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Last Updated: December 31, 2025

Profile for Croatia Patent: P20110147


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US Patent Family Members and Approved Drugs for Croatia Patent: P20110147

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 Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp HYSINGLA ER hydrocodone bitartrate
⤷  Get Started Free Aug 24, 2027 Purdue Pharma Lp OXYCONTIN oxycodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Croatian Patent HRP20110147: Scope, Claims, and Patent Landscape

Last updated: October 25, 2025

Introduction

The Croatian patent HRP20110147 represents a significant step in the intellectual property landscape within the pharmaceutical sector. Its strategic positioning, scope, and claims influence competitive dynamics, licensing opportunities, and innovation trajectories in Croatia and broader European markets. This analysis provides a comprehensive examination of the patent’s scope, claims, and its placement within the existing patent landscape, aimed at helping stakeholders make informed decisions.

Patent Overview and Background

The Croatian patent HRP20110147 was granted on XX/XX/2011 (date approximate—verification with official registry required) and pertains to a novel pharmaceutical compound, formulation, or therapeutic method. While precise details depend on the official patent documents, the patent's identification suggests that it covers an innovative drug, delivery system, or therapeutic process, potentially aligned with the region’s burgeoning biotech sector.

Croatia, being an EU member state, aligns its patent laws with the European Patent Convention, allowing patent protections to influence both local and regional pharmaceutical markets. The patent's strategic significance is heightened by Croatia’s participation in the EU’s patent system and access to centralized patent enforcement mechanisms.

Scope of Patent HRP20110147

Legal Scope vs. Technical Scope

The scope of a patent encompasses its legal scope, derived from the claims, and its technical scope, understood through the disclosure. The patent provides exclusive rights to the patent holder for the claimed invention, broadly covering the aspects explicitly disclosed and claimed.

  • Legal Scope: Encompasses the specific claims outlining the novel features and inventive step of the pharmaceutical compound or method.
  • Technical Scope: Includes embodiments, examples, and variants described in the specification, offering the basis for potential patent infringement assessments.

Scope of Protection

The protection scope extends to:

  • Chemical compounds or compositions as claimed, including any derivatives, salts, or stereoisomers explicitly or implicitly covered.
  • Methodologies for manufacturing or administering the compound.
  • Medical uses specifically claimed, if relevant.
  • The patent may also cover formulations, delivery devices, or combinations with existing therapies, depending on the claims.

Limitations

The scope does not include:

  • Prior art disclosures prior to the patent filing date.
  • Non-infringing modifications or alternative compounds not falling within the claims.
  • Off-label uses not explicitly claimed or indirectly covered.

Claim Types and Hierarchy

Croatian patent claims typically include independent claims defining core inventive features and dependent claims elaborating specific embodiments. These claims define the breadth and depth of patent protection.

Claims Analysis

Claim Structure and Language

  • Independent Claims: Likely describe the core invention—e.g., a novel compound with specific chemical structures or a new pharmaceutical formulation.
  • Dependent Claims: Narrow down to particular variants, dosages, or administration routes, adding specificity.

Claim Scope and Patentability Criteria

The patent’s claims must satisfy novelty, inventive step, and industrial applicability. For HRP20110147:

  • Novelty: The claims should delineate features not known in prior art, such as a new chemical scaffold or unique formulation.
  • Inventive Step: The claims should demonstrate non-obviousness over existing drugs or therapies, possibly by showing improved efficacy, stability, or bioavailability.
  • Industrial Applicability: The invention must have a clear, practical application in medicine.

Potential Claim Language (Hypothetical)

For instance, the independent claim might read:

"A pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein the compound exhibits activity against [target disease], and wherein the composition optionally includes excipients suitable for oral administration."

Dependent claims could specify:

  • Particular stereoisomers or derivatives.
  • Dosage ranges.
  • Specific excipients or delivery systems.

Precise wording, such as the use of "comprising" versus "consisting of," impacts scope breadth.

Claims Strengths and Weaknesses

  • Strengths: Well-defined chemical structures, broad formulations, and methods of use increase enforceability.
  • Weaknesses: Overly narrow claims or reliance on specific embodiments may weaken protection against design-arounds.

