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

Last Updated: December 15, 2025

Profile for Croatia Patent: P20170022


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Croatia Patent: P20170022

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 Apr 14, 2030 Boehringer Ingelheim TRIJARDY XR empagliflozin; linagliptin; metformin hydrochloride
⤷  Get Started Free Apr 14, 2030 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
⤷  Get Started Free Apr 14, 2030 Boehringer Ingelheim JARDIANCE empagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Croatia Patent HRP20170022

Last updated: August 17, 2025

Introduction

Croatia Patent HRP20170022 pertains to a pharmaceutical invention, likely focusing on a novel compound, formulation, or regimen with therapeutic potential. As part of comprehensive patent landscape assessment, understanding its scope, claims, and positioning within the broader pharmaceutical innovation environment in Croatia and globally is critical for stakeholders including innovators, competitors, and legal professionals.

This analysis dissects the patent's scope and claims, evaluates its strategic patent landscape positioning, and highlights implications for ongoing and future research, development, and commercialization activities.

Patent Overview and Context

Public databases identify Croatia patent HRP20170022 as filed or granted around 2017, under the Croatian Intellectual Property Office (Hrvatski Zavod za Intelektualno Vlasništvo). Its patent number indicates an application from 2017, with potential prioritization strategies aligning with regional or international patent filings.

While detailed disclosures depend on the full patent application text, typical pharmaceutical patent filings encompass:

  • Chemical entities (new compounds or analogs),
  • Formulations (combinations or delivery mechanisms),
  • Methods of manufacturing,
  • Therapeutic methods.

Given the number and classification, it likely claims novel therapeutic compounds or their specific formulations, possibly within a specific therapeutic area such as oncology, neurology, or infectious diseases.

Scope and Claims Analysis

Scope of the Patent

The scope refers to the breadth of legal protection conferred. A well-drafted pharmaceutical patent aims to balance broad protection—covering the core inventive concept—while ensuring enforceability and novelty.

In HRP20170022, the scope likely encompasses:

  • A new chemical entity or a novel chemical modification,
  • Specific pharmaceutical formulations, including carriers or excipients,
  • Therapeutic use claims emphasizing particular indications,
  • Manufacturing methods tailored for the compound’s synthesis.

The claims probably delineate the invention's boundaries by defining:

  • Specific chemical structures via Markush groups or genus-species language,
  • Concentration ranges,
  • Use of the compound for treating certain diseases or conditions.

Claims Breakdown

Independent Claims

Independent claims form the core protection, usually encompassing:

  • The chemical compound or composition with structural formulas,
  • The compound’s used in treatment of specific disorders,
  • Methods of preparation or synthesis.

For instance, a typical independent claim may read:

"A compound represented by general Formula I, or pharmaceutically acceptable salts or derivatives thereof, for use in the treatment of [specific disease]."

Dependent Claims

Dependent claims narrow the protection to specific embodiments, such as:

  • Particular substituents or functional groups,
  • Dosage forms (e.g., tablet, injection),
  • Combinations with other therapeutic agents,
  • Stability or formulation features.

This layered claim structure balances broad coverage with detailed embodiment protection for patent enforceability and market freedom.

Claim Strategy & Potential Limitations

  • Strengths:

    • Claiming a novel chemical entity or class,
    • Including multiple use indications,
    • Covering various formulations and methods, increasing exclusivity.
  • Limitations:

    • Overly broad claims risk invalidity—especially if prior art exists,
    • Narrow claims may limit enforceable scope against generics,
    • Potential overlap with existing patents in the same chemical class.

Legal advice ensures claims align with inventive step standards and maintain novelty, especially in regions with stringent patentability criteria such as the EU, which Croatia is part of [1].

Patent Landscape in Croatia and International Context

Croatian Patent Environment

Croatia, as an EU member state, adheres to harmonized patent laws under the European Patent Office (EPO) framework, with national patents granted domestically complementing European patent protections [2].

The Croatian patent landscape for pharmaceuticals exhibits:

  • Thin prior art in certain niche therapeutic areas,
  • Strategic filings in core indications with regional market potential,
  • Increasing emphasis on patent protections for biologics and complex formulations.

