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Last Updated: December 16, 2025

Profile for Slovenia Patent: 3357911


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US Patent Family Members and Approved Drugs for Slovenia Patent: 3357911

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
7,811,595 Mar 13, 2028 Akebia VAFSEO vadadustat
8,323,671 Apr 3, 2028 Akebia VAFSEO vadadustat
8,343,952 Aug 14, 2027 Akebia VAFSEO vadadustat
8,598,210 Jun 26, 2027 Akebia VAFSEO vadadustat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenia Patent SI3357911

Last updated: September 8, 2025


Introduction

Patent SI3357911 is a Slovene patent, which plays a pivotal role in delineating the innovative scope and patent protection landscape for a specific pharmaceutical compound or formulation. An analysis of its scope, claims, and surrounding patent landscape provides valuable insights for stakeholders such as biopharmaceutical companies, research institutions, and legal professionals involved in intellectual property rights (IPR) management, licensing, or development strategies.

This report aims to deliver a comprehensive evaluation of SI3357911, covering the technical scope defined by its claims, the scope’s breadth and limitations, and the broader patent landscape within which this patent resides. Such an analysis informs decisions related to patent validity, freedom-to-operate assessments, or potential licensing opportunities.


Patent Overview

Patent Number: SI3357911
Filing Date: [Insert filing date]
Publication Date: [Insert publication date]
Applicant/Owner: [Insert applicant/owner]
Jurisdiction: Slovenia, with possible European or international extensions

The patent grants exclusive rights pertaining to a novel chemical entity, pharmaceutical formulation, or therapeutic method, as per its detailed claims. The scope of patent SI3357911 hinges upon its broadness and particularity of its claims, which define the innovation’s boundaries.


Scope of the Patent

The scope of a patent encompasses the technical content protected by the claims, which specify the invention's exclusive rights. A comparison of the claims with prior art clarifies whether they are broad or narrow.

Claims Analysis

1. Independent Claims

The core of SI3357911 comprises one or more independent claims, which delineate the broadest scope of protection. Typically, in pharmaceutical patents, such claims specify:

  • The chemical structure(s) of the active ingredient(s),
  • The particular configuration or stereochemistry,
  • Specific pharmaceutical formulations or delivery devices,
  • Therapeutic uses or methods of treatment.

Example:
An independent claim might cover:

"A pharmaceutical composition comprising [chemical structure], in an effective amount for [therapeutic use], wherein the composition further comprises [excipients]."

This broad formulation aims to encompass various embodiments within the scope of the chemical or therapeutic innovation.

2. Dependent Claims

Dependent claims narrow the scope, providing specific embodiments or additional features. They often specify:

  • Particular substituents,
  • Specific formulation parameters,
  • Concentrations or dosages,
  • Delivery methods.

The combination of independent and dependent claims collectively define the patent's breadth.

Scope Consideration

The scope depends on claim language precision and technical breadth. Broad claims covering generic chemical structures or methods can impact competing inventions significantly, but they must be supported by a detailed description. Narrow claims limit enforcement but are less susceptible to invalidation.


Patent Claim Strategies and Legal Principles

  • Doctrine of Equivalence:
    The extent to which the claim scope covers variants outside explicit language. SI3357911’s claims’ language must be scrutinized concerning potential equivalents.

  • Supporting Disclosure:
    To maintain enforceability, the detailed description should adequately support all claim embodiments. Any gaps could weaken the patent's scope.

  • Claim Drafting:
    Effective claim drafting balances breadth (to deter competitors) with specificity (to withstand validity challenges). It’s essential to analyze whether SI3357911’s claims strike this balance.


Patent Landscape in Slovenia and Broader Context

1. National vs. International Patent Strategies

Slovenia, as an EPC contracting state, adheres to European patent procedures. Companies often file national patents like SI3357911 as part of wider strategies that include European patents and PCT applications to secure regional or global protection.

2. Patent Families and Priority Landscape

Examining whether SI3357911 forms part of a patent family, linked to earlier filings or priority applications (e.g., PCT), indicates the strategic importance and lifecycle stage of the invention. A well-referenced patent family suggests robust protection.

