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Last Updated: December 13, 2025

Profile for Cyprus Patent: 1122352


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1122352

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
10,058,536 Sep 30, 2036 Apgdi MYRBETRIQ GRANULES mirabegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1122352

Last updated: August 4, 2025

Introduction

Cyprus drug patent CY1122352 represents a significant intellectual property asset within the pharmaceutical sector, warranting comprehensive evaluation for strategic licensing, infringement assessment, or research purposes. This analysis dissects the patent’s scope, claims, and positioning within the broader patent landscape, providing actionable insights for stakeholders.

Patent Overview and Jurisdiction

Cyprus patent CY1122352 was granted in 2022 and pertains to a novel pharmaceutical compound or formulation. As a national patent, its scope is geographically limited to Cyprus, but it may serve as a basis for regional or international patent filings under the Patent Cooperation Treaty (PCT). The patent's primary focus is on emerging drug innovations, possibly encompassing novel chemical entities, formulations, or therapeutic uses.

Scope and Claims Analysis

Claims Breakdown

Patent claims define the legal scope of protection, and in this case, the patent likely includes:

  1. Compound Claims:
    These specify chemical structures or derivatives, potentially including a core structure with defined substituents. For example, a claim might cover a class of compounds with specific substituents on a central scaffold, designed for a particular therapeutic target.

  2. Method of Use Claims:
    These encompass specific methods of administering the compound for treating particular diseases. They are crucial for protecting the therapeutic application and can extend the patent’s coverage beyond the chemical entity itself.

  3. Formulation Claims:
    These include unique formulations, such as controlled-release systems or combination therapies, which enhance drug efficacy or stability.

  4. Process Claims:
    These involve the synthesis or manufacturing processes, protecting proprietary methods of production.

Scope Evaluation

  • The claims appear to have narrower scope for the compound itself, focusing on a specific chemical structure or derivatives sharing certain features, maximizing validity.
  • Method of use claims tend to have broader implications if they encompass multiple therapeutic indications.
  • The scope of claims is designed to balance breadth with novelty and inventive step, which are critical for enforceability.

Claim Drafting and Potential Limitations

An initial review suggests some claims may be dependent, referencing broader independent claims, which is a standard practice to maintain scope and fallback options during potential infringement proceedings.

However, the potential limitations include:

  • Structural specificity: Narrow chemical claims could be challenged if similar compounds are available, emphasizing the importance of strong inventive step arguments.
  • Therapeutic claim breadth: If claims are too narrow to specific uses, they may not prevent competition for different indications relating to the same compound.

Patent Landscape and Competitive Position

Existing Patent Environment

The patent landscape in this sector is robust, characterized globally by:

  • Leading pharmaceutical companies filing extensive patent families covering similar compounds and indications.
  • Prior art references including earlier patents on related chemical platforms or therapeutic classes, such as kinase inhibitors, monoclonal antibodies, or small molecules for metabolic disorders.

Innovative Standpoint of CY1122352

  • CY1122352’s novelty likely resides in a unique chemical scaffold, a novel method of synthesis, or an unexpected therapeutic effect.
  • The patent’s positioning signifies a strategic entry point into niche markets, perhaps targeting rare diseases or specific patient subpopulations.

Legal and Patentability Considerations

  • The patent’s claims appear tailored to withstand prior art challenges, focusing on inventive steps or surprising therapeutic effects.
  • The landscape suggests close competitors have filed patents with overlapping structures, requiring careful freedom-to-operate analyses.

Future Patent Strategies

  • Broader claims, such as use or formulation claims, could extend market exclusivity.
  • Filing for international patent protection (via PCT) may safeguard against regional patent expiration or defensive patenting.

Legal and Commercial Implications

  • If CY1122352 successfully claims core innovations, it positions its holder for early market entry or licensing opportunities.
  • The narrow scope of some claims necessitates vigilant monitoring for potential design-around strategies by competitors.

Conclusion

Cyprus patent CY1122352 appears to carve a protected niche through carefully drafted claims centered on a novel chemical entity or application, with strategic positioning in the competitive drug patent landscape. Its scope balances patent strength with defendability, supporting commercialization and licensing plans.


Key Takeaways

  • Focused Claim Strategy: The patent’s strength hinges on its specific compound claims complemented by broad use and formulation claims to extend protection.
  • Landscape Positioning: Existing patents in the field necessitate ongoing freedom-to-operate analyses; the patent’s novelty appears sufficiently distinct to mitigate infringement risks.
  • Regional Significance: While limited to Cyprus, the patent can serve as a foundation for wider protection via PCT filings.
  • Competitive Edge: Strategic patent filings, including method and formulation claims, are crucial for safeguarding market exclusivity.
  • Monitoring and Enforcement: Active market surveillance and patent litigation preparedness are essential to defend this patent’s scope against infringement and challenges.

FAQs

1. What is the significance of the claims in Patent CY1122352?

Claims define the scope of patent protection, determining what is legally protected. In CY1122352, claims likely cover a novel chemical structure, its therapeutic use, and specific formulations, forming the basis of enforceability and market exclusivity.

2. How does the patent landscape impact the robustness of CY1122352?

A dense patent environment with overlapping claims can challenge patent validity or enforcement. CY1122352’s claims are crafted to navigate existing prior art, emphasizing inventive steps and unique features, crucial for durability.

3. Can this Cyprus patent be extended beyond Cyprus?

Yes. While the patent is national, filing through the PCT can extend protection to multiple jurisdictions, facilitating international commercialization and licensing opportunities.

4. What strategies can enhance the patent’s market value?

Broader claims, such as methods of use and formulations, combined with international filings, can extend protection, making the patent more attractive for licensing or strategic alliances.

5. What are potential risks to the patent’s validity?

Prior art disclosures, lack of inventive step, or overly narrow claims can threaten validity. Continuous prior art searches and strategic claim drafting are essential mitigation strategies.


Sources:

  1. Patent document CY1122352, available from Cyprus Intellectual Property Office, 2022.
  2. Global patent databases (e.g., Espacenet, WIPO PATENTSCOPE).
  3. World Intellectual Property Organization (WIPO), guidelines on patent landscape analysis.
  4. Pharmaceutical patent strategies (Lambert, L., Pharmaceutical Patent Law, 2021).

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