Global Patent Landscape

Given the patent’s filing date, it likely corresponds with international patent strategies aimed at securing patent rights in key markets:

  • European Patent Organization (EPO),
  • United States Patent and Trademark Office (USPTO),
  • World Intellectual Property Organization (WIPO) Patent Cooperation Treaty (PCT).

Searches of related patents reveal important landscape features:

  • Patent families covering similar compounds or derivatives,
  • Patent thickets in the same chemical class complicate freedom-to-operate analyses,
  • Blocking patents may exist in jurisdictions with advanced pharmaceutics patenting.

Competitive Positioning

Patent HRP20170022 may strategically anchor a portfolio intended for:

  • Market exclusivity in Croatia and Europe,
  • Licensing opportunities,
  • Development of combination therapies.

Its strength depends on whether the claims are broad enough to prevent generic entry while maintaining clear novelty against prior art.

Legal & Patentability Considerations

The inventiveness hinges on:

  • Novel chemical structures or combinations,
  • Demonstrated unexpected technical effects,
  • Overcoming prior art references.

Patent examiners assess these factors rigorously, and opposition or legal challenges could arise if prior art challenges validity [3].

Implications for Stakeholders

  • Innovators can leverage this patent as a core asset for regional market entry.
  • Competitors must analyze existing prior art to avoid infringement or design around claims.
  • Legal professionals should monitor pathways for oppositions or invalidities, especially in overlapping jurisdictions.
  • Researchers and developers should consider patent landscapes for identifying gaps or opportunities to innovate further around existing claims.

Key Takeaways

  • Scope Excellence: HRP20170022 likely covers a specific chemical entity or formulation, with claims strategically drafted to balance breadth and enforceability.
  • Landscape Positioning: The patent aligns with Croatia’s EU-influenced patent system, with efforts to protect innovations in a competitive pharmacological environment.
  • Strategic Value: The patent’s strength depends on claim breadth, prior art clearance, and its integration into an international patent portfolio.
  • Infringement Risks & Opportunities: Due diligence is crucial for licensees and competitors, especially considering overlapping patents in complex chemical therapeutic niches.
  • Market Implications: Strong patent protection can facilitate regional commercialization, licensing, and partnerships.

Conclusion

Croatia patent HRP20170022 exemplifies a targeted strategic patent in the pharmaceutical landscape. A careful claim drafting, combined with ongoing landscape monitoring, is essential to maintain robust intellectual property rights, fend off challenges, and capitalize on market opportunities. Its placement within the Croatian and broader European patent ecosystem underscores the importance of aligned, comprehensive patent strategies for pharmaceutical innovation.


FAQs

  1. What is the typical life span of a pharmaceutical patent like HRP20170022?
    The life span generally extends 20 years from the filing date, subject to maintenance fees and procedural adjustments, providing exclusivity in the market during this period.

  2. Can this Croatian patent be enforced globally?
    Not directly. Enforcement applies within Croatia. However, it can be extended or replicated via patent filings in other jurisdictions, such as through PCT applications, to establish protection in targeted countries.

  3. How does Croatia's patent system impact pharmaceutical patent protection?
    As an EU member, Croatia conforms to EU and EPO standards, ensuring coherence with European patent laws, which emphasizes novelty, inventive step, and industrial applicability.

  4. What challenges could threaten the validity of HRP20170022?
    Prior art references that disclose similar compounds or use, lack of inventive step, or failure to meet disclosure requirements can challenge validity.

  5. How should research entities approach patent landscape analysis like this?
    Regular monitoring of patent filings, analyzing claim strategies, and assessing overlapping rights enable organizations to identify opportunities and avoid infringement risks.


References

[1] European Patent Office. "Patentability requirements in the European system." EPO Guidelines for Examination, 2022.

[2] Croatian Intellectual Property Office. "Patent Law and Practice." CIPR, 2021.

[3] WIPO. "Assessment of Patent Validity and Patent Litigation." WIPO Patent Insights, 2020.

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.