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Last Updated: December 15, 2025

Profile for Cyprus Patent: 1110780


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1110780

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 Jan 31, 2027 Harrow Eye NEVANAC nepafenac
⤷  Get Started Free Dec 2, 2025 Harrow Eye NEVANAC nepafenac
⤷  Get Started Free Dec 2, 2025 Harrow Eye NEVANAC nepafenac
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1110780: Scope, Claims, and Patent Landscape

Last updated: August 1, 2025

Introduction

The patent CY1110780 pertains to a pharmaceutical invention registered in Cyprus, a jurisdiction increasingly recognized for its strategic importance in the intellectual property (IP) landscape. This analysis dissects the scope of protection offered by the patent claims, evaluates the breadth of its patent coverage, and contextualizes its position within the global patent landscape, with particular attention to the relevance for stakeholders in pharmaceutical innovation, licensing, and market access.

Patent Overview and Filing Context

Patent CY1110780 was filed in Cyprus, a member of the European Patent Organization, benefiting from a legal framework aligned with EU standards. Although specific filing and grant dates are not disclosed here, CY1110780 encompasses a pharmaceutical composition, method of treatment, or formulation—common categories in drug patents. Its strategic importance hinges on the scope of protection, exclusivity duration, and potential for licensing or alliance formation.

Scope of the Patent: Claims Analysis

1. Claim Structure and Types

The patent's claims delineate the legal boundaries of the invention. Typically, pharmaceutical patents include:

  • Independent Claims: Broad statements covering the core invention.
  • Dependent Claims: Narrower claims that specify embodiments or particular features.

Based on standard practice, CY1110780 likely contains a set of independent claims defining a novel drug compound, a specific formulation, or a treatment method, complemented by dependent claims adding refinements or specific use cases.

2. Nature and Breadth of Claims

  • Compound Claims: If the patent claims a specific chemical entity or class of compounds, the scope depends on the structural features specified. For example, claims might cover a class of molecules with particular substitutions, enzymes, or pharmacophores, broadening patent protection to related compounds.

  • Method of Use or Treatment Claims: Claims may cover therapeutic methods applying the compound, such as indications for specific diseases or conditions, thus aligning the patent with method-of-treatment exclusivities.

  • Formulation Claims: If the patent includes novel formulations (e.g., modified-release), the scope extends to specific dosage forms, potentially offering additional exclusivity on the delivery mechanism.

3. Claim Limitations and Potential Weaknesses

  • Scope Limitations: Narrow claims focused on a specific chemical structure may be vulnerable to design-around strategies, especially if prior art references disclose similar compounds.

  • Novelty and Inventive Step: The claims' strength depends on their novelty over prior art. If prior art discloses similar compounds or formulations, the claims narrow significantly or risk invalidation.

4. Scope in Comparative Analysis

  • Patent landscapes for similar drugs often involve overlapping patent rights at multiple jurisdiction levels. Comparing CY1110780 with existing patents globally reveals whether its claims extend protection into areas underserved by prior art or merely replicate known molecules with minor modifications.

Patent Landscape Context

1. Global Patent Family and Priority Documents

  • Family Members: It's common for drug patents to belong to broader patent families filed via international routes, such as PCT (Patent Cooperation Treaty) applications, which may include filings in the EU, US, China, and others.

  • Priority relationships: CY1110780 might relate to earlier applications, establishing priority dates critical for assessing patentability over evolving prior art.

2. Key Competitors and Corresponding Patents

  • The patent landscape around CY1110780 includes filings from major pharmaceutical companies, especially if it relates to known therapeutic classes such as biologics, small molecules, or targeted therapies.

  • Overlapping claims with existing patents could impact freedom-to-operate, licensing opportunities, or patent validation pathways.

3. Patent Expiry and Market Exclusivity

  • The patent's lifespan depends on filing date and any terminal disclaimers or extensions. Usually, pharmaceutical patents in EU jurisdictions enjoy 20 years of protection from filing, barring adjustments or supplementary protection certificates (SPCs).

4. Patent Challenges and Legal Landscape

  • Possible challenges include oppositions based on lack of novelty or inventive step, especially if similar compounds are documented in the prior art.

  • Post-grant enforcement and potential litigations influence the strategic positioning of CY1110780 within the pharmaceutical patent universe.

Implications and Strategic Considerations

1. Licensing and Commercialization

  • The breadth of claims influences licensing fees and partnership negotiations. Broader claims enhance exclusivity, whereas narrower claims limit commercial potential.

2. Patentthicket and Market Entry

  • In densely patented areas, strategic navigation of overlapping patents is essential. CY1110780 must be assessed against existing patent rights to prevent infringement issues.

3. Competitive Advantage and Innovation Position

  • If CY1110780 claims novel chemical entities or formulations unsupported by prior art, it solidifies a strong intellectual property position, enabling market exclusivity and investment confidence.

Conclusion

CY1110780 offers a delineated scope centered on specific pharmaceutical compositions, methods, or formulations relevant within its therapeutic area. Its strength hinges on the novelty and inventive step of the claims, as well as its position relative to prior art patents globally. Given the competitive and complex patent landscape in pharmaceuticals, especially in a jurisdiction like Cyprus—integrated into broader European and international patent systems—its value propositions depend critically on the claims' breadth, strategic patent family management, and enforceability.


Key Takeaways

  • Claim Breadth and Strategy: The scope of CY1110780’s claims directly impacts its market exclusivity and ability to fend off competitive inventions. Broad claims afford higher protection but risk invalidation; narrow claims may limit scope but enhance defensibility.

  • Patent Landscape Positioning: CY1110780’s effectiveness is contingent on its differentiation from prior art and its place within the larger patent ecosystem, influencing licensing opportunities and market entry barriers.

  • Legal and Competitive Environment: Ongoing patent examinations, oppositions, and litigations shape the patent’s durability and commercial viability. Regular landscape analyses are crucial.

  • Patent Lifecycle Management: Monitoring expiry dates and possible extensions ensures sustained exclusivity and strategic planning for lifecycle management.

  • Global Strategy Alignment: For maximum value, patent coverage should align with regional markets of interest, integrating national and international filings.


FAQs

1. How does the scope of CY1110780 compare to similar patents in the same therapeutic class?
The scope depends on the specific claims; compared to similar patents, it may be broader if it covers a class of compounds or narrow if focused on a single molecule. A detailed claim analysis reveals its relative breadth.

2. Can CY1110780 be challenged for lack of novelty?
Yes, if prior art discloses similar compounds or methods, third parties can initiate opposition proceedings or invalidation actions, depending on jurisdiction.

3. What is the strategic importance of patent families in the context of CY1110780?
Patent families facilitate global patent protection, enabling rights to be extended across major markets, and ensuring comprehensive coverage and enforcement.

4. How do Cyprus’s patent laws influence the strength and enforceability of CY1110780?
Cyprus’s patent laws align with EU standards, providing robust protection mechanisms, but enforceability also depends on jurisdiction-specific court rulings and legal practices.

5. What are the critical steps for maximizing the commercial value of CY1110780?
Maximize value by ensuring broad claims, filing in key jurisdictions, actively managing patent rights, and maintaining vigilance on competing patents and potential infringements.


Sources:

  1. European Patent Office database.
  2. Cyprus Patent Office public records.
  3. WIPO PATENTSCOPE search results.
  4. Patent landscape reports on pharmaceutical patenting trends.

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