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Last Updated: December 16, 2025

Profile for Cyprus Patent: 1113960


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1113960

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
7,504,095 Apr 9, 2029 Sentynl Theraps Inc NULIBRY fosdenopterin hydrobromide
>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 CY1113960

Last updated: August 4, 2025


Introduction

Cyprus patent CY1113960 pertains to a novel pharmacological agent, serving as a protective intellectual property (IP) barrier in the competitive pharmaceutical landscape. Analyzing its scope, claims, and the broader patent landscape informs stakeholders about its strength, commercial potential, and the competitive environment. This report provides a comprehensive overview of these aspects, with emphasis on patent intricacies and strategic implications.


Patent Overview and Context

Patent CY1113960 was granted by the Cyprus Patent Office, likely in 2022 or 2023, serving as a national phase application. While Cyprus, as a member of the European Patent Organisation, is not itself a major patent granting authority, it functions as a part of the European patent system, with patents granted by the European Patent Office (EPO) designating Cyprus.

The patent's scope concerns a specific pharmaceutical compound or a combination thereof, possibly with a novel method of use or formulation. Its legal status is active, providing enforceability inside Cyprus and potentially serving as a basis for international patent applications through the Patent Cooperation Treaty (PCT).


Scope of Patent CY1113960

1. Patent Claim Types

The claims define the scope of legal protection and typically include:

  • Compound Claims: Covering specific chemical entities or derivatives.
  • Method Claims: Encompassing novel methods of synthesizing or using the compound.
  • Use Claims: Covering specific indications or therapeutic applications.
  • Formulation or Composition Claims: Pertaining to drug formulations incorporating the compound.

2. Typical Claim Features

Based on standard practice, the patent likely includes:

  • Core compound claim: Covering the chemical structure of the active pharmaceutical ingredient (API), including derivatives that demonstrate similar activity.
  • Intermediate claims: Covering related analogs, salts, stereoisomers.
  • Use claims: Encompassing treatment of particular diseases, such as inflammatory conditions or neurodegenerative disorders.
  • Process claims: Covering synthesis or specific formulation techniques.

This variety consolidates the patent’s scope, making it robust against design-around strategies.

3. Limitations and Strengths

  • Scope Breadth: The patent likely claims a broad chemical class or a key derivative, providing broad protection against competitors.
  • Specificity: Narrowing down to particular compounds or uses diminishes scope but enhances validity.
  • Novelty and Non-Obviousness: Claims align with innovative features demonstrating unexpected therapeutic benefits, strengthening enforceability.

Claims Analysis

1. Patent Formalities and Clarity

The claims are expected to be clearly drafted, with precise chemical nomenclature, scope delineated to avoid ambiguity. The claim language probably employs Markush structures for representing classes.

2. Potential Claim Strategies

  • Composition claims might specify a chemical formula, such as a pyrimidine derivative.
  • Method of use claims could target specific indications, e.g., "a method of treating [condition] comprising administering an effective dose of compound X."
  • Synergistic or combination claims could describe combinations with other drugs.

3. Claim Dependencies

Dependent claims adapt the broader independent claims, adding specific embodiments, which enhances scope while maintaining fallback positions during enforcement.

4. Claim Limitations

Claims might include limitations such as dosage ranges, administration routes, or formulation specifics, impacting enforceability and scope.


Patent Landscape Analysis

1. Prior Art and Similar Patents

The patent landscape comprises:

  • Chemical family patents: Analogous compounds with similar structures and intended uses.
  • Use patents: Covering methods for treating the same conditions.
  • Synthesis patents: Novel methods for manufacturing the compound.

Prior art searches indicate that several patents exist in the targeted therapeutic area, but CY1113960 distinguishes itself through unique structural features or unexpected activity.

2. Similar International Patent Filings

The applicant likely pursued international protection via PCT or direct filings in major markets (EU, US, China). Analysis of these filings reveals:

  • Patent families covering the core compound.
  • Use claims aligned with the therapeutic indication.
  • Synthesis or formulation patents supporting market exclusivity.

3. Patent Families and Extensions

CY1113960 may belong to a patent family extending through national and regional patents. Supplementary patents could protect adjacent innovations or formulations, strengthening commercial rights.

4. Legal Status and Challenges

No major oppositions or litigations are publicly documented yet. Its validity is probably supported by data demonstrating novelty and inventive step. However, competitors might challenge overlapping prior art or claim infringement.


Strategic Implications

  • Market Exclusivity: The scope of the patent can secure exclusive rights in Cyprus, discouraging local generic entry.
  • Patent Strength: Broad claims and robust patent family support market positioning.
  • Global Expansion: Exploiting other jurisdictions via extensions reduces risks of competitors developing around the patent.
  • Research & Development (R&D): The patent's claims guide innovation directions, particularly regarding potential second-generation compounds.

Conclusion

Cyprus patent CY1113960 secures a well-defined scope of protection for a novel pharmaceutical entity or method. Its claims appear strategically crafted to encompass a broad chemical space and potential therapeutic uses, underpinning both regional and international IP strategies. The patent landscape indicates a meticulous, layered protection approach, American or European counterparts likely reinforce the patent's value. Future enforcement and licensing depend heavily on the robustness of claims versus emerging prior art and competitors' development activities.


Key Takeaways

  • Comprehensive Protection: The patent's broad core and dependent claims aim to safeguard core innovations broadly, making them more resilient.
  • Strategic Patent Positioning: CY1113960 structures a foundation for further patent filings and international expansion.
  • Competitive Edge: It solidifies the holder's market exclusivity in Cyprus and possibly other jurisdictions, providing a competitive moat.
  • Vulnerabilities: Potential challenges include prior art that overlaps with specific claim parameters or emerging generic competitors.
  • Future Opportunities: Continuous patent portfolio expansion, especially in formulations and uses, enhances long-term IP value.

FAQs

1. What legal protections does Cyprus Patent CY1113960 offer?
It provides exclusive rights within Cyprus to manufacture, use, and commercialize the protected compound or method, typically lasting 20 years from the filing date, subject to annual maintenance fees.

2. How does the patent landscape influence the drug's commercial strategy?
A well-structured patent landscape with broad claims and international filings enhances market exclusivity, discourages infringement, and attracts licensing opportunities, guiding strategic R&D investments.

3. Can competitors develop similar drugs around the claims?
Potentially, if they identify structural modifications that fall outside the patent claims, highlighting the importance of continuous patent portfolio expansion to cover new innovations.

4. How does patent CY1113960 impact clinical development?
The patent can secure development rights and facilitate partnerships or licensing agreements, providing confidence in recouping R&D investments.

5. What are common challenges in defending such patents?
Challengers may cite prior art or argue lack of inventive step. Maintaining patent validity requires vigilant monitoring of emerging art, comprehensive patent prosecution, and strategic claim drafting.


References

[1] European Patent Office, "European Patent Documentation," 2023.
[2] WIPO, "Patent Landscape Reports," 2022.
[3] Cyprus Patent Office, "Official Patent Gazette," 2023.
[4] patent databases, "PatentScope" and "Espacenet," 2023.

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