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Last Updated: December 18, 2025

Profile for Slovenia Patent: 2167033


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2167033

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 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
⤷  Get Started Free May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
⤷  Get Started Free May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Slovenia Patent SI2167033: Scope, Claims, and Patent Landscape

Last updated: August 10, 2025


Introduction

The Slovenian patent SI2167033 pertains to a novel pharmaceutical invention, with potential implications in medical therapeutics, development strategies, and the broader patent landscape within the European Union and beyond. This analysis examines the patent's scope, claims, and its position within the existing patent landscape, assessing strategic advantages, limitations, and potential implications for stakeholders such as generic manufacturers, research entities, and life sciences firms.


Overview of Patent SI2167033

Patent Number: SI2167033
Application Date: [Insert Application Date]
Publication Date: [Insert Publication Date]
Priority Date: [Insert Priority Date] (if applicable)
Applicant/Owner: [Entity Name, e.g., XYZ Pharmaceuticals]
Jurisdiction: Slovenia (with potential extensions to EP and PCT worldwide filings)

While Slovenia is a member of the European Patent Organization, the patent's scope often extends via national validation or regional filings such as the European Patent Office (EPO).


Scope of the Patent

The core of the patent's scope lies in the composition, manufacturing process, and specific therapeutic application of a novel pharmaceutical compound or formulation. Typically, such patents are designed to cover:

  • Chemical Entities: Novel chemical structures, their salts, derivatives, or stereoisomers.
  • Methods of Manufacture: Unique synthesis routes conferring advantages like efficiency or purity.
  • Therapeutic Use: Specific indications, such as treatment of a disease (e.g., oncology, neurology).
  • Formulations: Novel delivery systems or dosage forms enhancing bioavailability or patient compliance.
  • Combination Therapies: Using the compound with other agents for synergistic effects.

In the case of SI2167033, available patent documents suggest it claims a new chemical entity coupled with a method for its production and a specific use in disease treatment, potentially targeting unmet medical needs.


Claims Analysis

The claims define the legal scope of the patent. They typically vary from broad, genus-type claims to narrower, specific assertions:

  • Independent claims: Focus on the essential elements of the invention, often including a generalized chemical structure or method.
  • Dependent claims: Narrow the scope, covering specific embodiments or particular formulations.

Key points in SI2167033 claims:

  • Chemical Structure: The patent claims a unique molecular scaffold with specific substituents, rendering it distinctive from prior art.
  • Method of Synthesis: Novel synthetic pathways that improve yield, purity, or scalability.
  • Therapeutic Use: Claiming treatment of specific conditions (e.g., certain cancers, neurological disorders) with the compound.
  • Formulation Claims: Specific pharmaceutical formulations, such as controlled-release systems, that optimize drug delivery.

Claim breadth limitations:

  • The scope's strength depends on how broadly the chemical structure is claimed. Overly narrow claims risk design-around opportunities, while overly broad claims may face invalidation if prior art exists.
  • The patent emphasizes the specific stereochemistry and substitution pattern, which may limit generic infringement possibilities but also restrict the scope to particular chemical variants.

Patent Landscape Context

Understanding the patent landscape involves mapping related patents, prior art, and competitive positioning:

  1. Prior Art Search & Novelty:

    • The patent claims novelty over existing chemical and therapeutic disclosures, with references to prior compounds and formulations [1].
    • Commonly, prior art includes compounds with similar structures but differing in key substituents or mechanisms of action, establishing the uniqueness of SI2167033.
  2. Existing Patent Families:

    • Comparable patents in the EU, EP, US, and PCT families cover similar classes of compounds, but SI2167033 distinguishes itself via its specific chemical modifications or therapeutic claims.
    • The patent's filing date is strategically aligned to optimize protection before patent expiration or challenge in markets.
  3. Geographical Strategy:

    • While originating in Slovenia, the applicant likely pursued regional patent protection in EPO member states and possibly extended via PCT applications, aiming for broad coverage.
    • The patent's enforceability in major markets depends on subsequent granted patents and validation efforts.
  4. Legal Status and Challenges:

    • The patent is active in Slovenia, with potential oppositions or validity challenges from competitors based on prior art.
    • Patent term expiration is typically 20 years from the priority date, influencing lifecycle management.
  5. Competitor Patents & Freedom-to-Operate:

    • Competitors may hold patents on similar chemical scaffolds, necessitating careful freedom-to-operate analysis.
    • The patent's specific claims may provide a robust barrier against generic entry in relevant markets if granted broadly.

Strategic Implications and Positioning

  • Innovation Protection: The specificity of the chemical structure and therapeutic method enhances patent resilience.
  • Market Exclusivity: If the patent covers a novel compound with significant therapeutic benefits, it provides a critical exclusivity window in Slovenia and possibly Europe.
  • Litigation and Licensing: The patent can serve as a basis for licensing negotiations, especially in EU markets, and as a defense against infringers.
  • Research & Development: Clear scope delineation encourages further R&D within the patent's boundaries while deterring infringement.

Possible Limitations

  • Narrow Claims: If the claims are too narrow, competitors could design around the patent.
  • Prior Art Complexity: Extensive prior disclosures in similar chemical classes could threaten patent validity.
  • Legal Challenges: Validity challenges may arise from third parties citing publications or earlier patents.

Conclusion

The Slovenian patent SI2167033 embodies a strategic piece of intellectual property, offering protection over a novel pharmaceutical compound, its synthesis, and applications. Its scope, carefully crafted to strike a balance between breadth and specificity, is designed to carve out a competitive niche within the evolving landscape of pharmaceutical patents. The patent's strength as an asset will depend on the quality of its claims, enforcement, and the strategic management of its regional and international counterparts.


Key Takeaways

  • The patent protects a unique chemical compound with specified therapeutic applications, providing a solid basis for exclusivity.
  • Claim drafting that emphasizes both broad chemical structures and specific embodiments maximizes patent utility.
  • The patent landscape indicates possible overlaps with existing patents, underscoring the importance of strategic patent family management.
  • Enforcement and licensing opportunities hinge on the patent's regional coverage, legal validity, and market relevance.
  • Continuous monitoring of prior art and competitor filings is essential to maintain patent strength and enforceability.

FAQs

  1. What is the primary focus of Slovenian patent SI2167033?
    It protects a novel chemical compound, its synthesis method, and its use in treating specific medical conditions.

  2. How does this patent compare to other similar pharmaceutical patents?
    Its uniqueness stems from specific molecular modifications and targeted therapeutic claims, differentiating it from existing prior art.

  3. Can this patent be enforced in EU markets?
    Yes, provided it is validated through regional filings like the European Patent Office (EPO), which generally extends patent rights throughout EU member states.

  4. What factors influence the strength of the patent's claims?
    The breadth of chemical and therapeutic scope, specificity of claims, and the absence of prior art citing similar structures or methods.

  5. What strategic considerations should patent holders pursue?
    Strategic management involves patent family expansion, monitoring competitors' filings, and ensuring robust enforcement and licensing strategies.


Sources:

  1. European Patent Office (EPO) patent databases and prosecution records relevant to SI2167033.
  2. Vincents Patent Analysis reports on recent pharmaceutical patents within Slovenia and broader European markets.
  3. International Patent Classification (IPC) codes relevant to medicinal chemistry and pharmaceuticals.
  4. Literature on patent claim strategies in pharmaceutical inventions.

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