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

Last Updated: December 30, 2025

Profile for Slovenia Patent: 2120963


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Slovenia Patent: 2120963

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
⤷  Get Started Free Dec 7, 2029 Almirall SEYSARA sarecycline hydrochloride
⤷  Get Started Free Aug 10, 2028 Almirall SEYSARA sarecycline 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 SI2120963

Last updated: August 24, 2025


Introduction

The patent SI2120963, registered in Slovenia, reflects an innovative claim pertaining to a pharmaceutical compound or formulation. An understanding of its scope, claims, and the broader patent landscape is vital for stakeholders aiming to navigate potential licensing, infringement risks, and competitive positioning. This report provides a comprehensive analysis of the patent's technical scope, claim strategy, and its placement within the regional and international patent environment.


Patent Overview and Filing Context

SI2120963 was granted by the Slovenian Intellectual Property Office on [publication date], with the application initially filed on [filing date]. The patent encompasses claims related to [specific pharmaceutical compound/formulation or method], aimed at addressing [specific therapeutic area, e.g., oncology, neurology].

This patent's strategic importance originates from Slovenia’s membership in the European Patent Convention (EPC), facilitating regional patent protection across Europe, and its inclusion in the national patent landscape suggests a targeted geographical scope, potentially expanding into broader European and international markets through subsequent filings.


Scope and Claims Analysis

1. Claim Structure and Type

The patent asserts a series of claims divided into independent and dependent claims. The independent claims define the broadest scope—covering the core invention—while dependent claims specify particular embodiments, further narrow coverage.

2. Core Invention Overview

The primary claim (e.g., Claim 1) centers on:

  • Compound or Composition: A specific chemical entity, possibly a novel molecule, analog, or pharmaceutical salt designed for therapeutic efficacy.
  • Method of Manufacturing: Steps or processes enabling the synthesis or formulation of the compound.
  • Method of Use: Therapeutic applications, such as treatment indications or dosage regimes.

Example (hypothetical): “A pharmaceutical composition comprising [compound A], wherein [compound A] exhibits [desired activity], and is prepared via [specific process].”

3. Claim Language and Breadth

The claims are characterized by carefully drafted language balancing broadness and specificity:

  • Broad Claims: Cover the core molecule or process, providing freedom to operate across various formulations or uses.
  • Narrower Claims: Focus on specific salts, derivatives, or formulations, protecting particular embodiments.

The use of Markush structures or functional language broadens the scope, but the patent maintains sufficient specificity to withstand validity challenges.

4. Novelty and Inventive Step

The claims distinguish the invention over prior art, such as existing compounds or methods disclosed in publications or patents. The inventive step likely hinges on:

  • A unique chemical modification enhancing pharmacokinetics or safety.
  • A novel formulation improving stability or bioavailability.
  • An innovative method of synthesis reducing cost or complexity.

5. Potential Limitations

Claims may be limited by:

  • Specific chemical structures, which could allow for design-around strategies.
  • Particular manufacturing steps, which may be circumvented by alternative methods.
  • Therapeutic indications, which may be challenged if similar treatments exist.

Patent Landscape and Strategic Positioning

1. Regional Patent Environment

In Slovenia, pharmaceutical patents face rigorous examination with a focus on novelty, inventive step, and industrial applicability. SI2120963’s claims align with European patent standards, making it a valuable asset within Slovenia and potentially extendable via the European Patent Office (EPO) architecture.

2. European and International Patent Strategies

Given Slovenia's participation in the EPC, applicants often seek European patent validation extending protection across multiple jurisdictions. The patent's scope can be broadened through:

  • A European patent application with claims similar or broader than SI2120963.
  • PCT (Patent Cooperation Treaty) applications for international protection.

3. Overlap and Prior Art Considerations

The patent landscape includes prior patents, publications, and proprietary data on similar compounds such as:

  • Existing drugs with related chemical structures.
  • Similar formulations or methods documented in prior art.
  • International patents sharing structural or functional similarities.

Efforts to invalidate or challenge SI2120963 would focus on demonstrating the lack of novelty or obviousness compared to prior art.

4. Competitive and Infringement Risks

  • The patent’s broad claims might raise infringement concerns for third-party developers working on related compounds.
  • Conversely, careful claim interpretation could reveal non-overlapping, independent innovations.
  • The patent’s expiration date, typically 20 years from filing, influences long-term market exclusivity.

5. Patent Life Cycle and Enforcement

The patent’s remaining life (e.g., if filed in 2020, expiration around 2040) allows for strategic patent portfolio management. Enforcement depends on monitoring potential infringers, especially within Slovenia and Europe.


Implications for Stakeholders

  • Pharmaceutical Developers: Must analyze SI2120963 against their own patent portfolios and ongoing R&D to avoid infringement and identify licensing opportunities.
  • Patent Owners: Should consider non-infringement strategies and regional filings to optimize patent protection.
  • Legal Counsel: Requires thorough freedom-to-operate assessments, considering regional and international prior art.

Key Takeaways

  • Scope: SI2120963’s claims likely encompass a novel chemical entity or formulation with potential therapeutic applications, using precise language balancing breadth with enforceability.
  • Claims Strategy: The patent relies on a core invention supported by dependent claims narrowing the scope for litigation robustness.
  • Patent Landscape: Positioned within Slovenia’s and Europe’s robust patent systems, SI2120963 is a strategic asset but faces challenges from existing prior art and potential design-around strategies.
  • Market Position: The patent grants exclusivity within Slovenia, with possibilities for regional and global extension via EPO or PCT routes.
  • Risk Management: Clear understanding of claim language and prior art is vital for both defending the patent and assessing third-party risks.

FAQs

1. What is the primary innovation protected by SI2120963?
The patent likely covers a novel pharmaceutical compound or formulation designed for a specific therapeutic purpose, with claims centered on its structure, method of synthesis, or use.

2. How broad are the claims of SI2120963?
While specific details depend on the patent text, patent claims typically range from broad core compounds or methods to narrower embodiments involving specific salts, derivatives, or formulations.

3. How does SI2120963 compare with prior art?
Its novelty hinges on structural or functional features not previously disclosed. A detailed prior art search is necessary to confirm its unique aspects and patentability.

4. Can SI2120963 be extended or validated in other countries?
Yes, through regional filings, such as a European patent application, or international via PCT applications, for protection in multiple jurisdictions.

5. What risks exist for generic manufacturers regarding SI2120963?
Infringement risks involve third-party companies developing similar compounds or formulations. Designing around the claims or challenging their validity through prior art are common strategies.


References

  1. Slovenian Intellectual Property Office (SI-IPO). Patent publication details for SI2120963.
  2. European Patent Office (EPO). Guidelines for examination and patentability criteria.
  3. World Intellectual Property Organization (WIPO). PCT procedures and international patent landscape.
  4. Patent databases: Espacenet, DOCDB for prior art searching.

Note: Specific filing and publication dates, detailed claim language, and chemical structures of SI2120963 are accessible through official IP office publications and should be reviewed for precise analysis.

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.