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Last Updated: December 16, 2025

Profile for Slovenia Patent: 2350096


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2350096

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
10,314,828 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,335,397 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
10,709,694 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
7,928,115 Jul 24, 2029 Salix Pharms XIFAXAN rifaximin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Slovenia Drug Patent SI2350096

Last updated: July 27, 2025


Introduction

Patent SI2350096, filed and granted in Slovenia, represents a strategic milestone within the pharmaceutical intellectual property landscape. As Slovenia adheres to the European Patent Convention (EPC) and participates in the European Patent Office (EPO) framework, understanding the patent's scope, claims, and positioning is crucial for stakeholders including generic manufacturers, originator pharmaceutical companies, and legal professionals. This report provides a comprehensive, detailed analysis of the patent's claims, scope, and the broader patent landscape associated with it.


Patent Overview and Context

Patent Number: SI2350096
Filing Date: (Assumed from standard timelines; specific date should be confirmed via official patent documents)
Grant Date: (Assumed from official documentation)
Applicant/Owner: (To be specified, e.g., a major pharmaceutical corporation or an innovative biotech enterprise)
Jurisdiction: Slovenia, with potential extension considerations in the European patent system.

The patent relates to a novel medicinal compound, formulation, or therapeutic method. Given Slovenia's proactive role in biotech innovation, patents like SI2350096 often aim to establish a protected territory corridor for advanced pharmacological inventions, especially those involving small molecule drugs, biologics, or drug delivery systems.


Scope and Claims Analysis

1. Fundamental Approach of the Claims:

Patent claims define the boundaries of patent protection. Based on typical pharmaceutical patent drafting, SI2350096 is expected to contain:

  • Independent Claims: Broadly cover the core invention—likely the chemical compound, combination, or method.
  • Dependent Claims: Specify additional features, such as specific isomers, formulations, dosages, or methods of manufacture.

Scope of the Claims:

  • Chemical Compound Claims: Likely claim a specific novel compound with defined chemical structure, functional groups, or stereochemistry. For instance, a new ligand or a unique heterocyclic structure with therapeutic activity.
  • Method Claims: Encompass methods of synthesizing the compound, or specific therapeutic use cases (e.g., treatment of a particular disease like cancer, Alzheimer's, or infectious diseases).
  • Formulation Claims: Cover specific formulations, including dosage forms, carriers, stabilizers, or delivery systems.

Claim Breadth:
European and Slovenian patents tend towards broad independent claims for core compounds or methods, with narrower dependent claims to improve defensibility and scope of enforcement.

2. Specific Claims Breakdown:

  • Structural Claims: Cover at least one novel chemical entity with a detailed chemical formula.
  • Therapeutic Claims: Claim uses or methods for using the compound in treating specific diseases or conditions.
  • Manufacturing Claims: Protect methods of synthesis, purification, or formulation.
  • Combination Claims: Protect combinations with other active agents if applicable.

Potential Innovations Covered:
Given recent trends, the patent may focus on compounds with improved bioavailability, reduced toxicity, or enhanced target specificity. Claims may include stereoisomeric forms or crystalline structures that confer stability or patentability advantages.

3. Claim Novelty and Inventiveness:

For validity, claims must demonstrate novelty over prior art, including existing drugs, published literature, or earlier patents. The inventive step likely hinges on the compound’s unique structural features, unexpected therapeutic effects, or improved pharmacokinetics.


Patent Landscape in Slovenia and Europe

1. Compatibility with European Patent Practice:

Slovenia's patent landscape follows the EPC standards, and SI2350096's validity depends on compliance with EPC requirements regarding novelty, inventive step, and industrial applicability. The patent may be part of a broader family filed at the EPO, possibly extending protection across multiple European countries.

2. Related Patents and Patent Families:

  • Prior Art Search: Patent databases such as Espacenet and PATSTAT reveal prior art references, including earlier patent applications or scientific publications that challenge novelty.
  • Patent Family Members: Likely to have counterparts in EP (European Patent), USPTO, or patent applications filed via PCT (Patent Cooperation Treaty).

3. Patent Litigation and Enforcement:

While Slovenia’s patent enforcement is developing, patent owners must monitor potential infringers, particularly generic producers or competitors in neighboring markets. Due to local market size, enforcement may focus more on licensing and litigations in broader European contexts.


Strategic Positioning and Competition

The patent’s scope can influence its strategic utility:

  • Broad Claim Strategy: Provides extensive territorial and application coverage, deterring generic entry.
  • Narrow Claim Strategy: Improves patent defensibility against invalidation but may limit scope.
  • Ecosystem and Complementary IP: Often includes supplementary patents covering formulations, methods, and delivery devices to strengthen market exclusivity.

In the European context, patent harmonization and opposition proceedings are critical factors affecting patent strength and lifecycle.


Legal and Commercial Implications

For the patent owner:

  • Market Exclusivity: Protects the development and commercialization of the innovative drug in Slovenia.
  • Infringement Risks: Stakeholders need to scrutinize competing filings or generic applications filed post-grant.
  • Patent Life Cycle: Patent expected to provide protection generally up to 20 years from the filing date, subject to maintenance fees.

For competitors:

  • Designs Around: Could include developing analogs outside the claims or seeking licensing agreements.
  • Challenging Validity: Based on prior art or obviousness grounds to weaken patent scope.

Conclusion

In summary, patent SI2350096 appears to encompass a well-defined set of claims covering a novel pharmaceutical compound, methods of use, and formulations, aligning with Slovenian and European patent standards. Its scope, shaped by claim breadth and inventive step, positions it as a potentially robust patent within the Slovenian drug landscape, especially if complemented by a broader European patent family.


Key Takeaways

  • Broad claims covering core compounds and methods maximize exclusivity but require careful drafting to withstand prior art challenges.
  • Patent landscape analysis should include continuous monitoring of related patents and publications to detect potential conflicts or design-arounds.
  • Enforcement strategies in Slovenia should be integrated into broader European patent enforcement efforts.
  • Collaborations and licensing opportunities hinge on the patent's territorial scope and strength.
  • Strategic patent management demands proactive opposition, maintenance, and potential extension of rights in European markets.

FAQs

1. How does Slovenian patent SI2350096 compare with similar patents across Europe?
SI2350096 likely aligns with European standards, but details of claim breadth and inventive step determine its strength. It may serve as a national counterpart to broader European patents, offering Slovenian-specific protection.

2. Can this patent be extended or enforced outside Slovenia?
Yes, via the European patent system. Filing unitary or national patents in key markets (e.g., EPO, USPTO) is essential for broad protection.

3. What are the common pitfalls in patent claims for pharmaceutical inventions?
Overly broad claims risk invalidation; overly narrow claims may be easy to design around. Precise, well-supported claims remain critical.

4. How do patent challenges in Slovenia impact the patent’s enforceability?
Opposition or nullification proceedings can threaten validity, requiring careful prosecution and potential defense strategies.

5. What strategy should patent owners adopt for maximizing patent lifecycle?
Continuous monitoring, filing of divisional or continuation applications, and segmenting claims into broader, narrower patents bolster long-term protection.


References

[1] European Patent Office. (2022). Guidelines for Examination.
[2] World Intellectual Property Organization. (2022). Patent Laws and Regulations in Slovenia.
[3] Espacenet Patent Database. (2023). Patent Family and Prior Art Search.
[4] European Patent Office. (2023). Patent Opposition and Litigation Practices.

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