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Last Updated: December 19, 2025

Profile for Slovenia Patent: 1971601


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1971601

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 Nov 15, 2026 Boehringer Ingelheim HERNEXEOS zongertinib
⤷  Get Started Free Apr 12, 2031 Seagen TUKYSA tucatinib
⤷  Get Started Free May 9, 2027 Seagen TUKYSA tucatinib
>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 SI1971601

Last updated: August 4, 2025


Introduction

The patent SI1971601, granted in Slovenia, represents a significant intellectual property asset within the pharmaceutical sector. To comprehensively evaluate its strategic value, it is essential to analyze its scope, claims, and the overall patent landscape surrounding it. This report synthesizes available information, examines the patent’s legal protection, compares it within the relevant domain, and explores implications for stakeholders.


Overview of Patent SI1971601

Patent SI1971601 was granted in Slovenia, a member of the European Union, benefiting from the harmonized patent system. While detailed textual claims are not publicly available here, typical pharmaceutical patents of this nature cover novel compounds, formulations, uses, or manufacturing processes.

Based on standard patent drafting practices, the patent likely encompasses:

  • A new chemical entity or a pharmaceutically active compound.
  • Novel formulations or administration methods.
  • Specific therapeutic applications.
  • Synthetic methods and intermediates.

Scope of Patent Claims

1. Core Claims

The core claims in pharmaceutical patents generally define the novel chemical compound(s) or therapeutic uses. For SI1971601, these likely specify:

  • The chemical structure of the active pharmaceutical ingredient (API).
  • Structural modifications that confer enhanced efficacy, stability, or bioavailability.
  • Specific salts, esters, or prodrugs of the compound.

2. Device and Formulation Claims

If the patent covers formulations, claims may specify:

  • Specific excipient combinations.
  • Delivery devices or administration routes.
  • Controlled-release systems.

3. Method of Use Claims

Patents often claim therapeutic methods, such as:

  • Treating particular diseases (e.g., oncology, neurology).
  • Dosage regimes and treatment durations.
  • Combination therapies.

Legal and Patentability Criteria in Slovenia

Under Slovenian patent law, compliant with EU directives, patent claims must meet criteria of:

  • Novelty—the claimed subject matter must be new.
  • Inventive step—not obvious to a person skilled in the art.
  • Industrial applicability—useful in industry.

The scope, therefore, is constrained by these requirements. The patent’s claims aims to carve out a non-obvious inventive territory within the pharmaceutical landscape.


Patent Landscape Analysis

1. International and Regional Patent Families

Given Slovenia’s participation in European Patent Convention (EPC), patents filed here often belong to broader European patent families. This means SI1971601 might be part of a larger patent family covering:

  • Multiple jurisdictions (EU member states, non-EU countries).
  • A common priority document, probably filed earlier (e.g., under PCT).

2. Major Competitors and Similar Patents

The patent landscape likely comprises:

  • Existing patents on similar compounds or mechanisms.
  • Patent thickets aimed at protecting innovations in the respective therapeutic area.
  • Generic challenges that could analyze freedom-to-operate.

Recent patent filings in the domain, especially in the EU, could impact the scope, especially if prior art overlaps or claims are narrow.

3. Patent Litigation and Cumulative Art

Slovenia’s patent office does not have a high profile for patent litigation; however, infringement risks may exist if competitors develop similar compounds or formulations. Prior art references and patent examination reports help assess claim robustness.


Scope Comparison with Similar Patents

  • The patent likely emphasizes specific structural features designed to improve efficacy or reduce side effects.
  • Compared to previous patents (e.g., in the same therapeutic class), SI1971601 may specify novel substituents or methodologies that distinguish it.
  • Its claims’ breadth or narrowness influences market exclusivity and the potential for licensing.

Potential Limitations and Challenges

  • Claim Breadth: Narrow claims may be easier for competitors to design around.
  • Prior Art: Similar compounds or formulations in existing patents could limit scope.
  • Patent Term: Typically 20 years from filing; approaching expiration could diminish exclusivity.
  • Regulatory Barriers: Patent protection is distinct from market approval; regulatory hurdles could impact market entry.

Strategic Implications

  • Patent strength hinges on the novelty and inventive step of the claims.
  • It protects a specific innovation, potentially providing market exclusivity.
  • The landscape analysis suggests the patent exists in a competitive domain, with opportunities for further extensions via subsidiary patents or improvements.

Conclusion

The Slovenian patent SI1971601 exemplifies a carefully scoped pharmaceutical IP right, tailored to protect a novel chemical entity, formulation, or therapeutic use. Its effectiveness depends on the breadth of claims, the robustness against prior art, and alignment with regional patent laws. For stakeholders, understanding this landscape informs investment decisions, licensing strategies, and R&D directions.


Key Takeaways

  • Patent Scope: Likely covers a specific chemical compound or formulation with claims designed to be novel and non-obvious.
  • Legal Context: Must satisfy novelty, inventive step, and industrial applicability under Slovenian and EU law.
  • Patent Landscape: Situated within a competitive arena with overlapping patents; protection strength depends on claim specificity.
  • Strategic Value: Acts as a barrier to generic entry, with potential for extension via additional patents or improvements.
  • Risk Factors: Narrow claims or existing prior art could limit enforcement and market exclusivity.

FAQs

1. What does the scope of patent SI1971601 protect?
It primarily protects the specific chemical compound, formulation, or therapeutic method described in its claims, preventing others from manufacturing, using, or selling the protected invention without license within Slovenia and possibly wider jurisdictions through family patents.

2. How do claims influence the patent’s enforceability?
Claims define the legal boundaries of protection. Broader claims may provide wider coverage but are harder to defend; narrower claims are easier to defend but may limit market exclusivity.

3. Can SI1971601 be challenged by competitors?
Yes. Challenges may include patent oppositions, invalidity actions based on prior art, or non-infringement claims. Its strength depends on the robustness of its claims and prior art landscape.

4. How does the patent landscape in Slovenia impact global strategy?
Since Slovenia is part of the EU, patents filed here often align with broader European filings, affecting strategies for regional and international patent protection.

5. What are potential future developments?
Further patent filings, supplementary protection certificates (SPCs), or research-based modifications can extend the lifecycle and scope of protection for the initial patent.


References

  1. European Patent Office. (2022). Guidelines for Examination.
  2. Slovenian Intellectual Property Office. (2022). Patent Law and Procedures.
  3. WIPO. (2022). Patent Cooperation Treaty (PCT) and International Patent Applications.
  4. EUIPO. (2022). European Patent System Overview.

Note: Specific patent claim texts are not publicly available; analyses are based on typical structures and standard practices in pharmaceutical patenting.

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