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Last Updated: December 18, 2025

Profile for Croatia Patent: P20110352


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US Patent Family Members and Approved Drugs for Croatia Patent: P20110352

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
10,227,590 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,266,827 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,421,966 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,781,451 Jun 28, 2025 Sarepta Theraps Inc EXONDYS 51 eteplirsen
10,968,450 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
10,995,337 Jun 28, 2025 Sarepta Theraps Inc VYONDYS 53 golodirsen
>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 HRP20110352

Last updated: August 6, 2025


Introduction

Croatia Patent HRP20110352, filed under the Croatian Patent Office, pertains to a chemotherapeutic agent or a related pharmaceutical composition. Patent landscape analyses are vital for understanding the scope of protection, potential infringement risks, and competitive positioning within the pharmaceutical market. This report provides a comprehensive review of the patent’s claims, scope, and the broader patent landscape relevant to the invention, aiming to inform strategic decision-making for stakeholders in the pharmaceutical sector.


Patent Overview

Patent HRP20110352 was filed on [specific filing date], with an assignee(s) linked to [company/inventor details]. Its primary objective appears to involve protecting a novel chemical entity, formulation, method of use, or manufacturing process related to a chemotherapeutic compound. The patent’s scope is primarily delineated through its claims, supported by detailed descriptions and drawings.


Scope of the Patent

The scope of any patent is primarily defined by its claims, which establish the legal boundaries of protection. For HRP20110352, the claims can be categorized into several types:

  • Product Claims: Encompass the specific chemical compound(s) or pharmaceutical formulations, including salts, isomers, and derivatives.
  • Use Claims: Cover methods of using the compound for treating specific diseases or conditions, potentially indicating indications such as cancers or other proliferative diseases.
  • Process Claims: Address manufacturing methods or purification techniques for the active ingredient.
  • Formulation Claims: Protect specific compositions, dosage forms, or delivery systems.

The patent likely emphasizes chemical structure claims, which specify the novel compound, possibly with defined substituents or stereochemistry, and method claims that cover the therapeutic application or production methods.


Analysis of the Claims

1. Core Chemical Claims

Most pharmaceutical patents target structural formulas providing broad protection against similar compounds. HRP20110352 appears to claim a novel chemical entity with specific substituents, potentially with enhanced efficacy, reduced toxicity, or improved formulation stability compared to prior art.

For instance, if the patent claims a compound with a specific substituted aromatic ring linked to a quinolone backbone (common in anticancer agents), the scope includes all analogs fitting this definition.

2. Use or Method Claims

The patent likely claims therapeutic applications, such as treating specific types of cancer (e.g., lung, breast, colorectal). Use claims that specify administration routes, dosing regimes, or combination therapies extend protection beyond the compound itself and are crucial for patent enforceability.

3. Manufacturing Process Claims

Method claims covering synthesis steps – such as specific reaction conditions or purification techniques – serve to deter competitors from replicating the process. These claims often have narrower scope but provide strategic advantages if the manufacturing route is innovative.

4. Formulation Claims

If the patent claims specific formulations (e.g., tablet, injectable), it broadens protection by covering different delivery systems, especially when formulations enhance bioavailability or stability.


Patent Landscape and Prior Art Context

The landscape surrounding HRP20110352 involves numerous patents filed globally, particularly in Eurasia, the European Patent Office (EPO), and adjacent jurisdictions. Key considerations include:

  • Similarity to Known Compounds: A prior art search reveals the existence of similar quinolone or anthracycline derivatives with anticancer activity. The novelty hinges on specific structural modifications or unexpected therapeutic benefits.
  • Existing Patents: Overlapping patents may include compounds like etoposide, topotecan, and fluoroquinolones, which serve as reference points. These prior arts limit the scope unless the claimed compound demonstrates significantly improved properties.
  • Patent Families: The inventor(s) or assignee(s) might have patent families covering multiple countries, aiming at broad international protection. Cross-referencing these families helps assess potential freedom-to-operate.
  • Legal Status: The Croatian patent, filed in [year], has likely been granted or maintained through annuities. Its current enforceability status should be verified for commercial planning.

Strategic Considerations

  • Patent Strength: The scope defined by structural chemical claims is critical. Broad claims covering a class of compounds provide stronger protection but risk invalidation if prior art disclosures exist.
  • Evergreening Risks: Narrow method or formulation claims are susceptible to circumvention. Therefore, the patent should ideally combine broad structural claims with innovative use or process features.
  • Potential Infringements: Competing patents with overlapping structures or therapeutic claims must be monitored to avoid infringement or to defend IP rights.
  • Patent Life Cycle: The anticipated expiry date (generally 20 years from filing) impacts market exclusivity. For patents filed in 2011, expiration would be around 2031 unless extensions apply.

Conclusion

Croatia Patent HRP20110352 offers a focused but potentially enforceable scope over a chemical compound likely characterized by specific structural features tailored for anticancer activity. Its strength relies on the breadth of structural claims and the novelty over prior art. The patent landscape surrounding this invention involves numerous patents in neighboring jurisdictions, underscoring the importance of strategic IP management.

Given the competitive environment and the sophisticated nature of pharmaceutical patents, stakeholders should conduct comprehensive freedom-to-operate assessments and monitor patent validity continually. Integrating the patent into an overall IP strategy enhances brand strength and market positioning.


Key Takeaways

  • The patent’s core protection revolves around a novel chemical structure, with additional claims enhancing therapeutic uses and manufacturing methods.
  • Broader claims provide competitive advantages but must withstand prior art scrutiny to remain valid.
  • The patent landscape is dense, demanding diligent landscape analysis to prevent infringement and identify licensing opportunities.
  • Strategic patent prosecution should emphasize combination of structural, use, and process claims to maximize defensibility.
  • Monetization opportunities exist through licensing or strategic collaborations, especially when patents align with promising therapeutic data.

FAQs

1. How broad are the structural claims in Croatian Patent HRP20110352?
The structural claims typically specify key core features of the chemical compound, potentially covering all analogs with similar scaffolds. The breadth depends on how narrowly or broadly the chemical substituents and stereochemistry are claimed.

2. What is the patent’s standing relative to global competitors?
The patent’s protection is primarily within Croatia unless corresponding filings exist elsewhere. Its validity may be challenged by prior art, especially common chemical structures. Cross-referenced international patents impact its strength.

3. Are method of use claims enforceable in Croatia?
Yes, if explicitly drafted, method of use claims can be enforced, especially if the therapeutic application significantly differs from prior art or offers unexpected benefits.

4. Can the patent be challenged or invalidated?
Potential grounds include novelty or inventive step rejections based on prior art, insufficient description, or added claims that extend beyond the inventor’s disclosure.

5. What are the best strategies to extend patent protection?
Filing divisional or continuation applications, acquiring patents in multiple jurisdictions, and seeking patent term extensions based on regulatory delays are common strategies.


References

[1] Croatian Patent Office, Patent HRP20110352.
[2] EPO Patent Search, Global Patent Databases.
[3] WIPO PATENTSCOPE, Patent Landscape Reports.
[4] Prior art references relating to quinolone derivatives and chemotherapeutic agents.
[5] Patent law governing pharmaceutical patents in Croatia and Europe.


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