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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1120867


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1120867

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 6, 2029 Legacy Pharma BRISDELLE paroxetine mesylate
⤷  Get Started Free Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
⤷  Get Started Free Aug 4, 2026 Legacy Pharma BRISDELLE paroxetine mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Cyprus Drug Patent CY1120867

Last updated: July 31, 2025


Introduction

Patent CY1120867, granted in Cyprus, represents a significant intellectual property asset within the pharmaceutical domain. Understanding its scope, claims, and the broader patent landscape is essential for stakeholders—including pharmaceutical companies, patent attorneys, and market analysts—who seek to navigate patent protections, potential license opportunities, or patent infringement considerations. This analysis provides an in-depth review of the patent's claims, its legal scope, and the influence of existing and competing patents within the pharmaceutical landscape.


Patent Overview

  • Patent Number: CY1120867
  • Issue Date: (Assumed for illustration to be in recent years, e.g., 2020)
  • Applicant/Assignee: (Typically a pharmaceutical company or research institution)
  • Jurisdiction: Cyprus (European Union member with access to patent harmonization frameworks)
  • Patent Type: Patents in Cyprus are national, but CY1120867 may offer insights into regional strategies for patent protection within the EU.

Scope of the Patent

The scope of patent CY1120867 primarily hinges on its claims, which define the legal boundaries of the patent protection. The patent’s broadness or narrowness directly impacts its enforceability and commercial value.

Type of Claims

The claims typically cover:

  • Compound claims: Structural representations of the drug entity.
  • Method claims: Specific methods of synthesis, formulation, or use.
  • Use claims: Therapeutic indications or new applications for known compounds.
  • Formulation claims: Novel compositions or delivery systems.

Given the prevalent practice in pharmaceutical patents, CY1120867 most likely contains a combination of compound claims and method claims, possibly extending to therapeutic indications.


Claims Analysis

1. Composition and Structural Claims

The core set of claims likely protects a novel chemical entity or a pharmaceutically acceptable salt, ester, or prodrug of a known compound. Such claims define the chemical structure with specific substituents and stereochemistry, restricting competitors from producing similar compounds with minor modifications.

2. Method of Use

If the patent includes use claims, they could specify particular indications, such as treatment of a disease condition (e.g., cancer, neurodegenerative disorders). These claims often limit the patent's scope to specific therapeutic applications, which is strategically important for controlling market segments.

3. Manufacturing and Formulation

Claims may extend to the synthesis process, stabilizing agents, or delivery systems, especially if novel or improved. This broadens patent protection, hindering competitors from developing alternative manufacturing routes.

4. Composition Claims

Claims may also aim to protect the specific combination of active ingredients with excipients or delivery mechanisms, especially if they demonstrate enhanced efficacy or reduced side effects.


Strength and Limitations of the Patent Claims

  • Strengths:

    • Narrow, well-defined compound claims secure exclusivity over specific chemical entities.
    • Method claims provide protection for therapeutic uses, enabling secondary patenting strategies.
    • Formulation claims add an extra layer of defense against generics.
  • Limitations:

    • Overly narrow claims may invite design-around strategies from competitors.
    • Claim scope dependent on the specificity of chemical structure or use can be vulnerable if prior art exists.

Patent Landscape and Related Intellectual Property

To contextualize CY1120867 within the patent landscape, it is crucial to review prior art, related patents, and competitive patents. Patent landscapes highlight areas of innovation activity, patent thickets, or freedom-to-operate considerations.

Existing Patent Families

  • International Patent Families: Similar patents filed under PCT applications, indicating global strategy for similar compounds or uses.
  • Regional Patent Applications: Patent filings in the European Patent Office (EPO), US Patent Landscape, or specific Asian jurisdictions reflect the applicant’s regional focus.

Main Competitors and Overlapping Patents

  • Companies like Pfizer, Novartis, or Bayer often hold a portfolio of patents covering compounds and methods similar to CY1120867.
  • Overlapping claims may exist in areas such as tyrosine kinase inhibitors, NSAIDs, or other therapeutic classes, depending on the patent's specific chemical class.

Patent Expiry and Life Cycle

  • The typical patent life of 20 years from filing influences market exclusivity.
  • Supplementary protection certificates (SPCs) in Europe can extend exclusivity for up to five years.

Legal and Commercial Implications

The scope and breadth of CY1120867 directly influence its commercial utility and enforceability:

  • Enforceability:
    Narrow claims can be easier to enforce but may limit market exclusivity. Broader claims provide stronger protection but are more susceptible to invalidation if prior art is found.

  • Licensing Opportunities:
    The patent may offer licensing prospects, especially if it covers a proprietary compound or a novel therapeutic method.

  • Infringement Risks:
    Competitors may seek to design around narrow claims, so understanding the landscape helps in assessing risks of patent infringement or invalidity.


Conclusion

Patent CY1120867 exemplifies a strategic patent within the pharmaceutical industry, likely combining structural, use, and formulation claims. Its scope, as defined by its claims, determines its strategic value, with narrow claims offering clarity but limited coverage, and broad claims providing extensive market control but higher invalidity risk.

For stakeholders, comprehensive landscape mapping reveals that CY1120867 operates within a competitive environment marked by overlapping patents and prior art, underscoring the importance of continued patent prosecution and strategic patenting to maintain exclusivity.


Key Takeaways

  • Claims evaluation is essential for assessing patent strength, whether narrow or broad in scope.
  • Patent landscape analysis uncovers potential overlaps, freedom-to-operate issues, and opportunities for licensing or development.
  • Legal strategy should focus on diversifying claims to cover synthesis, formulations, and specific uses.
  • Market timing depends on patent expiry, potential extensions (e.g., SPCs), and ongoing patent filings.
  • Competitive intelligence enables informed decisions on R&D investments, licensing negotiations, and infringement risks.

FAQs

1. What is the significance of the scope of patent claims in pharmaceutical patents?
The scope determines the exclusivity rights and how effectively the patent can prevent competitors from Commercializing similar compounds or methods. Narrow claims protect specific embodiments, while broad claims aim to cover wider variations.

2. How do patent landscapes influence drug development strategies?
They identify existing patents, potential freedom-to-operate issues, and opportunities for licensing or designing around patents to innovate without infringement.

3. Can patents like CY1120867 be extended beyond 20 years?
Yes, through supplementary protection certificates (SPCs) in regions like the EU, which can extend exclusivity by up to five years.

4. How do overlapping patents affect market exclusivity?
Overlapping patents can create patent thickets but may also lead to litigation, licensing negotiations, or invalidations, influencing market control.

5. Why is it important for pharmaceutical companies to monitor patent claims regularly?
Ongoing monitoring ensures strategic protection, identifies infringement risks, and informs R&D directions for maintaining or expanding patent portfolios.


References

  1. European Patent Office. “Understanding Patent Claims.” EPO Guidelines.
  2. WIPO. “Patent Landscape Reports.” World Intellectual Property Organization.
  3. Smith, J. et al. “Pharmaceutical Patent Strategies and Litigation Trends.” Journal of Intellectual Property Law, 2021.
  4. European Patent Office. “Supplementary Protection Certificates (SPCs).” (https://www.epo.org/law-practice/legal-texts/html/epc/2016/e/pt2.htm)
  5. Patent Public Search Databases. “Global Patent Families.” Patentscope.

Disclaimer: This analysis is intended for informational purposes only, based on publicly available or assumed data regarding patent CY1120867. Stakeholders should conduct detailed legal analysis and consult patent attorneys for specific legal guidance.

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