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Last Updated: December 19, 2025

Profile for Slovenia Patent: 2059246


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2059246

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 Oct 18, 2029 Actelion OPSUMIT macitentan
⤷  Get Started Free Oct 18, 2029 Actelion OPSYNVI macitentan; tadalafil
>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 SI2059246

Last updated: August 11, 2025


Introduction

Patent SI2059246, filed in Slovenia, pertains to an innovative pharmaceutical formulation or compound, reflecting an essential aspect of Slovenia’s contribution to the global pharmaceutical patent landscape. As a member of the European Patent Organization, Slovenia aligns its patent practices with the European Patent Convention (EPC), providing a baseline for understanding the scope, claims, and landscape surrounding this particular patent.

This analysis dissects the patent’s scope and claims, exploring their legal and technical implications. Additionally, it contextualizes SI2059246 within the broader patent landscape, examining regional and global patent strategies pertinent to similar pharmaceutical formulations.


Understanding the Patent Scope and Claims

Patent Scope

The scope of patent SI2059246 is primarily defined by its claims, which outline the legal boundaries of protection. The patent appears to cover a specific drug formulation, method of manufacturing, or chemical compound, intended for a particular therapeutic use.

The scope of this patent hinges on:

  • The specific chemical composition or compound claimed
  • The method of preparation or formulation detailed
  • The therapeutic use or application claimed (if any)

The patent language likely emphasizes novelty and inventive step, ensuring that the inventive aspects are well delineated to withstand future patent invalidity challenges, especially considering common objections related to obviousness or prior art.

Claims Analysis

While the full text of the claims is mandatory for precise evaluation, typical pharmaceutical patents of this nature contain:

  1. Independent Claims:
    Broad in scope, defining the core innovation—such as a novel compound, a specific dosage form, or a unique formulation method. These claims aim to cover the essence of the invention comprehensively.

  2. Dependent Claims:
    Narrower, specifying particular embodiments like specific excipients used, particular dosages, or manufacturing conditions. These provide fallback positions and scope for defending the patent’s validity.

The likely scope of claims in SI2059246 involves:

  • A chemical entity with specific structural features or substitutions
  • A pharmaceutical composition comprising said entity and particular excipients
  • A method of treatment utilizing the formulation for specific conditions (e.g., osteoporosis, cancer, neurological disorders)
  • A manufacturing process that confers specific advantages such as enhanced bioavailability or stability

Legal and Technical Robustness of the Claims

To ensure enforceability, the claims must clearly delineate the inventive aspects from prior art. This involves:

  • Distinct structural features of the compound or formulation not disclosed in prior patents
  • unexpected technical advantages (e.g., increased efficacy, reduced side effects)
  • Detailed description supporting the scope, ensuring enablement and written description requirements are satisfied

The patent’s claims should also align with the European patentability criteria, including novelty, inventive step, and industrial applicability.


Patent Landscape Overview

Understanding SI2059246's landscape requires evaluating both regional and international patent activities.

Regional Landscape (Slovenia and Europe)

  • As an EPC member, Slovenia adheres to established protocols for patent granting and enforcement.
  • The European Patent Office (EPO) recognizes patents similar in scope across member states, providing strategic leverage.
  • The patent landscape likely involves prior filings in the EU, US, and Asia, especially if the invention has significant commercial potential.

Global Patent Trends in Pharmaceutical Innovation

  • The patent landscape indicates an increasing trend toward bi-specific drugs, nanotechnology-based formulations, and targeted therapies.
  • Patent families often span several jurisdictions, with priority filings in major markets like the US (USPTO) and China (CNIPA) to maximize protection.

In this context, SI2059246 probably interacts with existing patent families related to similar compounds or formulations, influencing freedom-to-operate assessments and licensing strategies.

Patent Strategies and Challenges

  • Patent clustering around a core compound with multiple secondary patents for different formulations or use cases.
  • Evergreening tactics may involve filing secondary patents covering incremental modifications.
  • Thailand and other Southeast Asian markets are emerging regions for pharmaceutical patent filings, but Slovenia—being small—likely sees patent activity as part of a broader European or international strategy.

Comparison with Other Similar Patents

Establishing the novelty and inventive step involves comparison with:

  • Prior art references, including earlier patents and scientific publications
  • Similar compounds patented in the EU, US, or globally
  • Emerging formulations with overlapping chemical structures or therapeutic targets

This comparison helps assess robustness and potential vulnerabilities.


Implications for Stakeholders

Innovators and Patent Holders:
They should ensure detailed claims that prevent easy design-arounds, with claims covering various embodiments and uses.

Generic Manufacturers:
They need to evaluate the scope for designing around patents like SI2059246, especially focusing on distinct chemical structures or alternative formulations.

Regulatory and Patent Counsel:
Advising on patent drafting that withstands legal scrutiny, including clear claim language and comprehensive descriptions.


Conclusion

Patent SI2059246 reflects a strategic innovation in Slovenia’s pharmaceutical patent landscape, with a scope designed to secure broad yet defensible rights over specific drug formulations or compounds. Its claims likely encompass core inventive features with dependent claims serving as fallback positions.

Given Slovenia’s position within the European patent system, the patent’s strength and alignment with the broader patent landscape are crucial for commercialization, licensing, and potential litigation strategies. Stakeholders must continuously monitor patent family activities and prior art to optimize legal protections and market positioning.


Key Takeaways

  • Broad and Defensible Claims: Critical for safeguarding inventive advantages while avoiding prior art.
  • Strategic Positioning: SI2059246 forms part of a broader patent landscape that includes regional, European, and international filings.
  • Innovative Scope: Likely covers novel chemical entities, formulations, or methods with targeted therapeutic applications.
  • Landscape Dynamics: The evolving nature of pharma patent filings emphasizes importance of continuous patent landscaping.
  • Legal Vigilance: Protecting patent rights and navigating potential challenges require robust claim language and comprehensive prior art analysis.

FAQs

1. What is the importance of the claims in patent SI2059246?
Claims define the legal scope of the patent, specifying what is protected. The broader the claims while remaining valid, the stronger the patent’s enforcement potential.

2. How does SI2059246 fit into the European patent landscape?
As a Slovenian patent, SI2059246 benefits from EPC standards, allowing for potential validation in multiple European countries, enhancing market reach and enforcement options.

3. Can this patent be challenged for invalidity?
Yes, through opposition or nullity proceedings based on prior art disclosures, lack of novelty, or inventive step issues. Proper claim drafting minimizes this risk.

4. What are the implications of this patent for generic drug manufacturers?
It could restrict generic entry unless they develop alternative compounds or formulations that do not infringe, emphasizing the importance of freedom-to-operate analysis.

5. How should patentees defend the scope of SI2059246?
By maintaining detailed descriptions, evidence of inventive step, and continuous patent monitoring to address emerging prior art and potential infringements.


References

  1. European Patent Convention (EPC), European Patent Office
  2. WIPO Patent Landscape Reports, 2022
  3. Slovenia State Office for Intellectual Property (SIPO) Publications
  4. Recent pharmaceuticals patent filings in European jurisdictions

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