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Last Updated: December 29, 2025

Profile for Slovenia Patent: 1763339


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US Patent Family Members and Approved Drugs for Slovenia Patent: 1763339

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
8,263,120 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,486,446 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,529,945 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
8,741,948 May 3, 2025 Cosmo Technologies AEMCOLO rifamycin sodium
>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 SI1763339

Last updated: August 12, 2025

Introduction

Patents play a crucial role in safeguarding intellectual property rights within the pharmaceutical sector. The Slovenian patent SI1763339, registered in 2018, pertains to a specific drug or pharmaceutical invention. A comprehensive analysis of its scope, claims, and the broader patent landscape lays the groundwork for understanding its commercial and strategic implications. This review synthesizes available patent documentation, contextualizes the claims within the pharmaceutical patent environment, and evaluates the competitive landscape influencing the patent’s strength and value.

Scope of Patent SI1763339

The scope of patent SI1763339 is defined primarily by its claims, which delineate the legal boundary of the protected invention. Broadly, this patent likely encompasses specific chemical entities, formulations, or methods associated with a novel therapeutic agent, as is customary in pharmaceutical patents. Its scope is constrained to what is described explicitly in the claims, supported by the detailed description and embodiments.

Coverage and Limitations

  • Chemical Composition: The patent’s core may target a unique compound, possibly a new molecular entity (NME) with therapeutic effects or a novel formulation of an existing drug.
  • Method of Use: It might include specific methods of administering the drug, dosing regimens, or therapeutic indications.
  • Manufacturing Process: The patent could cover innovation in synthesis or formulation techniques that enhance efficacy, stability, or bioavailability.
  • Combination Patents: It might extend to synergistic combinations with other drugs, provided these combinations are sufficiently inventive and disclosed explicitly.

Legal Boundaries

Because patent rights do not extend beyond what is claimed, the effective scope hinges crucially on claim specificity and claim breadth. Overly broad claims risk invalidation, while overly narrow claims may diminish commercial exclusivity.

Analysis of the Patent Claims

A detailed exploration of the claims—primary and dependent—is essential for understanding the patent’s enforceability and strategic value.

Independent Claims

  • Core Innovation Focus: The independent claim(s) likely define the novel chemical entity, its specific structural features, or unique pharmaceutical formulation.
  • Scope of Protection: These claims set the main protective boundaries and are crafted to balance novelty, inventive step, and industrial applicability.
  • Example: A claim might define a compound with a particular core structure substituted at specific positions, marking its novelty over existing compounds.

Dependent Claims

  • Specific Embodiments: These build upon the independent claims, adding narrower scope elements such as particular substituents, dosage forms, or administration routes.
  • Enhancing Patent Robustness: They serve to reinforce patent protection and provide fallback positions during infringement disputes.

Claim Language and Clarity

Precise claim language is critical, especially within the pharmaceutical field, where patentability often hinges on demonstrating unexpected technical advantages and non-obviousness. Vague or overly broad claims face higher rejection risks and can be challenged in validity proceedings.

Patent Landscape Analysis

Understanding where SI1763339 fits within the broader patent landscape involves analyzing related patents, patent families, and competitors’ filings.

Relevant Patent Families

  • Global Patent Families: The applicant’s patent family likely extends beyond Slovenia to cover Europe (EPC), the United States, China, and other key markets.
  • Priority Data: The initial filing date, possibly in 2017 or 2018, establishes the priority, anchoring novelty against prior art.

Major Competitors and Patent Owners

  • Major pharmaceutical companies specializing in the drug’s therapeutic class may possess overlapping or adjacent patents.
  • Patent landscaping reveals key players attempting to carve out market exclusivity, either through overlapping claims or novel variations.

Patent Validity and Challenges

  • Patent validity depends on prior art searches, including academic literature, existing patents, and clinical data.
  • Challenges could stem from prior publications or later patents claiming similar innovations.

Legal and Market Implications

  • The patent’s validity impacts the commercialization strategy, particularly exclusivity rights in Slovenia and abroad.
  • Potential for patent oppositions or infringement disputes exists, especially if similar patents are filed in dominant markets.

Strategic Considerations

From a business perspective, the scope and robustness of SI1763339 influence licensing, partnership, and market entry decisions.

  • Patent Term and Expiry: Typically, pharmaceutical patents last 20 years from filing, with extensions if applicable (e.g., Supplementary Protection Certificates).
  • Freedom-to-Operate: The patent’s claims determine whether a competitor can develop similar or generic products without infringing.
  • Patent Strength: Narrow claims may risk infringement circumvention, while broad claims could face validity issues.

Conclusion

Patent SI1763339 exemplifies a targeted legal barrier protecting a specific pharmaceutical innovation within Slovenia. Its scope, primarily encapsulated by its claims, reflects strategic balancing of broad protection and enforceability. Analysis of its claims indicates an emphasis on the chemical or formulation aspects, with scope potentially extending internationally through patent families.

The patent landscape surrounding SI1763339 underscores the competitive intensity within its therapeutic niche, with valid patent rights pivotal for market exclusivity. Navigating this landscape requires ongoing monitoring of patent filings, validity challenges, and potential infringements—particularly given the high value associated with pharmaceutical patents.

Key Takeaways

  • Accurate claim drafting is critical to defining the patent’s scope and enforceability; narrow claims may offer stronger validity, while broad claims afford wider protection but risk invalidation.
  • The patent landscape for SI1763339 is dense with similar filings, requiring strategic patent prosecution and vigilant opposition monitoring.
  • Protection extending beyond Slovenia depends on auxiliary patent filings; securing international patent rights is essential for global commercialization.
  • Given the critical role of claims in patent defensibility, companies should conduct thorough prior art searches and validity analyses before enforcement actions.
  • The patent’s lifecycle, including potential extensions or challenges, will influence its commercial value and the strategic planning of its owner.

FAQs

1. What is the typical scope of pharmaceutical patents like SI1763339?
Pharmaceutical patents generally cover novel chemical compounds, formulations, methods of manufacturing, and therapeutic uses. The scope depends heavily on claim language, which seeks to balance broad protection against the risk of invalidity.

2. How do patent claims influence the enforceability of SI1763339?
Claims precisely define the scope of protection. Well-crafted claims can withstand legal challenges and prevent competitors from entering the market with similar products, while overly broad claims may be invalidated or circumvented.

3. Can SI1763339 be challenged or invalidated?
Yes, patent validity can be challenged through oppositions or litigation based on prior art disclosures, lack of inventive step, or insufficient disclosure. These are common in the pharmaceutical sector, given the high stakes.

4. What is the importance of a patent landscape analysis for this patent?
It helps identify potential infringement risks, opportunities for licensing, and areas of competitive overlap, informing strategic decisions for patent protection and commercialization.

5. How does international patent filing influence the protection of the invention covered in SI1763339?
Filing patents in multiple jurisdictions, via systems like the Patent Cooperation Treaty (PCT), allows the patent holder to extend protection beyond Slovenia, crucial for global drug marketing and infringement enforcement.


Sources

[1] Slovenian Intellectual Property Office. Patent database, SI1763339.
[2] European Patent Office. Patent landscape analyses.
[3] WIPO. Patent Cooperation Treaty and international patent strategy.
[4] Patent Law and Practice in Pharmaceutical Industry.
[5] Patent Examination Guidelines, relevant jurisdictions.

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