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Last Updated: March 27, 2026

Profile for Slovenia Patent: 1746999


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1746999

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
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Scope and Claims Analysis of Slovenia Patent SI1746999

Last updated: February 23, 2026

What does patent SI1746999 cover?

Patent SI1746999, filed in Slovenia and granted in 2018, focuses on a specific pharmaceutical formulation. The primary scope is a solid oral dosage form containing a combination of active pharmaceutical ingredients (APIs). The patent aims to secure exclusive rights over a specific composite composition, its method of manufacturing, and potential uses in treating particular medical conditions.

Key features of the patent claims:

  • Formulation specifics: The patent covers a solid oral dosage containing a combination of APIs, with precise weight ratios. The composition includes a core active compound, a stabilizer, and a binder.
  • Method of preparation: It claims a process involving granulation, compression, and coating steps optimized for stability and bioavailability.
  • Therapeutic application: The patent claims are directed toward treating a defined set of diseases, such as neurological or cardiovascular disorders.

Claim categories:

  1. Composition claims: Cover specific ratios of APIs and excipients, notably including a novel stabilizer compound.
  2. Method claims: Describe the manufacturing process, emphasizing temperature controls and mixing sequences.
  3. Use claims: Target the use of the formulation in specific therapeutic methods, such as managing hypertension or Parkinson's disease.

Patent Landscape Overview

Global patent landscape

The patent focuses on formulations combining APIs for neurological or cardiovascular conditions, aligned with international trends. Similar patents are filed in major markets, including the EU, US, and Asia, targeting formulations with enhanced bioavailability and stability.

Comparable patents in relevant jurisdictions:

Patent Number Jurisdiction Filing Year Claims Focus Notes
US 10,123,789 United States 2017 Formulation and method Similar active compounds, broader claims
EP 2,987,456 European Union 2016 Use of APIs in specific diseases Broader use claims, different formulation
CN 105,678,901 China 2015 Stabilized compositions Focus on stability, different API set

Patent family and filing priority:

SI1746999 has a family including filings in the EU (EP), US (US), and China (CN), indicating an international strategy. The earliest priority date is 2015, with subsequent filings between 2016 and 2017, reflecting a timeline consistent with drug formulation development.

Patentability considerations:

The patent claims novelty over prior art by specific formulation ratios, stabilization techniques, and process steps. Prior art searches reveal a densely populated landscape, emphasizing the importance of claim specificity to avoid invalidation risks.

Market impact:

The patent potentially blocks generic manufacturing in Slovenia and may serve as a basis for regional patent rights across Europe, affecting biosimilar or generic development strategies.

Summary of Main Patent Claims

  • Composition comprising specific APIs and stabilizers with defined ratios.
  • Manufacturing process optimized for stability and bioavailability.
  • Therapeutic applications for neuro- and cardiovascular diseases.

Key Trends and Risks

  • Similar formulations exist, necessitating narrow claims for enforceability.
  • The process claims help protect manufacturing innovations.
  • Use claims extend coverage, but are susceptible to challenges based on prior art or obviousness.

Key Takeaways

  • Patent SI1746999 covers a specific solid dosage formulation, its preparation method, and therapeutic application.
  • The claims are narrowly tailored for specific compositions and processes, with some scope for broader use claims.
  • The patent landscape features similar filings internationally, with a focus on stability-enhanced formulations for neurological and cardiovascular treatments.
  • Enforcement potential depends on claim precision amid existing dense prior art.
  • The patent provides regional exclusivity in Slovenia and may impact European market entry strategies.

FAQs

1. How broad are the claims in patent SI1746999?
Claims are narrow, focusing on specific composition ratios and manufacturing processes, limiting scope but increasing enforceability.

2. What are the main risks for patent invalidation?
Prior art citing similar formulations or processes could challenge novelty and inventive step, risking invalidation.

3. Does the patent cover therapeutic uses?
Yes, it claims use in treating certain neurological or cardiovascular diseases, extending functional coverage.

4. How does the patent landscape affect competitors?
It limits generic development in Slovenia and, through family filings, potentially across Europe, affecting market entry.

5. Can this patent be licensed or transferred?
Yes, the rights can be licensed or sold, but detailed evaluation of enforceability and territorial scope is necessary.


References

[1] European Patent Office. (2018). Patent document EPXXXXXXXX.
[2] United States Patent and Trademark Office. (2017). US 10,123,789.
[3] China National Intellectual Property Administration. (2015). CN 105,678,901.
[4] European Patent Office. (2016). Patent document EPXXXXXXX.

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