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Last Updated: December 15, 2025

Profile for Croatia Patent: P20150678


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US Patent Family Members and Approved Drugs for Croatia Patent: P20150678

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 Nov 10, 2032 Pf Prism Cv TORISEL temsirolimus
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Drug Patent HRP20150678

Last updated: July 29, 2025


Introduction

The Croatian patent HRP20150678 pertains to a pharmaceutical invention filed and granted in Croatia, offering insights into the specific protections, scope, and strategic positioning within the broader pharmaceutical patent landscape. This detailed analysis aims to dissect the patent's claims, scope, and the current patent landscape, facilitating informed decision-making for businesses, research institutions, and legal practitioners involved in pharmaceutical innovation.


Patent Overview

The patent HRP20150678 was filed to protect a novel medicinal compound or formulation (assumed from the context, as the precise structure is not provided here). Croatian patents, governed primarily by the Croatian Patent Office and aligned with European patent standards, tend to feature claims focusing on inventive steps, specific formulations, or use indications.


Scope of the Patent

The scope of HRP20150678 primarily relates to the claimed invention’s technical features, which could include:

  • Chemical Composition: The core compounds or their derivatives.
  • Method of Use: New therapeutic methods, dosage regimens, or administration routes.
  • Formulation: Specific formulations, including excipients, delivery matrices, or controlled-release systems.
  • Manufacturing Process: Novel synthesis steps or processing techniques.

Based on general patent strategies in the pharmaceutical sector, HRP20150678 most likely encompasses a combination of product claims (covering the compound or composition), use claims (indicating therapeutic applications), and possibly process claims (methods of synthesis or formulation).


Claims Analysis

Although the specific claims are not provided here, typical claims in a Croatian drug patent follow standard patterns:

1. Compound Claims

  • Cover the chemical entity or its pharmaceutically acceptable salts, solvates, or stereoisomers.
  • Define the scope through chemical formulae, such as generic Markush claims.

2. Use Claims

  • Specify therapeutic benefits, such as treatment of a particular disease or condition.
  • Could include second medical use claims, quite common in pharmaceutical patents.

3. Formulation Claims

  • Include specific delivery forms, e.g., tablets, capsules, injectables.
  • Possibly claim combinations with other active ingredients.

4. Process Claims

  • Cover synthesis or manufacturing methods that produce the compound or formulation.

The scope hinges heavily on how broadly or narrowly these claims are drafted. Broad claims risk art rejections but afford stronger exclusivity, while narrow claims might be easier to defend but less protective.


Patent Landscape

Croatia's patent landscape for pharmaceuticals exhibits increasing activity, aligned with European patent developments, given Croatia's accession to the EU and participation in the European Patent Convention.

1. Patent Families and Priority

  • Croatian patents are often part of wider European or international patent families.
  • HRP20150678 may claim priority from an earlier application, possibly filed under the Patent Cooperation Treaty (PCT), with subsequent national phase entry.

2. Competition and Overlap

  • The landscape features patents targeting similar molecular targets or indications.
  • Overlapping patents can lead to licensing opportunities or litigation risks.
  • The National Drug Registry and international patent databases reveal comparable filings, especially by multinational corporations and biotech firms.

3. Patent Validity and Challenges

  • Croatian patents undergo examination for novelty, inventive step, and industrial applicability.
  • The patent’s robustness depends on prior art analysis, especially regarding similar chemical entities or therapeutic uses.
  • Potential for oppositions from third parties exists within the Croatian post-grant proceedings window.

Legal and Commercial Strategy Considerations

  • Claim Strength: Broad, structurally comprehensive claims provide higher protection but face increased scrutiny during examination. Narrow claims simplify differentiation but limit market exclusivity.
  • Novelty and Inventive Step: The invention's uniqueness relative to prior art determines enforceability and licensing value.
  • Patent Term and Maintenance: Generally, Croatian patents are granted for 20 years from the filing date, subject to annual maintenance fees.
  • Freedom to Operate: Careful landscape analysis is crucial to avoid infringing third-party rights and to identify licensing opportunities.

Implications for Stakeholders

  • Pharmaceutical Companies: Businesses should assess the patent’s breadth when developing new drugs targeting similar indications.
  • Research Institutions: Can gauge potential licensing agreements or collaborative opportunities if the patent covers promising compounds.
  • Legal Practitioners: Need to scrutinize the claims over existing patents for potential infringements or invalidation strategies.

Conclusion

Croatia patent HRP20150678 exemplifies a focused effort to protect a specific pharmaceutical innovation within the local and broader European landscape. Its scope likely combines compound, use, and formulation claims, designed to safeguard a novel medicinal entity or application. The patent landscape remains dynamic, shaped by ongoing filings, challenges, and multi-jurisdictional strategies, emphasizing the importance of comprehensive patent management and landscape analysis.


Key Takeaways

  • The scope of HRP20150678 hinges on well-drafted claims balancing breadth and defensibility.
  • Patent landscape analysis reveals potential overlaps with international filings, affecting freedom to operate.
  • Strengthening patent claims with precise language enhances enforceability amid competing innovations.
  • Maintaining robust prosecution and monitoring proceedings in Croatia and Europe is crucial for sustained exclusivity.
  • Strategic licensing and litigation considerations depend on thorough prior art and landscape assessments.

FAQs

Q1: How does Croatian patent law influence the scope of pharmaceutical patents like HRP20150678?
Croatian patent law follows the European Patent Convention, emphasizing novelty, inventive step, and industrial applicability. Patent claims must meet these criteria, impacting how broadly claims can be drafted and enforced in Croatia.

Q2: Can the patent HRP20150678 be enforced outside Croatia?
Enforcement depends on whether the patent is part of a broader international patent family or has equivalent filings in other jurisdictions. Without territorial equivalents or extensions, enforcement is limited to Croatia.

Q3: What are common strategies to broaden the scope of pharmaceutical patents in Croatia?
Using Markush structures for chemical claims, drafting multiple use claims, and including various formulations can extend the patent’s protective scope while maintaining validity.

Q4: How does the patent landscape impact drug development in Croatia?
A crowded landscape can hinder innovation by increasing patent infringement risks. Conversely, a clear landscape aids in designing non-infringing products and identifying licensing opportunities.

Q5: What steps can innovators take to strengthen patent protection for pharmaceutical inventions in Croatia?
Thorough prior art searches, detailed claim drafting, strategic filing of multiple claims, and timely prosecution are essential to secure strong, enforceable rights.


Sources:

  1. Croatian Intellectual Property Office. Patent Law. https://dziv.hr
  2. European Patent Office. Guidelines for Examination.
  3. World Intellectual Property Organization. Guide to Patentability Standards.

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