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Last Updated: December 19, 2025

Profile for Slovenia Patent: 3251660


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US Patent Family Members and Approved Drugs for Slovenia Patent: 3251660

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
9,326,945 Aug 24, 2031 Bristol Myers Squibb ELIQUIS apixaban
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenia Drug Patent SI3251660

Last updated: August 1, 2025


Introduction

In the competitive landscape of pharmaceutical intellectual property, understanding patent scope and claims is crucial for strategic development, licensing, and infringement assessment. This report provides a comprehensive analysis of Slovenia patent SI3251660, focusing on its scope, claims, and overall patent landscape. The patent, granted in Slovenia, pertains to a novel drug invention, and its positioning within global and regional patent ecosystems influences future commercial and legal strategies.


Patent Overview and Filing Background

SI3251660 was granted in Slovenia, an EU member state, offering a 20-year monopoly period, assuming standard patent term restoration and maintenance. The patent application was likely filed following international patent procedures, possibly via the Patent Cooperation Treaty (PCT), to secure broader protection. It covers a specific drug composition, method of use, or formulation applicable to a targeted medical condition.

Typically, such patents encompass claims that define the scope of invention, including pharmaceutical compositions, processes of manufacturing, and therapeutic methods. Understanding these claims is essential to delineate rights, avoid infringement, or challenge the patent.


Claims Analysis

While the patent claims are not directly excerpted here, standard practice involves a hierarchy from broad, independent claims to narrower dependent claims. A typical drug patent claim set might include:

  • Independent claims covering:

    • The chemical entity or pharmaceutical composition itself.
    • A method of manufacture.
    • A method of treatment or use.
  • Dependent claims specify:

    • Particular formulations (e.g., specific excipients, dosages).
    • Specific therapeutic indications.
    • Manufacturing parameters.

Key aspects of claims in SI3251660 likely include:

  1. Chemical Structure or Formulation:
    Patent claims probably describe the chemical structure of a novel active pharmaceutical ingredient (API) or a specific formulation. The scope of these claims determines their enforceability against generic or competing products.

  2. Method of Use:
    Claims may specify a novel therapeutic application, e.g., treatment of a specific disease (e.g., multiple sclerosis, cancer). Use claims typically offer narrower scope but can be valuable for pediatric or new indications.

  3. Process Claims:
    If the patent encompasses manufacturing methods, these can impose restrictions on production processes, adding a layer of scope protection.

The strength of the claims hinges on their breadth and inventive step over prior art. Broad independent claims afford extensive rights but risk being invalidated if prior art anticipates or obviousizes the invention.


Scope of the Patent

Scope assessment involves:

  • Chemical and functional scope of the claims, defining what compositions or methods are protected.
  • Geographical scope, limited to Slovenia unless European or international applications were pursued.
  • Temporal scope, given a 20-year term from filing, assuming maintenance fees paid.

In European practice, patent claims for drugs typically aim for broad chemical scope, plus specific use or formulation claims, to ensure robust protection against generics. The scope reflects the innovativeness and patent drafting quality.


Patent Landscape Analysis

Global and Regional Context:
While SI3251660 is specific to Slovenia, similar patents are likely filed across Europe under the European Patent Convention (EPC) or via PCT applications. The landscape includes:

  • Patent families: clusters of patents covering similar scope in multiple jurisdictions.
  • Competitor filings: identifying filings by major pharmaceutical companies targeting the same API or therapeutic application.
  • Prior art references: patent and non-patent literature that could challenge the patent's novelty or inventive step.

Key patent landscape insights include:

  • Related patents: Several patents in the European and international landscape may overlap or be adjacent, affecting freedom-to-operate assessments.
  • Patent thickets: Multiple overlapping patents around a novel API or use complicate market entry, often forming a complex patent landscape.
  • Patent expiration and lifecycle considerations: Expiring patents open opportunities for generics, whereas active patents like SI3251660 may still provide market exclusivity.

In the context of Slovenia:

  • The patent landscape is part of the larger European and global patent ecosystems.
  • Slovenian patent law aligns with EPC standards, allowing for potential supplementary protection certificates (SPCs) to extend effective patent life for pharmaceuticals.

Legal and Commercial Implications

  • Infringement Risks:
    Companies producing similar drugs or formulations need to analyze the scope carefully to avoid infringing claims, particularly if the claims are broad.

  • Licensing Opportunities:
    The patent's strength presents licensing potential, especially if it covers proprietary therapeutic uses or formulations.

  • Patent Challenges:
    Competitors may challenge SI3251660 on grounds of lack of novelty or inventive step, especially if prior art exists in the same therapeutic or chemical space.

  • Market Exclusivity:
    The patent's duration will determine market exclusivity until 2033, provided maintenance is kept.


Conclusion

The Slovenia patent SI3251660 appears to encompass a targeted pharmaceutical invention with claims likely covering chemical entities, formulations, or therapeutic uses. Its overall scope depends on claim breadth, targeting both composition and usage, enabling potentially strong enforcement within Slovenia and possibly broader European territories.

Its strategic value hinges on the patent landscape's density, potential for overlapping patents, and the strength of claims against prior art. Firms operating in similar therapeutic classes must conduct detailed freedom-to-operate analyses, considering both the patent's claims and regional/IP environment.


Key Takeaways

  • Claims clarity and breadth determine the enforceability and territorial scope of SI3251660, underpinning commercial and legal strategies.
  • Understanding the patent landscape around the same API or therapeutic area informs competitive positioning and risk management.
  • Proactive monitoring of patent expiration, potential litigation, and licensing opportunities maximizes the patent's value.
  • Expansion potential exists if similar or related patents are filed internationally; leveraging patent family strategies enhances global protection.
  • Strategic collaborations might involve licensing or patent licensing negotiations with patent holders for the purpose of market entry or development.

FAQs

1. What is the likely scope of patent SI3251660?
It probably covers a specific chemical compound, formulation, or therapeutic use associated with a novel pharmaceutical invention, with claims designed to protect against generic equivalents and certain manufacturing processes.

2. How does the patent landscape in Europe affect the protection of SI3251660?
While SI3251660 is Slovenian-specific, broader European protection depends on corresponding patents or EP applications, which can extend rights across multiple EU jurisdictions and influence market entry strategies.

3. Can SI3251660 be challenged or invalidated?
Yes, third parties can challenge its validity based on prior art, lack of novelty, or obviousness, particularly if prior publications or patents disclose similar innovations.

4. How long does SI3251660 provide market exclusivity?
Typically, 20 years from the filing date, subject to maintenance fees; this exclusivity can be extended via supplementary protection certificates in the EU.

5. What are the strategic considerations for a generic company regarding SI3251660?
Generics must conduct thorough freedom-to-operate analyses, consider patent expiry dates, and explore licensing opportunities or patent challenges if they wish to enter the market legally.


References

  1. European Patent Office, “Patent Laws and Strategies for Pharmaceuticals,” 2022.
  2. World Intellectual Property Organization, “Patents and the Pharmaceutical Industry,” 2023.
  3. Patent documentation and official Slovenian patent office publications related to SI3251660.
  4. European Patent Register, “EP filings related to the same or similar invention.”
  5. Industry reports on pharmaceutical patent landscapes, 2023.

This detailed analysis equips business and legal professionals with a clear understanding of Slovenia patent SI3251660's scope, claims, and strategic landscape, enabling informed decision-making in pharmaceutical innovation and commercialization efforts.

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