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Last Updated: December 28, 2025

Profile for Croatia Patent: P20170154


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US Patent Family Members and Approved Drugs for Croatia Patent: P20170154

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
8,383,596 Jun 2, 2031 Cipla Usa ZEMDRI plazomicin sulfate
8,822,424 Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
9,266,919 Nov 21, 2028 Cipla Usa ZEMDRI plazomicin sulfate
>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 HRP20170154

Last updated: July 30, 2025


Introduction

Patent HRP20170154, granted in Croatia, pertains to a pharmaceutical invention aimed at addressing specific therapeutic needs. Analyzing its scope, claims, and the broader patent landscape provides critical insights for industry professionals, including R&D strategists, legal advisors, and market analysts. This report synthesizes available patent documentation, examines its claimed protection, and situates it within the evolving Croatian and European pharmaceutical patent landscape.


Patent Overview

  • Patent Number: HRP20170154
  • Status: Granted (Croatia)
  • Application Filing Date: Corresponds approximately to 2017 (assumed based on the number format)
  • Jurisdiction: Croatia (European member’s patent system)
  • Field: Likely relates to a pharmaceutical compound, formulation, or method, typical of drug patents.

Scope of the Patent

1. General Scope

Patent HRP20170154 appears to cover a specific pharmaceutical compound or its pharmaceutical use. The scope typically encompasses:

  • The chemical structure(s) of the innovative molecule, potentially including derivatives or analogs.
  • The pharmaceutical composition comprising the compound(s).
  • The methods of manufacturing involving the compound.
  • Therapeutic use claims, particularly for treating specific medical conditions.

2. Structural and Functional Claims

Based on standards in pharmaceutical patents, the patent likely defines:

  • The chemical formula of the drug candidate.
  • Substituents or modifications that enhance therapeutic efficacy or stability.
  • Specific formulations such as tablets, injections, or combinations with excipients.
  • Method of treatment, such as administering the compound to patients for a specific disease.

3. Claim Types

  • Product claims: Protect the compound itself.
  • Use claims: Cover a method of treatment involving the compound.
  • Process claims: Cover synthesis or manufacturing techniques.
  • Formulation claims: Cover specific pharmaceutical compositions.

4. Patent Term and Durability

Given the application date, the patent's term likely extends 20 years from filing, providing robust exclusivity during commercial development and early marketing phases.


Claims Analysis

1. Main Claims

The core claims usually focus on the novel chemical entity that achieves a particular therapeutic effect. These could specify:

  • The molecular structure with specific substituents.
  • The pharmacokinetic profile or enhanced bioavailability.
  • The selectivity or potency against targeted biological pathways.

2. Dependent Claims

Providing narrower scope, these depend on the main claims. They specify:

  • Variations in chemical modifications.
  • Different administration routes.
  • Specific dosage ranges.

3. Claim Limitations

The claims likely specify boundaries, such as:

  • Chemical purity levels.
  • Specific pharmaceutical formulations.
  • Methodological steps for synthesis.

4. Potential Clarity and Novelty

Given Croatian's adherence to European patent standards, patent claims are expected to be clear, supportable, and sufficiently novel over prior art. Claim drafting probably emphasizes:

  • Unique chemical scaffolds.
  • Unexpected therapeutic advantages.
  • Specific combinations or formulations not previously disclosed.

Patent Landscape in Croatia and Europe

1. European Patent System

Croatia, as an EPC member, adopts harmonized patent practices aligned with the European Patent Convention (EPC). This allows for:

  • Parallel patent filings within the European Patent Office (EPO).
  • Croation patent grants often derived from or related to broader European applications.

2. Competitor and Prior Art Analysis

  • Internationally, similar compounds or treatment methods are patented.
  • The patent landscape likely features prior art from major pharmaceutical companies, especially around major drug classes such as kinase inhibitors, anti-inflammatory agents, or biologics.

3. Patent Family and Related Patents

  • HRP20170154 probably belongs to a patent family covering multiple jurisdictions.
  • Related applications may include continuations, divisional applications, or provisional filings.

4. Landscape Trends

  • A shift toward precision medicine and targeted therapies influences claim scopes.
  • Increased patenting of biologics and biosimilars impacts the scope of drug patents.
  • Croatia's local innovation protections complement EU-wide patent strategizing.

Legal and Commercial Implications

1. Patent Strengths

  • A well-drafted patent with broad claims could hinder competitors from developing similar compounds.
  • Inclusion of method-of-use claims broadens the scope of protection.

2. Limitations and Challenges

  • The scope may face challenges if prior art discloses similar compounds or uses.
  • Patent validity depends on novelty, inventive step, and industrial applicability under Croatian and EPO standards.

3. Market Implications

  • The patent fortifies exclusivity in Croatia for the claimed therapeutic indications.
  • Secures a competitive edge for the patent holder during commercial launch phases.
  • Potential to license or enforce against infringing parties.

Conclusion

Patent HRP20170154 offers significant protection for a specific pharmaceutical compound or application within Croatia, with an emphasis likely on chemical structure and therapeutic use claims. Its strength and scope depend heavily on claim drafting, prior art landscape, and patent prosecution strategies aligned with European standards. Understanding its precise claims and related patent family members is essential for assessing competitive advantages and potential licensing opportunities.


Key Takeaways

  • The patent protects a specific chemical compound or therapeutic indication, with broad claims likely covering structure and use.
  • Its scope aligns with European patent practices, providing robust protection potentially extendable through international filings.
  • Competitors must navigate the detailed claims to avoid infringement, emphasizing the importance of claim interpretation.
  • Ongoing monitoring of related patents is crucial due to rapid innovation in pharmaceutical chemistry.
  • Patent enforcement and licensing are strategic tools to optimize commercial advantage in Croatia and beyond.

FAQs

1. How does Croatia's patent system influence the scope of pharmaceutical patents like HRP20170154?
Croatia follows EPC standards, emphasizing novelty, inventive step, and industrial applicability. Patent claims must be clear, supported by description, and sufficiently broad to prevent easy workarounds, shaping overall patent scope and enforceability.

2. Can this Croatian patent be enforced across Europe?
While the Croatian patent grants protection within Croatia, similar enforcement requires filing or relying on European or international patent applications. The patent family and related patents in the EPO facilitate broader European protection.

3. What are common challenges in patenting pharmaceutical compounds?
Challenges include demonstrating sufficient novelty over prior art, drafting claims that adequately cover the invention without being overly broad, and overcoming arguments related to obviousness or obvious combinations.

4. How might patent claims impact generic drug development?
Restrictive or very narrow claims can be circumvented, whereas broad claims can delay generic entry. Patent litigation or opposition proceedings may also influence the scope and lifecycle of protection.

5. Why is understanding the patent landscape vital for pharmaceutical innovation?
It enables innovators to identify freedom-to-operate, avoid infringement, strategize patent filings, and maximize market exclusivity, ultimately enhancing R&D investments' return.


References:

[1] Croatian Intellectual Property Office (HIPO) Patent Database
[2] European Patent Office (EPO) patent documents
[3] European Patent Convention (EPC) Guidelines
[4] Latest market and patent trend analyses in pharmaceutical patenting

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