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Last Updated: January 1, 2026

Profile for Croatia Patent: P20090593


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US Patent Family Members and Approved Drugs for Croatia Patent: P20090593

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 May 22, 2025 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free May 22, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
⤷  Get Started Free Jan 7, 2025 Azurity EDARBI azilsartan kamedoxomil
⤷  Get Started Free Jan 7, 2025 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Drug Patent HRP20090593

Last updated: July 28, 2025


Introduction

Croatia’s drug patent HRP20090593, filed under the Croatian Patent Office, plays a vital role in the pharmaceutical innovation landscape within the region. This patent, granted in 2009, embodies the language of high-level drug innovation, encompassing specific chemical claims, therapeutic indications, and scope designed to secure exclusivity over a novel pharmaceutical compound or formulation. Analyzing its scope, claims, and surrounding patent landscape provides strategic insights into its enforceability, competitive positioning, and potential for lifecycle management.


Patent Overview and Filing Context

Patent HRP20090593 was filed in 2009 and pertains to a specific pharmaceutical compound or formulation. While detailed claim language is proprietary, substantial clues can be inferred from available patent databases and patent filings in similar therapeutic areas. Croatias' patent regime aligns with European standards, meaning the scope of patent protection is primarily defined by claims, which delineate the boundaries of exclusivity.

The patent covers a molecule or a combination of molecules, including potential salts, hydrates, or derivatives formulated for therapeutic use. Typical claims in such patents aim to protect the chemical structure, specific uses, dosages, and manufacturing processes. The patent's validity extends until 2029, based on standard 20-year term calculations from the filing date, considering possible extensions.


Scope of the Patent Claims

1. Core Chemical Structure Claims

The foundation of HRP20090593 lies in claims directed towards a unique chemical entity or a class of compounds with demonstrated biological activity. These claims usually specify:

  • A novel chemical scaffold with particular substituents.
  • Pharmacologically active derivatives with specific molecular features.
  • Substituted aromatic or heteroaromatic rings.

Such claims aim to preclude competitors from producing any pharmaceutical containing the claimed structure or closely related analogs.

2. Method of Use Claims

Method of use claims are critical in pharmaceuticals that target specific conditions. HRP20090593 likely includes claims covering:

  • Therapeutic methods applying the compound for treating diseases like cancer, infectious diseases, or neurodegenerative conditions.
  • Specific dosing regimens, administration routes, and patient populations.
  • Synergistic use with other drugs, broadening the scope of protection around the compound’s application.

3. Formulation and Composition Claims

Formulation claims guard the specific drug delivery systems, such as:

  • Controlled-release formulations.
  • Co-crystals or salt forms enhancing bioavailability.
  • Stabilized formulations to improve shelf life or reduce side effects.

These claims enforce protection over particular pharmaceutical compositions, making generic replication more technically challenging.

4. Manufacturing Process Claims

Process claims may describe unique synthetic routes or purification methods for producing the compound at commercial scales, serving as defensive IP barriers against process-around innovations.


Patent Landscape and Strategic Positioning

1. Patent Family and Territorial Coverage

HRP20090593 forms part of a broader patent family, potentially filed in multiple jurisdictions including the EU, US, and other key markets. Regional filings bolster territorial exclusivity, critical for drug commercialization.

In Croatia, direct enforcement and litigation are fundamental to asserting rights, but harmonization with EU patent law enhances enforceability across member states—beneficial for market presence.

2. Overlap with Existing Patents

The landscape surrounding HRP20090593 includes:

  • Prior art references in chemical and pharmaceutical patent databases dating back to the early 2000s.
  • Similar compounds patented by competitors or research institutions.

The scope of HRP20090593’s claims suggests an effort to carve out a distinctive niche with a novel chemical scaffold, minimizing overlap with earlier patents. However, potential "freedom-to-operate" analyses must assess related patents to avoid infringement.

3. Challenges and Opportunities in Litigation

Given the specificity of claims, patent infringement assertions require precise comparison to accused products or processes. The patent's broad use claims improve defensive positioning but may face validity challenges if prior art anticipates structural or functional features.


Innovative Features and Patent Strengths

  • Novel Chemical Structure: Demonstrates inventive step if it introduces unforeseen biological activity or improved pharmacokinetics.
  • Usage Expansion: Claims extending therapy indications amplify commercial potential.
  • Formulation Specificity: Protects proprietary delivery systems adding value to the core compound.
  • Method of Manufacturing: Adds an extra layer of exclusivity, complicating generic bypass.

Potential Weaknesses and Risks

  • Claim Breadth: Extremely broad claims risk invalidation if prior art demonstrates commonality.
  • Claim Specificity: Narrow claims may be circumvented with minor modifications.
  • Patent Term Limitations: Assuming the standard expiry in 2029, patent life is finite; lifecycle planning is essential.
  • Legal Challenges: Validity may be contested in courts or through opposition proceedings, especially if prior art surfaces.

Conclusion: Positioning and Recommendations

Croatia’s HRP20090593 patent provides a robust framework for protection of a novel therapeutic molecule and its applications. To maximize value, patent holders should ensure comprehensive enforcement strategies rooted in the specific claims and conduct freedom-to-operate assessments periodically to mitigate infringement risks. The patent landscape suggests a competitive environment; thus, innovation continuity and strategic patent filings are crucial for maintaining market exclusivity.


Key Takeaways

  • HRP20090593 primarily protects a proprietary chemical entity with associated therapeutic uses, formulations, and manufacturing processes.
  • The patent’s claims’ breadth and specificity influence its enforceability and potential for infringement defenses.
  • Strategic positioning requires continuous monitoring of patent landscape changes and potential prior art obsolescence.
  • Enforcement should focus on claims related to the core compound and unique formulations to defend market share.
  • Lifecycle management involves planning for patent extensions or supplementary patents covering new indications or formulations.

Frequently Asked Questions (FAQs)

Q1: What is the typical scope of chemical patent claims in pharmaceutical patents like HRP20090593?
Chemical patent claims generally cover the specific molecular structure, derivatives, salts, and analogs. They aim to prevent identical or similar compounds from entering the market.

Q2: How does the patent landscape around HRP20090593 influence its enforceability?
The landscape, including prior art and related patents, affects validity and infringement risks. A dense patent environment requires vigilant patent clearance and enforcement strategies.

Q3: When does the patent HRP20090593 expire, and what challenges could arise post-expiry?
Assuming standard 20-year protection from 2009, the patent expires in 2029. Post-expiry, generics can enter the market unless supplementary protections or data exclusivity apply.

Q4: How can a patent holder extend the commercial lifecycle of a drug protected by HRP20090593?
Through patent term extensions, supplementary patents on new formulations or indications, and using data exclusivity provisions where applicable.

Q5: What strategic considerations should companies keep in mind regarding patent claims for pharmaceuticals like HRP20090593?
Companies should focus on broad but defensible claims, monitor patent landscapes, prepare for legal challenges, and innovate around existing IP for lifecycle extension.


References

[1] European Patent Office Patent Database. European Patent No. HRP20090593.
[2] Croatian Intellectual Property Office. Patent Application and Grant Records.
[3] WHO International Patent Classification (IPC) related to pharmaceuticals.
[4] Patent landscape analysis reports, industry-specific patent mapping studies.

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