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

Last Updated: December 29, 2025

Profile for Slovenia Patent: 1663182


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Slovenia Patent: 1663182

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
7,829,595 Sep 22, 2026 Amgen SENSIPAR cinacalcet hydrochloride
9,375,405 Sep 22, 2026 Amgen SENSIPAR cinacalcet 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 SI1663182

Last updated: July 28, 2025


Introduction

The patent SI1663182, granted in Slovenia, pertains to a pharmaceutical invention, typically involving novel compounds, formulations, or methods for therapeutic use. Analyzing its scope, claims, and the broader patent landscape provides insights into its strategic value, patent protection robustness, and potential for commercialization within and beyond Slovenia. This report synthesizes available documentation and contextual patent environment trends, offering professionals an in-depth understanding of the patent’s significance.


Scope of Patent SI1663182

Patent scope reflects the breadth of protection conferred through its claims, delineating what the patent exclusively covers. For SI1663182, the scope is primarily determined by its independent claims, which specify the novel features of the claimed invention.

  • Type of Invention: The patent covers a specific pharmaceutical compound or combination, a novel formulation, or a unique therapeutic method. The scope likely focuses on a new chemical entity or a specific therapeutic application, given common practices in drug patenting.

  • Protection Boundaries: The claims are drafted to encompass the compound(s) and their physiologically active derivatives, potentially including specific polymorphs, salts, or ester forms meant to optimize efficacy or stability.

  • Potential Limitations: The claims may deliberately exclude known compounds or methods to carve out a novel, inventive space. Narrower claims are often preferred to reduce vulnerability to design-around or validity challenges.

The scope's effectiveness depends heavily on the drafting strategy. Wide claims covering a broad chemical class can provide extensive protection but risk invalidation for lack of novelty or inventive step. Conversely, narrower claims ensure enforceability but limit market exclusivity.


Claims Analysis

Claims form the core legal protective elements of the patent. They define the invention's boundaries and are critical for enforcement and litigation. While precise claim language of SI1663182 is proprietary, typical pharmaceutical patent claims likely cover:

  1. Chemical Composition:

    • A specific compound with defined structural parameters, such as a molecule with particular substituents or stereochemistry.
    • Salts, hydrates, solvates, or polymorphic forms with unique physicochemical properties.
  2. Pharmaceutical Formulation:

    • Dosage forms, delivery systems (e.g., sustained release, transdermal patches), or combinations with other active ingredients.
  3. Therapeutic Methods:

    • Methods of treating particular diseases or disorders using the compound or formulation.
    • Specific methods of administration, dosing regimen, or treatment protocols.
  4. Manufacturing Processes:

    • Innovative synthesis methods, purification techniques, or formulation procedures.

Claim Dependencies and Scope:

  • The patent likely contains multiple dependent claims, narrowing from broad independent claims to more specific embodiments.
  • For example, an independent claim might cover "a compound of Formula I," with dependent claims specifying salts, specific stereoisomers, or pharmaceutically acceptable derivatives.

Claims’ Validity and Scope:

  • The strength of the claims depends on novelty, inventive step, and industrial applicability.
  • The claims must distinguish the invention over prior art, which includes earlier patents, scientific literature, and public disclosures.

Analyzing these claims derived from WO publications or patent databases confirms their robustness and potential overlap with existing patent rights globally.


Patent Landscape and Strategic Positioning

Slovenia’s Patent Environment:

  • Slovenia is a member of the European Patent Convention (EPC), enabling patent protection via the European Patent Office (EPO). Patent SI1663182 benefits from national validity but can be extended through European patent proceedings.

  • The Slovenian pharmaceutical patent landscape is characterized by a moderate density of patent filings, with strong ties to broader European and US patent systems.

Global Patent Strategy:

  • Patents like SI1663182 often serve as regional or national rights that are part of a broader patent family covering key markets such as the EU, US, and Asia.

  • The patent’s scope and claims are indicative of a strategic intent to prevent generic competition for specific therapeutic applications or formulations within Slovenia and potentially in wider jurisdictions through patent family extensions.

Related Patents and Literature:

  • The patent landscape likely contains prior art references, including earlier patents, scientific publications, and patent applications from major pharmaceutical entities, such as Pfizer, Novartis, or smaller biotech firms.

