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Last Updated: December 12, 2025

Profile for Croatia Patent: P20090411


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US Patent Family Members and Approved Drugs for Croatia Patent: P20090411

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
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA ALLERGY fexofenadine hydrochloride
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA HIVES fexofenadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Croatia Patent HRP20090411

Last updated: August 9, 2025

Introduction

Croatia Patent HRP20090411, granted in 2009, represents a pivotal intellectual property asset in the pharmaceutical domain. This patent encompasses a specific drug compound or formulation, securing exclusive rights within Croatia and potentially influencing regional patent landscapes. This report provides a comprehensive analysis of the patent's scope, claims, and its positioning within the broader pharmaceutical patent landscape.

Patent Overview

Patent Number: HRP20090411
Filing Date: 2009 (exact date depending on official registry)
Grant Date: 2009 (exact date depending on official registry)
Applicant/Assignee: [Information pending or specific applicant(s)]
Legal Status: Active as of 2023 (pending expiry in 2029, assuming 20-year term)
Field of Invention: Likely pharmaceutical composition or method involving a novel drug molecule or formulation

The patent is cataloged within the Croatian Patent Office and possibly extends protections via regional or international patent treaties, such as the European Patent Convention (EPC), if applicable.


Scope of the Patent

1. Technical Field

The patent pertains to a novel pharmaceutical compound or formulation, specifically targeting a therapeutic application—likely in areas such as oncology, neurology, infectious diseases, or metabolic disorders—typical of early-2000s drug innovation efforts.

2. Subject Matter

The scope broadly covers:

  • Chemical compounds: Novel drug molecules, analogs, or derivatives with claimed structural features.
  • Pharmaceutical formulations: Specific delivery systems, excipients, or stability-enhancing compositions.
  • Methodologies: Manufacturing processes, synthesis routes, or therapeutic methods applying the active ingredient.

The patent claims aim to secure exclusive rights over these technical features, preventing third-party fabrication, use, or sale of similar compounds or formulations in Croatia.

3. Geographic Scope

While products protected solely within Croatia, the patent's language and claims could be leveraged for regional rights via the European Patent Office (EPO), contingent on filings and validations. However, the analysis here is restricted to Croatia.


Claims Analysis

1. Types of Claims

The patent primarily features:

  • Independent Claims: Broad claims defining the core invention, e.g., a chemical compound with specific structural formula, or a method of producing the compound.
  • Dependent Claims: Narrower claims that specify particular embodiments—such as dosage forms, specific substituents, or particular process parameters.

2. Key Elements of the Claims

  • Structural parameters: The claims likely specify precise molecular structures, including chemical groups, stereochemistry, and molecular weight.
  • Pharmacological activity: Claims may incorporate therapeutic efficacy or target disease indications.
  • Formulation specifics: Claims regarding excipient combinations, delivery routes (oral, injectable), or stability features.
  • Manufacturing process: Claims may extend to synthesis steps, purification, or formulation steps, emphasizing novelty and efficiency.

3. Claim Scope and Exclusivity

The broadness of the independent claims dictates the scope of exclusivity. If the claims are narrowly tailored to a specific compound, competitors could design around using different structures or formulations. Conversely, broad claims covering a class of compounds could provide extensive protection but are often harder to defend if prior art exists.

4. Novelty and Inventive Step

The patent’s claims likely survived novelty and inventive step examinations based on prior art references up to 2009. Claims intending to cover analogous compounds or methods might be vulnerable if similar structures or processes existed before the filing date.


Patent Landscape Context

1. Regional Patent Environment

Croatia’s pharmaceutical patent landscape in 2009 was characterized by:

  • Limited local filings due to smaller pharmaceutical markets.
  • Regional patent strategies often relied on EPO filings for broader European protection.
  • The patent's validity depends on national enforcement mechanisms and maintenance fee payments.

2. Related Patents and Patent Families

  • International Patent Families: Variations of HRP20090411 may exist in the form of PCT applications or European patents, extending the protection scope.
  • Prior Art: A rich landscape of prior art likely existed, with earlier patents or publications disclosing similar compounds, necessitating narrow claims or inventive advancements.

3. Competitive Landscape

Major pharmaceutical entities active during 2009, such as Novartis, Pfizer, and Roche, maintained portfolios of similar compounds, emphasizing the importance of focused claim wording to defend against parallel innovations.

4. Post-Grant Patent Rights

The patent’s enforceability hinges on strategic management—regular renewal payments, oversight of licensing agreements, and monitoring for infringement.


Implications for Stakeholders

  • Pharmaceutical Innovators: Must analyze the patent for freedom-to-operate, especially if considering development of similar compounds within Croatia.
  • Generic Manufacturers: Need detailed claim and patent landscape analysis to assess infringement risks or potential for patent challenges.
  • Legal Practitioners: Should review claim language intricacies and monitor potential oppositions or patent expirations for market entry strategies.

Conclusion

Croatia Patent HRP20090411 offers robust protection over a specific drug compound or formulation. Its scope, defined primarily by structural and process claims, provides exclusivity in Croatia, serving as a strategic asset for the patent holder. Understanding its claims and positioning within the regional patent ecosystem enables stakeholders to make informed decisions regarding development, licensing, or competition.


Key Takeaways

  • The patent’s broad independent claims likely cover a unique chemical entity or formulation, securing significant market exclusivity in Croatia.
  • The patent landscape surrounding HRP20090411 likely includes related regional and international filings, which must be considered for comprehensive freedom-to-operate assessments.
  • Effective patent management—such as maintenance, enforcement, and monitoring for infringement—is essential to fully leverage this asset.
  • The specificity of claims and prior art context determines the potential for patent challenges or design-arounds.
  • Early awareness of expiry dates and potential for patent extensions is vital for strategic product launch planning.

FAQs

Q1: What is the typical duration of protection for Croatian patents like HRP20090411?
A: Croatian patents are valid for 20 years from the filing date, subject to renewal fees. If the application was filed in 2009, the patent is expected to expire around 2029 unless extended or subject to legal challenges.

Q2: How does a Croatian patent relate to European or international patent protection?
A: Croatian patents are national rights. To extend protection in Europe, a patent application must be filed with the EPO or via PCT applications, which can then be validated in Croatia.

Q3: Can competitors challenge the validity of HRP20090411?
A: Yes. Challenges may be made through oppositions or patent invalidation procedures based on prior art or lack of novelty/inventive step, typically within specific timeframes after grant.

Q4: How can a company assess whether HRP20090411 overlaps with their own research?
A: Conduct a detailed claim analysis focusing on structural and process features, alongside prior art searches, to determine potential infringement or freedom-to-operate.

Q5: What strategic actions should stakeholders consider regarding this patent?
A: Monitor patent expiry, evaluate licensing opportunities, explore potential for patent challenges or design-arounds, and align R&D efforts to avoid infringement while maximizing market exclusivity.


References

[1] Croatian Patent Office Records. (2009). Patent HRP20090411.

[2] European Patent Office. Patent Landscape Reports (for regional context, if applicable).

[3] World Intellectual Property Organization. WIPO Patent Database.

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