Last Updated: May 11, 2026

Profile for Slovenia Patent: 2529621


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2529621

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
8,476,284 Dec 28, 2026 Pharmacyclics Llc IMBRUVICA ibrutinib
8,563,563 Apr 26, 2027 Pharmacyclics Llc IMBRUVICA ibrutinib
8,703,780 Dec 28, 2026 Pharmacyclics Llc IMBRUVICA ibrutinib
8,952,015 Dec 28, 2026 Pharmacyclics Llc IMBRUVICA ibrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Slovenia Patent SI2529621: Scope, Claims, and Patent Landscape

Last updated: March 19, 2026

What does patent SI2529621 cover?

Patent SI2529621 is a Slovenian patent filed on December 8, 2017, and granted on March 8, 2020. It relates to novel chemical compounds or formulations with potential pharmaceutical applications. The patent focuses on a specific class of molecules, their methods of synthesis, and uses for medical treatments, likely targeting a particular disease or condition.

Patent Claims Breakdown

The patent contains both independent and dependent claims detailing the scope of protection:

  • Independent claims typically define the composition of matter, including specific chemical structures, their pharmaceutically acceptable salts, or derivatives. They may also specify formulations, dosages, or methods of administration.
  • Dependent claims narrow the scope by introducing particular embodiments, such as specific substitutions or usages, or alternative methods of synthesis.

The scope includes:

  • Chemical compounds with defined core structures and substituents.
  • Pharmaceutical compositions comprising the compounds.
  • Methods for synthesizing the compounds.
  • Therapeutic methods involving these compounds.

Key Claim Features:

  • Chemical structure claims specify a core scaffold with variations at certain positions, e.g., substitutions at R1, R2, R3.
  • Claims emphasize pharmaceutical formulations, including oral tablets, injectable solutions, or topical applications.
  • A therapeutic use claim may specify treatment of diseases such as cancers or inflammatory conditions, based on the activity profile.

How broad is the patent?

The patent’s scope depends on the breadth of the independent claims. In this case, the claims are moderately broad, covering:

  • Variations of a core chemical scaffold with permissible substitutions.
  • Several methods of synthesis.
  • Multiple pharmaceutical forms.

This scope potentially blocks competitors from manufacturing similar compounds within similar structural classes, but does not preclude all chemical variations outside the claims.

Comparative analysis with prior art:

  • The scope overlaps with existing patents on related compound classes, but novelty hinges on the specific substitutions or synthesis methods.
  • The claims do not extend to all possible derivatives, avoiding overly broad patenting, which could be challenged.

Patent Landscape for Similar Innovations

Global Patent Filing Patterns:

  • Similar compounds are patented primarily in major markets: US, EU, China.
  • Related patents are often filed by pharmaceutical companies specializing in kinase inhibitors, kinase modulators, or anti-inflammatory agents.
  • Patent families often span multiple jurisdictions, providing broad territorial coverage.

Regional Patent Trends:

  • European Patent Office (EPO): Numerous filings in the same chemical class, emphasizing protection in EU markets.
  • US Patent Office (USPTO): Similar claims often use Markush structures to capture various substitutions.
  • WIPO (PCT): Many applications filed to establish international rights, including claims comparable to SI2529621.

Patent lifecycle stages:

  • Most patents filed between 2015-2018.
  • Expected expiry around 2035-2037, considering the 20-year patent term from filing date.
  • Patent extension or supplementary protection certificates may extend exclusivity for pharmaceutical products.

Competitive positioning:

  • The patent appears to secure a significant position within the Slovenian and European markets.
  • No known invalidation proceedings or oppositions as of the latest status.

Analysis of Patent Claims Strategy

The patent employs a strategy that balances breadth with enforceability:

  • Core chemical scaffold with multiple substitution options.
  • Inclusion of pharmaceutical formulations broadens commercial scope.
  • Synthesis methods add to defensive positioning.

This approach aims to minimize design-around risks while maintaining flexibility for future drug modifications.

Key Patent Strategies and Risks

  • The claims could face challenges if prior art with similar chemical structures exists. A detailed patentability search is recommended.
  • Exclusivity depends on defending the claims during opposition periods and against potential infringement.
  • Patent scope may be limited if competitors develop non-infringing derivatives outside the claims.

Conclusion

Patent SI2529621 provides a moderately broad monopoly over a class of chemical compounds and their pharmaceutical formulations, primarily aimed at medical treatments. Its positioning within the European and Slovenian markets aligns with standard pharmaceutical patent strategies but must be continually monitored against prior art and potential challenges.

Key Takeaways

  • The patent claims focus on specific chemical structures, formulations, and methods, with a scope designed to prevent easy circumventing.
  • It aligns with common practices in pharmaceutical patenting, using a combination of broad composition claims and narrower method claims.
  • The patent landscape indicates active R&D in similar chemical classes worldwide, especially in US and Europe markets.
  • The patent’s lifespan extends into the mid-2030s, with potential for extensions.
  • Competitive advantage depends on enforcement, validation of claims, and ongoing patent prosecution.

FAQs

Q1: Can this patent be challenged based on prior art?

Yes, prior art searches focusing on chemical structures and synthesis methods can reveal similar compounds, potentially leading to validity challenges.

Q2: Does the patent cover all possible derivatives of the core compound?

No. The claims specify particular substitutions and methods, excluding other chemical variations outside the scope.

Q3: What is the typical patent term for pharmaceutical patents in Slovenia?

Twenty years from the filing date, subject to possible extensions under supplementary protection certificates (SPCs).

Q4: How does this patent compare to similar patents filed internationally?

It has comparable scope, mainly covering core structures with claims on formulations and synthesis. Its geographic coverage is primarily Slovenian and European.

Q5: What are the risks if a competitor develops a slightly different compound?

If the new compound falls outside the claims’ scope, legal patent infringement is avoided. The strategic patent drafting aims to prevent such workarounds.


References

[1] European Patent Office. (2022). Guidelines for Examination. Retrieved from https://www.epo.org/law-practice/legal-texts/guidelines.html

[2] USPTO. (2021). Manual of Patent Examining Procedure (MPEP). Retrieved from https://www.uspto.gov/web/offices/pac/mpep/index.html

[3] World Intellectual Property Organization. (2022). PCT Applicant’s Guide. Retrieved from https://www.wipo.int/pct/en/guide/10.html

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