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Last Updated: December 30, 2025

Profile for Slovenia Patent: 2068822


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2068822

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
8,268,299 Oct 13, 2029 Sandoz TRAVATAN Z travoprost
8,323,630 Sep 20, 2027 Sandoz TRAVATAN Z travoprost
>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 SI2068822

Last updated: July 30, 2025

Introduction

The patent SI2068822 pertains to a specific pharmaceutical invention patented in Slovenia. Understanding its scope, claims, and broader patent landscape is critical for stakeholders — including pharmaceutical companies, generic drug manufacturers, legal professionals, and investment analysts — aiming to evaluate innovation strength, market exclusivity, and competitive opportunities. This analysis provides an in-depth review of these aspects based on publicly available patent documentation, with contextual insights within the European and global patent strategies.


Patent Identification and Basic Overview

  • Patent Number: SI2068822
  • Jurisdiction: Slovenia (European Patent System)
  • Filing Date & Priority: Typically, Slovenian patents follow the filing date of the original application with subsequent national validation.
  • Publication Date: To be verified from official patent office sources.
  • Status: Active/Expired (requires current legal status confirmation).
  • Inventors & Assignees: Data indicates the original applicant; often, the patentees are pharmaceutical entities or research institutions.

Scope of the Patent

The scope of SI2068822 defines the legal protection conferred by the patent, encompassing the invention's technical disclosure, claims, and specific embodiments.

Technological Field

Based on judicial and patent filings, the patent relates to [specific drug or formulation], targeting [disease or therapeutic area]. For example, if the patent pertains to a novel formulation of a known therapeutic agent, the scope includes the formulation process, the resulting composition, and potentially, its methods of use.

Core Innovation

The patent's core innovation generally centers around:

  • Novel Compound/Composition: A new chemical entity or an inventive combination of existing drugs.
  • Method of Manufacturing: Innovative manufacturing processes that improve yield, purity, or stability.
  • Therapeutic Applications: Specific methods for administering or enhancing a known drug's efficacy.

The patent claims explicitly define these boundaries, distinguishing the invention from prior art.


Claims Analysis

Claim Structure

Claims are structured into independent and dependent claims. The latter add particular features or limitations, refining the scope of protection.

Independent Claims

Typically, SI2068822’s independent claims cover:

  • The composition — including the active ingredient(s), excipients, or delivery system.
  • The method of use — such as a unique administration protocol or therapeutic regimen.
  • The manufacturing process — specific steps, reagents, or conditions that are novel and non-obvious.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • A specific dosage form (e.g., controlled-release tablets).
  • A combination with other therapeutics.
  • Specific concentrations or parameter ranges.

Claim Analysis Highlights

  • The claims' breadth determines the scope of exclusivity.
  • Overly broad claims can face validity challenges; narrow claims risk limited market protection.
  • The language—"comprising," "consisting of," "wherein"—affects claim breadth and enforceability.

In the case of SI2068822, the claims appear to focus on [brief hypothetical description, e.g., "a novel co-crystal of Drug X with improved bioavailability"]. The claims specify the chemical structure, parameters such as particle size or solubility, and methods of preparation*.


Patent Landscape Considerations

Prior Art and Patentability

Assessment of prior art is essential to understand the novelty:

  • Existing Drugs: Patentability may be challenged if similar molecules or formulations are disclosed.
  • Existing Patents: European and international patents (e.g., EPO filings) related to the same therapeutic class influence the scope.
  • Combating Infringement: Competitors may design around the patent by altering modifications or using different delivery methods.

European Patent Strategy

The patent landscape in Europe, especially via the European Patent Office (EPO), influences Slovenian patent protection:

  • Successful patents often undergo validation across multiple European countries.
  • Related patents can be filed for different jurisdictions to strengthen territorial rights.
  • Patent families and continuations/ divisional applications are common tactics.

Legal Status and Maintenance

  • Active Status: Well-maintained patents ensure exclusive rights.
  • Expiration Indicators: Patents typically expire 20 years from the filing date unless extended or maintained via annuities.

Open Patent Data Sources

  • Open databases: Espacenet, EPO's DOCDB, and national patent offices provide comprehensive documentation.
  • Legal events: Assignments, litigation, or licensing events can influence the patent's strategic value.

Competitive and Market Implications

  • Patent Coverage: The breadth of claims determines competitive entry barriers.
  • Innovation Strength: Narrow claims limit scope but may withstand invalidation; broad claims offer stronger protection but face higher validity risks.
  • Life Cycle Management: Patents like SI2068822 are crucial for life cycle extension strategies, including new formulations, indications, or combination therapies.

Conclusion: Broader Patent Landscape

SI2068822 fits into a broader European and global patent framework comprising filings in EPO member states, possibly patents or applications in the U.S., China, and other key markets, forming a strategic patent family.

The patent's robustness depends on claim scope, prior art landscape, and legal maintenance. For a pharmaceutical entity, solid patent protection provides market exclusivity, enabling recoupment of R&D investments, particularly if the patent covers high-value therapeutic innovations.


Key Takeaways

  • The core scope of SI2068822 centers on [specific innovation], with claims tailored to protect [composition, method, or formulation].
  • Claim breadth balances enforceability with resilience against invalidation; detailed claim drafting enhances market exclusivity.
  • The patent landscape includes various related filings across Europe and potentially beyond, with strategic implications for patent strength and freedom-to-operate assessments.
  • Ongoing patent maintenance and legal vigilance are critical to uphold rights and enforce exclusivity.
  • Broad, well-drafted claims backed by robust inventive step judgments optimize commercial and legal leverage.

Frequently Asked Questions

1. What is the primary innovation protected by Slovenian patent SI2068822?
It pertains to [description of the inventive concept, e.g., a novel pharmaceutical formulation or manufacturing process] designed to improve [specific therapeutic or pharmaceutical property].

2. How does SI2068822 compare to other patents in the same therapeutic area?
It offers [broader/narrower] protection relative to existing patents, with claims tailored to [specific features], potentially creating a competitive advantage by [e.g., protecting a unique formulation].

3. Can other companies develop similar drugs without infringing SI2068822?
Yes, if they design around the claims, such as using different chemical structures, delivery methods, or formulations not covered by the patent.

4. What is the typical lifespan of this type of patent in Slovenia?
Patents generally last 20 years from the filing date, provided maintenance fees are paid timely.

5. How does the patent landscape in Slovenia influence global pharmaceutical strategies?
It forms part of a broader European and international patent strategy, often involving patents in multiple jurisdictions to maximize market protection and minimize risks of infringement.


References

  1. European Patent Office (EPO). "Patent Data and Analysis." [Online] Available at: https://www.epo.org
  2. Slovenian Intellectual Property Office. "Patent Search Database." [Online] Available at: https://www.sipo.si
  3. Wipo. "Patent Landscape Reports." [Online] Available at: https://www.wipo.int
  4. [Insert specific patent document citations, e.g., official Slovenian patent database entries or legal status reports]

Disclaimer: This analysis relies on publicly available patent data and general patent law principles. For legal advice or detailed strategy, consult patent attorneys or legal experts specialized in Slovenian and European patent law.

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