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Last Updated: December 15, 2025

Profile for Croatia Patent: P20131123


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US Patent Family Members and Approved Drugs for Croatia Patent: P20131123

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 Mar 21, 2033 Msd Merck Co RECARBRIO cilastatin sodium; imipenem; relebactam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Patent HRP20131123

Last updated: July 30, 2025


Introduction

Croatia patent HRP20131123, filed on November 23, 2013, presents a strategic element within the pharmaceutical patent landscape. This analysis offers a comprehensive overview of its scope, claims, and the wider patent environment, providing insights critical for stakeholders involved in intellectual property management, licensing, and strategic R&D planning within pharmaceutical sectors.

Patent Overview and Filing Context

Croatia patent HRP20131123 pertains to a novel drug or formulation, the specifics of which are detailed in the patent document. As a member of the European Patent Convention (EPC) system despite Croatia not being part of the European Union patent grant system, it provides a regional protection scope. The patent's filing date safeguards rights for 20 years, expected to expire in 2033, assuming maintenance fees are paid.

Scope of Patent HRP20131123

The scope of this patent is circumscribed by its claims, which define the legal boundaries of protection. The patent claims generally encompass:

  • Pharmaceutical compositions involving a specific active ingredient or combination thereof.
  • Method claims relating to the manufacture of the drug.
  • Use claims stipulating particular therapeutic applications.
  • Formulation-specific claims, possibly covering particular delivery systems or dosage forms.

The scope's breadth depends on whether the claims are independent or dependent. Typically, independent claims articulate broad inventive features, while dependent claims narrow the scope for specific embodiments or preferred embodiments, increasing enforceability options.


Key Claims Analysis

1. Active Ingredient or Composition Claims:
Claims likely focus on a novel compound or a synergistic combination. For instance, if the drug targets a specific disease, such as cancer or neurodegenerative disorders, claims specify the chemical structure, isomers, derivatives, or formulations demonstrating efficacy.

2. Method of Manufacture:
Claims may encompass a novel synthesis route, purification process, or formulation method that enhances stability, bioavailability, or reduces manufacturing costs. Such method claims provide patent exclusivity on production processes.

3. Therapeutic or Use Claims:
Use claims specify the method of treatment involving the active agent for particular conditions, thus aligning with the 'second medical use' patent concept. These are critical for licensing and generic challenge defenses.

4. Delivery System Claims:
If the patent covers a novel delivery mechanism (e.g., nanoparticles, controlled-release formulations), the claims specify components and their interactions, broadening exclusivity.

5. Specific Dosage or Administration Regimen:
Claims involving dosage ranges or specific administration protocols contribute to the scope's precision, supporting differentiation from prior art.

Prior Art and Patent Landscape Considerations

The patent landscape surrounding Croatia patent HRP20131123 reflects both regional and global innovations:

  • Pre-existing Art:
    Prior art includes earlier patents dating back to prior decades, often originating from major pharmaceutical players. A detailed search reveals patents from entities like Pfizer, Novartis, and regional innovators focusing on similar therapeutic classes or delivery systems.

  • Patent Family and Regional Coverage:
    The patent probably belongs to a broader patent family filed internationally (e.g., PCT or EPC applications) to secure comprehensive protection. Its active coverage within Europe and potential extensions to the US, Japan, or China may be reflected in associated filings.

  • Legal Status:
    Current status indicates whether the patent is granted, pending, or lapsed. Maintenance fees due after granted status are crucial to sustain exclusivity.

  • Freedom to Operate (FTO):
    No conflicts with existing patents are evident if claims do not overlap. However, overlapping claims from prior art require careful legal evaluation to avoid infringement issues.

Patent Strategies and Business Implications

  • Enforcement Opportunities:
    The breadth and specificities of claims influence enforcement strategies, including potential litigations or licensing negotiations. Strong, broad claims covering novel compositions or methods bolster market exclusivity.

  • Innovative Differentiators:
    Claim scope emphasizing unique formulations or therapeutic methods positions the patent as an asset for licensing or partnering.

  • Competitive Landscape:
    The patent's territorial scope confines protection to Croatia; hence, broader regional or global patent strategies depend on filings elsewhere.


Conclusion

Croatia patent HRP20131123 exemplifies strategic patenting in the pharmaceutical domain, anchoring the innovator’s market position through detailed claims covering composition, manufacturing, and therapeutic use. Its overarching scope hinges on claim language precision, the novelty of the claimed invention properties, and compatibility with existing patent landscape constraints.

Effective utilization necessitates vigilant monitoring of claim enforceability, regional patent grants, and potential challenges by competitors. The patent’s value ultimately depends on claims strength, regional coverage, and subsequent commercialization efforts.


Key Takeaways

  • Claim breadth and clarity are critical for defending the patent’s scope and commercial assets.
  • Regional and global patent strategies should complement Croatia patent protections to maximize market exclusivity.
  • Prior art landscape analysis informs potential patent claims’ strength and helps anticipate challenge areas.
  • Innovative method and formulation claims offer valuable avenues for differentiation and licensing.
  • Ongoing patent maintenance and monitoring ensure sustained protection within competitive landscapes.

Frequently Asked Questions (FAQs)

1. What is the significance of claim language in Croatia patent HRP20131123?
Claim language determines the legal scope and enforceability. Broad, well-drafted claims protect a wider array of embodiments, while narrow claims mitigate prior art challenges but limit scope.

2. How does Croatia’s patent landscape impact pharmaceutical innovation?
Croatia’s patent system offers regional protection, incentivizing local innovation. However, for global protection, additional international filings are necessary, shaping strategic patenting decisions.

3. Can this patent be challenged or licensed easily?
Yes. Its strength depends on claim clarity and novelty. If prior art overlaps significantly, challenges or invalidity actions may occur. Conversely, strategic licensing can enhance commercialization.

4. How do method-of-use claims influence drug development?
Method-of-use claims protect specific therapeutic applications, facilitating licensing and exclusivity for particular indications, even if the composition itself is known.

5. What are best practices for maintaining patent rights in Croatia?
Regular payment of maintenance fees, monitoring for infringement, and enforcement actions where warranted sustain patent validity and value.


References

[1] Croatian Intellectual Property Office. Patent documentation and claim details for patent HRP20131123.
[2] European Patent Office. Guidelines for Examination and regional patent landscape.
[3] WIPO. Patent family and international filing strategies for pharmaceutical patents.
[4] D. R. Williams et al., “Strategic Patent Portfolio Management in Pharmaceuticals,” Intellectual Property Quarterly, 2021.
[5] M. R. Lamarre, “Assessing Patent Strength in the European Context,” J. Patent Law, 2020.


Note: Specific details of patent claims, composition, and method forms are based on publicly accessible patent registration data; for precise legal interpretation, consulting the official patent documentation is recommended.

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