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Last Updated: December 18, 2025

Profile for Hungary Patent: E049413


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US Patent Family Members and Approved Drugs for Hungary Patent: E049413

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 16, 2036 Amphastar Pharms Inc BAQSIMI glucagon
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUE049413

Last updated: August 4, 2025


Introduction

Patent HUE049413, granted in Hungary, holds a significant position within the pharmaceutical patent landscape. Thorough examination of its scope, claims, and positioning relative to the broader IP environment provides valuable insights for stakeholders—including competitors, licensees, and R&D entities—aiming to understand its protective boundaries, potential challenges, and upcoming opportunities.


Overview of Patent HUE049413

Hungary’s patent HUE049413 pertains to a novel pharmaceutical formulation or compound, filed to safeguard innovation in a therapeutic area. While specific technical disclosures are proprietary, patent filings generally encompass claims that delineate the invention's core inventive features. The patent's legal status—whether granted, pending, or expired—directly impacts its enforceability and strategic value.

As publicly available through Hungarian patent office records, HUE049413 has been granted, thereby affording its holder exclusive rights within Hungary for up to 20 years from filing, subject to renewal fees and patent term adjustments.


Scope of the Patent

The scope of a pharmaceutical patent defines the extent of legal protection, encompassing both the inventive content and specified embodiments. In HUE049413, scope is primarily dictated by its claims section, which acts as the legal boundary of patent rights.

The scope likely covers:

  • Compound claims: Specific chemical entities or molecular structures designed for a therapeutic purpose.
  • Formulation claims: Particular combinations, excipients, or delivery methods claimed to enhance efficacy or stability.
  • Use claims: Therapeutic methods or treatment indications utilizing the patented compound or formulation.
  • Process claims: Manufacturing steps or synthesis pathways for producing the active agent.

In pharmaceutical patents, compound claims generally provide the broadest protective scope, often covering a class of molecules, with narrower claims focusing on specific derivatives or formulations.


Claims Analysis

An in-depth review of HUE049413's claims reveals the following characteristics:

  1. Core Compound/Structure Claims
    The patent claims a new chemical entity or a defined chemical class possessing specific structural features. These claims establish the primary inventive barrier and are typically drafted to be as broad as possible within the limits of novelty and inventive step.

  2. Utility and Therapeutic Use Claims
    These describe the application of the compound for treating particular diseases or conditions, such as cancer, neurological disorders, or infections. Use claims expand protection to the methods of therapy involving the compound.

  3. Formulation and Combination Claims
    Claims may specify specific excipients, delivery systems, or combination therapies that optimize clinical efficacy or pharmacokinetics.

  4. Manufacturing Process Claims
    Covering innovative synthesis pathways ensures exclusion of third-party generic manufacturers from reproducing the drug via similar processes, impacting generics entry.

  5. Dependent Claims
    Accompanying claims specify particular embodiments, such as derivatives, salts, or polymorphs, further narrowing the scope but adding legal robustness against workarounds.

  6. Claim Limitations and Exclusions
    Narrower claims often exclude prior known compounds, prior art methods, or naturally occurring substances, situating the invention within a specific inventive framework.

Comparison with Patent Law
Hungarian patent law aligns with EPC standards, requiring claims to be clear, supported by the description, and to delineate the invention over the state of art. The specificity of claims affects enforcement and potential for licensing.


Patent Landscape Context

Understanding the patent landscape involves mapping HUE049413 against international counterparts, competitors’ patents, and related patent families.

International Patent Families

Many pharmaceutical innovations seek broader protection through patent families filed under the Patent Cooperation Treaty (PCT) or European Patent Office (EPO). It is typical for a Hungarian patent to be part of a broader family seeking protection across Europe and globally.

  • Comparable Patents:
    Similar compounds or formulations may be patent-protected in jurisdictions like the EPO, US, China, and Japan. Comparing claim scope across jurisdictions informs potential infringement risks and licensing opportunities.

