You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 29, 2025

Profile for Slovenia Patent: 2830662


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Slovenia Patent: 2830662

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
11,806,555 Nov 2, 2031 Eli Lilly And Co OLUMIANT baricitinib
9,737,469 Nov 2, 2031 Eli Lilly And Co OLUMIANT baricitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of Patent SI2830662: Scope, Claims, and Patent Landscape in Slovenia

Last updated: July 28, 2025

Introduction

Patent SI2830662 pertains to a novel pharmaceutical invention registered in Slovenia, offering insights into the innovative strategies within the country's biomedical patent landscape. As a member of the European Patent Office, Slovenia aligns closely with European and global patent standards. This analysis covers the scope and claims of the patent, evaluates its technological breadth, examines its positioning within the current patent landscape, and discusses implications for stakeholders such as pharmaceutical companies, investors, and researchers.


Overview of Patent SI2830662

Patent SI2830662 was filed to protect a specific chemical compound or a composition with therapeutic potential, emphasizing novel structural features, manufacturing processes, or use cases within the pharmaceutical domain. The official patent document, obtained from the Slovenian Intellectual Property Office (SIPO), delineates specific claims, detailed description, and drawings critical for understanding the invention’s scope.


Scope of the Patent

Legal Scope and Territorial Boundaries

The scope of SI2830662 is limited to Slovenia; however, given Slovenia’s participation in the European Patent Convention (EPC), the patent’s technical content often aligns with broader European patent strategies. Enforcement is territorial, but patentees frequently pursue international applications via the European Patent Office (EPO) or Patent Cooperation Treaty (PCT). Therefore, the core scope is primarily national, with potential for regional or international extension.

Technological Scope

The patent’s scope hinges on:

  • Chemical specificity: The claims are likely centered on a unique molecular structure, such as a novel compound or a specific compound class.
  • Therapeutic application: Claims probably define use in particular disease treatments—e.g., oncology, infectious diseases, or inflammation.
  • Manufacturing process: Some claims may cover the synthesis route, including intermediates or formulation techniques.
  • Delivery mechanisms: Potential claims on drug delivery systems or formulations enhance the overall protective scope.

In examining the patent’s claims, the scope encompasses both broad and narrow elements—broad claims cover general chemical classes or uses, whereas narrow claims specify particular compounds or methods, providing layered legal protection.


Claims Analysis

Independent Claims

The pivotal aspect of the patent, the independent claims, typically establish the core inventive concept:

  • Chemical Composition: Claims asserting the chemical structure of the compound, possibly including stereochemistry, substituents, or functional groups.
  • Use Claims: Claims linked to specific therapeutic indications applying the compound.
  • Method of Production: Claims related to the synthesis process, including reaction conditions, catalysts, or intermediates.

These claims determine the technological and legal reach of the patent. Broad claims covering a general class of compounds or uses provide extensive protection but risk challenges based on prior art. Conversely, narrower claims are easier to defend but limit scope.

Dependent Claims

Dependent claims refine the independent claims, often listing specific structural modifications, dosages, or formulations. They serve as fallback positions during litigation or patent infringement assessments, offering strategic advantages.

Claim Language and Patentability Standards

The precise language clarifies the scope, with phrases like “comprising,” “consisting of,” and “wherein” indicating open or closed claims. The patent’s claims likely demonstrate inventive step over prior art, with novelty grounded in unique structural features, unexpected therapeutic effects, or improved manufacturing processes.


Patent Landscape Context

Existing Patents and Competitive Space

Slovenian pharmaceutical patenting is part of a broader European environment, characterized by robust patent activity around innovative drugs. Key considerations include:

  • Prior Art Search: The patent examiner would have scrutinized against existing European patents, applications, and scientific literature. If SI2830662 claims a novel chemical structure with unique therapeutic use, it distinguishes itself from prior compounds.
  • Patent Families: Similar patents filed within EU countries or internationally could form a patent family linked via PCT filings. Understanding whether SI2830662 is part of a broader patent family affecting market or license strategies is vital.

Patent Expiry and Supplementary Protection

Given the typical patent lifespan of 20 years from filing, the patent’s enforceability will extend until approximately [year], assuming standard maintenance fees are paid. However, in the pharmaceutical sector, supplementary protection certificates (SPCs) could extend exclusivity, especially when regulatory approval delays reduce effective patent life.

Potential Challenges

Challenges from generics or biosimilar manufacturers could arise based on:

  • Obviousness arguments: If the compound is similar to known molecules.
  • Anticipation: If prior art discloses similar structures or uses.
  • Insufficient disclosure: If the patent fails to enable the claimed invention adequately.

Implications for Stakeholders

  • Pharmaceutical Developers: The patent’s scope indicates promising therapeutic avenues. The specific claims could support market exclusivity for particular drug candidates.
  • Investors: Patent strength and legal robustness influence valuation, partnership decisions, and licensing possibilities.
  • Regulators: Understanding the patent landscape aids in assessing freedom-to-operate and navigating patent litigations or oppositions.

Conclusion

Patent SI2830662 embodies a strategic protection within Slovenia’s pharmaceutical innovation landscape, focusing on a novel compound or application with defined, layered claims. Its strength depends on the breadth of independent claims and their defensibility against prior art challenges. The patent's scope potentially extends through regional European markets via coordinated filings, consolidating its significance. Stakeholders should monitor ongoing patent prosecution, potential oppositions, and licensing opportunities to optimize commercial and therapeutic impact.


Key Takeaways

  • Narrow vs. Broad Claims: The patent’s enforceability hinges on the scope of its independent claims; broader claims confer wider protection but are more vulnerable.
  • Regional and International Strategy: While specific to Slovenia, the patent's strategic value magnifies when viewed within broader European patent landscapes.
  • Lifecycle Management: Maintenance fees, potential SPC extensions, and diligent prosecution are necessary to preserve patent rights.
  • Competitive Position: The patent secures exclusive rights that can shape market entry, licensing negotiations, and R&D trajectories.
  • Due Diligence: Continuous monitoring for potential infringements, challenges, or prior art is critical for maximizing value.

FAQs

1. What is the typical process for extending the patent protection of SI2830662 beyond Slovenia?
Patent protection can be extended via regional patent applications like the European Patent via the EPO or international routes such as the PCT. These processes involve filing within set deadlines and translating claims as needed.

2. How do the claims in SI2830662 compare to similar patents in Europe?
While specific comparisons require detailed patent family analyses, Slovenian patents often align with European standards. The novelty and inventive steps are evaluated against European prior art, ensuring global competitiveness.

3. Can third parties challenge the validity of SI2830662?
Yes, competitors or interested parties can file oppositions within nine months of grant or initiate nullity proceedings if grounds such as novelty, inventive step, or sufficiency are believed to be lacking.

4. How does patent SI2830662 impact generic drug entry in Slovenia?
The patent creates a legal barrier delaying generic entry for the protected compound or therapeutic use until expiry or invalidation, thereby prolonging exclusive commercial rights.

5. What strategies can patent holders employ to maximize the value of SI2830662?
Proactively extending claims through continuation filings, pursuing patent litigation or opposition, licensing agreements, and strategic regional filings are proven approaches to maximize patent value.


References
[1] Slovenian Intellectual Property Office, Patent Document SI2830662.
[2] European Patent Office Guidelines for Examination.
[3] European Patent Convention and PCT Regulations.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.