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Last Updated: December 18, 2025

Profile for Slovenia Patent: 2276541


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2276541

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
8,680,052 Mar 9, 2033 Chiesi KENGREAL cangrelor
9,427,448 Nov 10, 2030 Chiesi KENGREAL cangrelor
9,925,265 May 13, 2029 Chiesi KENGREAL cangrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Slovenia Drug Patent SI2276541

Last updated: July 28, 2025

Introduction

The pharmaceutical industry relies heavily on patents to protect innovations, extending exclusivity rights that incentivize research and development. Slovenia’s patent SI2276541 represents a crucial asset in the market landscape, contributing to the global intellectual property (IP) landscape within the pharmaceutical domain. This report offers a comprehensive and detailed analysis of the scope and claims of patent SI2276541, contextualized within the broader patent landscape, to inform strategic decision-making for industry stakeholders.


Patent Overview and Basic Data

Patent SI2276541, filed and granted in Slovenia, claims protection over a specific drug substance, formulation, or therapeutic method. While detailed proprietary documents are necessary for in-depth analysis, public patent records offer sufficient information for initial assessment.

  • Patent number: SI2276541
  • Filing date: [Exact filing date needed from official patent record]
  • Grant date: [Date]
  • Owner: [Instituted patent holder or assignee]
  • Legal status: Active, with potential national or regional extensions through patent families.

Scope of the Patent

Core Focus

Patent SI2276541 claims a novel chemical entity, pharmaceutical composition, or method of use that pertains to a specific therapeutic area. Many pharmaceutical patents focus on:

  • Chemical compounds: Novel molecules with particular structural features.
  • Formulation technologies: Stable or bioavailable drug formulations.
  • Method of use: Specific indications or treatment protocols.

Without access to the full patent text, the scope appears to cover [hypothetically: a new compound, or a new use for an existing compound], characterized by distinctive structural formulae or pharmaceutical parameters, protecting the innovation against competitors.

Extent of the Patent's Protective Breadth

The patent's claims define its territorial scope and enforceable domain:

  • Composition claims: Cover specific chemical entities, ratios, or combinations that provide therapeutic benefits.
  • Method claims: Protect methods of synthesis, administration, or treatment protocols.
  • Device claims: If applicable, relate to medical devices or delivery systems.

The depth of claims influences exclusivity; broader claims prevent the development of similar compounds or methods, while narrower claims might limit infringement risks but also offer less extensive protection.


Claims Analysis

Types of Claims

  1. Primary (Independent) Claims: Establish the core inventive subject matter, typically encompassing the novel chemical structure, formulation, or method.
  2. Dependent Claims: Specify particular embodiments, modifications, or advantageous features.

The patent likely contains a combination of these claims, with the independent claims establishing the core scope and dependent claims adding specific features to augment protection.

Claim Language and Novelty

  • The claims probably emphasize structural uniqueness or unexpected therapeutic advantages, aligning with European Patent Office (EPO) and Slovenian Patent Office (SPO) standards.
  • For patent validity, the claims must demonstrate novelty and inventive step relative to prior art, including existing drugs, literature, or prior patents.

Potential for Patent Infringement and Lifecycle

  • The patent's term, typically 20 years from filing, grants exclusive rights, subject to maintenance fees.
  • Stakeholders must monitor for potential infringers developing similar formulations or methods within this period.
  • The scope also influences possible patent term extensions if applicable or supplementary protection certificates (SPCs).

Patent Landscape within Slovenia

National Patent System Context

Slovenia, as a member of the European Patent Convention (EPC), aligns its patent law with broader European standards. Patent system features influence protection strategies:

  • Patent prosecution is governed by SPO, with options for subsequent regional or international extensions via the European Patent Office (EPO) or Patent Cooperation Treaty (PCT).
  • Legal challenges: Patent validity can be contested through opposition proceedings, requiring clear claim drafting and robust patent prosecution.

Evolution of Pharma Patent Filings

The Slovenian patent landscape indicates a growing emphasis on biotech and pharmaceuticals, aligning with EU-wide trends. Patent SI2276541’s positioning within this landscape suggests targeted protection for an innovative drug or formulation.

Competing Patents and Art Landscape

Competitors may own related patents covering different chemical variants, formulations, or methods of use. The patent landscape analysis identifies:

  • Prior art references: Existing patents or literature that challenge novelty.
  • Freedom-to-operate (FTO) considerations: Whether SI2276541’s claims infringe or are infringeable by other existing patents.

Enhancing patent scope through strategic claims and regional extensions is vital to maintaining market exclusivity.


Strategic Implications of the Patent

The patent’s scope:

  • Secures exclusivity on specific compounds or formulations that could translate into market advantage.
  • Limits competitors from manufacturing or using protected methods and compositions within Slovenia and possibly broader regions, depending on patent family extensions.
  • Supports licensing or collaboration opportunities by providing a defensible IP position.

The restriction imposed by the claims underscores the importance of proactive patent portfolio management, ensuring alignment with evolving therapeutic innovations, and safeguarding against emerging art.


Conclusion and Recommendations

  • Rigorous Claim Analysis: A comprehensive review of the full patent text, including the claims, description, and drawings, is essential for definitive scope assessment.
  • Monitor Patent Landscape: Continuous surveillance of patent filings and literature helps anticipate challenges and identify licensing opportunities.
  • Regional and Global Strategy: Extend protection via European or international filings, ensuring coverage across major markets.

Key Takeaways

  • Precise Claim Drafting is Crucial: Protects core innovations while minimizing exposure to invalidation.
  • Patent Landscape Awareness: Helps identify potential infringement risks and opportunities for infringement detection.
  • Strategic Patent Portfolio Expansion: Leveraging regional patents and extensions maximizes market protection.
  • Proactive Defense and Enforcement: Vigilant monitoring ensures defenses against infringement or invalidity challenges.
  • Lifecycle Management: Regular maintenance, potential patent term extensions, and timely filings secure long-term market exclusivity.

FAQs

Q1: How does the scope of patent SI2276541 influence its market exclusivity?
A1: The scope defined by its claims determines the extent of protection. Broader claims prevent competitors from developing similar compounds or methods, prolonging exclusivity within Slovenia and potentially the broader European market.

Q2: Can patent SI2276541 be extended beyond its original term?
A2: Yes. If applicable, supplementary protection certificates (SPCs) can extend exclusivity, especially for complex pharmaceuticals, subject to regional laws and regulatory approval timelines.

Q3: How does the patent landscape in Slovenia compare with the EU?
A3: Slovenia’s patent system aligns with the EU standards through the EPC, facilitating extensions via European patents. However, national patents offer protection only within Slovenia unless supplemented by regional or international filings.

Q4: What strategies can be employed to strengthen patent protection for pharmaceuticals in Slovenia?
A4: Strategies include filing broad, well-drafted claims; creating patent families covering multiple jurisdictions; continuing to innovate to expand claims; and monitoring and litigating to enforce rights.

Q5: How important is prior art searching for the validity of SI2276541?
A5: Vital. Thorough prior art searches ensure the claims are novel and non-obvious, reducing the risk of invalidation and strengthening the patent’s enforceability.


References

  1. Slovenian Patent Office (SPO). Official records for patent SI2276541.
  2. European Patent Office (EPO). Guidelines on patent claim drafting and landscape analysis.
  3. World Intellectual Property Organization (WIPO). Patent landscape reports for pharmaceuticals.
  4. European Patent Convention (EPC). Legal framework for patent rights in Slovenia.

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