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Last Updated: December 17, 2025

Profile for Slovenia Patent: 3169307


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US Patent Family Members and Approved Drugs for Slovenia Patent: 3169307

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
11,213,498 Jan 14, 2036 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
11,389,416 Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
12,083,087 Jul 17, 2035 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>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 SI3169307

Last updated: July 31, 2025

Introduction

Slovenia Patent SI3169307 pertains to pharmaceutical innovations within the country’s patent framework, reflecting the intellectual property protections available for novel drug compositions, methods, or uses. This analysis offers a comprehensive overview of its scope and claims, contextualizes it within the patent landscape, and evaluates its strategic significance for stakeholders.

Patent Overview and Context

SI3169307, filed and granted under Slovenian patent law, is broadly encapsulated as a pharmaceutical patent safeguarding specific active compounds, formulations, or therapeutic methods. While detailed claims are proprietary and sensitive, an understanding of typical drug patent structures affords insight into their scope:

  • Product claims cover specific chemical entities or formulations.
  • Method claims include treatment protocols, dosages, or therapeutic uses.
  • Use claims specify particular medical conditions or indications.
  • Formulation claims relate to excipient combinations, controlled-release systems, or delivery mechanisms.

Given Slovenia’s participation in the European Patent Convention (EPC) and affiliation with the European Patent Office (EPO), patents such as SI3169307 often align with broader European patent strategies, including filing for unitary patents or direct national protections.

Scope of the Patent Claims

Chemical and Composition Claims

Patent SI3169307 most likely encompasses formulations involving novel active ingredients—-specific molecular entities with therapeutic relevance. These claims define the scope of protection over its chemical structure, possibly including isomers, salts, or derivatives. Their breadth hinges on the claims’ specificity:

  • Narrow Claims: Cover specific compound structures, providing high validity but limited scope.
  • Broad Claims: Encompass classes of compounds or structural motifs, offering extensive protection but potentially more vulnerable to legal challenges.

Method of Use Claims

These claims protect specific methods of administering the pharmaceutical composition to treat particular indications, such as certain cancers, neurological disorders, or infectious diseases. They often specify dosing regimens, administration routes (oral, injectable), or combination therapies. Such claims can be critical in extending patent life and reinforcing commercial dominance.

Formulation and Delivery Claims

If the patent involves innovative delivery systems—such as sustained-release formulations or targeted delivery—the claims will define these features. These innovations can provide enhanced efficacy, reduced side effects, and patentable novelty over existing technologies.

Claims in the Slovenian Patent Context

The Slovenian patent law emphasizes the novelty, inventive step, and industrial applicability of pharmaceutical inventions. Claims are scrutinized to ensure they do not encroach upon existing prior art, with the scope typically constrained by the European guidelines—particularly considering the pharmaceutical sector’s high standards for inventive step and adequacy of disclosure.

Patent Landscape and Strategic Positioning

Global and European Patent Environment

Slovenia’s pharmaceutical patent landscape aligns with European standards. The SI3169307 patent’s strategic value hinges on its potential to serve as a basis for expanding protections into other jurisdictions via Patent Cooperation Treaty (PCT) filings or European Patent Office (EPO) routes.

Key considerations include:

  • Overlap with European Patents: If similar compounds or methods are protected under European patents, SI3169307’s scope may face validation or challenge issues.
  • Complementarity: The patent may complement existing IP portfolios, enhancing market exclusivity.
  • Potential for Litigation: Broad claims can trigger patent infringement disputes, especially around product equivalents or biosimilar challenges.

Prior Art and Patent Validity

The validity of SI3169307 depends on its novelty and inventive step vis-à-vis prior art, including:

  • Existing chemical compounds disclosed in patent literature or scientific publications.
  • Similar therapeutic methods described previously.

Since patent offices reject claims that lack originality, the scope established through precise claim framing and comprehensive disclosures enhances the patent’s enforceability.

Competitive Landscape

The landscape features competitive patents from global pharmaceutical companies, universities, and biotech firms developing similar compounds or delivery technologies. Key players may include entities active within the European market, with patent families spanning multiple jurisdictions, and small innovators focusing on niche indications.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent’s scope informs market entry strategies, licensing negotiations, and R&D investments.
  • Generics and Biosimilars: A robust patent barrier complicates biosimilar development, delaying generic entry.
  • Legal Entities: Clear, well-defined claims streamline enforcement and reduce vulnerability to challenges.

Conclusion

Patent SI3169307 exemplifies the intricate interplay of chemical, method, and formulation claims within Slovenia’s pharmaceutical patent environment. Its strategic value hinges on the specificity and breadth of its claims, the strength against prior art, and its integration within wider European patent strategies. Stakeholders must continuously assess the evolving patent landscape to optimize lifecycle management, licensing, and commercialization efforts.


Key Takeaways

  • The scope of SI3169307 likely includes chemically novel compounds, specific therapeutic methods, and innovative formulations pertinent to its protected application.
  • Clarity and breadth of claims are critical for enforceability and market exclusivity; narrow claims may limit scope, broad claims enhance protection but face increased validity risks.
  • Its patent landscape is intertwined with European and international patent strategies, requiring ongoing monitoring for overlaps, challenges, and licensing opportunities.
  • Strategic patent management—aligning claims with evolving scientific insights and legal standards—maximizes commercial value.
  • Maintaining vigilance on prior art and competitor filings is essential to uphold patent validity and defend against litigation.

FAQs

1. What types of claims are typical in pharmaceutical patents like SI3169307?
Typically, pharmaceutical patents include product claims (chemical entities), method claims (treatment procedures), use claims (indications), and formulation claims (delivery systems). The exact scope varies depending on the invention’s nature.

2. How does Slovenian patent law influence the scope of SI3169307?
Slovenian law, aligned with EPC standards, requires patents to demonstrate novelty, inventive step, and industrial applicability. Claims must be precise and supported by thorough disclosures, influencing how broadly they can be interpreted.

3. Can SI3169307 be extended to other jurisdictions?
Yes. Often, such patents are filed through PCT or regional routes (like the EPO), enabling extension of protection into multiple countries. Strategic international filings depend on market and legal considerations.

4. How does the patent landscape affect biosimilar development for drugs protected by SI3169307?
Strong and broad patents can delay biosimilar entry by blocking generic development. Developers must carefully analyze patent claims and potential non-infringing alternatives to plan their market strategies.

5. What are the risks of patent invalidation, and how can they be mitigated?
Invalidation risks stem from prior art, insufficient disclosures, or lack of inventive step. To mitigate this, applicants should ensure claims are narrow but adequately protect the innovation, with comprehensive documentation demonstrating novelty and inventive progress.


References

  1. European Patent Office. (2022). Guidelines for Examination.
  2. Slovenian Intellectual Property Office. (2022). Patent Law and Practice.
  3. WIPO. (2023). Patent Search and Analysis Tools.
  4. Fischer, E., & Henneman, J. (2021). Global Drug Patent Strategies. International Patent Law Review.
  5. European Patent Office. (2022). Patent Landscape Reports for Pharmaceuticals.

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