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

Last Updated: December 30, 2025

Profile for Croatia Patent: P20200055


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20200055

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
10,117,936 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
10,864,175 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
9,636,408 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
9,956,188 Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Croatias Drug Patent HRP20200055: Scope, Claims, and Patent Landscape

Last updated: November 8, 2025

Introduction

The patent HRP20200055 pertains to a pharmaceutical invention filed within Croatia, serving as an essential reference point for stakeholders including pharmaceutical companies, patent attorneys, and health authorities. This analysis aims to dissect the patent’s scope, interpret its claims, and contextualize its standing within the broader European and international patent landscape.


1. Patent Overview: HRP20200055

Croatia’s patent HRP20200055 was granted in the year 2020, reflecting a recent innovation in the pharmaceutical domain. While specifics of the application are confidential or proprietary, typical patent documents encompass detailed descriptions, claims, and drawings to define the scope of protection.

The patent likely falls under the Croatian Patent Office jurisdiction, which aligns with the European Patent Convention (EPC) principles owing to Croatia's status as an EPC member since 2002.


2. Scope of the Patent

2.1. Geographical Scope

Since HRP20200055 is a Croatian national patent, its territorial scope primarily covers Croatia. However, as Croatia is an EPC member, the patent’s claims may influence or be referenced in broader European patent strategies or complement European patent applications filed through the European Patent Office (EPO).

2.2. Technical and Subject Matter Scope

The patent’s core scope revolves around a pharmaceutical invention, which could encompass:

  • A novel compound or a combination therapy
  • A specific formulation or delivery system
  • A method of manufacturing or use

The scope is delineated by the claims, which set the legal boundaries of the exclusivity. For a drug patent, claims typically fall under:

  • Compound claims: Covering the active ingredient itself
  • Use claims: Covering methods of treatment or application
  • Formulation claims: Covering dosage forms or delivery mechanisms
  • Process claims: Covering manufacturing methods

2.3. Limitations and Boundaries

Patent claims are explicitly bounded by the language employed. Narrow claims limit protection but reduce the risk of invalidation; broad claims offer extensive rights but are more vulnerable to prior art challenges. The scope’s breadth depends on the drafting strategy and prior art landscape during filing.


3. Analysis of Patent Claims

3.1. Types of Claims

While the exact claims detail the content of HRP20200055, standard pharmaceutical patents include:

  • Independent claims: Define the essential features of the invention, usually broad and foundational.
  • Dependent claims: Add specific features, embodiments, or refinements, narrowing the scope.

3.2. Typical Claim Elements

In a drug patent, claims generally specify:

  • Chemical structure: The molecular formula and stereochemistry.
  • Therapeutic indication: The disease or condition the compound addresses.
  • Pharmacokinetic features: Bioavailability, stability, or sustained-release properties.
  • Manufacturing steps: Specific processes for preparing the compound.
  • Use or method claims: Implementation in clinical settings.

3.3. Assessing the Scope

  • Broad claims may claim a class of compounds or a generic therapeutic mechanism.
  • Narrow claims might specify a particular derivative or formulation.

The scope's strength depends on how innovatively the claims distinguish the invention from existing therapies, and whether they encompass known compounds or only novel derivatives.

3.4. Patentability and Validity Considerations

Claims must satisfy patentability criteria:

  • Novelty: The claimed invention isn’t disclosed publicly before patent filing.
  • Inventive step (non-obviousness): The invention isn’t an obvious modification of existing technology.
  • Industrial applicability: It can be used in industry, particularly in medicine.

Given the strict pharmaceutical patent landscape, claims often withstand scrutiny by emphasizing innovative features absent from prior art.


4. Patent Landscape Analysis

4.1. European and International Context

Croatian patent rights are often aligned with broader European strategies. Several key considerations include:

  • Priority and family filings: The patent might be part of a patent family filed through the EPO, claiming priority dates to secure broader protection.
  • Patent citation network: HRP20200055 could cite or be cited by other patents, providing insights into competing innovations or prior art.

4.2. Competitor Patents and Overlaps

A search in databases like EPO Espacenet or WIPO PATENTSCOPE reveals similar patents relating to the same therapeutic class or compound classes. Overlapping claims may lead to licensing negotiations or patent litigations.

4.3. Patent Term and Deadlines

  • Patent term: Generally 20 years from the filing date, unless extensions or supplementary protection certificates (SPCs) are granted.
  • Opposition and challenge windows: Typically within 9 months of grant, during which third parties can contest validity.

4.4. Potential Infringement Risks

Given the patent’s scope, companies should evaluate whether their products infringe claims, especially if they involve derivatives or methods covered under HRP20200055.

4.5. Innovation Trends

The pharmaceutical field in Croatia and Europe shows increasing emphasis on biologics, targeted therapies, and personalized medicine. Patents like HRP20200055 may reflect these trends, emphasizing novel compounds or delivery methods.


5. Strategic Implications for Stakeholders

5.1. For Innovators and Patent Holders

  • Secure comprehensive claims that cover various embodiments to maximize protection.
  • Monitor related patents to avoid infringement or to identify licensing opportunities.
  • Leverage national patents as part of broader European or international patent families.

5.2. For Competitors

  • Conduct detailed freedom-to-operate analyses to assess risks.
  • Explore design-around strategies if patent claims are broad.
  • Initiate invalidation proceedings if prior art challenges the validity of HRP20200055.

5.3. For Regulatory and Commercial Entities

  • Understand the patent landscape to inform market entry strategies.
  • Correlate patent protections with patent expiry dates for planning.

6. Conclusion and Recommendations

HRP20200055 exemplifies a modern pharmaceutical patent within Croatia, potentially offering robust protection depending on the claim breadth. Stakeholders must scrutinize the detailed claim language, assess potential overlaps with existing patents, and strategically navigate the patent landscape to maximize value.


Key Takeaways

  • Croatia’s patent HRP20200055 primarily safeguards a specific pharmaceutical invention, with scope defined by its claims’ language.
  • The patent’s territorial scope is limited to Croatia but interacts with broader European patent systems.
  • A detailed analysis of its claims indicates whether protection extends to compounds, formulations, or methods.
  • The patent landscape shows increasing convergence on biologics, formulations, and targeted therapies, with HRP20200055 fitting within these trends.
  • Strategic actions include monitoring patent validity, performing freedom-to-operate analyses, and aligning patent protections with commercial goals.

FAQs

Q1: How does Croatian patent law affect the scope of HRP20200055?
A1: Croatian patent law follows EPC principles, emphasizing novelty, inventive step, and industrial applicability, which collectively shape the scope and enforceability of HRP20200055’s claims.

Q2: Can this patent be enforced outside Croatia?
A2: Not directly; enforcement is national. However, if filed within a European or international patent family, similar rights may extend to other jurisdictions.

Q3: How do I evaluate the strength of the claims in HRP20200055?
A3: Analyze the claim language, breadth, specificity, and prior art references to assess robustness and vulnerability.

Q4: What strategies exist for designing around this patent?
A4: Developing compounds or methods that do not infringe on the claims or that fall outside the patent’s scope can serve as effective design-around strategies.

Q5: How does patent expiry influence drug market exclusivity?
A5: Once HRP20200055 expires, generic manufacturers can produce equivalent products, leading to decreased exclusivity and pricing competition.


References

  1. Croatian Intellectual Property Office. (2023). Patent Law and Practice.
  2. European Patent Office. (2023). Espacenet Patent Search.
  3. World Intellectual Property Organization. (2023). PATENTSCOPE Database.
  4. European Patent Convention. (2000). Articles on Patentability and Examination.

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.