilars or generics post-expiry could erode market exclusivity.

  • Patent Thickets and Litigation: The presence of multiple overlapping patents forms a thicket, affecting market entry and licensing strategies.

  • Life Cycle Management Opportunities: Follow-up patents, such as secondary patents on formulations or uses, can extend protection or improve product positioning.


Strategic Implications

  • Enforcement: Broad, well-defined claims enhance enforcement potential; narrow claims increase vulnerability but may be easier to defend.

  • Infringement Risks: Companies developing similar drugs must scrutinize claim language to avoid infringement.

  • Licensing and Partnerships: The patent offers leverage for licensing negotiations. Its scope and validity influence licensing value.

  • Patent Expiry Planning: Patent filing dates, term adjustments, and potential extensions (e.g., data exclusivity) affect commercial planning.


Key Takeaways

  • Clarity of Claims is Crucial: Precise, well-drafted claims define enforceability and scope; ambiguity reduces litigation resilience.
  • Patent Landscape Integration: Mapping similar patents globally is essential for assessing market entry, infringement risks, and licensing opportunities.
  • Strategic Portfolio Building: Complementary patents on formulations, methods, and indications bolster patent life-cycle management.
  • Regional Considerations: Patent validity is limited geographically; multijurisdictional strategies necessitate filings in key markets.
  • Dynamic Environment: Patent rights can be challenged or invalidated; ongoing monitoring and defensive strategies are vital.

FAQs

1. What is the significance of the claims in patent HUE043732 for pharmaceutical companies?
Claims define the scope of the patent's protection, determining what constitutes infringement. Precise claims allow companies to safeguard their innovations while avoiding infringing on others’ rights, thereby shaping legal and commercial strategies.

2. How does the patent landscape in Hungary impact global pharmaceutical patent strategies?
Hungary’s national patents are limited geographically; companies seeking global protection must pursue European and international filings. The landscape informs licensing, partnership, and market entry decisions within Hungary and across Europe.

3. Can the scope of HUE043732 be broadened through subsequent patents?
Yes, follow-up patents on formulations, new uses, or improved processes can extend protection and supplement the original patent, creating a more robust patent portfolio.

4. How might competitors challenge the validity of patent HUE043732?
By presenting prior art that anticipates or renders the invention obvious, competitors can contest validity through legal invalidation procedures, which are common in Hungary and European jurisdictions.

5. What are the strategic considerations for maintaining or challenging this patent?
Maintaining the patent requires timely payments and monitoring for potential infringements, while challenging it necessitates thorough prior art searches and legal expertise to demonstrate invalidity on grounds like lack of novelty or inventive step.


References

  1. European Patent Office. (2023). Patent and Patent Search Resources.
  2. Hungarian Intellectual Property Office. (2023). Patent Law and Practice.
  3. World Intellectual Property Organization. (2023). Patent Landscape Reports.
  4. European Patent Convention. (2023). Guidelines for Examination.
  5. WIPO. (2023). Patentability and Patent Law Fundamentals.

In conclusion, patent HUE043732 represents a strategic asset with scope defined through its claims—whether protecting a chemical compound, process, or use. The effectiveness of its enforceability hinges on claim drafting, global patent landscape considerations, and ongoing patent management strategies. Continuous monitoring and proactive patent portfolio development are essential in the dynamic pharmaceutical field.

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