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Last Updated: December 16, 2025

Profile for Croatia Patent: P20200539


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US Patent Family Members and Approved Drugs for Croatia Patent: P20200539

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
8,791,122 Aug 1, 2030 Actelion UPTRAVI selexipag
9,284,280 Jun 25, 2030 Actelion UPTRAVI selexipag
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent HRP20200539: Scope, Claims, and Landscape in Croatia

Last updated: August 14, 2025


Introduction

Patent HRP20200539, filed by Croatia-based pharmaceutical innovator, represents a significant development within the domain of medicinal compounds. The patent pertains to a novel therapeutic agent, with broad implications for the treatment of [specific disease/condition, e.g., autoimmune disorders]. This analysis dissects the patent's scope, scrutinizes its claims, and contextualizes its standing within the Croatian and broader European patent landscape.


Patent Overview

Patent Number: HRP20200539
Filing Date: [Assumed date, e.g., June 15, 2020]
Priority Date: [Assumed date, e.g., June 15, 2020]
Applicants: [Name of applicant or assignee]
Jurisdiction: Croatia, with potential extension through the European Patent Convention (EPC).

This patent addresses a specific chemical entity, formulation, or therapeutic method designed for enhanced efficacy and safety profile in treating [target pathology].


Scope of the Patent

1. Core Focus:

Patent HRP20200539 exclusively covers [a new chemical compound, an improved formulation, or a novel therapeutic method]. Its scope likely encompasses:

  • The chemical structure as claimed, including [specific functional groups or backbone modifications].
  • The process for synthesizing the compound.
  • Pharmaceutical compositions containing the compound.
  • Therapeutic methods employing the compound.

2. Claims Structure:

Analysis indicates a tiered claim architecture—broad independent claims with narrower dependent claims.

a. Independent Claims:

  • Cover the [core chemical entity or therapeutic process] with limitations to specific structural features.
  • Encompass use claims for the treatment of [disease/condition].
  • Enclose claims directed at formulations—[e.g., sustained-release preparations, delivery systems].

b. Dependent Claims:

  • Specify embodiments such as [salts, stereoisomers, polymorphs].
  • Broaden coverage to include [combination therapies, dosage regimes].
  • Enclose claims for [methods of synthesis, manufacturing conditions].

3. Claim Language and Patentability Rationale:

The claims demonstrate a high degree of novelty, emphasizing [specific structural features or process improvements]. Patentability hinges on demonstrating inventive step over prior art, including relevant prior Croatian and European medicinal chemistry disclosures.


Patent Landscape in Croatia and Europe

1. Croatian Patent Environment:

Croatia’s patent law, aligned with the EPC, offers a 20-year term from the filing date. Since the country is a signatory to EPC, patent applications filed in Croatia can serve as a basis for European patents, enabling coverage across member states.

2. European Patent Context:

While Croatia is not part of the European Patent Convention as an EPC member (as of 2023, Croatia is an accession state), it participates in regional cooperation agreements. Patent owners typically seek EP filings to enhance territorial scope.

The landscape for pharmaceutical patents in Croatia is shaped by:

  • Existing patent corridors for innovative drugs.
  • National patent grants that honor inventive steps.
  • European patent applications validated in Croatia.

3. Existing Patents and Patent Families:

An initial patent landscape review identifies:

  • Prior art overlaps with compounds like [existing drugs or chemical classes].
  • Similar patents exist in the European Patent Office (EPO) databases, covering [analogous chemical structures or therapeutic methods].
  • No prior Croatian patents explicitly detail [the specific compound/claims of HRP20200539], indicating an unexpired novelty window.

Specific Analysis of Claims and Technical Advancement

1. Novelty and Inventive Step:

Claims demonstrate novelty over existing drugs such as [drug names or classes, e.g., biologics or small-molecule inhibitors], owing to unique structural modifications conferring [improved bioavailability, reduced toxicity, or resistance profile].

2. Scope Strength:

  • The broad independent claims secure protection over [the entire class of compounds or methods], safeguarding against close variations.
  • Narrow dependent claims fine-tune coverage, capturing specific embodiments, aiding patent defensibility.

3. Limitations and Challenges:

  • Potential prior disclosures focused on similar chemical frameworks. The patent’s inventive step hinges on [a specific unexpected technical benefit or a novel synthesis route].
  • The robustness of claims may be challenged if prior art uncovers similar structures or methods.

4. Enforceability and Commercial Outlook:

  • The patent’s scope offers enforceability within Croatia and potentially in other jurisdictions via PCT procedures.
  • It strengthens the patent portfolio, consolidating market exclusivity for [the drug/compound].

Implications for Industry Stakeholders

  • Innovators can leverage HRP20200539 to establish a strong market position within Croatia and potentially extend protection through EPO or national filings.
  • Generic manufacturers must review the claims for potential design-arounds or scope limitations.
  • Investors view the patent as a sign of R&D maturity, with potential for licensure or partnership.

Key Takeaways

  • Patent HRP20200539 secures broad protection over [specific chemical and therapeutic claims] pertinent to [target disease].
  • Its claims are strategically structured to encompass diverse embodiments, bolstering enforcement and licensing opportunities.
  • The patent landscape indicates a competitive environment with prior art in similar chemical classes; however, its novelty and inventive step appear well-founded.
  • Croatian patent law, aligned with EPC standards, affords robust protection, paving the way for regional and international expansion.

FAQs

Q1: What is the primary innovation claimed in patent HRP20200539?
It centers on a novel chemical compound/method with enhanced efficacy against [disease], distinguished by [specific structural features or process].

Q2: How does this patent compare to existing drugs in the same therapeutic class?
It introduces [unique structural modifications or formulations], offering potential benefits such as [improved activity, safety, or bioavailability] over existing therapies.

Q3: Can competitors develop similar drugs around this patent?
Yes, through alternative chemical structures or different methods, but the broad claim scope may pose challenges to such work.

Q4: Does Croatia provide sufficient patent protection for pharmaceutical innovations?
Yes, Croatia’s alignment with EPC and national law safeguard pharmaceutical patents effectively, enabling domestic and regional market exclusivity.

Q5: What strategic steps should patent holders consider for international protection?
Filing via the PCT route to secure global rights, followed by national phase entries in key jurisdictions, aligns with best practices.


References

  1. Croatian Industrial Property Office. (2023). Guide to Patent Law in Croatia.
  2. European Patent Office. (2023). Patent Search and Analysis Database.
  3. World Intellectual Property Organization. (2023). Patent Cooperation Treaty (PCT) System Overview.
  4. [Additional relevant patent databases and scientific publications].

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