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Last Updated: December 29, 2025

Profile for Slovenia Patent: 1638574


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1638574

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
8,575,146 Dec 2, 2030 Novartis RYDAPT midostaurin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenian Drug Patent SI1638574

Last updated: July 30, 2025

Introduction

The Slovenian patent SI1638574 pertains to a pharmaceutical invention aimed at addressing a specific medical condition through a novel compound, formulation, or method. This patent's scope and claims critically influence its enforceability, licensing opportunities, and potential for commercial development within Slovenia and internationally. Analyzing these aspects alongside the patent landscape provides a comprehensive understanding of its strategic position.


Patent Overview

Patent SI1638574 was granted in Slovenia and is classified under the Cooperative Patent Classification (CPC) codes related to pharmaceutical compositions and methods of treatment. It reflects an inventive contribution in the therapeutic space, possibly covering a new active compound, a combination therapy, or an improved formulation designed to enhance efficacy or reduce side effects.

The patent filing date, priority date, and expiration date (likely 20 years from the earliest filing) establish its patent term and novelty window. The patent's family members probably extend into key jurisdictions, including the European Patent Office (EPO) and possibly the United States or other major markets, indicating its strategic reach.


Scope of the Patent

The scope defines the breadth of protection conferred by SI1638574 and is primarily encapsulated through its independent and dependent claims. Understanding these claims is essential to assess the patent's enforceability and licensing potential.

Independent Claims

Typically, the independent claims in pharmaceutical patents set out the core inventive concept, such as:

  • A novel chemical compound with specific structural features.
  • A pharmaceutical composition comprising the compound and excipients.
  • A method of treatment involving the administration of the compound to a patient in need.

For SI1638574, the independent claims likely include a formula or set of formulas representing the active compound(s). They may also encompass the specific dosing regimen, administration route, or treatment indications. The claims are structured to protect not only the compound itself but also its specific uses and methods of manufacture.

Dependent Claims

Dependent claims narrow the scope, specifying variations such as:

  • Different salts, esters, or stereoisomers of the core compound.
  • Specific dosage ranges.
  • Specific formulations (e.g., controlled-release).
  • Use in particular patient populations or disease indications.

By covering these variants, the patent aims to prevent the emergence of workarounds and expand the scope of protection.


Claim Strategy and Patent Strength

The strength of SI1638574 hinges on:

  • Novelty and Inventive Step: Demonstrated through unique structural motifs or surprising therapeutic effects not disclosed in prior art.
  • Claim Defensibility: Well-drafted claims that avoid overly broad language but retain meaningful scope.
  • Utility: Clear demonstration of the compound's therapeutic benefit.

For example, if the patent claims a specific stereoisomer with superior activity, this enhances its strength by focusing on a particular chemical entity rather than a broad class.


Patent Landscape Analysis

The patent landscape surrounding SI1638574 encompasses the broader ecosystem of existing patents, patent applications, and literature related to the same or similar compounds or therapeutic areas.

Existing Patents and Prior Art

  • The therapeutic domain's maturity influences overlapping patents. In areas like oncology, immunology, or chronic disease management, extensive patenting activity exists.
  • Prior art searches reveal whether the claimed compound or method is indeed inventive. For instance, if similar compounds are disclosed in existing patents or scientific literature, SI1638574's claims need to carve out a non-obvious inventive step.
  • European and international patent applications published prior to SI1638574's filing can be cited as prior art, potentially limiting scope or providing freedom-to-operate insights.

Competitor Patent Activities

  • Major pharma players may have filed patents on related compounds. For example, if a competitor has an expired patent predating SI1638574, it might facilitate generic development.
  • Conversely, active patent filing around the same active ingredient might lead to patent thickets, necessitating careful interpretation of claim scope.

Patent Family and Extension Strategy

  • The patent family likely extends into EPO and other jurisdictions, protecting key markets for commercial viability.
  • Supplementary patent applications or divisionals might serve to broaden coverage or clarify scope.

Legal and Commercial Implications

The enforceability of SI1638574 depends on:

  • The clarity and support of the claims.
  • Successful prosecution history, including any amendments made during examination.
  • The extent of prior art overlapping with the claimed invention.

Commercially, this patent positions the holder to:

  • Engage in licensing negotiations, especially if the claims are broad.
  • Limit competitors from marketing similar compounds or treatment methods.
  • Seek regulatory exclusivity alongside patent rights, particularly in the EU market.

Potential Challenges and Opportunities

  • Challenges: Narrow claims, prior art disclosures, or overly broad language could lead to infringement disputes or invalidation proceedings.
  • Opportunities: A strong patent scope covering specific, inventive compounds and their uses can underpin a successful drug development strategy, attract licensing partners, or serve as a basis for further innovation.

Conclusion

Patent SI1638574 exemplifies a strategic IP asset within Slovenia's pharmaceutical landscape. Its strength hinges on how well its claims delineate a novel, inventive compound or method, and its position relative to the existing patent landscape. Ongoing patent monitoring, landscape analysis, and strategic planning are necessary to maximize its value and mitigate risks.


Key Takeaways

  • The patent's scope is primarily defined by structured independent and dependent claims, targeting specific chemical entities and their therapeutic uses.
  • Its strength depends on clear novelty, non-obviousness, and comprehensive coverage of variations.
  • The patent landscape surrounding SI1638574 includes prior art, competitor patents, and existing literature, which influences its enforceability.
  • Effective patent family strategy and claims drafting extend its market exclusivity and licensing potential.
  • Continuous monitoring of technological advancements and patent filings is critical to maintain competitive advantage.

FAQs

Q1: Can the scope of SI1638574 be broadened through amendments?
Yes, during prosecution, claims can be amended to broaden or clarify scope, provided they do not extend beyond the original disclosure (no added matter) and conform to patent laws.

Q2: How does SI1638574 compare with similar patents in the EU?
Comparison requires detailed patent mining; however, if similar patents exist, SI1638574's claims should be strategically crafted to occupy a unique niche, such as a specific compound stereoisomer or a novel use.

Q3: What is the potential for patent infringement if a competitor develops a related drug?
Infringement depends on whether the competitor's drug falls within the scope of SI1638574's claims; detailed claim charts and legal analysis are necessary for definitive assessment.

Q4: Are there any limitations on patent enforcement in Slovenia?
Enforcement is consistent with EU patent law, requiring legal action in Slovenian courts. Limitations include validity challenges based on prior art or claim clarity issues.

Q5: How does patent SI1638574 support commercialization?
It provides exclusive rights to prevent others from manufacturing or selling the covered pharmaceutical product in Slovenia, creating a foundation for licensing, strategic partnerships, or independent commercialization.


References

  1. European Patent Office, "Guidelines for Examination," 2022.
  2. World Intellectual Property Organization, "Patent Landscape Reports," 2021.
  3. Slovenian Industrial Property Office, Patent Database, 2023.
  4. European Patent Office, "EPO Patent Search," 2023.
  5. PatentScope, WIPO, "Global Patent Database," 2023.

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