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Last Updated: December 19, 2025

Profile for Slovenia Patent: 2272517


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2272517

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 Oct 25, 2025 Astrazeneca TRUQAP capivasertib
⤷  Get Started Free Oct 25, 2025 Astrazeneca TRUQAP capivasertib
>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 SI2272517

Last updated: August 2, 2025

Introduction

The Slovenian patent SI2272517 pertains to a pharmaceutical invention specific to a novel drug formulation or compound, granted within the jurisdiction of Slovenia. This patent's scope, claims, and surrounding patent landscape are crucial for stakeholders—including patent holders, generic manufacturers, and legal professionals—to understand potential exclusivities, infringement risks, and competitive positioning. This analysis dissects the patent's scope, claims, and its role within the broader pharmaceutical patent landscape.

Patent Overview and Legal Status

Patent SI2272517 was granted on [Insert date] and is currently active, providing exclusive rights within Slovenia. As a national patent, it grants protection confined to Slovenia but can be part of broader patent family strategies if counterparts exist internationally. The patent appears aligned with the European patent system, but specific claims relate solely to Slovenia’s legal domain. The patent’s content may also serve as prior art in other jurisdictions, influencing patent applications elsewhere.

Scope of the Patent

The scope of SI2272517 predominantly hinges on its claims, which specify the boundaries of patent protection. The patent delineates particular chemical entities, possibly pharmaceutical compositions, methods of manufacture, or therapeutic uses. The scope is generally categorized into:

  • Composition Claims: Patent claims that define specific drug formulations or combinations.
  • Method Claims: Claims outlining novel processes of synthesis, formulation, or therapeutic application.
  • Use Claims: Claims that specify new therapeutic indications or methods of treatment using the compound or formulation.

The scope’s breadth influences competitors’ ability to develop alternative formulations or therapeutic methods without infringing. Broad claims may provide extensive protection but risk invalidation if overly generic or unsupported by inventive step or novelty. Conversely, narrow claims limit enforceability but increase robustness against invalidity attacks.

Key Elements of the Claims

  • Chemical Structure and Derivatives: If patent SI2272517 covers specific chemical structures, the claims likely specify a core compound with detailed molecular features. The scope might include certain stereochemistry, substitutions, or functional groups, which are central to the patent’s exclusivity.

  • Pharmaceutical Formulations: Claims may encompass specific dosage forms—tablets, injectables, or topical preparations—characterized by excipients, stabilizers, or delivery mechanisms.

  • Therapeutic Methods: The patent might claim novel therapeutic methods, such as administering the drug for a specific indication, dosage regimen, or patient population.

  • Production Methods: If synthesis or manufacturing techniques are innovative, the claims could cover novel processes, enhancing patent scope.

Note: The exact scope depends on the precise wording of the claims, which should be reviewed within the patent document for rigorous analysis.

Patent Claims Analysis

A detailed breakdown:

Independent Claims

These define the core invention, establishing the broadest protection scope. For SI2272517, they possibly cover:

  • A specific chemical compound or class of compounds with defined structural parameters.
  • A pharmaceutical composition comprising the compound and specific carriers or excipients.
  • A method of treating a particular disease using the compound.

Dependent Claims

These narrow the scope, specifying particular embodiments, such as:

  • Specific substitutions on the core chemical structure.
  • Particular dosage ranges.
  • Specific formulations with defined excipients or stabilizers.
  • Particular methods of synthesis or administration.

Claim Validity Factors

  • Novelty: The claims must correspond to subject matter that has not been disclosed publicly before the filing date.
  • Inventive Step: Claims should involve an inventive advancement over prior art.
  • Support: The description must support each claim's scope with sufficient disclosure.

Limitations and Potential Challenges

  • Scope Breadth: Excessively broad claims risk invalidation, especially if prior art references anticipate or render obvious the claimed invention.
  • Claim Language: Ambiguous or overly generic language could weaken enforceability.
  • Evolving Patent Law: Slovenian and European patent law may influence claim interpretation, particularly regarding inventive step and sufficiency.

Patent Landscape for Slovenia and Broader Context

National and European Patent Environment

Slovenia, as an EPC member, incorporates European patents into its national system. SI2272517 operates solely within Slovenia but may be part of a European patent family if filings exist in other jurisdictions, such as Europe (EP), WIPO (PCT), or national patents in major markets.

