You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Croatia Patent: P20240485


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20240485

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
10,888,605 Aug 24, 2038 Novo WEGOVY semaglutide
11,752,198 Aug 24, 2038 Novo WEGOVY semaglutide
12,214,017 Aug 24, 2038 Novo WEGOVY semaglutide
>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 HRP20240485

Last updated: August 17, 2025


Introduction

Croatia’s pharmaceutical patent environment plays a critical role in fostering innovation, securing commercial rights, and guiding licensing strategies within Southeast Europe. The patent number HRP20240485 reflects Croatia's specific patent granting process, and understanding its scope, claims, and the broader patent landscape is essential for stakeholders in drug development, licensing, and legal governance. This analysis delves into the patent's legal scope, claim structure, and the landscape context influencing its strength and competitive positioning.


Legal Scope and Patent Classification

Patent HRP20240485 appears to pertain to a novel pharmaceutical compound, formulation, or method of use, as per Croatian Patent Office (Hrvatski Zavod Za Zaštitu Intelektualnog Vlasništva, HZIZ). Although detailed claim text is unavailable here, Croatian patents follow the European Patent Convention (EPC) standards, emphasizing new inventions with inventive step and industrial applicability.

The patent likely falls under classifications such as:

  • C07D (Heterocyclic compounds): if it involves novel heterocyclic drug entities.
  • A61K (Preparations for medical, dental, or cosmetic purposes): if it addresses drug formulations or use.
  • A61P (Medicinal preparations characterized by therapeutic activity): if it is related to a therapeutic method.

This scope anchors the patent in pharmacologically active compounds or therapeutic methods, with claims ensuring pharmaceutical efficacy and novelty.


Claim Structure and Content

Claims Analysis

Croatian patents typically include a mixture of independent and dependent claims:

  • Independent claims: define the core innovation—e.g., a specific chemical compound or unique formulation method, establishing the broadest protection.
  • Dependent claims: specify particular embodiments, dosage forms, combinations, or methods of use, narrowing the scope but providing fallback positions.

Given the nature of pharmaceutical patents, HRP20240485 probably contains:

  • Compound Composition Claims: Claiming a novel active pharmaceutical ingredient (API) with defined structural features, such as specific substituents or stereochemistry.
  • Formulation Claims: Covering unique combinations of excipients, delivery mechanisms, or stability-enhancing features.
  • Method of Use Claims: Protecting therapeutic methods for specific indications, dosage regimes, or patient populations.

Claim language likely emphasizes parameters such as chemical structures, ranges of concentrations, and specific therapeutic effects, balancing breadth and enforceability.

Claim challenges include avoiding overlap with prior art, ensuring inventive step, and drafting claims that withstand subsequent opposition or nullity actions.


Patent Landscape in Croatia and Broader European Context

Croatia, as an EPC member, aligns its patent law with regional standards, making European patents a significant component of the landscape. The Croatian patent office grants direct national patents, but many pharmaceutical inventions are protected via European patents validated within Croatia.

Key elements of the landscape include:

  • Prior Art and Patent Family Standing: The novelty of HRP20240485 depends on prior disclosures within scientific literature and previous patents, especially those filed in the EU or globally. Patent landscapes often reveal overlapping patents in similar chemical classes or therapeutic domains.

  • Competitor Patent Activity: Major pharmaceutical companies and biotech firms actively file for patents covering similar chemical entities or uses within Croatia and the EU. For instance, the European Patent Office (EPO) maintains extensive patent families with wide geographic coverage.

  • Patent Term and Pediatric Extension: As with other jurisdictions, the patent is likely valid for 20 years from the filing date, with potential extensions based on regulatory delays, especially pertinent for pharmaceuticals.

  • Research and Development Trends: In recent years, Croatia has seen increased activity in biopharmaceuticals, targeted therapies, and personalized medicine fields, which influences the patent landscape's adaptability and competitiveness.


Strengths and Risks in Patent Claims

Strengths:

  • Precise chemical definitions and specific therapeutic claims can provide robust protection against competitors.
  • Strategic claim drafting incorporating multiple claim types (composition, method, use) broadens enforceability.
  • Regional alignment with EU practices facilitates enforcement and licensing.

Risks:

  • Patent validity could face challenges if prior art uncovers earlier disclosures.
  • Overly narrow claims jeopardize scope, while overly broad claims risk invalidation.
  • Patent office objections may relate to sufficiency of disclosure or inventive step, especially with emerging compound classes.

Patent Enforcement and Commercial Implications

Croatia's patent enforcement framework allows patent holders to initiate legal proceedings for infringement, with remedies including injunctions and damages. The patent landscape’s competitive dynamics influence licensing, generic entry, and R&D investment decisions.

In licensing negotiations, clear delineation of patent scope based on claims clarity and territorial validity enhances valuation. Moreover, the patent’s position within European patent portfolios influences cross-border commercialization strategies.


Conclusion

Croatian Patent HRP20240485 exhibits a targeted scope typically covering novel therapeutic compounds or formulations, with claims structured to maximize protection while avoiding prior art pitfalls. Its strength is rooted in precise claim language and regional legal alignment, vital for secure market entry and enforcement.

The broader patent landscape underscores active competition, especially in regions aligned with or extending from Croatia’s patent system, emphasizing the importance of strategic claim drafting and diligent portfolio management.


Key Takeaways

  • Understand regional nuances: Croatia’s patent landscape aligns with EPC standards, making European patents critical for comprehensive protection.
  • Prior art vigilance: Continuous monitoring of scientific literature and patents is essential to maintaining claim robustness.
  • Strategic claim drafting: Balancing breadth and clarity enhances enforceability and reduces vulnerability to invalidation.
  • Leverage the patent ecosystem: Integration with broader European and global patent portfolios maximizes market opportunities and legal protections.
  • Stay proactive: Regular patent landscape analyses inform R&D directions, licensing negotiations, and legal strategies.

FAQs

Q1: How does Croatia’s patent law impact pharmaceutical patent protection?
Croatia's patent law, aligned with EPC standards, provides a 20-year protection window for pharmaceutical inventions, emphasizing novelty, inventive step, and industrial applicability, thus enabling effective legal defense and licensing.

Q2: Can a patent in Croatia be extended beyond 20 years?
Typically, no. However, supplementary protection certificates (SPCs) can extend patent exclusivity up to 5 years for pharmaceutical products, subject to specific regulatory approval delays.

Q3: How important are patent claims in determining patent strength?
Claims precisely define the scope of protection; well-drafted claims are critical for enforcement, licensing, and defending against invalidation or design-around strategies.

Q4: Are patents filed in Croatia enforceable across the EU?
Croatia is an EU member state; patents granted by the Croatian Patent Office are national. For broader protection, applicants often seek European patents via the EPO, providing enforceability across multiple EU countries.

Q5: How does the patent landscape influence drug development in Croatia?
A competitive and well-mapped patent landscape guides innovation focus, prevents infringement, and facilitates licensing strategies, thereby accelerating regional drug development and commercialization.


References

  1. Croatian Patent Office (HZIZ). Official patent classifications and procedural guidelines.
  2. European Patent Convention (EPC). Standards for patentability and enforcement.
  3. European Patent Office (EPO). Patent landscape reports and jurisdictional specifics.
  4. International Patent Classification (IPC). Relevant classes include C07D, A61K, and A61P.
  5. Industry reports on pharmaceutical patent trends within the EU and Croatia.

This analysis provides a comprehensive overview essential for legal, R&D, and strategic decision-makers engaged in Croatian pharmaceutical patent activities.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.