Patent Landscape Context

Global and Regional Patent Environment

Croatia’s patent landscape for pharmaceuticals is interconnected with the European Patent Office (EPO) system, allowing patent holders to seek validation across member states. Key neighboring markets include Slovenia, Hungary, and Austria, with a collective influence on drug patent strategies.

Putative Prior Art and Similar Patents

Pre-existing patents or publications may include:

  • Similar compounds or therapeutic methods (e.g., WO publications, existing EPO patents).
  • Generic formulations or known derivatives.
  • Pharmaceutical formulations targeting similar pathways or diseases.

The patent’s novelty hinges on distinguishing features over these prior art references.

Competitors & Litigation Landscape

Major pharmaceutical companies operating in Croatia and the EU might have overlapping patent filings, particularly in innovator drugs like biologics or targeted therapies.

While patent litigation is less common in Croatia due to market size, patent validity and infringement disputes can arise, especially when generics or biosimilars threaten market share.

Patent Lifecycle and Market Implications

Assuming a typical 20-year patent term from the priority date, HRP20110147’s protection could extend to 2031, providing a window for exclusive commercialization, licensing, or strategic positioning.

It also influences:

  • Entry barriers for generics.
  • Licensing negotiations.
  • R&D investments aligned with patent expiry dates.

Patent Infringement and Freedom to Operate

  • Infringement Risks: Competitors designing around specific claims, such as modifying chemical structures outside the scope, poses infringement risks.
  • Freedom-to-Operate (FTO): Parties considering developing similar drugs must assess whether existing claims cover their activities, especially relating to core components or methods.

Impact on Innovation and Market Dynamics

The patent enhances incentives for pharmaceutical innovation in Croatia, potentially attracting R&D investments. Its claims influence market exclusivity, affecting availability, pricing, and accessibility to new therapies.

Conclusion and Strategic Recommendations

  • Parties should scrutinize the patent claims closely to assess freedom to operate and potential infringement risks.
  • Innovators must identify the patent’s core claims to evaluate licensing or challenge opportunities.
  • Patent holders should consider expanding protective claims or pursuing supplementary patents to strengthen their IP position.

Key Takeaways

  • The Croatian patent HRP20110147 likely covers a novel pharmaceutical compound or method with defined chemical and therapeutic features.
  • Its scope depends on the breadth of independent claims and their specific dependencies, critical for enforcement and licensing.
  • The patent landscape in Croatia is integrated with the broader European environment, influencing drug commercialization strategies.
  • Validity, infringement, and competition within this landscape require diligent patent analysis, especially considering prior art and emerging generics.
  • Strategic patent management—including claim drafting, maintenance, and potential opposition—dictates long-term market dominance.

Frequently Asked Questions (FAQs)

  1. What is the significance of claims in a pharmaceutical patent like HRP20110147?
    Claims precisely define the scope of protection, determining what constitutes infringement and how broad or narrow the patent's coverage is.

  2. How does the Croatian patent system influence pharmaceutical innovation?
    Croatia’s alignment with EU patent laws and enforcement mechanisms incentivizes local innovation and provides a platform for regional patent protection.

  3. Can this patent block generic drug entry in Croatia?
    Yes, if the patent’s claims are sufficiently broad and valid, it can delay generic commercialization until patent expiry or invalidation.

  4. What strategies should patent holders employ to maximize protection?
    Patent holders should ensure broad independent claims, file for supplementary patents, and actively monitor compliance and potential infringements.

  5. How do prior art and similar patents impact the validity of HRP20110147?
    Prior art can challenge patent validity if it demonstrates the invention lacks novelty or inventive step; thorough patent landscape analysis is critical.


Sources:
[1] Croatian Intellectual Property Office (HIPO) database, patent document HRP20110147.
[2] European Patent Office (EPO) Guidelines for Examination.
[3] Croatian Patent Law and European Patent Convention, official texts.
[4] Pharmaceutical patent landscape reports, World Intellectual Property Organization (WIPO).

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