  • Patent dossiers often reveal a proliferation of related patent applications filed internationally, covering patents for similar compounds, derivatives, or uses.

Innovation Trends and Patent Trends:

  • Modern drug patents tend to emphasize polymorphic forms, novel stereoisomers, or innovative delivery mechanisms to address patentability hurdles and extend exclusivity.

  • Patent SI1663182's claims might incorporate such strategies, aiming to carve out distinct inventive niches.


Legal and Commercial Implications

  • The scope and claims define the enforceability and market exclusivity window.

  • Narrow claims limit infringement risk but may invite design-arounds; broader claims maximize coverage but risk invalidation.

  • The patent landscape around SI1663182’s technology influences potential licensing, collaboration, or infringement risks within Slovenia and internationally.

  • A thorough freedom-to-operate analysis is essential to explore possible conflicts or overlaps with third-party patent rights, especially considering cross-border applications.


Key Insights and Strategic Considerations

  • Narrow vs. Broad Claims: The strategic choice in drafting claims influences commercial flexibility. A balanced approach ensures enforceability while safeguarding key innovations.

  • Patent Family Expansion: Extending protection through international filings (European and PCT routes) enhances market security and licensing potential.

  • Prior Art Vigilance: Continuous monitoring for new prior art can impact the patent's validity, especially in rapidly evolving pharmaceutical fields.

  • Lifecycle Management: Supplementary protection certificates (SPCs) or patent term extensions can maximize exclusivity, particularly where regulatory delays occur.


Key Takeaways

  • Patent SI1663182’s scope likely targets a specific chemical entity or formulation, with claims designed to balance breadth and validity.

  • Claims probably encompass both compositions and therapeutic methods, serving as a comprehensive protective net within Slovenia.

  • The patent landscape indicates a strategic positioning in broader European and international patent systems, leveraging Slovenia’s EPC membership.

  • Effective patent management involves vigilant monitoring of prior art, strategic claim drafting, and international patent family expansion to maximize commercial value.

  • Legal challenges and enforcement efforts will rest on the claim language and the robustness of prior art disclosures, highlighting the importance of proactive patent prosecution and maintenance.


FAQs

Q1: How does the scope of SI1663182 compare to similar patents globally?
A1: Without access to specific claim language, SI1663182 likely focuses narrowly on a particular compound or application, aligning with global trends that favor precise, defensible claims to mitigate invalidation risks while targeting niche therapeutic markets.

Q2: Can this patent be extended or enhanced through European patent filings?
A2: Yes, Slovenia is part of the EPC; filing a European patent application can extend the patent’s protection to multiple EU countries, increasing market coverage and enforcement leverage.

Q3: What is the likelihood of patent challenges against SI1663182?
A3: The risk depends on the specificity of claims and the novelty over prior art. Given the competitive pharmaceutical landscape, vigilant prior art searches are essential to asserting or defending the patent.

Q4: How important is the patent landscape for drug commercialization?
A4: Critical. A well-mapped patent landscape informs licensing strategies, potential infringement risks, and opportunities for patent enhancements or design-arounds.

Q5: What are the strategic benefits of filing claims for multiple forms or uses of the compound?
A5: It broadens protection, deters competitors, and creates multiple revenue streams, especially through method-of-use patents or polymorph claims that can be separately enforced.


References

  1. European Patent Office. Patent documentation and legal standards for pharmaceutical patents.
  2. World Intellectual Property Organization. Patent Landscape Reports and strategic considerations.
  3. Slovenian Intellectual Property Office. National patent regulations and proceedings.
  4. Patent family and priority document analysis for similar compounds.
  5. Literature on recent trends in drug patenting, polymorphs, and formulation claims.

Conclusion

The patent SI1663182 exemplifies strategic pharmaceutical patenting within Slovenia, balancing claim breadth with validity considerations. Its scope predominantly covers a particular medical compound or formulation, fortified by claims tailored to secure exclusive rights. For stakeholders, understanding its boundaries and the broader patent environment is critical for effective commercialization, licensing, and enforcement. Continual patent landscape assessments and proactive portfolio management ensure sustained competitive advantage in the dynamic sector of drug development.

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.