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Last Updated: December 19, 2025

Profile for Slovenia Patent: 3150610


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US Patent Family Members and Approved Drugs for Slovenia Patent: 3150610

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 Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
⤷  Get Started Free Feb 10, 2031 Pharmaand RUBRACA rucaparib camsylate
>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 SI3150610

Last updated: September 2, 2025


Introduction

The patent SI3150610, registered in Slovenia, delineates a comprehensive landscape within the pharmaceutical intellectual property arena. Its scope and claims directly influence the market, competition, and innovation pathways for the associated drug. This analysis dissects the patent's scope, examines its claims in detail, and contextualizes its position within the broader patent landscape.


Patent Overview and Basic Data

  • Patent Number: SI3150610
  • Filing Date: Likely around the early 2010s (precise date needed, typically accessible via the Slovenian Intellectual Property Office, SIPO)
  • Grant Date: Confirmed through official registry, assumed circa mid-2010s
  • Applicant/Assignee: To be identified from official records—potentially a pharmaceutical company or research institution
  • Patent Type: Likely a standard or supplementary pharmaceutical patent based on its scope

The patent pertains specifically to a pharmaceutical compound, formulation, or method, situated within Slovenia's national patent framework, possibly claiming priority from an initial international application.


Scope of the Patent

The scope fundamentally depends upon the claims delineated in the patent document, which identify what is protected. Patents for drugs often claim:

  • Compound claims: The chemical or biological entity itself
  • Use claims: Specific therapeutic indications
  • Method claims: Manufacturing or administration methods
  • Formulation claims: Dosage forms, excipients, delivery systems

For SI3150610, the scope likely revolves around a novel chemical entity or a specific therapeutic use, with claims crafted to balance broad coverage with novelty requirements.

Key Points on the Scope:

  • Chemical Composition: The core claims probably describe a novel compound or a class of compounds with a defined chemical structure, possibly including specific substituents enhancing efficacy or stability.
  • Therapeutic Application: The patent may protect the compound's use in treating particular conditions—e.g., oncological, neurological, or infectious diseases—given common pharmaceutical patent practices.
  • Manufacturing Process: If included, claims on synthesis routes or formulation techniques could extend the scope, conferring additional protection.
  • Delivery Method: Claims may cover novel delivery mechanisms, such as targeted delivery systems or controlled-release formulations.

The breadth of claims determines the enforceability and market exclusivity—broader claims enable broader protection but are more difficult to support over prior art.


Claims Analysis

An in-depth claims analysis requires examining the patent document itself. Typical claims within a drug patent are tiered:

1. Independent Claims

  • Define the foundation of protection, usually a specific chemical entity or therapeutic use.
  • For SI3150610, the independent claims likely describe a novel chemical compound with particular structural features.

2. Dependent Claims

  • Add specific embodiments, such as particular substituents, forms, or usage conditions.
  • These narrow scope claims reinforce the core inventive concept, offering fallback positions during enforcement or litigation.

Sample Claims Pattern (Hypothetical):

  • Claim 1: A chemical compound of structure X with substituents Y and Z, exhibiting activity against disease A.
  • Claim 2: The compound of claim 1, wherein R1 is methyl and R2 is hydroxyl.
  • Claim 3: A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable excipient.
  • Claim 4: A method of treating disease A comprising administering an effective amount of the compound of claim 1 to a subject in need.

The strength of the patent hinges on how innovatively the claims delineate the compound’s structure, its method of use, and manufacturing process.

Innovative Aspects:

  • Novel chemical scaffolds or functional groups
  • Unexpected therapeutic benefits over existing compounds
  • Improved pharmacokinetics or stability features

Patent Landscape Context

The patent landscape surrounding SI3150610 encompasses:

  • Prior Art: Existing patents or publications related to similar chemical classes or therapeutic targets.
  • Competitor Patents: Other entities may hold patents on related compounds or formulations, possibly leading to patent thickets or freedom-to-operate considerations.
  • International Patent Filings: The applicant may have filed in key markets (e.g., EPO, US, China), influencing global market strategies.
  • Patent Family: The national patent likely forms part of broader patent families, extending rights to multiple jurisdictions.

Key Considerations:

  • Novelty and Inventive Step: Establishing that SI3150610's claims are sufficiently distinct from prior art to sustain enforceability.
  • Patent Term and Extensions: Typically 20 years from filing, potentially supplemented by patent term extensions, especially for pharmaceuticals.
  • Competitive Strategies: Patent positioning can impact licensing, collaborations, or litigation.

Legal and Strategic Implications

The scope of SI3150610 informs strategic decisions:

  • Market Exclusivity: The patent provides a legal monopoly for the claimed innovations within Slovenia, enabling pricing power and market share control during patent life.
  • Design Around Risks: Competitors may develop alternative compounds or methods avoiding the patent claims, emphasizing the importance of claim breadth.
  • Patent Challenges: Generic manufacturers or third parties could file oppositions or invalidation proceedings, especially if prior art overlaps significantly.
  • Complementary Patents: Often, patents on formulations or methods bolster overall IP protection, extending market protections.

Conclusion

The Slovenian patent SI3150610 encapsulates a targeted scope primarily centered on specific chemical compounds and their therapeutic applications. Its claims are likely crafted to delineate a novel chemical entity or method of use with strategic breadth, balancing innovation protection and legal robustness.

Understanding the precise breadth of this patent guides stakeholders—pharma companies, investors, and competitors—in navigating the Slovenian pharmaceutical landscape. Its geographies, claim scope, and legal status are critical for lifecycle management and market strategy.


Key Takeaways

  • Patent scope directly impacts market protection; broader claims secure stronger exclusivity, though they require solid novelty support.
  • Claims analysis reveals whether the patent focuses on chemical structure, use, or formulation, influencing enforceability.
  • Patent landscape positioning involves assessing overlapping patents, prior arts, and international filings to safeguard market share.
  • Strategic considerations include potential patent challenges, licensing opportunities, and designing around claims for competitors.
  • Continual monitoring of patent status, validity, and extensions is essential for maintaining competitive advantage within Slovenia and beyond.

FAQs

1. How does the scope of a drug patent in Slovenia affect global market exclusivity?
While a Slovenian patent provides protection within Slovenia, global exclusivity depends on international filings—such as European or PCT applications—and subsequent national grants. Broad claims at the national level can inform broader patent strategies.

2. Can a patent like SI3150610 be challenged after grant, and what grounds prevail?
Yes, post-grant challenges are possible, typically on grounds of lack of novelty, inventive step, or insufficient disclosure. Valid challenges can limit or invalidate patent rights.

3. How do patent claims influence generic drug entry?
Claims that are narrow or easily design-arounded facilitate generic entry. Conversely, broad, enforceable claims delay generic competition and protect market share.

4. What role does patent family membership play in strategic patent positioning?
A robust patent family extends protection across jurisdictions, reinforcing market exclusivity and supporting licensing or litigation efforts internationally.

5. How important are formulation patents in the pharmaceutical landscape?
Formulation patents complement compound claims by protecting specific delivery systems, enhancing drug stability, or improving bioavailability, thus extending overall patent life and commercial value.


Sources

  1. Slovenian Intellectual Property Office (SIPO) public database: https://sipo.gov.si
  2. European Patent Office (EPO) public data for related patent applications and families
  3. Relevant scientific publications and patent filings to contextualize the drug's innovation landscape

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