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

Last Updated: December 29, 2025

Profile for Slovenia Patent: 3143990


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Slovenia Patent: 3143990

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
9,592,208 Sep 30, 2032 Novartis GILENYA fingolimod hydrochloride
>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 SI3143990

Last updated: August 27, 2025

Introduction

Patent SI3143990 pertains to a specific pharmaceutical invention filed and granted within Slovenia, representing an essential component of the country's intellectual property landscape in the biopharmaceutical sector. This analysis examines the scope and claims of the patent, evaluates its positioning within the broader patent landscape, and offers insights into strategic considerations for stakeholders in pharmaceutical innovation and patent management.

Overview of Patent SI3143990

Patent SI3143990 was granted by the Slovenian Intellectual Property Office (SIPO), securing exclusive rights to a specific drug-related invention. While detailed information from the patent document is necessary to understand the scope precisely, typical patents in this domain reflect innovations around chemical compounds, formulations, methods of treatment, or manufacturing processes.

Publication Details

  • Filing Date: Typically, the patent’s filing date influences its term and prior art considerations.
  • Grant Date: The date of patent grant marks the beginning of exclusivity.
  • Patent Term: Standard patent protection lasts 20 years from the filing date, subject to maintenance fees.

Type of Patent

SI3143990 appears to be a utility patent concerning a novel compound, formulation, or method of treatment for a given disease, assuming typical pharmaceutical patents.

Scope and Claims Analysis

Claims Structure

Patent claims define the legal scope of protection. For drug patents, claims typically delineate the compound’s chemical structure, specific formulations, or methods of use. They can be categorized into:

  • Independent Claims: Broad and cover the core invention.
  • Dependent Claims: Narrower, referencing independent claims to encompass specific embodiments or improvements.

Scope of the Patent

Based on standard practice, the scope of SI3143990 likely covers:

  • Chemical Entities: Novel compounds or derivatives with specified structural formulas.
  • Pharmaceutical Compositions: Formulations combining the active ingredient with excipients.
  • Method of Use: Therapeutic methods for treating particular diseases or conditions.

The precise scope hinges on language specificity and claim breadth. Broad claims provide extensive protection but risk invalidity if challenged by prior art, while narrower claims offer more limited exclusion but potentially less strategic coverage.

Claim Language Analysis

Without the actual claim text, typical features include:

  • Structural Definition: Claims might specify a compound’s molecular formula, key functional groups, stereochemistry, or substituents.
  • Purity and Formulation: Claims may extend to specific concentrations or delivery vehicles.
  • Target Indications: Claims could encompass use in treating diseases like cancer, autoimmune disorders, or neurological conditions.

It is common to see claims such as:

"A compound of formula [X], wherein substituents R1, R2, and R3 are defined, and the compound exhibits improved bioavailability."

or

"A method of treating [disease] comprising administering an effective amount of compound [Y]."

Scope Limitations and Potential Challenges

Legal and strategic considerations include:

  • Prior Art: The broader the claims, the more susceptible they are to invalidation by existing prior art disclosures.
  • Overbreadth Risks: Overly broad claims may be contested or invalidated.
  • Patent Clarity: Precise claim language improves enforceability.

In the context of Slovenia, a member of the European Patent Convention (EPC), the patent’s scope may also align with European patent standards, influencing its validation and enforceability across EPC member states.

Patent Landscape and Competitive Positioning

National and Regional Patent Ecosystem

Slovenia’s pharmaceutical patent landscape is characterized by:

  • EPC Membership: Patent protection in Slovenia is often aligned with European patent applications, enabling broader regional coverage.
  • Complementarity with EP Patent: Developers often file European patents covering multiple jurisdictions, with Slovenian patents providing national rights.

Global Patent Environment

For drugs, patent protection extends beyond Slovenia:

  • International Filing Strategies: Likely, applicants filed PCT applications or direct filings in key jurisdictions such as the EU, US, and Asia.
  • Patent Families: The patent probably belongs to a family encompassing multiple jurisdictions, with Slovenian rights serving as part of broader strategic patent portfolios.

Innovative Positioning

  • Novelty and Inventive Step: The patent claim’s validity hinges on demonstrating novelty over existing prior art and an inventive step.
  • Potential for Generic Entry Delay: As a national patent, SI3143990 may delay generic competition within Slovenia and provide leverage for licensing deals or partnerships.

Infringement and Enforcement

  • Enforceability: Given the patent’s scope, patent holders can pursue enforcement within Slovenia to prevent unauthorized manufacturing, use, or sale of infringing products.
  • Cross-Border Considerations: Due to European integration, enforcement might also be coordinated via European patent mechanisms.

Impact of Regional Harmonization

Slovenia’s adherence to EU patent laws and agreements enables patent rights to be extended or validated in other EU Member States, augmenting the patent’s commercial value and geographic coverage.

Key Strategic Insights

  • Scope Precision: Clear, well-crafted claims supported by detailed description maximize enforceability.
  • Portfolio Management: Strategic patent family management ensures comprehensive protection across jurisdictions.
  • Litigation Preparedness: Patent scope should be balanced to withstand legal scrutiny and challenges.
  • Innovation Lifecycle: Ongoing R&D and patent filings are vital to maintain competitive advantage.

Conclusion

Patent SI3143990 exemplifies a targeted effort to secure exclusive rights in the evolving Slovenian pharmaceutical landscape. Its scope likely encompasses specific chemical compounds and therapeutic methods, aligning with typical pharmaceutical patent strategies. To sustain market position, patent holders should maintain vigilant portfolio management, pursue strategic regional filings, and ensure precise claim drafting.


Key Takeaways

  • The patent's scope is central to its enforceability and strategic value; broad claims require careful crafting to avoid invalidation.
  • Slovenia’s patent landscape offers vital regional protection, particularly through EPC co-membership, allowing for multi-jurisdictional enforcement.
  • Positioning within the broader patent landscape demands alignment with international filing strategies, including PCT and European filings.
  • Continuous innovation and patent portfolio expansion are essential to safeguard against patent cliffs and generic challenges.
  • Effective enforcement hinges on clear claim language, thorough prior art searches, and regional legal compliance.

FAQs

1. What is the typical validity period of Slovenian drug patents like SI3143990?
Most pharmaceutical patents in Slovenia are valid for 20 years from the filing date, subject to maintenance fees and legal compliance.

2. How does Slovenia’s membership in the EPC influence patent protection?
It allows patent applicants to seek regional protection via the European Patent Office, which can be validated in Slovenia and other EPC member states, streamlining international patent rights.

3. Can SI3143990 be extended beyond its initial term?
While patent rights generally last 20 years, extensions such as Supplementary Protection Certificates (SPCs) may be available in Europe for medicinal products, potentially prolonging exclusivity.

4. How important is claim drafting in securing effective patent protection?
Crucial. Well-drafted claims define the infringement boundaries, influence enforceability, and determine the scope of monopoly rights.

5. What strategic steps should patent holders take regarding such patents?
They should continuously monitor patent validity, file strategic filings in key jurisdictions, draft precise claims, and prepare enforcement actions to maximize patent value.


References

[1] European Patent Office, "European Patent Convention," 2023.
[2] Slovenian Intellectual Property Office, "Patent Law and Practice," 2023.
[3] World Intellectual Property Organization, "Patent Cooperation Treaty," 2023.
[4] European Patent Office, "Guidelines for Examination," 2023.

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.