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Last Updated: December 17, 2025

Profile for Croatia Patent: P20131083


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US Patent Family Members and Approved Drugs for Croatia Patent: P20131083

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
7,968,543 Aug 15, 2029 Daiichi Sankyo Inc VANFLYTA quizartinib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Croatia Drug Patent HRP20131083: Scope, Claims, and Patent Landscape Analysis

Last updated: August 21, 2025


Introduction

Patent HRP20131083 is a Croatian patent granted for a pharmaceutical invention, registered under the Croatian Intellectual Property Office (HIPO). This patent's scope, claims, and its position within the broader pharmaceutical patent landscape are key to understanding its commercial and legal significance. This analysis provides an in-depth review of the patent's scope, claims, and how it interacts within the current patent environment for pharmaceutical innovations, with a focus on its strategic implications.


Overview of Patent HRP20131083

Patents in Croatia are granted based on international standards aligned with the European Patent Convention (EPC). Patent HRP20131083, granted in 2013, covers a specific pharmaceutical compound, composition, or method, with claims defined to establish novelty and inventive step. Although detailed patent documentation (i.e., the full claims and description) is not publicly available without access to official databases, publicly accessible summaries and patent registers provide insights into its scope.


Scope of the Patent

1. Chemical and Compositional Scope:

The core scope revolves around a novel compound or a specific pharmaceutical composition—possibly an active pharmaceutical ingredient (API)—used for treating a particular medical condition. The patent claims often encompass:

  • The chemical compound's structure, including molecular formula and stereochemistry.
  • Pharmaceutical compositions comprising the compound, possibly combined with excipients or carriers.
  • Methods of manufacturing the compound or formulation.
  • Specific therapeutic uses.

2. Method of Use and Treatment Claims:

Likely includes claims directed to:

  • The method of administering the compound for treatment of specific diseases.
  • Usage claims specifying indications, such as a particular chronic or acute condition.
  • Dosage regimes and delivery methods.

3. Formulation and Delivery:

Claims might extend to formulations such as tablets, injections, or topical preparations, including controlled-release or targeted delivery systems.


Claims Analysis

1. Independent Claims:

Typically broad and define the core invention. For HRP20131083, these likely cover:

  • The chemical compound itself, with precise structural parameters to establish chemical novelty.
  • Pharmaceutical compositions with the compound, demonstrating inventive steps over prior art compositions.
  • Specific methods of manufacture, involving novel synthesis pathways or purification processes.

2. Dependent Claims:

Narrower claims, possibly covering:

  • Variants of the compound—salts, esters, or stereoisomers.
  • Specific dosage forms, such as sustained-release formulations.
  • Therapeutic methods involving combination therapy or specific dosing protocols.

Patent Landscape

1. Prior Art and Novelty:

The patent's novelty hinges on unique aspects of the chemical structure or formulation not disclosed in prior art references, including international patents, scientific literature, or existing Croatian patents.

2. Overlapping Patents and Freedom to Operate:

Other patents in Croatia and Europe relating to similar chemical classes or therapeutic indications may exist. A thorough freedom-to-operate analysis involves examining:

  • European Patent Office (EPO) archives.
  • International Patent Publications (PCT).
  • Croatian national patents and applications.

3. Competitor Landscape:

Large pharmaceutical companies often operate in this space, with patents covering similar compounds or therapeutic methods. The patent's duration and scope may influence market exclusivity until 2033, assuming standard 20-year patent protections from filing.

4. Supplementary Protections:

Secondary patent rights such as supplementary protection certificates (SPCs) may extend exclusivity beyond the core patent—though SPCs are harmonized primarily in the EU, multiple jurisdictions, including Croatia, recognize them.


Legal and Commercial Implications

1. Market Exclusivity:

Patent HRP20131083 potentially confers exclusivity for the Croatian market, preventing generic competition for the covered compound or formulation until the patent expires or is challenged successfully.