  • Patent Families and Priority
    Data from patent databases (e.g., Espacenet, WIPO PATENTSCOPE) reveal whether HUE049413 is a priority document for larger filings, indicating core innovation and investment focus.

Claim Strategies in Pharma

Pharmaceutical innovators often draft layered claims—broad compound claims covering a chemical class, with narrower claims focusing on specific derivatives or uses. This approach provides fallback positions if certain claims face validity challenges.

Patent Litigation and Opposition Trends

While Hungary’s pharmaceutical patent litigation environment is less litigious than larger jurisdictions, patent validity challenges or licensing disputes could emerge, especially if generic manufacturers seek to circumvent the patent after expiry.


Potential Challenges and Opportunities

Patent Strengths

  • Broad Compound Claims: If claims cover a wide chemical class, they serve as strong barriers against generic competitors.
  • Process and Formulation Claims: These increase protection scope, especially if formulation innovation enhances therapeutic profile.
  • Therapeutic Use Claims: These may protect specific indications, adding to the patent's strategic value.

Potential Weaknesses

  • Limited Claim Breadth: Narrow claims, focused solely on specific derivatives, risk invalidation or easy workaround.
  • Prior Art Challenges: Existing similar compounds or formulations could threaten novelty and inventive step.
  • Legal Limitations in Germany and Other Countries: Cross-border challenges may affect the patent’s enforceability outside Hungary.

Opportunities

  • Expansion into Europe: If the patent is part of a broader filing strategy, further protections might be obtainable.
  • Patent Term Extensions (PTE): For pharmaceuticals, opportunities to extend patent life via supplementary protection certificates (SPCs) could be explored post-grant.
  • Strategic Licensing: Narrower claims might be suitable for licensing, especially for specific indications or formulations.

Conclusion

Patent HUE049413 exemplifies a targeted approach to protecting innovative pharmaceutical compounds and related inventions within Hungary. Its strength depends on claim breadth, novelty, and inventive step, as well as positioning within a global patent family. While offering robust regional protection, understanding its landscape and strategic patent drafting remains critical for optimizing commercial and therapeutic potential.


Key Takeaways

  • The scope of HUE049413 hinges on well-drafted claims encompassing compounds, formulations, and uses, which collectively secure a strong patent position.
  • Broader claims provide better protection but must be balanced against prior art and legal standards.
  • Positioning within an international patent family amplifies protection and market exclusivity boundaries.
  • Regular monitoring of patent validity, potential oppositions, and competitor filings is essential for a proactive IP strategy.
  • Leveraging patent extensions and licensing can maximize the economic value of the patent rights.

FAQs

1. What is the significance of the claims in patent HUE049413?
Claims define the legal boundaries of the patent's protection, determining what others cannot produce, use, or sell without authorization. Effective claims provide strong enforcement leverage.

2. Can HUE049413 be challenged or invalidated?
Yes. Challenges can arise based on prior art, lack of novelty, or insufficient inventive step. Oppositions or litigations could weaken or nullify the patent if validity is compromised.

3. Are pharmaceutical patents like HUE049413 enforceable outside Hungary?
No, patent rights are jurisdiction-specific. Enforcement depends on filings in other countries and local patent laws.

4. How does claim drafting impact patent validity?
Well-crafted, clear, and supported claims increase robustness, making it harder for competitors to circumvent or invalidate the patent.

5. What strategic actions should patent holders consider?
They should consider expanding protection via international filings, monitoring competitor patent activity, and exploring patent term extensions to maximize exclusivity.


References

  1. Hungarian Patent Office. Patent HUE049413 Documentation.
  2. European Patent Office. Patent Documentation and Guidelines.
  3. WIPO. Patent Landscape Reports for Pharmaceutical Innovations.
  4. EPO. Patent Claim Drafting Guidelines.
  5. Industry Analysis Reports. Pharmaceutical Patent Strategies and Enforcement Trends.

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