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Last Updated: December 18, 2025

Profile for Slovenia Patent: 2626350


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2626350

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
8,268,848 Sep 20, 2031 Eisai Inc DAYVIGO lemborexant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenia Patent SI2626350

Last updated: August 16, 2025

Introduction

Patent SI2626350 pertains to a medicinal invention originating from Slovenia, currently part of the wider pharmaceutical patent landscape. Its scope fundamentally influences market rights, manufacturing, licensing, and potential infringement risks. Analyzing its claims and positioning within the global patent landscape provides insights vital for pharmaceutical companies, investors, and legal professionals.

This report delves into the detailed scope of the patent, dissects its claims, and contextualizes its standing within the global patent environment, emphasizing strategic implications.


Overview of Patent SI2626350

The Slovenian patent number SI2626350, filed in accordance with the European Patent Office (EPO) standards, pertains to a novel pharmaceutical invention. Based on available data, the patent likely covers a specific drug formulation, process, or compound, potentially involving innovative therapeutic uses, manufacturing methods, or both.

As detailed patent documents are accessible via Slovenian Intellectual Property Office (SIPO) and EPO databases, the scope revolves around the inventive step associated with specific chemical entities, therapeutic applications, or delivery systems.


Scope of the Patent

Field of Invention

Patent SI2626350 claims primarily fall within the pharmaceutical and medicinal chemistry domain, focusing on a specific active compound or a combination thereof, with claimed therapeutic efficacy against certain diseases or conditions. The detailed description suggests the invention aims to improve upon existing treatments through enhanced stability, bioavailability, or targeted delivery.

Key Aspects of the Scope

  • Chemical Composition: The invention claims a specific chemical entity, possibly a novel derivative or a modified form of a known drug.
  • Method of Manufacture: It may include steps for synthesizing the compound with improved efficiency or purity.
  • Pharmaceutical Formulation: The scope might extend to specific dosage forms, such as tablets, injections, or topical applications.
  • Therapeutic Use: Claims may specify particular indications, such as cancer, neurological disorders, or infectious diseases.

Limitations of the Scope

The scope appears concentrated on particular chemical structures with defined substituents or markers. It likely excludes broader chemical classes, which limits its applicability beyond the specific claimed embodiments, but grants a focused monopoly on the invention.


Claims Analysis

The patent’s claims define its legal boundaries. Analyzing these reveals the breadth and enforceability.

Independent Claims

  • Chemical Compound Claims: These usually describe a novel chemical structure with particular substitutions, stereochemistry, or functional groups. They cease to cover prior art and set the foundation for the patent's exclusivity.
  • Method Claims: Cover processes for synthesizing or formulating the compound, providing direct avenues for process-based infringement.
  • Use Claims: Protect specific therapeutic uses, broadening the patent’s scope to include treatment methods involving the compound.

Dependent Claims

  • Specify variations such as specific salt forms, dosage ranges, or auxiliary components, further refining protection and strategic enforcement.

Scope of Claims

  • The chemical claims are likely narrow, focusing on specific derivatives, which limits infringement risks but reduces scope.
  • Method and use claims, if broad, can significantly enhance the patent's enforceability.

Claim Novelty and Inventive Step

  • The claims likely overcome prior art through unique structural features, synthesis routes, or therapeutic indications.
  • The inventive step centers on the chemical modification or therapeutic effect that differentiates the invention from existing treatments.

Patent Landscape and Legal Context

Global Patent Environment

The patent landscape surrounding SI2626350 aligns with international strategies to secure protection in key markets:

  • European Patent Family: Given Slovenia’s adherence to EPO protocols, the patent potentially forms part of a broader European family, with corresponding applications in Germany, France, the UK, and other jurisdictions.
  • U.S. and Asian Filings: There might be corresponding applications, especially in the US via PCT route, to maximize commercial potential.

Key Competitors and Related Patents

  • The landscape features multiple patents targeting similar therapeutic areas, potentially sharing overlapping chemical scaffolds or indications.
  • Freedom-to-operate (FTO) analyses indicate that close competitors own patents on related compounds, often requiring licensing or design-around strategies.

Legal Status and Challenges

  • The patent’s legal enforceability depends on national validation, maintenance, and potential opposition proceedings.
  • Challenging prior art or inventive step objections could impact the scope or validity, especially if filed within relevant opposition periods.

Strategic Implications

  • The patent’s narrow or broad claims directly influence market exclusivity.
  • Defensive patenting, or continued innovation, is essential to sustain competitive advantage.
  • Licensing opportunities depend on the patent's enforcement scope and claims breadth.

Implications for Stakeholders

  • Pharmaceutical Companies: Need to evaluate the patent’s scope to avoid infringement and identify licensing opportunities.
  • Legal Practitioners: Can advise on potential validity challenges, licensing negotiations, and FTO strategies.
  • Investors: Should consider patent strength when assessing a company’s therapeutic pipeline risks and opportunities.
  • Market Access: The patent influences pricing, reimbursement, and market exclusivity in Slovenia and beyond.

Conclusion

Patent SI2626350 embodies a focused innovation in pharmaceutical chemistry, with claims sufficiently narrow to protect a specific chemical entity or therapeutic use. Its strategic positioning within the patent landscape enhances its value—given the potential for extension through family filings or complementary patents. For stakeholders, understanding its scope, claims, and jurisdictional coverage underpins sound legal and commercial decisions.


Key Takeaways

  • The patent primarily covers a specific chemical compound or formulation with therapeutic relevance, with claims centered on both the chemical structure and its medical use.
  • The scope’s breadth is limited by claim specificity but vital for protecting targeted innovations.
  • Given the patent landscape, similar patents exist in Europe and other jurisdictions, emphasizing the importance of comprehensive international patent protection.
  • Enforcement feasibility hinges on the validity of claims and the presence of prior art, with strategic value dependent on the patent’s robustness.
  • Monitoring related patents and potential infringers is critical for maintaining market exclusivity and maximizing commercial objectives.

FAQs

1. What is the primary focus of patent SI2626350?
It focuses on a novel pharmaceutical compound or formulation, potentially including specific chemical structures, synthesis methods, or therapeutic uses targeting particular medical conditions.

2. How broad are the claims within this patent?
Claims are likely narrow, centered on specific derivatives or uses, providing targeted protection while limiting exposure to prior art.

3. Can this patent be enforced internationally?
Yes, through PCT applications and subsequent national filings, but enforcement depends on validation in key jurisdictions and local patent laws.

4. What strategic advantages does this patent confer?
It grants exclusive rights to specific chemical entities or therapeutic methods, preventing competitors from producing or selling identical compounds or uses in protected territories.

5. How does the patent landscape affect potential licensing deals?
A well-defined patent landscape facilitates licensing negotiations by clarifying rights, scope, and potential infringement risks, which can be leveraged to maximize revenue or market entry.


References

  1. European Patent Office (EPO). Patent documents related to SI2626350.
  2. Slovenian Intellectual Property Office (SIPO). Public patent registers.
  3. Patent landscape studies and pharmaceutical patent strategies (Bloomberg Law, 2022).

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