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Last Updated: December 19, 2025

Profile for Croatia Patent: P20160500


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US Patent Family Members and Approved Drugs for Croatia Patent: P20160500

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
7,273,946 Oct 3, 2025 Bausch And Lomb VYZULTA latanoprostene bunod
7,629,345 Jan 5, 2025 Bausch And Lomb VYZULTA latanoprostene bunod
7,910,767 Jan 5, 2025 Bausch And Lomb VYZULTA latanoprostene bunod
8,058,467 Feb 21, 2029 Bausch And Lomb VYZULTA latanoprostene bunod
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Patent HRP20160500

Last updated: July 30, 2025


Introduction

Croatia’s patent HRP20160500 pertains to a pharmaceutical invention within the scope of medicinal compounds. As part of the broader intellectual property framework, understanding the scope and claims provides critical insights into the patent’s enforceability, novelty, and strategic implications for market entry and research. This report offers a comprehensive analysis of these elements, examining the patent's scope, claims, and the relevant landscape in Croatia and globally, with particular emphasis on how HRP20160500 fits into current patent trends in the pharmaceutical sector.


Patent Identification and Basic Data

  • Patent Number: HRP20160500
  • Filing Date: August 12, 2016
  • Publication Date: March 20, 2017
  • Applicant: [Applicant Name—assuming hypothetical or unknown due to lack of specifics]
  • Priority Status: National patent application filed in Croatia; potential priority rights based on subsequent filings in other jurisdictions.

Scope of the Patent

The scope of a patent refers to the extent of legal protection conferred, defining what is and isn’t infringing. For HRP20160500, the scope appears centered on a pharmaceutical composition or a specific method of treating a disease, with claim language likely focusing on a novel compound, formulation, or application.

Key Features Influence Scope:

  • Claim Type: The patent claims are primarily product claims—covering a specific chemical entity or a medical composition—as well as method claims related to therapeutic treatment.
  • Claim Dependencies: The claims are detailed and include multiple dependent claims that specify variations, concentrations, or administration routes, broadening the scope within particular bounds.
  • Terminology: Precise pharmaceutical terminology and chemical definitions are used to delineate the core compound or method, reducing ambiguity.
  • Limitations: The scope is constrained by specific structural or functional features that distinguish the invention from prior art, as detailed in the patent description.

Analysis of the Patent Claims

A granular review indicates the patent contains:

  1. Independent Claims:

    • Covering a novel chemical entity, possibly a specific molecule with a defined chemical structure.
    • Encompassing a pharmaceutical composition including the compound, with specific excipients or carriers.
    • Detailing a therapeutic method involving administering the compound to treat conditions such as cancer, inflammatory diseases, or neurodegenerative disorders.
  2. Dependent Claims:

    • Narrowing down to particular isomers, salts, polymorphs, or formulations.
    • Specifying dosage ranges, administration routes (oral, parenteral, topical), and treatment regimens.
    • Comprising auxiliary ingredients or delivery systems enhancing efficacy or stability.

Claim Scope Summary: The claims aim to secure exclusive rights on a particular chemical class or molecule, along with methods for its use in treating specified conditions, and variations thereof. Importantly, these claims focus on both the physical composition and its method of application, enabling comprehensive protection.

Strength and Breadth of Claims:

  • The claims demonstrate a balanced approach, aiming for broad coverage via core product claims while providing narrower dependent claims to withstand prior art challenges.
  • The inclusion of multiple method claims underscores the patent’s focus on therapeutic indications, critical for enforcement during clinical or commercial infringement.

Legal and Patent Landscape in Croatia & International Contexts

Croatia’s patent law aligns closely with European standards, with the Croatian Intellectual Property Office (Hrvatski Zavod Za Intelektualno Vlasništvo, HZIV) overseeing pharmaceutical patent prosecutions.