3. Prior Art and Novelty

The patent’s novelty hinges on prior art, including previously disclosed compounds, methods, or formulations. The patent office in Slovenia likely conducted an examination based on nearby chemical or therapeutic prior art, which defines the boundaries of patentability.

4. Competitive Patent Activity

Patent landscapes in the specified therapeutic area reveal the development intensity within Slovenia, the European Patent Office (EPO), and globally. For example, in the field of oncology or neurology, overlapping patent families signal active R&D and potential patent thickets.

5. Patent Expiry and Freedom-to-Operate

Understanding the patent’s expiry date is critical for assessing market entry opportunities. If SI3357911 is still within its enforceable term, license negotiations are pertinent. Conversely, expiration can open opportunities for generics or biosimilar development.


Legal and Commercial Significance

  • Protection Scope:
    The breadth of protection confines competitors and influences licensing negotiations. Broad claims enable the patent holder to assert rights against a wide variety of infringing activities.

  • Innovation Differentiation:
    The patent guards unique chemical entities or formulations, providing a competitive advantage and incentivizing further R&D investment.

  • Potential Challenges:
    Classification of the claims as "obvious" or lacking inventive step could threaten validity. An analysis of prior art cited during prosecution provides insights into the strength of SI3357911’s claims.


Conclusion

Patent SI3357911 encapsulates a strategic element within the Slovene and European pharmaceutical patent landscape, potentially covering a novel drug compound, formulation, or therapeutic method. Its scope is defined by carefully drafted claims balancing breadth and specificity, tailored to withstand challenges and optimize commercial value.

Professionals must monitor related patent activities, validate the scope against evolving prior art, and evaluate licensing or infringement risks based on this patent's positioning within the broader patent landscape.


Key Takeaways

  • Scope Clarity Matters:
    The patent’s enforceability hinges on the precision and breadth of its claims, impacting freedom-to-operate and licensing strategies.

  • Patent Family Dynamics:
    Recognizing SI3357911’s place within a broader patent family informs its strategic importance and validity over time.

  • Landscape and Competitive Position:
    Active patent filing in the VII field signals ongoing R&D; assessing overlaps is essential for strategic decision-making.

  • Legal Robustness:
    Ensuring claims are well-supported and non-obvious strengthens enforceability, especially in contested approvals.

  • Strategic Planning:
    Monitoring patent expiry dates and potential challenges enables optimal timing for market entry or licensing negotiations.


FAQs

1. What is the significance of claim breadth in patent SI3357911’s protection?
Claim breadth determines how much territory the patent covers. Broader claims protect against more variants but risk being invalidated if too vague or unsupported, whereas narrower claims provide specific protection but may be easier for competitors to circumvent.

2. How does the patent landscape around SI3357911 influence its commercialization?
A dense landscape with overlapping patents can complicate licensing and entry strategies. Identifying potential infringers and freedom-to-operate is critical, especially if similar patents have overlapping claims.

3. Can SI3357911 be challenged based on prior art?
Yes. A challenge against its novelty or inventive step could be based on prior disclosures, which may include earlier patents, publications, or existing products. The strength of SI3357911 relates to its ability to demonstrate novelty and inventive step over prior art.

4. How does Slovenia’s patent law impact the enforceability of SI3357911?
Slovenia’s adherence to European patent standards aligns patent scope and validity criteria with broader European practices, including the requirement for inventive step and support by the description.

5. What strategic steps should patent owners pursue regarding SI3357911?
Owners should monitor patent expiry dates, enforce against infringement, consider patent extensions where available, and evaluate licensing opportunities, especially if the patent covers a high-value therapeutic area.


Sources:

[1] European Patent Office - Guidelines for Examination.
[2] EPO Patent Law and Practice.
[3] Slovenian Industrial Property Office (SPI) – Patent Database.
[4] World Intellectual Property Organization (WIPO) – Patent Landscape Reports.
[5] Relevant scientific and patent literature in the therapeutic field pertaining to the patent’s claims.


Note: Due to limited access to the full text and detailed prosecution history of SI3357911, the above analysis is based on standard patent principles and recognized practices within pharmaceutical patent law. For definitive patent scope and legal standing, consulting the official patent documentation and legal counsel is recommended.

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