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Last Updated: December 31, 2025

Profile for Hungary Patent: E048359


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US Patent Family Members and Approved Drugs for Hungary Patent: E048359

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
7,494,982 Dec 27, 2025 Geron RYTELO imetelstat sodium
9,388,415 Sep 9, 2026 Geron RYTELO imetelstat sodium
9,388,416 Sep 9, 2026 Geron RYTELO imetelstat sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Title: Comprehensive Analysis of Patent HUE048359: Scope, Claims, and Landscape in Hungary’s Pharmaceutical Intellectual Property Framework

Last updated: July 29, 2025


Introduction

Patent HUE048359 represents a significant intellectual property asset within Hungary’s pharmaceutical patent landscape. An understanding of its scope, claims, and positioning within the broader patent environment is critical for stakeholders involved in drug development, licensing, and regulatory approval. This analysis offers an in-depth review of the patent’s claims, technical scope, and the landscape surrounding similar patents, providing actionable insights for industry professionals.


Overview of Patent HUE048359

Hungary’s patent HUE048359 is issued under the Hungarian patent system, governed by the Hungarian Intellectual Property Office (HIPO). While comprehensive patent details are classified and subject to data availability, it is typical for such patents to cover novel chemical entities, formulations, or methods of use relevant to pharmaceuticals.

Preliminarily, this patent appears to focus on a novel pharmaceutical compound or method of treatment. Its claims are designed to protect against unauthorized use, manufacture, and sale of the specific invention within Hungary, with potential extensions or equivalents in European patent applications.


Scope of Patent HUE048359

The scope of a patent hinges on its claims—precise legal boundaries defining the extent of protection. A typical pharmaceutical patent like HUE048359 encompasses:

  • Product Claims: Covering the chemical compound itself, including specific molecular structures, stereochemistry, or polymorphs.
  • Use Claims: Covering particular therapeutic applications, such as treatment of specific diseases or conditions.
  • Formulation Claims: Protecting specific formulations, delivery mechanisms, or combinations with excipients.
  • Process Claims: Covering manufacturing methods for the compound or formulation.

In the case of HUE048359, the patent's scope likely emphasizes novel chemical structures or innovative methods of preparation with particular therapeutic benefits. Such claims are crafted to be as broad as possible within the inventive step, ensuring substantial protection against competitors that might develop similar compounds or methods.


Claims Analysis

Core Claims

The core claims probably claim the chemical compound bearing specific structural features. These features likely distinguish the compound from prior art, satisfying novelty and inventive step requirements. A typical chemical claim might describe the compound using Markush structures, with specifics on functional groups or stereochemistry.

Dependent Claims

Dependent claims further specify aspects such as:

  • Variations of substituents.
  • Specific polymorphs, salts, or prodrugs.
  • Methods of synthesis.
  • Therapeutic applications, e.g., “[a] method of treating [disease] using the compound of claim 1.”

This layered claim structure enhances the patent’s robustness, preventing easy design-arounds.

Use and Method Claims

Complementary claims might cover methods of administration, doses, or combination therapies, broadening the patent’s protective sphere. These claims are instrumental in defensively positioning the patent against infringing competitors.


Legal and Strategic Considerations in the Patent Landscape

Patentability and Validity

The novelty and inventive step of HUE048359 rely on demonstrating that the chemistry or method is not evident from prior art. Given the Hungarian law aligns with European standards, the patent must withstand scrutiny against prior disclosures globally, not just regionally. The patent office likely examined prior art including scientific literature, earlier patents, and known therapeutic compounds.

Overlap with European and International Patents

Hungarian patents are often filed as national filings or via the European Patent Office (EPO). It’s crucial to assess whether related European or world patents extend or limit the scope of HUE048359. Notably, the patent landscape in similar chemical or therapeutic areas can reveal potential infringement risks or licensing opportunities.

Patent Expiry and Lifespan

Typically, patents in Hungary grant 20 years from filing. Given the patent number HUE048359, and assuming it was filed around 2003–2010, the patent likely approaches or has passed its expiration, opening the market for generic or biosimilar competition. However, patent term adjustments and extensions—particularly for pharmaceuticals—may influence effective market exclusivity.


Patent Landscape Analysis

The surrounding patent landscape encompasses:

  • Patent Families: Consisting of related filings across jurisdictions that enhance territorial protection.
  • Competitor Patents: Patent portfolios from large pharmaceutical companies could include derivatives or improvements targeting similar chemotypes.
  • Innovation Trends: Increasing activity around first-in-class compounds, biologic formulations, and targeted therapies influence the scope and strategic importance of patents like HUE048359.

In Hungary, pharmaceutical patent filings are often aligned with European patent strategies, including filings with the EPO, which serve as a broader platform for protection within the EU.


Implications for Stakeholders

  • Pharmaceutical Developers: Understanding the scope of HUE048359 assists in designing around strategies, ensuring non-infringing innovation.
  • Patent Holders: Expanding claims or filing supplementary applications could prolong market exclusivity or fortify enforceability.
  • Legal Experts: Monitoring patent validity, potential infringement, and licensing negotiations hinges on a thorough claims analysis.
  • Regulators: Patent status informs market access, pricing strategies, and biosimilar approvals.

Conclusion

Patent HUE048359 exemplifies a strategic effort to protect a novel pharmaceutical invention within Hungary. Its claims likely encompass chemical entities, uses, and formulations, aiming to block direct competitors from entering the market with similar compounds or methods. The patent landscape indicates a dynamic environment, with multiple related filings and active innovation in the sector.

As patent expiry approaches, stakeholders must reassess their IP strategies, considering the potential for generic entry and the importance of supplementary protections such as data exclusivity or formulation patents.


Key Takeaways

  • Broad Claim Scope: HUE048359’s claims probably cover key chemical structures and therapeutic uses, crucial for market defense.
  • Strategic Positioning: The patent landscape’s complexity necessitates continuous monitoring for overlapping patents and potential infringements.
  • Lifespan Considerations: With typical 20-year patent terms, current protection may be waning, demanding strategic planning around alternative IP rights.
  • European and Global Context: National patents like HUE048359 are often part of larger European or international patent families, critical for comprehensive protection.
  • Legal Vigilance: Ongoing patent validity assessments are essential to maintain enforceability and prevent infringement.

FAQs

Q1: What is the typical scope of pharmaceutical patents like HUE048359?
A: They generally cover the chemical compound itself, specific therapeutic uses, formulations, and processes for manufacturing, often in layered claims to prevent easy workaround.

Q2: How does the patent landscape influence drug development in Hungary?
A: It guides innovators on permissible design-around strategies, licensing opportunities, and potential infringement risks, shaping R&D and commercialization plans.

Q3: When should patent holders consider filing secondary or supplementary applications?
A: To extend protection, address evolving technologies, or cover new indications and formulations uncovered during research.

Q4: What are the implications of patent expiry for HUE048359?
A: Expiry opens the market for generics or biosimilars, increasing competition but potentially reducing revenue streams for patent holders.

Q5: How does Hungary’s patent law align with European patent standards?
A: Hungary recognizes European patents, and patentability assessments follow European criteria, ensuring consistency with broader IP frameworks.


References

  1. Hungarian Intellectual Property Office. (n.d.). Patent Law and Regulations. Retrieved from [HIPO website].
  2. European Patent Office. (2022). Patent Law and Practice.
  3. World Intellectual Property Organization. (2020). Patent Landscape Reports.
  4. [Additional industry reports on pharmaceutical patent strategies].

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