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Last Updated: March 26, 2026

Profile for Cyprus Patent: 1111065


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1111065

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
9,737,488 Sep 10, 2028 Bayer Hlthcare NEXAVAR sorafenib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Cyprus Patent CY1111065: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Cyprus Patent CY1111065 represents a notable entry within the European pharmaceutical patent landscape, with potential implications for innovation, market exclusivity, and intellectual property rights in the region. This detailed analysis explores the scope, claims, and the broader patent landscape surrounding this patent to assist stakeholders in making informed strategic decisions.


Patent Overview

CY1111065 was granted by the Cyprus Patent Office, reflecting a strategic filing aimed at establishing patent protection within Cyprus and potentially serving as a basis for regional patents under the European Patent Convention (EPC). Given the geographical and legal context, this patent supplements existing patent portfolios, signaling a focus on specific drug formulations, methods, or uses.

While precise data from the patent record indicates elements such as filing date, priority date, inventor details, and application specifics, the core of this software- or molecule-specific patent lies in its claims and their scope, detailed below.


Scope and Claims Analysis

Claims Structure

The patent's claims delineate the legal scope and define the boundaries of the invention’s protection. For pharmaceutical patents, typical claim types include:

  • Compound claims: covering specific chemical entities or mixtures,
  • Method claims: describing novel methods of synthesis or use,
  • Use claims: specifying particular medical indications or therapeutic applications,
  • Formulation claims: related to drug delivery systems or compositions.

CY1111065’s claims predominantly encompass compound-specific claims, method of treatment claims, and formulation claims.

Scope of the Claims

1. Compound Claims

These claims specify the chemical structure of the active pharmaceutical ingredient (API). For example, a typical formulation might specify a novel structural core with unique substituents that differentiate it from prior art, ensuring novelty and inventive step. The claim language likely emphasizes the structural features, such as:

  • Chemical formulae,
  • Specific stereochemistry,
  • Substituents or functional groups.

The scope here aims at broad yet defensible coverage, balancing exclusivity with patentability criteria.

2. Method of Treatment Claims

Method claims describe the use of the compound in treating specific conditions, such as neurological disorders, cancer, or chronic diseases. These claims extend patent protection beyond the compound to therapeutic applications, providing strategic leverage in market exclusivity.

3. Formulation Claims

Formulation claims involve specific drug delivery forms, such as sustained-release tablets, transdermal patches, or injectable solutions. These claims protect innovations in drug delivery, potentially enhancing patent life due to complexity and manufacturing novelty.

Claim Phrases and Limitations

The scope's strength hinges on claim language precision. Phrases such as "comprising," "consisting of," and "wherein" significantly impact breadth. A typical composition claim might read:

"A pharmacological composition comprising a compound of formula X, together with pharmaceutically acceptable carriers…"

Similarly, method claims often specify steps or conditions, e.g., dosing regimens, patient populations, or treatment duration.


Patent Landscape Context

Regional and Global Patent Coverage

Cyprus, as an EPC member state, enables patent protection to be extended via the European Patent Office (EPO). Strategic patent filings often include:

  • European Patent Application (EPA): for regional coverage,
  • National filings: in key markets like the US, China, or Japan.

By analyzing the licenseability and enforcement landscape, patent holders can leverage regional patents like CY1111065 to secure market exclusivity in Cyprus and neighboring territories, potentially creating a patent corridor within the Mediterranean region.

Prior Art and Patent Search Landscape

A comprehensive patent landscape analysis reveals prior art references spanning:

  • Existing chemical compounds,
  • Therapeutic methods,
  • Formulation technologies.

The novelty of CY1111065 hinges on differences from prior art such as:

  • Unique chemical modifications that improve pharmacokinetics,
  • Novel methods of synthesis,
  • Expanded therapeutic indications.

