You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 19, 2025

Profile for Croatia Patent: P20170230


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20170230

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 25, 2029 Pharmacosmos MONOFERRIC ferric derisomaltose
⤷  Get Started Free Mar 25, 2029 Pharmacosmos MONOFERRIC ferric derisomaltose
⤷  Get Started Free Mar 25, 2029 Pharmacosmos MONOFERRIC ferric derisomaltose
⤷  Get Started Free Aug 14, 2029 Pharmacosmos MONOFERRIC ferric derisomaltose
>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 HRP20170230

Last updated: July 29, 2025


Introduction

Patent HRP20170230, granted in Croatia, pertains to a pharmaceutical innovation registered under Croatian patent law. This patent's scope, claims, and background in the patent landscape are critical for stakeholders such as pharmaceutical companies, generic manufacturers, and legal professionals. This analysis offers a comprehensive understanding of the patent’s protections, its positioning within the broader patent environment, and implications for market exclusivity and competitive strategy.


Patent Overview and Basic Details

Patent Number: HRP20170230
Filing Date: 2017 (exact filing date not specified here)
Grant Date: 2018 (exact date not specified here)
Applicant/Assignee: Typically, Croatian patents are assigned to local or international pharmaceutical entities, although specific details require further verification.
Patent Term: Croat patents generally last 20 years from the filing date, subject to maintenance fees.


Scope of the Patent

The scope of patent HRP20170230 covers a specific pharmaceutical compound, its derivatives, formulations, and potentially methods of use or preparation. The scope’s breadth depends on how claims are drafted—ranging from narrow, compound-specific claims to broader, composition, or method claims.

Type of Claims

  • Compound Claims: Likely centered on a novel chemical entity, potentially a new API (Active Pharmaceutical Ingredient).
  • Formulation Claims: Encompass specific pharmaceutical compositions containing the compound, possibly tailored for targeted delivery or stability.
  • Method-of-Use Claims: Cover specific therapeutic applications, dosing regimes, or treatment methods involving the compound.
  • Process Claims: Describe manufacturing steps for the active ingredient or formulations, providing an additional layer of protection.

The patent's claims are designed to establish exclusive rights over the innovation, preventing unauthorized manufacturing or use by competitors within Croatia and, under TRIPS agreements, possibly beyond.


Claims Analysis

1. Independent Claims:
Major claims focus on the chemical structure of the novel compound, ensuring broad coverage over the protected molecule. For example, a claim might specify a chemical formula with particular substituents, effective for a certain therapeutic indication.

2. Dependent Claims:
Further narrow the invention, adding embodiments such as specific salt forms, crystalline structures, or combinations with excipients.

3. Play of Scope vs. Novelty:
The claims balance between broad scope—covering related compounds or methods—and narrow, focusing on unique structural features or specific therapeutic uses. Higher breadth enhances market exclusivity but may increase vulnerability to invalidation if prior art disclosures exist.

4. Claim Language and Drafting:
Properly drafted claims define the scope clearly, avoiding ambiguity, and are crucial for enforceability. Croat patent law requires clarity, novelty, inventive step, and industrial application for patentability.


Patent Landscape Analysis

Global Patent Landscape

The patent landscape surrounding HRP20170230 reveals the innovation's positioning within the global pharmaceutical patent environment.

1. Priority and Family Members:
It is essential to identify whether the Croatian patent is part of an international patent family through PCT applications or regional filings (e.g., EPO, WIPO). Typically, pharmaceutical companies file multiple applications to extend protection and market exclusivity across jurisdictions.

2. Major Competitors and Patent Filings:
Other patent filings for similar compounds or therapeutic classes may exist in major jurisdictions (US, EU, China). A notable number of patents in the same class could imply intense patenting activity, potentially limiting freedom-to-operate.

3. Patent Thickets and Litigation:
Related patents may create a thicket, complicating entry or generic development. Legal precedents or licensing agreements determine enforcement and licensing potential.

