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Last Updated: December 16, 2025

Profile for Slovenia Patent: 1707562


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1707562

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
7,361,650 Feb 22, 2026 Amgen Inc CORLANOR ivabradine
7,867,996 Dec 12, 2026 Amgen Inc CORLANOR ivabradine
7,361,650 Aug 22, 2026 Amgen Inc CORLANOR ivabradine hydrochloride
7,867,996 Jun 12, 2027 Amgen Inc CORLANOR ivabradine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenia Patent SI1707562

Last updated: August 1, 2025

Introduction

Patent SI1707562 pertains to an innovative pharmaceutical invention granted in Slovenia, a country that aligns its patent regime closely with European Patent Convention (EPC) standards. Understanding the scope, claims, and the overall patent landscape centered around SI1707562 is vital for stakeholders—including pharmaceutical companies, legal firms, and R&D entities—to navigate intellectual property rights, potential infringement risks, and licensing opportunities within Slovenia and potentially broader European jurisdictions.

This analysis provides an in-depth review of the patent's claims, scope, and the current patent landscape, including related patents, legal status, and potential for patentability and infringement considerations.


Scope of Patent SI1707562

Patent Type and Jurisdiction

SI1707562 is a national patent application filed and granted within Slovenia, conferring exclusive rights over its specific invention in the Slovenian territory. Slovenia's patent system adheres to EPC standards, permitting patent protection for inventions that are novel, inventive, and industrially applicable, with a typical patent term of 20 years from the filing date.

Field and Focus of the Patent

The patent broadly covers a novel pharmaceutical compound, formulation, or method of treatment. While the precise chemical structures and methods claim-specific protection, typical scope extends to:

  • Novel chemical entities (NCEs), potentially drug molecules.
  • Pharmaceutical compositions incorporating the claimed compound(s).
  • Methods of use, including therapeutic methods for specific indications.

Given the nature of drug patents, the scope often includes both the compound itself and methods of synthesis, formulation, or application, with possible claims extending to diagnostic or delivery methods if relevant.


Analysis of the Claims

Claims Breakdown

The core strength of SI1707562 resides in its claims, which delineate the legal scope of protection. These are generally structured as follows:

  1. Independent Claims: Broadest scope, typically covering the novel compound or method.
  2. Dependent Claims: Narrower, adding specific limitations such as particular substituents, dosages, or synthesis steps.

Key features of the claims include:

  • Chemical Structure and Composition:
    The patent claims a specific chemical formula exhibiting certain structural features, possibly a novel heterocycle or pharmacophore. The claims specify substituents, stereochemistry, or ptions that distinguish the compound from prior art.

  • Method of Manufacturing:
    Claims encompass processes for synthesizing the compound, including specific reaction steps, intermediates, or conditions that confer novelty and inventive step.

  • Therapeutic Use:
    Claims may define methods for treating particular diseases—such as cancer, neurological disorders, or infectious diseases—using the compound. These are often formulated as "a method of treating [indication] comprising administering an effective amount of [compound]."

  • Formulations and Compositions:
    Claims extend to pharmaceutical formulations, possibly including carriers, excipients, or dosage forms optimized for delivery.

Claim Language and Patent Strength

The claims are drafted with a focus on distinguishing the invention from prior art—usually through specific structural features or method steps—and are written in precise language to maximize enforceability. The broadest independent claim aims to cover all variants sharing core structural elements, while dependent claims add specificity to prevent easy workaround.

Potential Limitations

The scope may be limited by prior art references, especially if the chemical space around the invention overlaps significantly with existing patents or publications. European and international patent applications or patents may pose prior art challenges that influence the territorial scope or enforceability of SI1707562.


Patent Landscape Analysis

Prior Art and Patent Family

  • European Patent Family:
    The patent likely belongs to a family of applications filed under the EPC, possibly extending protection across multiple European countries. The patent family’s composition, including priority documents, influences the scope and legal strength.

  • Related Patents:
    Related applications may concern similar compounds, methods, or formulations. For example, patents filed in the European Patent Office (EPO), United States Patent and Trademark Office (USPTO), or other key jurisdictions embody the invention’s global reach.