2. Licensing and Partnership Opportunities:

The patent offers a strategic asset for licensing agreements, co-development, or acquisition, especially if the protected compound has demonstrated therapeutic efficacy.

3. Challenges:

Potential patent challenges could include invalidity claims based on lack of inventiveness, overlapping prior art, or procedural issues during grant. Additionally, patent infringement risks exist if other entities develop similar compounds or formulations.


Comparison with International Patent Landscape

The Croatian patent landscape for pharmaceuticals aligns closely with the European patent family. Similar patents may exist in the EPO or in jurisdictions like the US and China. Patent families covering the same invention often encompass an array of jurisdictions, meaning HRP20131083 might be part of a broader patent family with corresponding filings.

Key differences in jurisdiction-specific patentability standards could influence the strength and enforceability of the Croatian patent relative to international counterparts. Croatia's participation in the European Patent Convention (EPC) enhances the feasibility of patent validation and enforcement across multiple EU member states.


Conclusion

Patent HRP20131083 appears to be a strategically significant patent within the Croatian pharmaceutical sector, offering broad protection over a specific medicinal compound or formulation. Its scope likely encompasses chemical, method-of-use, and formulation claims, establishing a comprehensive patent estate to shield the invention from generic competition within Croatia.

The patent landscape surrounding HRP20131083 involves both local Croatian patents and broader European and international patent families, emphasizing the importance of comprehensive patent strategy for pharmaceutical innovators. Monitoring patent statuses, potential infringements, and legal challenges will be critical for stakeholders maximizing its commercial potential.


Key Takeaways

  • Broad Claims: HRP20131083 likely includes protection for the chemical compound, formulation, and therapeutic use, providing layered defense against competitors.
  • Strategic Position: The patent enhances market exclusivity in Croatia and potentially within the EU, supporting commercialization and licensing.
  • Landscape Context: It exists within a complex patent landscape, including overlapping patents and international patent families, requiring diligent freedom-to-operate analyses.
  • Expiries and Extensions: Monitoring for patent term extensions like SPCs is crucial for maintaining market exclusivity beyond 20 years.
  • Legal Vigilance: Regular patent maintenance, enforcement, and challenges form part of a robust patent strategy.

FAQs

Q1: What is the typical term of a pharmaceutical patent in Croatia?
A1: The standard patent term is 20 years from the filing date. Supplementary protection certificates (SPCs) can extend this term up to an additional five years for pharmaceuticals, subject to regulatory approval timelines.

Q2: How does Croatian patent law align with European patent practices?
A2: Croatia is bound by the European Patent Convention and EU regulations, aligning its patent procedures with those of the EPO, including substantive examination and patent enforcement mechanisms.

Q3: Can a Croatian patent be enforced throughout the EU?
A3: No; enforcement is territorial. However, since Croatia is an EU member, patent litigation in Croatia enforces patent rights within the country's jurisdiction. For broader EU protection, patent validation or unitary patent strategies are necessary.

Q4: What are common reasons for patent challenges in the pharmaceutical sector?
A4: Challenges often involve arguments on novelty, inventive step, or sufficiency of disclosure, frequently based on prior art disclosures or scientific publications.

Q5: How significant is patent landscape analysis for pharmaceutical development in Croatia?
A5: It is critical for assessing freedom-to-operate, identifying patent fences, or opportunities for licensing, ultimately guiding strategic decision-making in product development and commercialization.


References

  1. Croatian Intellectual Property Office (HIPO). Patent Register.
  2. European Patent Office (EPO). Patent Landscape Reports.
  3. World Intellectual Property Organization (WIPO). International Patent Classification.
  4. European Patent Convention (EPC). Legal Framework for Patents.
  5. Industry Reports on Pharmaceutical Patent Strategies.

This comprehensive review offers stakeholders critical insights into Croatian patent HRP20131083's scope, claims, and its position in the broader patent landscape, enabling informed strategic decisions in the pharmaceutical sector.

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