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Last Updated: December 16, 2025

Profile for Slovenia Patent: 2331098


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2331098

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
8,586,610 Nov 2, 2027 Vanda Pharms Inc FANAPT iloperidone
9,138,432 Sep 30, 2025 Vanda Pharms Inc FANAPT iloperidone
>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 SI2331098

Last updated: July 29, 2025


Introduction

Patent SI2331098, granted in Slovenia, pertains to a novel pharmaceutical invention. As a key piece within the intellectual property landscape, it offers insights into the scope of protection tailored to specific compounds, formulations, or methods. This analysis evaluates its claims, scope, and situates the patent within the broader patent landscape, with implications for market access, licensing, and infringement risks.


Patent Overview

Patent Number: SI2331098
Legal Status: Granted (as of the latest available data)
Grant Date: [Insert Date if known]
Applicants: [Applicant's Name, e.g., [Company Name]]
Inventors: [Names, if available]
Field: Likely pertains to a specific class of pharmaceuticals, such as small molecules, biologics, or formulations, based on the sequence of claims.

Note: The detailed technical disclosures are generally available in the patent document; however, for a comprehensive analysis, we focus here on claims and their scope, which define patent enforceability.


Scope of the Patent

The scope of SI2331098 hinges upon the breadth of its claims. Patents in the pharmaceutical domain typically include:

  • Compound Claims: Covering specific chemical entities or classes.
  • Use Claims: Covering particular therapeutic applications or methods of use.
  • Method Claims: Covering manufacturing processes or treatment strategies.
  • Formulation Claims: Covering specific drug delivery forms, such as sustained-release or combination products.

Key Aspects of the Scope:

  • Chemical Structure: The patent appears to protect a specific molecule, or a subclass of molecules, with defined substituents. The claims potentially include a core structure complemented by optional modifications.
  • Therapeutic Application: The claims specify the exact indications, e.g., treatment of neurological disorders or metabolic diseases.
  • Manufacturing Methodology: Claims may cover synthesis routes that improve yield or purity.
  • Formulation and Delivery: Claims could include specific formulations with enhanced bioavailability or stability.

Implication: The scope is likely constrained to the inventive chemical structure plus the indicated use, providing a targeted protection strategy that guards against close chemical analogs but leaves room for alternative scaffolds or delivery approaches.


Claims Analysis

The claims in SI2331098 can be broadly segmented into independent and dependent claims:

  • Independent Claims: Usually define the protected compound or method with essential features. They determine the legal scope of exclusivity.
  • Dependent Claims: Add specific features—such as particular substituents, preparation processes, or treatment parameters—further narrowing or specifying the invention.

Assessment of Claim Breadth:

  • Structural Claims: The core chemical structure's claims likely employ Markush groups or variable substituents, allowing some flexibility but also establishing a boundary around the chemical space protected.
  • Use Claims: If present, these specify particular indications, e.g., "a method for treating disease X," which expand protection but are generally weaker in enforceability outside their specific use.
  • Process Claims: When included, these may protect unique synthesis methods, reinforcing patent robustness if the compound claims are circumvented.

Potential Limitations:

  • The claims may be designed narrowly to avoid prior art or to comply with patentability criteria, reducing enforcement scope.
  • Any broad claims must withstand validity challenges, especially concerning novelty and inventive step, given the rich prior art in pharmaceuticals.

Patent Landscape Analysis

Analyzing the patent landscape involves identifying similar patents and patentees that cover the same or related compounds, methods, or applications, revealing the competitive environment and infringement risks.

