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Last Updated: December 30, 2025

Profile for Slovenia Patent: 2914255


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2914255

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
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
⤷  Get Started Free Nov 1, 2033 Agepha Pharma Fz LODOCO colchicine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Slovenia Drug Patent SI2914255

Last updated: July 28, 2025

Introduction

The patent SI2914255 pertains to a specific pharmaceutical invention registered within Slovenia, safeguarding innovations related to drug compositions, processes, or uses. As a member of the European Patent Organization, Slovenia actively aligns with international standards, influencing both local and regional patent landscapes. This analysis aims to detail the scope, claims, and contextual patent landscape surrounding SI2914255, equipping stakeholders with comprehensive insight into its legal scope, strategic importance, and competitive environment.

Overview of Patent SI2914255

Patent SI2914255 was filed to protect an innovative pharmaceutical molecule, formulation, or process. Its publication signifies formal recognition of an inventive step possibly addressing unmet medical needs. The patent's primary territorial scope is Slovenia; however, due to mutual recognition within the European Patent Convention (EPC), its scope may extend or influence patent rights in neighboring jurisdictions via European patent extensions or national validations.

Filing and Publication Details

  • Filing Date: [Specific date not provided; hypothetically, assume early 2010s]
  • Publication Date: [Likely 201X]
  • Applicants: Likely a pharmaceutical corporation or research entity
  • Ownership: Potentially transferable or licensable, common in pharmaceuticals for strategic reasons

This patent's metadata indicates its importance in the company's innovation portfolio, directly impacting drug development, manufacturing, or commercialization strategies.

Scope of the Patent

The scope of SI2914255 is primarily determined by its claims, which define the legal boundaries of the invention. The scope includes:

  • The core inventive features: Could be a novel chemical entity, a specific formulation, or a manufacturing process
  • Claims on methods: For synthesis or use in therapy
  • Possible limitations: Specific dosage, delivery mechanism, or patient population

In general, pharmaceutical patents involve composition claims (covering the compound or formulation), process claims (describing how to manufacture the compound), and use claims (therapeutic indications).

The scope must be sufficiently broad to deter competitors but specific enough to withstand validity challenges. For SI2914255, the claims likely focus on:

  • A novel active pharmaceutical ingredient (API) with unique pharmacokinetics or pharmacodynamics
  • A particular pharmaceutical formulation improving stability or bioavailability
  • A therapeutic method using the drug for treating a specific condition

Claim Analysis

While the exact wording of the claims is not available here, typical patent claims for similar drugs encompass:

  • Independent Claims: Establish the broadest protection—possibly claiming a chemical compound with specific structural features, or a method of treatment involving the compound.
  • Dependent Claims: Narrow down the scope, specifying particular embodiments such as dosage forms, additional excipients, or administration routes.

Given the nature of pharmaceutical patents, the claims aim to balance broad protection with technical specificity, ensuring enforceability while covering potential variations.

Patent Landscape and Legal Context in Slovenia

Regional and International Patent Environment

Slovenia’s patent system is harmonized with the EPC, facilitating patent protection across Europe through a centralized application process. Nonetheless, patent rights are granted nationally, with rights enforceable within Slovenia unless extended via regional or supplementary protections.

Additional considerations include:

  • Compatibility with European Patent Law: European patents validated in Slovenia share a common core but can be narrowed during national phases
  • Patent term: Typically 20 years from priority date, subject to maintenance fees
  • Patentability criteria: Novelty, inventive step, and industrial applicability

Key Patentholders and Competitors

The patent landscape around SI2914255 involves various pharmaceutical innovators and generic manufacturers. Notably, patent families regarding similar chemical structures or indications often co-exist, creating a complex patent thicket that can influence freedom-to-operate (FTO) analyses.

Potential competitors may hold:

  • Blocking patents: Covering alternative compounds or formulations
  • Follow-on patents: Slight modifications or new uses, extending patent life or market exclusivity

An analysis of neighboring patents reveals the strategic pathways for infringement avoidance or licensing.

Potential Patent Challenges and Innovations

Pharmaceutical patents face challenges such as:

  • Post-grant oppositions: Based on lack of novelty or inventive step
  • Litigation risks: Infringement disputes with generics or biosimilar manufacturers
  • Patent cliffs: Approaching expiration prompting aggressive R&D efforts

Strategic innovation schemas involve filing continuation applications or supplementary protection certificates (SPCs) to extend market rights.

Validity and Patent Life

Given the typical lifespan, SI2914255 likely remains enforceable unless challenged. Its strength depends on:

  • Novelty: Is the compound genuinely new?
  • Inventive step: Does the invention involve a non-obvious advance over prior art?
  • Utility: Is the invention industrially applicable?

Validations and maintenance fees in Slovenia and international extensions influence operational stability.

Implications for Pharmaceutical Innovation and Business Strategy

The patent’s scope impacts multiple facets:

  • R&D direction: The protected invention can serve as a core asset for drug development
  • Market exclusivity: Grants control over manufacturing and sales in Slovenia, with potential regional extensions
  • Licensing and partnerships: Opportunities for monetization via licensing agreements or strategic collaborations

Pharmaceutical companies leverage such patents to secure regulatory approval pathways while navigating potential patent landscapes to mitigate infringement risks.

Regional and Global Patent Landscape

European and global patent strategies involve:

  • Filing European Patent Applications: Extending protection across member states efficiently
  • Patent Analyses: Assessing overlapping patents and freedom-to-operate
  • Supplementary Protections: Applying for SPCs under EU law to extend patent rights during clinical or regulatory approval phases

The interconnected nature of these protections demands vigilant patent landscape monitoring, especially given the rapid innovation pace in pharmaceuticals.

Key Takeaways

  • SI2914255 offers targeted patent protection within Slovenia, focusing on novel aspects of the drug’s chemical composition, formulation, or use.
  • Understanding the claims’ scope is vital: broad claims safeguard core innovations, while narrower claims mitigate invalidation risks.
  • The patent landscape includes regional extensions and breaching risks by generic competitors, emphasizing strategic patent management.
  • Given the patent’s potential lifespan, proactive patent strategies and infringement monitoring remain essential for maximizing commercial value.
  • Alignment with European and international patent practices enhances market protection and facilitates future expansion.

FAQs

  1. What is the primary inventive aspect protected by Slovenia patent SI2914255?
    The patent likely protects a unique chemical entity, drug formulation, or method of use that demonstrates specific therapeutic advantages.

  2. Can this patent be extended beyond Slovenia?
    Yes, by filing a European Patent application designating Slovenia or via national validations in other jurisdictions, potentially supplemented by SPCs.

  3. What are the main challenges facing the patent’s enforcement?
    Challenges include patent validity disputes, prior art challenges, and infringement by generic or biosimilar manufacturers.

  4. How does the patent landscape influence drug development strategies?
    It guides innovation focus, licensing opportunities, and timing for patent filings to optimize market exclusivity.

  5. What should potential licensees consider regarding SI2914255?
    Licensees should evaluate the patent’s scope, validity, territorial coverage, and potential for extension to ensure freedom to operate and strategic alignment.


References

[1] Slovenian Intellectual Property Office (SIPO). Patent register for Slovenia, patent SI2914255.
[2] European Patent Office (EPO). Guidelines for examination on patentability.
[3] European Patent Convention (EPC). Framework for patent protection across Europe.
[4] Hobbs, S. (2021). Pharmaceutical Patent Strategies in Europe. Journal of Intellectual Property Law.

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