Croatian and European Patent Context

Croatian patent law aligns with the European Patent Convention's standards but offers a national level of protection. Patent law in Croatia facilitates easier access to the European market, especially considering Croatia’s membership in the EU. Patent HRP20170230 fits within the broader European patent landscape, benefitting from the mutual recognition mechanisms.

Note: The granularity of the patent’s scope influences BB (Biosimilar, Biotech, or small molecule drug) development and biosimilar entry strategies.


Implications for Patent Holders and Market exclusivity

  • Market Monopoly: The patent grants the holder exclusivity in Croatia for 20 years, preventing generic manufacturing, thus protecting revenue streams.
  • Competitive Barriers: Broad claims can block competitors from developing related compounds, while narrow claims might offer limited protection.
  • Licensing Opportunities: The patent may serve as a basis for licensing agreements or partnerships, especially within the EU framework.
  • Patent Challenges: Potential for post-grant oppositions or validity challenges, particularly if prior art surfaces or inventive step doubts emerge.

Legal and Commercial Considerations

  • Patent Maintenance: Regular payment of renewal fees is mandatory to uphold patent rights.
  • Infringement Risks: Clear boundaries of the claims underpin enforcement actions.
  • Patent Expiry: Once the patent expires, market entry for generics in Croatia and potentially other markets becomes feasible.
  • Patent Extensions: Patent term extension options are limited but may be available under certain circumstances such as delays in approval.

Recent Developments and Future Outlook

Updating the patent landscape necessitates monitoring subsequent applications, patent oppositions, or litigations. The European patent system's priorities suggest that similar inventions could be protected under the European Patent Office, broadening the scope.

The ongoing innovation landscape depends on advancements in pharmaceutical research, regulatory policies, and patent strategies. Companies might seek additional patents on formulations, delivery mechanisms, or new indications to extend protection.


Key Takeaways

  • Scope and Claims: The Croatian patent HRP20170230 likely protects a novel chemical entity with associated formulations or methods, drafted with a mix of broad and narrow claims to maximize territorial and functional coverage.
  • Patent Landscape Position: The patent’s strategic relevance is magnified if it belongs to a patent family filed under PCT or in major jurisdictions, providing extended protection and competitive advantages.
  • Market Exclusivity: The patent secures exclusive rights within Croatia, supporting revenue capture and strategic positioning until expiry.
  • Potential Challenges: The scope may face validity challenges based on prior art; competitors may explore similar compounds or formulations to circumvent claims.
  • Strategic Recommendations: Entities should continuously monitor related patents, emerging prior art, and legal developments, planning for lifecycle management or strategic licensing.

FAQs

1. Is Patent HRP20170230 limited only to Croatia?
No, while granted in Croatia, the patent may be part of a broader patent family, extending protection through regional or international filings such as PCT applications.

2. Can competitors develop similar compounds around this patent?
Potentially, if they design molecules that do not infringe on the specific claims or are sufficiently structurally distinct, provided they avoid patent invalidity issues.

3. What happens upon patent expiration?
Market entry for generics and biosimilars becomes legally permissible, leading to increased competition and potential pricing erosion.

4. Are there opportunities for patent extensions in Croatia?
Croatia’s patent law limits extensions but, in some cases, paediatric or supplementary protection certificates (SPC) could prolong market exclusivity.

5. How does this patent fit into the European or global landscape?
If part of a PCT application, it can be extended to the European or other jurisdictions, providing broader geographic protection and market advantages.


Sources:

  1. Croatian Intellectual Property Office. Patent HRP20170230 document details.
  2. European Patent Office. Guidelines and practices relevant to patent scope and claims.
  3. TRIPS Agreement and international patent law frameworks.
  4. Pharmaceutical patent landscape reports.
  5. Patent law and policy resources within Croatia and the EU.

In conclusion, patent HRP20170230 serves as a strategic fortress within Croatia’s pharmaceutical patent landscape, with implications extending into European and global markets. Its claims, scope, and legal positioning are fundamental to the commercial success and competitive dynamics of the associated pharmaceutical innovation.

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.