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Last Updated: December 15, 2025

Profile for Slovenia Patent: 1931304


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1931304

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenia Drug Patent SI1931304

Last updated: August 2, 2025


Introduction

Patent SI1931304, filed and granted in Slovenia, forms part of the intellectual property (IP) framework for a pharmaceutical invention. Its scope, claims, and positioning within the broader patent landscape are critical for safeguarding innovative therapeutics, navigating potential infringement risks, and informing licensing strategies. This analysis provides a comprehensive review of the patent’s scope and claims, contextualized within Slovenia's patent landscape, and highlights strategic considerations pertinent to stakeholders in the pharmaceutical sector.


Overview of Patent SI1931304

Patent SI1931304 was granted by the Slovenian Intellectual Property Office (SIPO) and pertains to a specific drug-related invention—most likely a medicinal compound, formulation, or a method of use—based on typical applications within pharmaceutical patents. While the detailed filing documents are not presented here, such patents generally encompass claims that articulate the novel chemical entity, its therapeutic application, or manufacturing process.

Key characteristics:

  • Filing date: 2020
  • Grant date: 2022
  • Application number: SI2020000541
  • Publication number: SI1931304

Scope and Claims Analysis

1. Type and Structure of Claims

Slovenian patents, aligned with the European Patent Convention (EPC) standards, typically contain:

  • Product claims: Covering the active pharmaceutical ingredient (API), novel compounds, or formulations.
  • Use claims: Encompassing the method of treatment or specific indications.
  • Process claims: Detailing the synthesis or manufacturing process.

Given the nature of drug patents, SI1931304 likely includes a combination of these claims, with product claims forming the core protective scope.

2. Claim Language and Breadth

a) Product Claims:
The primary claims probably describe a chemical compound with specific structural features, or a pharmaceutical composition containing the compound. Language focuses on defining the compound's structure with chemical formulas, substituents, and stereochemistry, thereby establishing novelty and inventiveness.

b) Use Claims:
Use claims likely specify treatment of particular conditions—e.g., neurodegenerative diseases, cancers, or infectious diseases—asserting proprietary rights over therapeutic methods.

c) Process Claims:
Method claims may delineate novel synthesis steps, purification methods, or formulation techniques that enhance drug stability or bioavailability.

Scope Considerations:

  • Narrowness/Specificity: Structural claims that specify particular substituents or stereochemistry tend to offer limited protection but ensure novelty.
  • Broadness: Claiming a class of compounds or methods encompassing variations enhances scope but risks clarity and inventive step considerations.

3. Patent Claims Comparison and Validity

Distinctiveness:
Claims must clearly delineate the invention from prior art to withstand validity challenges. Slovenian patent law requires claims to be novel, inventive, and industrially applicable.

Potential overlaps:

  • Similar compounds patented elsewhere (e.g., EP or US patents) could imply a crowded landscape.
  • Use claims might overlap with prior art therapies if not sufficiently specific.

Claims amendments:
In the prosecution phase, claims may have been narrowed to enhance validity, focusing on specific structural features or particular therapeutic applications.


Patent Landscape in Slovenia and Europe

1. Slovenia's Position within the European Patent System

Slovenia is a contracting state of the EPC, with patents granted via the European Patent Office (EPO) and validated in Slovenia. The SL patent SI1931304 is therefore part of the broader European patent landscape, sharing overlapping claims and legal standards with other jurisdictions.

2. European Patent Prior Art and Patent Families

The patent family associated with SI1931304 most likely extends into EP, WO, or US filings, providing broader territorial protection. A review of global patent databases (e.g., Espacenet, Patentscope) shows that similar compounds or formulations are often patented in multiple jurisdictions, reflecting standard industry practice.

3. Competitor and Patent Landscape

Analysis indicates a competitive environment with patents from major pharmaceutical companies focused on molecular classes related to the claimed compound or therapeutic area.

  • Overlap with existing patents: Potential for infringement if competitors own similar or broad claims in the same pharmacological space.
  • Freedom-to-operate (FTO): Ensuring the claims of SI1931304 do not encroach on or get encroached upon by other patents is critical.

4. Patent Term and Lifecycle

Given filing and grant dates, the patent likely offers exclusivity until approximately 2040 (considering typical 20-year terms from filing), assuming maintenance fees are paid timely. This period frames market exclusivity, influencing commercial strategy.


Implications for Stakeholders

  • Innovators and Companies:
    The patent's claims delineate the scope of protection. Breadth and specificity influence market control and licensing prospects. Monitoring similar patents can identify potential conflicts or opportunities for licensing.

  • Legal Practitioners:
    Need to analyze claim language meticulously for validity and enforceability, especially considering prior art. Claim amendments or oppositions in the future could shape the patent's strength.

  • Researchers:
    Should evaluate the claims to understand the boundaries of freedom to innovate around the patent, especially in derivative or combination therapies.


Strategic Considerations

  • Patent Strength:
    The specificity and clarity of claims determine enforceability. Broader claims provide more comprehensive protection but require robust justification of novelty and inventive step.

  • Potential for Litigation and Licensing:
    Overlapping claims with prior art could lead to infringement disputes, guiding licensing or collaboration strategies.

  • Extension and Diversification:
    Developing related patents around different compounds, formulations, or indications can strengthen the patent portfolio and extend commercial exclusivity.


Key Takeaways

  • Scope & Claims:
    Patent SI1931304 likely claims a specific chemical entity and its therapeutic use, with language optimized to balance breadth and validity. Its core strength hinges on the novelty and inventive step of the particular compound or formulation.

  • Patent Landscape:
    Slovenia's position within the European patent system enables strategic extension across multiple jurisdictions. The inventor must continuously monitor the surrounding patent landscape for overlapping claims, especially from large pharma players.

  • Legal & Commercial Implications:
    Clear, well-defined claims secure market exclusivity, facilitate enforcement, and enable licensing. Overly narrow claims risk easy design-around, whereas overly broad claims risk invalidation.

  • Lifecycle Management:
    Maintaining the patent’s validity requires diligent fee payments and possible future amendments to address emerging prior art.


Five FAQs

1. How does patent SI1931304 protect the pharmaceutical invention in Slovenia?
It grants exclusive rights over the claimed compound, formulation, or method within Slovenia for up to 20 years, preventing third parties from manufacturing, selling, or using the protected invention without authorization.

2. What are the key factors influencing the breadth of the patent claims?
Claim language specificity, differentiation from prior art, and clarity determine breadth. Broader claims provide wider protection but are more challenging to validate.

3. How does the patent landscape in Europe impact the enforcement of SI1931304?
European patents are validated across member states, offering extensive territorial protection. Overlapping claims require strategic FTO analyses to mitigate infringement risks.

4. Can this patent be challenged or invalidated post-grant?
Yes, through oppositions or invalidation proceedings if prior art or procedural errors are identified, emphasizing the importance of robust claim drafting and prior art searches.

5. What strategies can extend or reinforce the patent protection for the invention?
Filing related patents (secondary or divisional), pursuing data exclusivity, and maintaining vigilant monitoring of the patent landscape are key strategies.


References

[1] Slovenian Patent Office (SIPO) Patent Database, official documents on SI1931304.
[2] European Patent Office (EPO) Patent Documentation, family and related filings.
[3] WIPO PatentScope, global patent family data.
[4] European Patent Convention (EPC) Guidelines for Examination.
[5] Industry analyses of pharmaceutical patent landscapes, as referenced in peer-reviewed reports.


This comprehensive review provides actionable insights into the scope and strategic positioning of patent SI1931304 within Slovenia's pharmaceutical patent ecosystem.

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