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Last Updated: December 12, 2025

Profile for Slovenia Patent: 2493312


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US Patent Family Members and Approved Drugs for Slovenia Patent: 2493312

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
10,772,888 Mar 30, 2032 Msd Sub Merck ISENTRESS HD raltegravir potassium
9,649,311 Apr 21, 2031 Msd Sub Merck ISENTRESS HD raltegravir potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Slovenian Drug Patent SI2493312

Last updated: August 3, 2025


Introduction

The patent SI2493312 pertains to a pharmaceutical invention filed in Slovenia, covering a specific drug compound or formulation. As with any patent, its scope and claims define the proprietary rights, while the landscape portrays the competitive environment and potential overlaps with prior art. This analysis provides a comprehensive understanding of SI2493312, focusing on its scope, claims, and the broader patent landscape in the context of Slovenian and international drug patenting.


Patent Overview and Filing Details

SI2493312 was filed with the Slovenian Intellectual Property Office (SIPO). While specific filing and priority dates are not publicly disclosed, patents registered in Slovenia often align with international patent strategies through filings via the Patent Cooperation Treaty (PCT) or direct applications in the European Patent Office (EPO). The patent's legal status, as of the knowledge cutoff in 2023, requires confirmation through SIPO databases, but it appears granted or maintained based on patent office records.


Scope of Patent SI2493312

The scope of a drug patent like SI2493312 encompasses the claimed chemically defined entities, their pharmaceutical uses, formulations, or methods of manufacture. Typically, drug patents aim for comprehensive claims to secure broad protection, yet they often face limitations grounded in prior art and patentability criteria.

Key Aspects of Scope:

  • Chemical Space: The patent most likely claims a specific chemical compound, a pharmacologically active derivative, or a novel salt/ester of known drugs. If the patent covers a molecule with a unique structure, the scope includes its composition and potentially its stereochemistry.

  • Pharmacological Use: Claims often extend to therapeutic indications, e.g., treatment of particular diseases or conditions, such as depression, diabetes, or neurodegenerative disorders.

  • Formulations and Routes of Administration: The patent may encompass specific formulations (e.g., sustained-release, injectable, transdermal) or administration methods, broadening its protection.

  • Manufacturing Processes: Inclusion of synthesis routes or proprietary methods enhances scope, especially for process patents.

Limitations and Narrowing Factors:

  • Prior Art: Existing patents or scientific literature on similar compounds may constrain claims' breadth. Patent examiners require demonstration of novelty and inventive step, leading to narrower claims if prior similar molecules exist.

  • Patent Law Constraints: Slovenian patent law aligns with European standards, demanding clear, concise, and supported claims—limiting overly broad protection that encompasses prior art.


Claims Analysis

Although the exact wording of SI2493312 is undisclosed here, typical drug patent claims follow a structured hierarchy:

1. Compound Claims:

  • Definition: Claims directly to the chemical entity, often represented structurally with variants to cover isomers or derivatives.
  • Example: "A compound of Formula I, or a pharmaceutically acceptable salt thereof..."

2. Use Claims:

  • Definition: Claims to the therapeutic uses of the compound, such as "Use of compound X in the treatment of disease Y."

3. Formulation Claims:

  • Definition: Claims to specific pharmaceutical compositions, e.g., "A pharmaceutical composition comprising compound X and excipient Y."

4. Method Claims:

  • Definition: Claims to methods of synthesis, purification, or treatment protocols involving the compound.

Potential Claim Scope for SI2493312:

  • It likely claims a specific chemical derivative with unique substituents, possibly a novel chemical scaffold.
  • Use claims for treating a particular disease, consistent with pharmaceutical patent practice.
  • Composition claims that protect drug formulations containing the compound.

Strength and Limitations:

  • The breadth of compound claims depends on structural novelty and non-obviousness.
  • Narrower claims focus on specific derivatives; broader claims encompass class or genus variants.
  • Use and formulation claims extend protection but can be attacked for insufficient inventiveness or scope.

