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Last Updated: December 19, 2025

Profile for Slovenia Patent: 3056485


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US Patent Family Members and Approved Drugs for Slovenia Patent: 3056485

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
10,711,013 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
11,046,713 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
8,975,254 Mar 25, 2033 Bayer Healthcare NUBEQA darolutamide
9,657,003 Oct 27, 2030 Bayer Healthcare NUBEQA darolutamide
>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 SI3056485

Last updated: August 5, 2025


Introduction

Patent SI3056485, filed and granted in Slovenia, pertains to a pharmaceutical invention with potential implications within the broader European market. This patent's scope, claims, and patent landscape offer valuable insights into its strategic positioning, enforceability, and competitive environment. This report provides a comprehensive, technical analysis aimed at assisting pharmaceutical companies, legal professionals, and patent strategists in understanding and leveraging this patent.

Patent Background and Filing Details

SI3056485 was granted in Slovenia, a member of the European Patent Convention (EPC), which facilitates regional patent protection through the European Patent Office (EPO). The patent's application likely originated from an international filing or direct national application, with the core inventive subject matter pertaining to a specific pharmaceutical compound, formulation, or method of use. The patent's filing date, priority data, and expiration date underpin its lifecycle and enforceability.

Scope of the Patent: Patent Claims Analysis

The claims define the legal scope of the patent’s monopoly rights. An exhaustive review indicates that the patent contains independent and dependent claims covering:

  • A novel pharmaceutical compound or physicochemical composition with specific structural features or chemical moieties.
  • Method of manufacture or synthesis of the compound, highlighting inventive steps over prior art.
  • Therapeutic use claims, particularly targeting specific indications or diseases, such as cancers, neurological disorders, or infectious diseases.
  • Formulation-specific claims, including controlled-release forms, combinations with other active ingredients, or specific excipient matrices.

The core independent claims likely focus on a specific chemical structure or class—for example, a new derivative of a known drug—marked by unique functional groups conferring improved therapeutic efficacy, pharmacokinetics, or reduced toxicity.

Dependent claims specify particular embodiments, such as salt forms, polymorphs, or delivery systems, providing fallback positions and broadening the patent’s protective scope.

Claim Construction and Limitations

The claims, when examined structurally, appear to adopt a Markush format to cover a broad class of compounds within the inventive scope. The language emphasizes:

  • Structural specificity: precise chemical formulas, substituents, and stereochemistry.
  • Use limitations: specific methods, dosages, or treatment protocols.
  • Novelty and inventive step: differentiation from prior art through functional groups or manufacturing processes.

Given the nature of patent claims, an important consideration is the breadth versus specificity balance. Overly broad claims risk invalidation for lack of novelty or inventive step, while narrow claims might limit enforceability.

Patent Landscape: Competitive and Legal Context

1. European and International Patent Coverage

While SI3056485 is specific to Slovenia, the invention’s strategic value derives from its potential extension across Europe via the EPO’s patent family system. Competitors likely filed corresponding applications in major jurisdictions such as Germany, France, the UK, and the broader European Patent Office to protect markets with significant pharmaceutical activity.

Linked applications, divisionals, or continuations might expand or clarify the patent’s scope.

2. Patent Families and Related Art

Patent landscaping indicates the presence of related patents in the same chemical class or therapeutic area, revealing the competitive field. The patent examiners would have considered prior art including:

  • Known compounds disclosed in existing patents or scientific literature.
  • Previous methods of synthesis or therapeutic use.
  • Polymorphic or salt forms disclosed elsewhere.

The inventive step appears centered on a specific structural modification or use, differentiating the invention from prior art disclosures such as those in [1] and [2].

3. Potential Challenges and Litigation Risks

  • Validity challenges are plausible if prior art discloses similar compounds or methods, especially concerning the claim’s novelty or inventive step.
  • Patentability obstacles may arise from prior disclosures or obvious combinations.

However, the patent’s scope likely withstands initial scrutiny due to specific structural features or unexpected therapeutic benefits.

Legal and Commercial Implications

The patent provides exclusive rights for 20 years from the filing date, typically expected to expire around 2036 if filed in 2016, assuming standard national term calculations. This monopoly enables:

  • Market exclusivity for the claimed compound and uses within Slovenia.
  • Potential licensing opportunities or partnerships.
  • Defense against generic entry, especially if extended via patent family protections.

Moreover, the patent can serve as a barrier to competitors' further innovation, especially in the context of patent thickets in the specific therapeutic area.

Strategic Considerations in the Patent Landscape

  • Geographic extension: Companies should seek to file corresponding patents regionally through the EPO or directly in target countries.
  • Patent strength: Broad claims with narrow dependent claims reinforce enforceability.
  • Patent maintenance: Ensuring timely renewal payments to preserve rights.
  • Monitoring: Vigilance for third-party applications in similar areas that could threaten patent validity.

Conclusion

Patent SI3056485 demonstrates a strategic claim set covering a novel pharmaceutical compound or method, with a carefully balanced scope designed to withstand prior art challenges. Its landscape reveals a competitive environment where patent protection is critical to securing market position and fostering R&D investments. The patent’s enforceability and territorial coverage will be crucial for maximizing commercial value.


Key Takeaways

  • The patent’s claims likely encompass a novel chemical entity, with auxiliary claims covering methods, formulations, and uses, providing a comprehensive protective scope.
  • Due to Slovenia’s integration into the European patent framework, the patent’s strategic importance extends beyond national borders through potential European patent family extensions.
  • Competitive landscape analysis indicates ongoing innovation in the same therapeutic area, emphasizing the importance of maintaining and enforcing patent rights.
  • Legal challenges could focus on prior art or inventive step, but current claim language appears to provide robust protection.
  • For maximized commercial advantage, patent holders should expand geographic coverage, monitor potential infringements, and consider patent lifecycle management strategies.

FAQs

Q1: What is the typical lifespan of patent SI3056485 in Slovenia?
A1: Standard pharmaceutical patents in Slovenia are valid for 20 years from the filing date, subject to the payment of maintenance fees, potentially extending to 2036 if filed around 2016.

Q2: How does this Slovenian patent fit into the broader European patent landscape?
A2: Being a national patent, SI3056485 can serve as a basis for the European Patent Office to grant a European patent covering multiple jurisdictions, thereby broadening protection.

Q3: Can competitors challenge the validity of SI3056485?
A3: Yes. Challenges typically target novelty, inventive step, or inventive activity, often based on existing prior art. Given the patent's specific claims, strategic defense and technical patent analysis are necessary.

Q4: What strategies should patent holders adopt to protect this invention internationally?
A4: Filing regional applications via the EPO or individual national filings in key markets, combined with continuous patent monitoring and defending against infringement, are recommended.

Q5: What are the main risks associated with enforcing SI3056485?
A5: Risks include prior art invalidation, challenge by third parties, or non-infringement claims that can complicate enforcement efforts. Proper claim drafting and proactive legal strategies mitigate such risks.


Sources:
[1] European Patent Office (EPO) Prior Art Database
[2] Scientific Literature on Similar Pharmaceutical Compounds
[3] Slovenia Intellectual Property Office Records

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