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Last Updated: December 31, 2025

Profile for Croatia Patent: P20140667


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US Patent Family Members and Approved Drugs for Croatia Patent: P20140667

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 21, 2028 Gilead Sciences Inc VOSEVI sofosbuvir; velpatasvir; voxilaprevir
⤷  Get Started Free Sep 26, 2029 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
⤷  Get Started Free Sep 26, 2029 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
>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 HRP20140667

Last updated: August 1, 2025


Introduction

The patent HRP20140667, filed or granted in Croatia, constitutes a crucial legal barrier protecting a specific pharmaceutical compound or formulation. This analysis examines the scope of the patent, its claims, and its position within the broader patent landscape, offering insights vital for stakeholders interested in market exclusivity, innovation, and potential challenges.


Patent Overview and Context

HRP20140667 is identified as a pharmaceutical patent granted or filed in Croatia, a member of the European Patent Organization. While specific patent documentation details require access to the Croatian Intellectual Property Office (HIPO), typical patent documentation for pharmaceutical inventions encompasses claims covering active compounds, methods of use, manufacturing processes, and compositions.

The patent's commercial relevance hinges on the scope of its claims — whether they are narrow, covering a specific compound, or broad, encompassing multiple related structures or formulations. Such scope impacts both market exclusivity and potential freedom-to-operate considerations.


Scope of the Patent

The scope of HRP20140667 generally falls into two categories:

  1. Product Claims: Covering specific chemical entities, such as a novel active pharmaceutical ingredient (API) or derivatives. These claims define exact molecular structures or classes related to a therapeutic agent.

  2. Use and Process Claims: Encompassing methods of treatment, dosing regimens, or manufacturing processes associated with the compound.

Given standard patent drafting practices for pharmaceuticals, HRP20140667 is likely to include:

  • Compound Claims: Covering the specific chemical structure(s) that demonstrate novelty and inventive step.
  • Substituent and Derivative Claims: Broadening coverage to include structurally similar compounds with potential therapeutic activity.
  • Formulation Claims: Covering specific compositions, delivery systems, or excipients ensuring product stability or bioavailability.
  • Method of Use Claims: Protecting particular therapeutic indications or administration protocols.

The patent’s scope is especially relevant if it claims a broad chemical class, which could affect generic entry and market competition.


Claims Analysis

A detailed claims analysis requires access to the full patent document. However, standard considerations include:

  • Claim breadth: Broader claims may include generic structures or functional features, offering extensive protection but risking invalidation for lack of inventive step or insufficient disclosure.
  • Dependent claims: Usually narrow claims that specify particular embodiments or preferred embodiments, enabling fallback positions during infringement or validity challenges.
  • Novelty and inventive step: Claims must demonstrate innovations over prior art, relevant in Europe and Croatia, which often scrutinizes pharmaceutical patents for inventive merit.

For HRP20140667, the typical claims could specify:

  • A chemical formula with defined substituents (e.g., a new heterocyclic compound).
  • A process for synthesizing the compound.
  • Therapeutic use of the compound in treating specific conditions (e.g., cancer, autoimmune diseases).

The patent likely emphasizes the novelty of the chemical structure and its specific application, aligning with European patent standards.


Patent Landscape in Croatia and Europe

Croatia's patent landscape for pharmaceuticals is aligned with European standards, governed by the European Patent Convention (EPC) and local law. The following points highlight market positioning:

  1. European Patent System:
    Croatia, as an EPC member, recognizes European patents validated locally. If HRP20140667 is a European patent application validated in Croatia, it benefits from post-grant exclusivity until expiry, usually 20 years from the priority date.

  2. Patent Families and Priority Zones:
    If the patent originated from a broader family, protection may extend across multiple jurisdictions, impacting competition and generic entry across Europe.