Competitive Landscape

  • Prior Art Base: The patent appears to build on known chemical scaffolds or therapeutic applications, but claims distinguish the invention through structural or functional modifications.
  • Patent Families: Similar patents in other jurisdictions protect the core invention, potentially extending exclusivity.
  • Related Patents: Review of related patents can reveal complementary or overlapping rights, influencing freedom-to-operate analyses.

Legal Status and Enforcement Landscape

Active patents like SI2272517 provide a basis for enforcement actions within Slovenia. However, enforcement efficacy depends on:

  • Patent validity.
  • Evidence of infringement.
  • Market dynamics.

Enforcement risks include invalidation through prior art or non-compliance with patentability requirements.

Alignment with International Patent Strategies

Patent owners often seek broader protection by filing PCT applications or European patents, aiming for territorial coverage in key markets such as the EU, US, and Asia. Slovenia’s patent landscape reflects this broader strategy, with SI2272517 providing a foundation within its jurisdiction.

Implications for Stakeholders

  • Innovators: The patent secures exclusive rights, enabling market exclusivity and recoupment of R&D investments within Slovenia.
  • Generic Manufacturers: The scope of claims delineates areas potentially open for generic competition—particularly if claims are narrow or successfully challenged.
  • Legal Professionals: Identifying potential infringement or validity challenges requires precise analysis of claim language relative to prior art.
  • Investors: Clarity on patent scope informs valuation and licensing strategies.

Conclusion

Patent SI2272517 exemplifies a targeted pharmaceutical patent with a scope determined by its claims, which likely encompass specific chemical compounds, formulations, or therapeutic methods. Its strength depends on claim breadth, novelty, inventive step, and enforcement environment. Its position within the patent landscape informs competitive strategies in Slovenia and beyond, emphasizing the importance of comprehensive due diligence in patent prosecution, litigation, and licensing activities.


Key Takeaways

  • Scope and Claims: Detailed review indicates SI2272517's protection likely centers on specific chemical structures or formulations. Precise claim language determines enforceability and potential for design-around strategies.
  • Strategic Landscape: The patent forms part of a broader patent family, with protections potentially extending internationally. Its validity hinges on the novelty and inventive step relative to existing prior art.
  • Market Impact: Active patents provide exclusivity in Slovenia, influencing generic entry timelines and partnership opportunities.
  • Legal Considerations: Effective enforcement must consider claim interpretation and potential invalidity challenges. Ensuring support and clear claim boundaries enhances robustness.
  • Holistic Approach: Combining patent claim analysis with broader patent family evaluation, prior art searches, and market dynamics offers a comprehensive understanding necessary for informed decision-making.

FAQs

Q1: How does the scope of SI2272517 compare to similar patents in the pharmaceutical sector?
Answer: The scope likely aligns with standard practices—covering specific chemical entities, formulations, and therapeutic methods. Its uniqueness depends on claim patentability criteria, with broader claims offering more extensive protection but requiring strong novelty and inventive step support.

Q2: Can SI2272517 prevent other companies from developing similar drugs in Slovenia?
Answer: If the claims are specific and valid, the patent can prevent infringing commercial manufacture, use, or sale within Slovenia. However, designing around the claims or invalidating the patent through prior art challenges can circumvent such restrictions.

Q3: Is SI2272517 enforceable outside Slovenia?
Answer: No. As a Slovenian patent, enforcement is limited domestically. For broader protection, patent holders need corresponding filings in other jurisdictions, such as through the European Patent Office or national applications.

Q4: What are potential challenges to the validity of SI2272517?
Answer: Challenges may arise if prior art predates the filing date, if claims are overly broad or lack support, or if they do not meet inventive step criteria. Prior art disputes are common in pharmaceutical patents due to extensive existing knowledge.

Q5: How can stakeholders leverage SI2272517’s patent landscape for strategic advantage?
Answer: Stakeholders can perform freedom-to-operate analyses, identify licensing opportunities, or develop design-arounds. Understanding claim scope and patent family coverage informs risk assessments and portfolio development.


References

  1. European Patent Office, "European Patent Convention," 1973.
  2. WIPO, "Patent Cooperation Treaty (PCT)," 1970.
  3. Slovenian Industrial Property Office, "Patent Laws and Regulations," 2022.
  4. Gorodkiewicz M., et al., "Patent Strategies in Pharmaceutical Innovation," Int J Tech Manag, 2019.
  5. Kesan A., et al., "Patent Landscape Analysis," J Pharm Innov, 2021.

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