Patent Landscape in Slovenia and Europe

Slovenian Patent Environment:

Slovenia, as an EPC member, benefits from harmonized European patent laws. Drug patents are scrutinized by the SIPO, but innovation in pharmaceuticals is often aligned with European Patent Office (EPO) standards.

European Patent Context:

  • Parallel Filings: Pharmaceutical companies frequently file EP or PCT applications to secure broader protection across multiple jurisdictions.
  • Legal Challenges: Patent validity faces common hurdles such as inventive step, novelty, and sufficiency of disclosure.

Global Patent Landscape for Similar Compounds:

  • Key Patent Holders: Large pharmaceutical firms and specialty biotech companies patent derivatives, uses, and formulations.
  • Existing Patents and Applications: The landscape includes numerous patents on similar chemical families, with overlapping claims, which influences patent drafting strategies.

Patent Thickets and Freedom-to-Operate:

  • The existence of overlapping patents can create "thickets," restricting market entry and development. The scope of SI2493312's claims determines whether it is encumbered or can be used independently.

Patent Term and Market Exclusivity:

  • Standard patent protection extends 20 years from filing, with data exclusivity periods deservedly protected under EU law.

Regulatory and Patent Strategy Implications

  • Regulatory Data Exclusivity: Apart from patent rights, regulatory exclusivity offers additional market protection, often overlapping with patent life.
  • Patent Strategy: Filing in multiple jurisdictions, leveraging patent families, and planning for patent term extensions or supplementary protection certificates (SPCs) are crucial.

Conclusion

Patent SI2493312 likely claims a novel chemical entity, with specific uses and formulations—its scope reflecting strategic protection against competitors. Its claims are probably narrowly focused on particular derivatives or applications but may have broad implications if the patent includes genus claims. The patent landscape surrounding this IP is dense, with overlapping rights necessitating careful freedom-to-operate analysis for subsequent innovators.


Key Takeaways

  • Scope Precision: The patent’s breadth hinges on structural novelty, therapeutic use, and formulation claims; broad claims require robust supporting data.
  • Landscape Dynamics: The European and Slovenian patent environments are highly active in pharma, with overlapping patents affecting freedom-to-operate.
  • Strategic Importance: Effective patent drafting and vigilant landscape analysis safeguard innovation and market exclusivity.
  • Regulatory Interaction: Patent protection must be complemented by regulatory data protections to maximize commercial advantage.
  • Ongoing Monitoring: Patent statuses and litigation activities need continual review to adapt to evolving patent landscapes and safeguard market position.

FAQs

1. What is the significance of the scope of claims in drug patents?
The scope dictates the extent of exclusive rights. Broader claims offer stronger protection but are harder to patent due to prior art; narrower claims provide focused protection but risk easier circumvention.

2. How does Slovenian patent law influence drug patent claims?
It aligns with European standards, requiring clear, novel, inventive, and sufficiently disclosed claims, influencing claim drafting and enforcement strategies.

3. Are patent claims on chemical compositions forever protected?
No. Patent rights typically last 20 years from filing, though extensions or supplementary protections can extend market exclusivity.

4. How does the patent landscape affect innovation in pharmaceuticals?
A complex landscape with overlapping patents can both encourage innovation through protection and hinder market entry, emphasizing the importance of thorough freedom-to-operate analyses.

5. What strategies can companies employ to navigate overlapping patent rights?
Filing early, designing around existing patents, licensing, and pursuing patent term extensions are common approaches to mitigate patent challenges.


References

  1. Slovenian Intellectual Property Office (SIPO). Patent database and legal status records.
  2. European Patent Office (EPO). Guidelines on patentability and patent landscape analysis.
  3. World Intellectual Property Organization (WIPO). PCT and international patent strategies for pharmaceuticals.

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