  3. Patent Challenges and Litigation:
    Pharmaceutical patents frequently face validity and infringement challenges. The scope of claims in HRP20140667 influences its vulnerability: narrow claims are easier to circumvent, whereas broad claims offer stronger protection but are scrutinized more intensely.

  4. Expiration and Follow-up Patents:
    Patent lifecycle management involves potential extensions via supplementary protection certificates (SPCs) in Europe, potentially prolonging exclusivity beyond 20 years.

Related Patents and Innovation Ecosystem

The patent landscape involves:

  • Prior Art and Similar Patents:
    Analysis of similar inventions or earlier patents reveals the novelty and inventive steps of HRP20140667. The existence of close existing patents may limit scope or influence claim amendments.

  • Active Competitors:
    Major pharmaceutical players developing similar compounds could influence the patent's strength and market strategy.

  • Research and Development Trends:
    Emerging trends in targeted therapies or biologics might affect the patent's relevance and potential for follow-up innovation.


Legal and Commercial Implications

  • Market Exclusivity:
    In Croatia, patent protection provides a vital competitive advantage, allowing the patent holder to recoup R&D investments and establish market dominance.

  • Generic Entry Risks:
    If the patent’s claims are narrow, generic manufacturers may design around them, leading to potential patent challenges. Conversely, broad claims might delay or prevent generic entry.

  • Potential for Patent Litigation:
    Patent litigation strategies, either for asserting rights or defending validity, are influenced by the patent’s claim scope and the surrounding patent landscape.


Conclusion

The Croatian patent HRP20140667, representing a pharmaceutical innovation, likely encompasses a combination of specific compound claims and possibly use or process claims. Its scope determines its enforceability, market longevity, and freedom to operate.

Stakeholders should examine the patent claims meticulously, considering potential for narrow interpretation or possible invalidation. The patent landscape’s complexity necessitates continuous monitoring for prior art, competing filings, and legal challenges, especially within the European context where the patent might be extended or challenged.


Key Takeaways

  • Claim Breadth Is Critical: Broader claims offer stronger exclusivity but face higher validity scrutiny; narrower claims are easier to design around but provide limited protection.
  • European Patent System Alignment: Croatia’s patent landscape aligns with the EPC, facilitating mutual recognition but requiring rigorous prosecution and validation strategies.
  • Data-Driven Decision-Making: Detailed claim analysis, prior art review, and competitor intelligence are essential to assess patent strength and freedom to operate.
  • Lifecycle Management: Extended protection through SPCs can prolong market dominance beyond 20 years, crucial for long-term ROI.
  • Legal Vigilance Essential: Regular monitoring for potential infringing activities and patent challenges safeguards commercial interests.

FAQs

1. What is the typical scope of pharmaceutical patents like HRP20140667?
They usually cover specific chemical compounds, their derivatives, manufacturing processes, formulations, and therapeutic methods associated with the active ingredient.

2. How does Croatia’s patent law influence pharmaceutical patent protection?
Croatia follows EPC standards and national laws, granting 20-year patent terms, with possibilities for extensions via SPCs, but scrutinizes patent validity based on novelty and inventive step.

3. Can the claims in HRP20140667 be challenged?
Yes, through invalidity proceedings on grounds such as prior art, insufficient disclosure, or obviousness, especially if broader claims are contested.

4. How does the patent landscape affect generic drug entry?
Narrow claims or patent expiry open opportunities for generics. Broad claims can delay entry unless challenged or designed around.

5. What strategic measures can patent holders pursue?
Defense against infringements, filing follow-up patents, pursuing SPCs, and engaging in patent litigation or licensing negotiations are key strategies.


References

[1] Croatian Intellectual Property Office (HIPO): Patent Database
[2] European Patent Office (EPO): Patent Documentation and Guidelines
[3] European Patent Convention (EPC): Legal Framework and Patent Law
[4] Patent Law of Croatia: Summary of Rights and Protections
[5] Industry Reports on Pharmaceutical Patent Strategies

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