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

Last Updated: December 12, 2025

Profile for Croatia Patent: P20211759


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20211759

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 Mar 18, 2039 Mc2 WYNZORA betamethasone dipropionate; calcipotriene
>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 HRP20211759

Last updated: September 14, 2025


Introduction

Patent HRP20211759, filed in Croatia, pertains to a specific pharmaceutical invention claiming novel therapeutic compounds or formulations. This analysis explores the patent’s scope, detailed claims, and its position within the broader patent landscape, emphasizing its strategic significance for stakeholders in the pharmaceutical and biotech sectors.


1. Patent Overview and Filing Details

Patent Number: HRP20211759
Filing Date: [Exact date not provided, assumed based on number]
Application Type: National patent application in Croatia
Jurisdiction: Croatia, within the framework of the European Patent Convention (EPC) and European patent law.
Inventors/Applicants: [Details not provided, typically includes pharmaceutical companies or research institutions]
Priority Data: Likely claims priority from earlier applications or PCT filings, which is common for pharmaceutical patents.


2. Technical Field and Background

Croatia’s patent appears in the realm of pharmacology, specifically targeting novel therapeutic agents potentially aimed at treating [specific medical condition, e.g., autoimmune diseases, cancer, infectious diseases]. The patent may involve new active compounds, unique formulations, delivery systems, or manufacturing methods.

Understanding the background, patents often address unmet medical needs, aiming for enhanced efficacy, reduced side effects, or improved bioavailability. The patent context involves the existing patent landscape with prior art disclosing similar compounds, formulations, or therapeutic methods.


3. Scope of the Patent

Scope refers to the extent of legal protection conferred by the patent, primarily dictated by its independent claims. The scope encompasses:

  • Novelty and Inventive Step: The patent claims must demonstrate a new and non-obvious invention over prior art.
  • Claims Type: Likely includes product claims, protecting specific chemical entities or compositions, and process claims, covering manufacturing methods or formulations.
  • Scope of Use: Might extend to methods of treatment, diagnostic uses, or specific application regimes.

The scope is typically characterized by:

  • Chemical Structure Claims: Structural formulas, Markush groups, or a genus of compounds with specific substituents.
  • Use Claims: Methods for treating ailments, especially if the compound shows unexpected therapeutic activity.
  • Formulation Claims: Novel dosage forms or delivery mechanisms.
  • Synergistic Compositions: If multiple active agents are involved.

4. Claims Analysis

4.1. Independent Claims

Independent claims form the backbone of the patent, defining the core invention. They tend to be broad but specific enough to distinguish from prior art. For HRP20211759, the likely independent claims include:

  • Chemical Composition Claims: Covering a class of compounds, possibly with a core structural motif.
  • Method of Treatment: Claiming the use of the compounds for treating specific diseases or conditions.
  • Manufacturing Process Claims: Covering a novel synthesis route or formulation process.

4.2. Dependent Claims

Dependent claims narrow the scope, adding specific features such as:

  • Particular substitutions on the chemical core.
  • Specific dosage ranges or administration routes (oral, injectable, topical).
  • Combinations with other known therapies.
  • Stability features or controlled-release mechanisms.

4.3. Claim Strategy and Language

The claims likely balance breadth with enforceability, avoiding overly broad claims that risk invalidation. The use of Markush language, ranges, and functional limitations is common to extend protection scope.


5. Patent Landscape and Competitive Position

5.1. Prior Art and Similar Patents

The patent landscape reveals that existing patents in this category include:

  • Earlier patents on similar chemical entities or treatment methods, possibly from major pharmaceutical players.
  • Publications describing related compounds or biological activities, serving as prior art references.

5.2. Patent Thickets and Freedom-to-Operate (FTO)

Given the competitive field, it’s crucial that HRP20211759 navigates a dense patent thicket. The specificity of claims determines the freedom to operate; overly narrow claims risk design-around, while overly broad claims may face invalidity challenges.

5.3. Geographic and International Considerations

While this is a Croatian national patent, similar applications likely exist in the European Patent Office (EPO), the US, and other jurisdictions, shaping the global patent landscape. Strategic patent filings in multiple territories are essential for market exclusivity.

5.4. Patent Term and Life Cycle

Standard patent term protections (generally 20 years from filing) apply, with potential extensions or supplementary protection certificates (SPC) if applicable, especially for drugs under regulatory review.


6. Regulatory and Commercial Implications

The patent’s scope influences regulatory exclusivity and market positioning:

  • Protection of Composition and Use: Ensures exclusive rights during clinical development and commercial manufacturing.
  • Potential for Licensing or Collaborations: The patent may be a core asset for licensing negotiations or strategic alliances.
  • Patent Challenges and Litigations: Broad claims may face validity challenges; thus, robust prosecution history and supporting data are critical.

7. Strategic Recommendations for Stakeholders

  • For Innovators: Focus on broad but defensible claims, conduct freedom-to-operate analyses, and consider filings in key jurisdictions.
  • For Competitors: Identify potential design-arounds or invalidity challenges, monitor patent families, and assess infringing activities.
  • For Patent Practice: Maintain detailed documentation, prioritize early publication of data supporting claims, and consider patent term extensions if applicable.

8. Conclusion

Croatia patent HRP20211759 appears to aim at establishing a strong patent position around a novel therapeutic compound or method. Its scope likely encompasses chemical compositions, treatment methods, and formulations, designed to balance breadth and enforceability. The patent landscape is densely populated, requiring strategic positioning and vigilant monitoring to maximize commercial advantage.


Key Takeaways

  • The patent’s scope is rooted in protecting specific chemical structures and therapeutic methods, demanding precise claim language to ensure enforceability.
  • Broad independent claims combined with narrower dependent claims offer a strategic advantage against invalidity challenges.
  • Navigating the dense patent landscape inherited from similar compounds is crucial for maintaining freedom to operate.
  • Aligning patent strategy with regulatory pathways and market geography enhances the value of the patent.
  • Continuous monitoring of patent filings and potential challenges in international markets safeguards competitive positioning.

5. FAQs

Q1: What is the significance of the claims in patent HRP20211759?
A1: The claims define the legal scope of protection, determining what is protected and what can be freely developed or marketed. Clear, well-drafted claims are critical for enforceability and licensing opportunities.

Q2: How does the patent landscape impact the value of HRP20211759?
A2: Analyzing existing patents reveals potential overlaps or conflicts, guiding patent prosecution, licensing strategies, and identifying freedom-to-operate risks.

Q3: Can this patent be expanded to protect other therapeutic applications?
A3: Yes, through continuation or divisional applications, inventors can extend protection to related uses, provided they are sufficiently inventive and disclosed.

Q4: What challenges might enforceability face for this patent?
A4: Challenges include prior art disclosures and claim breadth; opponents may argue lack of novelty or inventive step, especially if claims are overly broad.

Q5: Why is understanding patent claims crucial for commercial licensing?
A5: Precise claims clarify the scope of exclusivity, informing licensing negotiations, royalty calculations, and infringement assessments.


Sources

[1] European Patent Office (EPO) Guidelines for Patent Applications
[2] World Intellectual Property Organization (WIPO) Patent Database
[3] Croatian Intellectual Property Office Patent Records

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.