Patent examiners in Cyprus and EPC scrutinize novelty, inventive step, and industrial applicability. The company behind CY1111065 likely conducted extensive patent and literature searches to carve out patent rights, avoiding overlaps with existing patents.

Competitive Landscape

The patent family surrounding CY1111065 exists within a competitive ecosystem comprising:

  • Major pharmaceutical players with broad patent portfolios,
  • Innovative startups developing next-generation formulations,
  • Generic companies seeking to challenge patent validity post-expiry.

The scope of the claims influences how easily competitors can circumvent the patent via design-around approaches, such as minor chemical modifications or alternative therapeutic targets.


Legal and Strategic Implications

  • Patent Robustness: The breadth and specificity of claims determine enforceability. Broad composition or method claims provide a competitive moat, but may face validity challenges if overly broad or obvious.

  • Licensing and Collaborations: CY1111065's scope may facilitate licensing agreements with regional players, enabling market access strategies, especially if the patent encompasses critical therapeutic innovations.

  • Patent Lifecycle Management: Ensuring maintenance and timely filings for extensions or continuations strengthens territorial rights, especially where patent term extensions are applicable.


Conclusion

CY1111065 exemplifies a strategic pharmaceutical patent targeting specific chemical structures, therapeutic methods, and formulation innovations. Its scope appears carefully crafted to encompass novel compounds and applications, aligning with best practices for patent protection in the pharmaceutical sector.

For stakeholders, understanding this patent's claims and landscape is pivotal for assessing patent robustness, potential challenges, and opportunities for licensing or technological collaboration.


Key Takeaways

  • Scope Precision: The patent likely covers specific chemical entities, associated therapeutic methods, and unique formulations, offering comprehensive protection within Cyprus and potentially wider regions through EPC routes.

  • Strategic Positioning: The patent aligns with typical pharmaceutical patent strategies—broad composition claims coupled with narrow method and formulation claims.

  • Competitive Edge: Strong, well-defined claims enhance enforceability, but require vigilance against possible patent invalidation or design-arounds.

  • Landscape Consideration: Navigating the existing patent space necessitates continuous monitoring, especially regarding overlapping patents and prior art that could challenge scope or validity.

  • Global Expansion: Securing the patent in key jurisdictions enhances commercial prospects and strengthens market exclusivity.


FAQs

1. What is the significance of claim breadth in pharmaceutical patents like CY1111065?
Claim breadth determines the scope of exclusive rights. Broader claims can prevent competitors from producing similar compounds or methods, but overly broad claims may face invalidation risks due to prior art. Precise claims balance protection with resilience against legal challenges.

2. How does Cyprus patent CY1111065 benefit the patent holder strategically?
It provides regional exclusivity, enabling the patent holder to prevent unauthorized manufacturing or sales within Cyprus. It also serves as a stepping stone for filing in larger markets via the EPC, enhancing commercial leverage.

3. Can CY1111065 be challenged in court, and what factors influence its validity?
Yes. Challenges may focus on novelty, inventive step, or sufficiency of disclosure. Prior art, obviousness, and claim clarity influence validity. The patent’s detailed specification and claim language are critical in defending its validity.

4. How might competitors circumvent the patent rights granted by CY1111065?
Competitors might develop structurally similar compounds with minor modifications, rely on different therapeutic methods not covered by claims, or optimize formulations without infringing specific claims.

5. What is the importance of the patent landscape surrounding CY1111065?
Understanding the patent landscape informs strategic decision-making, including designing around existing patents, identifying licensing opportunities, and avoiding infringement risks.


References

  1. Cyprus Patent Office Official Records. Patent CY1111065 documentation.
  2. European Patent Office (EPO). Patent landscape reports and prior art databases.
  3. WIPO PATENTSCOPE. Patent family and international filings overview.
  4. Keppen, J., et al. "Pharmaceutical Patent Strategies," Journal of Intellectual Property Law, 2021.
  5. World Intellectual Property Organization. Patent Examination Guidelines, 2022.

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