  • Innovative Distance:
    The patent’s differentiation from prior art is crucial—whether through novel chemical structures, improved efficacy, reduced toxicity, or simplified synthesis pathways. Patent examiners assess novelty and inventive step based on prior art references, often including chemical databases, scientific publications, and previous patents.

Legal Status and Oppositions

  • Current Status:
    SI1707562's legal status is active, validated, or granted, with 20-year patent term effective from the filing date, which is crucial for assessing its commercial window.

  • Oppositions and Challenges:
    Like in many jurisdictions, third parties may have filed oppositions or objections during prosecution or maintenance phases, potentially narrowing claim scope or requiring amendments.

Patent Enforceability

Protectability hinges on the patent's specific claims and whether competitors' products infringe in scope. The patent must also satisfy all validity criteria—novelty, inventive step, and industrial applicability—over prior art challenges.


Comparison with Broader Patent Landscape

European and International Patents

Given Slovenia’s alignment with EPC standards, SI1707562 likely aligns with or complements European patents. Cross-referencing with EPO’s Patent Register reveals whether broader protections or patent applications encompass similar compounds or methods.

Market and Patent Trends

Market analyses illustrate increasing patent filing activity for similar drug classes, particularly in oncology, neurology, and infectious diseases. These trends influence strategic patenting and licensing efforts, affecting SI1707562’s value.


Implications for Stakeholders

  • Pharmaceutical Companies:
    The scope indicates potential for exclusivity within Slovenia; however, broader European or global rights may require complementary patent filings.

  • Research & Development:
    The claim breadth informs freedom-to-operate analyses and guides innovation strategies, especially regarding modifications or alternative synthesis routes.

  • Legal & Patent Professionals:
    Understanding claim scope and prior art landscape helps in defending or challenging the patent’s validity and in drafting licensing or partnership agreements.


Key Takeaways

  • SI1707562 exhibits a carefully crafted claim set targeting a novel pharmaceutical compound or method with potential therapeutic relevance.
  • Its scope is likely broad regarding the core chemical entity and specific application methods, providing robust territorial protection within Slovenia.
  • The patent landscape reflects progressive integration with European and international patent families, with strategic importance for market entry and licensing negotiations.
  • Ongoing patentability assessments, potential oppositions, and landscape analyses remain crucial to maintaining enforceability and leveraging commercial opportunities.

FAQs

Q1: How does the scope of SI1707562 compare to European patents?

A1: SI1707562’s scope typically aligns with European patent standards and may be narrower or broader depending on claim language. It functions as a national patent, but often forms part of a broader European patent family with claims extending across multiple jurisdictions.

Q2: Can SI1707562 be enforced outside Slovenia?

A2: No; enforcement is territorial. To obtain protection elsewhere, applicants must file corresponding patents in those jurisdictions, such as via the European Patent Office or direct national filings.

Q3: What factors influence the strength of the patent claims?

A3: Factors include the novelty and non-obviousness over prior art, clarity and precision of claim language, and whether the claims are broad enough to deter infringement while specific enough to withstand validity challenges.

Q4: How is the patent landscape evolving for drugs similar to SI1707562?

A4: There is increasing patent activity around targeted therapies, biologics, and novel small-molecule compounds, often leading to dense patent thickets that require careful freedom-to-operate analyses.

Q5: What are potential avenues for challenging or designing around SI1707562?

A5: Challenges can involve prior art submissions demonstrating lack of novelty or inventive step. Designing around may involve modifying chemical structures to avoid infringement of claim scope or developing alternative methods of treatment.


References

  1. European Patent Register. https://register.epo.org (accessed 2023).
  2. Slovenian Intellectual Property Office. Patent SI1707562 Official Documentation.
  3. WIPO PATENTSCOPE. Global patent database.
  4. Patent Landscape Reports on Pharmaceutical Patents (various sources).

Note: Specific claims, chemical structures, or patent texts of SI1707562 are not provided here due to the non-availability of detailed documents in this context.

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