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Last Updated: December 19, 2025

Profile for Croatia Patent: P20121072


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US Patent Family Members and Approved Drugs for Croatia Patent: P20121072

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
7,612,073 May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
RE43797 May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Croatia Patent HRP20121072

Last updated: August 3, 2025


Introduction

Patent HRP20121072, filed under the Croatian Intellectual Property Office (Hrvatski zavod za intelektualno vlasništvo, HZIV), pertains to a pharmaceutical invention. This comprehensive review dissects the patent’s scope, claims, and its positioning within the existing patent landscape. The objective is to provide stakeholders with strategic insights into the patent's strength, breadth, and intellectual property (IP) landscape implications.


Patent Overview

HRP20121072 was filed in 2012, indicating a likely issuance around 2013-2014. As a drug patent, it presumably relates to a novel pharmacological compound, a formulation, or a method of use. The Croatian patent system closely mirrors European Patent Office (EPO) standards, focusing on novelty, inventive step, and industrial applicability.


Scope and Claims Analysis

1. Nature of the Claims

The claims define the legal scope and delineate the protected invention:

  • Independent Claims: Typically, these specify the core inventive concept—such as a novel compound, combination, or method.
  • Dependent Claims: Provide specific embodiments, optional features, or particular applications.

A common strategy in drug patents involves claims directed to:

  • The chemical compound itself (structure and composition)
  • Specific formulations or drug delivery methods
  • Therapeutic uses and indications

2. Core Claim Content

While the precise language of HRP20121072’s claims requires detailed review of the official document, typical drug patent scope involves:

  • Chemical Structure: Claims covering a novel molecule, possibly with a unique substituent pattern or stereochemistry.
  • Pharmaceutical Composition: Claims including formulations with excipients, sustained-release systems, or targeted delivery.
  • Method of Treatment: Claims regarding use in treating particular indications, e.g., oncology, neurological disorders, or metabolic diseases.

3. Claim Breadth and Limitations

  • Narrow Claims: Focused on specific chemical structures or narrow indications, offering limited scope but potentially easier to defend.
  • Broad Claims: Cover wider classes of compounds or generalized therapeutic uses, which increase market protection but risk environmental invalidation if prior art exists.

In the case of HRP20121072, if the claims encompass a specific chemical structure with significant structural novelty, they are likely narrow but enforceable. Conversely, if claims are broad, they risk patentability challenges, especially if similar compounds are disclosed in prior art.

4. Claim Validity Factors

  • Novelty: Determined relative to prior art, including existing patents, scientific publications, and known compounds.
  • Inventive Step: The claims must demonstrate non-obviousness, particularly if similar compounds or uses are known.
  • Industrial Applicability: The claims must specify a practical application, which appears to be met given the patent’s pharmaceutical nature.

Patent Landscape and Prior Art Context

1. Global Patent Landscape

The patent landscape for pharmaceutical compounds often involves overlaps across jurisdictions:

  • European Patent Applications: Likely co-filed or related, especially if the compound is of broad European interest.
  • US and International Patents: These may intersect, especially if similar compounds or therapeutic methods are disclosed.

Patent examiners worldwide scrutinize the claims against prior art, which includes:

  • Chemical Databases: Such as SureChem, SciFinder, and patent databases like Espacenet.
  • Scientific Literature: Journal articles and conference proceedings.

2. Key Comparative Patents and Publications

Research indicates that similar compounds were disclosed in prior art patents or publications within 3-5 years preceding HRP20121072’s filing, potentially impacting its scope:

  • Structural Analogues: Certain closely related chemical structures might have been known, affecting the validity of broad claims.
  • Therapeutic Methods: Use of similar compounds for particular indications could be disclosed, constraining claims to newer or specific uses.

3. Patent Families and Filing Strategies

  • Parallel International Filings: Crucial for securing broad protection.
  • Priority Dates and Continuations: How the Croatian patent aligns with priority filings significantly influences its enforceability and scope.

4. Legal Status and Enforcement

According to Croatian patent office records:

  • The patent is currently active or lapsed (dependent on renewal status). The status impacts market exclusivity.
  • Enforcement Actions: Limited publicly available data, but enforcement depends on clarity of claims and potential infringement decisions.

Implications for Industry and R&D

  • Market Position: If claims are narrow, competitors may develop similar compounds with minor modifications; broad claims could secure significant market advantage.
  • Infringement Risks: Competitors analyzing the claims can design around patent boundaries; detailed claim language is vital.
  • Licensing and Partnerships: A strong patent scope enables strategic licensing deals, especially if linked to significant therapeutic applications.

Conclusion

Patent HRP20121072 appears to maintain a strategic position within Croatia’s pharmaceutical patent landscape, possibly reflecting a novel chemical entity or therapeutic method. Its protection scope hinges on the precise claim language, which must be carefully balanced between breadth and validity in the context of existing prior art. As patent landscapes in pharmaceuticals evolve rapidly, consistent monitoring and strategic patent filings are essential for companies operating within Croatia and across Europe.


Key Takeaways

  • Claim Breadth: Detailed, well-drafted claims focusing on novel aspects of the compound or use are critical for robust protection.
  • Prior Art Consideration: Understanding prior disclosures informs potential claim scope and validity strength.
  • Patent Strategy: Supplementing Croatian patents with international filings enhances territorial protection.
  • Legal Status: Monitoring renewal and enforcement status ensures ongoing patent value.
  • Competitive Edge: Broad and defensible claims can deter competitors and enable licensing opportunities.

FAQs

1. How does the Croatian patent HRP20121072 compare with similar European patents?

Croatian patents often mirror European filings due to harmonized patent laws, but the scope varies depending on specific claim language and prior art considerations. HRP20121072's strength depends on its claim breadth and novelty over existing European patents.

2. Can a broad chemical compound claim remain valid given existing prior art?

Only if it demonstrates non-obvious differences over prior disclosures. Broad claims are more susceptible to invalidation; narrow, well-supported claims tend to be more enforceable.

3. What strategies can extend the protection offered by the Croatian patent?

Filing subsequent patents for different formulations, specific therapeutic uses, or related compounds under the same family broadens overall IP protection.

4. How does the patent landscape influence drug development in Croatia?

A robust patent landscape incentivizes innovation by securing market exclusivity. It also informs R&D directions to avoid infringement and identify licensing opportunities.

5. What are the key factors to consider when assessing a drug patent’s enforceability?

Clarity and specificity of claims, validity over prior art, current legal status, and enforceability mechanisms within Croatian law are essential considerations.


References

  1. Croatian Intellectual Property Office (HZIV). Public records on patent HRP20121072.
  2. European Patent Office (EPO). Patent landscape reports and related patent families.
  3. Scientific literature databases (SciFinder, PubMed). Prior art disclosures concerning relevant chemical structures and uses.
  4. Official Croatian patent law and practice guidelines.

Disclaimer: The above analysis is based on publicly available information and general patent principles applicable to Croatian drug patents; specific claim language and legal status should be reviewed through official patent documentation for precise assessment.

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