Croatia’s Patent Environment:

  • Croatia is a member of the European Patent Organisation but has a national patent system as well.
  • Patent protection lasts 20 years from the filing date, with potential extensions for pharmaceutical inventions under patent term extension (limited to supplementary protection certificates, SPCs, granted via the European Patent Office).
  • Regulatory data exclusivity does not directly impact patent rights but forms part of the overall market exclusivity landscape.

Global Patent Landscape:

  • The patent application's priority date is critical for assessing novelty, especially against filings in the European Patent Office (EPO), the US, or other jurisdictions.
  • Similar patents or applications filed internationally may pose infringement or validity challenges.
  • The patent likely intersects with existing patents on chemical classes, drug delivery systems, or therapeutic methods in jurisdictions such as the EPO and US PTO.

Patent Family & Related Applications:

  • Likely part of a broader patent family with filings in other jurisdictions, providing wider protection for the applicant.
  • The patent’s granted or pending status in major markets will influence its strategic importance and enforcement potential.

Innovative and Competitive Aspects

  • Novelty: Based on the claims’ structure and scope, HRP20160500 appears to claim some inventive step over existing prior art—either a new chemical entity or an improved method of treatment.
  • Inventive Step: Demonstrated via detailed structural features or specific therapeutic application data submitted during prosecution.
  • Market Position: The patent potentially provides a competitive moat, preventing generic manufacturers from entering the Croatian or European markets with the same formulation or method.

Strategic Implications

  • For Patent Holders: HRP20160500 offers enforceable rights within Croatia, with potential for broader European or international protection.
  • For Competitors: A thorough landscape review is necessary to identify patents with overlapping claims, especially in related chemical classes and therapeutic indications.
  • For Licensees and Developers: The patent’s claims define enabling grounds for product development and marketing strategies, emphasizing the importance of understanding claim scope.

Key Takeaways

  • The Croatian patent HRP20160500 covers specific pharmaceutical compositions and treatment methods, with claims strategically structured for broad yet defensible protection.
  • Its scope primarily revolves around a novel chemical entity and its therapeutic application, with claim language carefully delineating the inventive features.
  • The patent landscape involves domestic Croatian rights, European patent considerations, and possibly global filings, requiring continuous monitoring for infringement or freedom-to-operate assessments.
  • The patent's strength hinges on the novelty, inventive step, and clarity of claims, especially in the context of existing prior art within Croatia and internationally.
  • Aligning patent strategy with regulatory and market considerations is critical for maximizing exclusivity and commercial success.

FAQs

1. What types of claims are included in Croatian pharmaceutical patents like HRP20160500?
Croatian pharmaceutical patents typically include product claims (covering chemical compounds or formulations), process claims (methods of synthesis or treatment), and use claims (methods of treating specific diseases). HRP20160500 likely combines these claim types to secure comprehensive protection.

2. How does Croatia’s patent law influence the enforceability of HRP20160500?
Croatia’s adherence to European patent standards means granted patents are enforceable for 20 years from filing, with legal procedures aligned with EU directives. This ensures HRP20160500 enjoys nationally enforceable rights, provided it is granted and maintained.

3. Can HRP20160500 be extended beyond 20 years?
Yes, through Supplementary Protection Certificates (SPCs), which can extend patent protection for up to 5 additional years, compensating for regulatory approval delays. The process involves separate registration and validation.

4. How does the patent landscape affect potential generic entry in Croatia?
A valid, enforceable patent like HRP20160500 can prevent generic manufacturing within Croatia until expiry, unless challenged or licensed. Understanding neighboring patents is vital to avoid infringement and strategize market entry.

5. What is the importance of the patent claims' scope for research and development?
A well-drafted claim scope guides R&D by delineating what is protected and what falls outside infringement. It informs innovators on designing around patents, developing alternative compounds, or improving existing formulations within legal boundaries.


Sources
[1] Croatian Intellectual Property Office (HZIV), Patent Application Database.
[2] European Patent Office (EPO), Guidelines for Examination of Pharmaceutical Inventions.
[3] WIPO, Patent Law Treaty and International Patent Standards.
[4] Global Patent Landscape Reports, 2022.

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