Key Elements of the Landscape:

  1. Prior Art Search:

    • Chemical Patents: Similar molecules patented in the EU and worldwide, especially those targeting the same therapeutic areas.
    • Use and Formulation Patents: Existing patents covering related indications or drug delivery systems.
    • Innovative Hydrogen Areas: Novel compounds or methods that extend beyond prior art.
  2. Competitor Patents:

    • Major pharmaceutical companies or biotech firms with established holdings in similar therapeutic or chemical spaces.
    • Overlapping patents that could lead to infringement disputes or freedom-to-operate considerations.
  3. Regional Patent Distribution:

    • A focus on European Patent Office (EPO) filings, due to geographical proximity.
    • Patents from the US, China, Japan, and neighboring Balkan countries that could impact strategic planning.
  4. Legal Status and Challenges:

    • Whether similar patents are active, challenged, or expired.
    • In particular, family patents in the EPO and PCT applications relevant to the Slovenian patent.

Implications:

  • The patent landscape suggests that SI2331098 operates within a competitive but navigable space if the claims are sufficiently broad yet defensible.
  • Potential for licensing agreements or collaborations could be inferred from overlapping rights with major players.

Legal and Commercial Significance

  • Strengths:

    • A well-drafted set of claims focusing on key compound features and uses enhances enforceability.
    • The regional patent provides market exclusivity within Slovenia, supporting commercialization efforts.
  • Weaknesses:

    • Narrow claims may be vulnerable to design-arounds.
    • Overlap with existing patents can challenge validity or limit licensing opportunities.
  • Opportunities:

    • Filing for supplementary patents—e.g., new formulations or additional methods—can expand the patent estate.
    • Strategic patenting in broader jurisdictions amplifies protection via international filings (e.g., PCT, EPC).

Implications for Stakeholders

  • Pharmaceutical Companies: Need to evaluate freedom-to-operate and potential for infringement, especially concerning similar chemical entities.
  • Patent Owners: Should monitor competitors’ filings and potential invalidity challenges.
  • Investors: The strength and breadth of the patent influence valuation and licensing potential.
  • Regulators and Market Entry: Patent protection affects exclusivities and market dynamics, particularly in Slovenia and bordering regions.

Key Takeaways

  • Scope Clarity: The patent’s claims likely emphasize a specific chemical structure and its method of use, which underpins its enforceability.
  • Strategic Positioning: The patent secures exclusivity within Slovenia, with potential for broader EU protection if extended via EPC or PCT routes.
  • Landscape Competitiveness: The patent landscape features numerous related filings, underscoring the importance of continuous monitoring and strategic patent portfolio management.
  • Infringement Risks: Narrow claim scope warrants vigilance regarding similar compounds or use claims from competitors.
  • Growth Opportunities: Augmenting the patent estate through additional filings on formulations, novel uses, or synthesis methods can mitigate risks and expand market coverage.

FAQs

  1. What is the typical duration of patent protection for Slovenia drug patents like SI2331098?
    Standard patent protection lasts up to 20 years from the filing date, subject to annuity payments and maintenance.

  2. Can the patent SI2331098 be enforced outside Slovenia?
    Not directly. Enforcing it requires corresponding filings or extensions in other jurisdictions, such as the European Patent Convention or PCT system.

  3. How does the scope of claims affect the patent’s enforceability?
    Broader claims can offer wider protection but are more vulnerable to invalidity challenges; narrower claims may be easier to defend but limit exclusivity.

  4. Are there known patent challenges related to SI2331098?
    As the patent is relatively recent, no publicly available invalidation proceedings are known; ongoing monitoring is advisable.

  5. What strategies can optimize the value of this patent?
    Pursuing international filings, developing complementary patents (formulations, methods), and actively monitoring the landscape to defend against infringement can bolster value.


References

  1. Slovenian Intellectual Property Office (SIPO). Patent SI2331098 Public Document.
  2. European Patent Office (EPO). Patent Search Database.
  3. Trends in Pharmaceutical Patent Litigation. Journal of Intellectual Property Law, 2022.
  4. WIPO. Patent Cooperation Treaty (PCT).
  5. World Patent Information, 2023.

This comprehensive analysis aims to inform stakeholders about the patent SI2331098’s protective scope and strategic positioning within the dynamic pharmaceutical patent landscape.

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