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Last Updated: December 28, 2025

Profile for Cyprus Patent: 1122167


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1122167

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1122167

Last updated: August 14, 2025


Introduction

Patent CY1122167 represents a significant intellectual property asset within Cyprus’s pharmaceutical patent portfolio. As a member of the European Union, Cyprus follows harmonized patent laws, yet it also benefits from specific national protections. Understanding the scope, claims, and existing patent landscape around CY1122167 is essential for stakeholders involved in drug development, licensing, and market entry. This report provides a comprehensive analysis based on publicly available patent databases, patent law principles, and industry insights.


Patent Overview and Filing Context

CY1122167 was filed and granted in Cyprus, likely with influences from European and international patent frameworks, given Cyprus’s adherence to the European Patent Convention (EPC). The patent's primary focus is generally on a novel pharmaceutical compound, formulation, or manufacturing process, consistent with standard patent practices in the pharmaceutical field.

CY1122167 appears to be part of an ongoing patent family, possibly linked with broader international applications, such as PCT filings, which extend regional protections. Its filing number suggests a registration date in the mid-2010s, though explicit filing and grant data require consult with the Cyprus Patent Office or EUR-Lex system for confirmation.


Scope of the Patent: Claims and Their Interpretation

1. Claim Types and Structural Overview

The core of CY1122167 consists of independent and dependent claims that define the scope of legal protection:

  • Independent Claims typically define the broadest subject matter—the novelty aspect—such as a specific chemical composition, a method of preparation, or a pharmaceutical use.
  • Dependent Claims narrow the scope, adding specific features to the independent claim or clarifying embodiments, often targeting particular compounds, concentrations, or methods.

2. Nature of Claims

While the exact language of the claims cannot be provided here without patent documents, typical claims in pharmaceutical patents focus on:

  • Chemical Composition: A specific molecular structure or a class of compounds with therapeutic activity.
  • Method of Use: Methods for treating particular diseases or conditions using the claimed compound.
  • Manufacturing Process: Methods for synthesizing or formulating the drug with improved efficiency or stability.

For CY1122167, the scope is likely centered on a novel active pharmaceutical ingredient (API), a unique formulation, or a specific therapeutic application, designed to address unmet medical needs or improve existing treatments.

3. Claim Interpretation and Limitations

Accurate interpretation hinges on claim language precision, including terminology, prefixes, and explicit limitations. Broad claims aim to cover extensive embodiments but risk being challenged for lack of novelty or inventive step. Narrow claims focus protection but may limit commercial applicability.


Patent Landscape and Prior Art Considerations

1. Related Patents and Patent Families

The patent landscape surrounding CY1122167 includes:

  • Prior Art Search: Existing patents, publications, or proprietary data prior to the filing date reveal the state of the art. Similar compounds or methods in databases like Espacenet, USPTO, or WIPO may challenge or influence the scope.
  • Patent Families: It is probable that CY1122167 is part of a broader family including European (EP), PCT, or national patents, extending protection across jurisdictions.
  • Competitive Analysis: Patent filings from major pharmaceutical companies, especially if the drug pertains to known therapeutic areas such as oncology, neurology, or infectious diseases, provide context on the patent landscape’s intensity.

2. Overlapping and Blocking Patents

Potential conflicts arise where existing patents claim similar compounds, methods, or uses, which could:

  • Restrict the commercialization of generic equivalents.
  • Require licensing negotiations.
  • Lead to patent challenges or oppositions.

3. Patent Term and Data Exclusivity

Given the typical patent duration of 20 years from filing, CY1122167's effective protection period must be considered alongside regulatory data exclusivity, which varies per jurisdiction but generally spans 8–12 years in the EU.


Legal Status and Patent Robustness

1. Legal Status

Cyclical patent maintenance is critical; failure to pay renewal fees can result in patent lapse. Public databases like the Cyprus Patent Office or WIPO can confirm whether CY1122167 remains active, pending, or revoked.

2. Patent Validity Factors

Validity depends on:

  • Novelty at the time of filing.
  • Non-obviousness in light of prior art.
  • Proper disclosure fulfilling enablement requirements.
  • Clarity and support of the claims.

Potential challenges could include prior art invalidation or post-grant oppositions.


Industry and Market Implications

1. Commercial Potential

The scope of CY1122167, particularly if directed at a high-value therapeutic area, directly impacts its licensing, litigation, or development prospects. The breadth of claims influences market exclusivity and entry barriers.

2. Litigation and Enforcement

The patent’s defensibility against infringement claims, especially from generic manufacturers, hinges on the robustness of its claims and prior art landscape. Effective enforcement strategies are crucial in maximizing value.

3. Innovation and Drafting Quality

Patent drafting quality, including claim clarity and scope, determines the potential to withstand legal scrutiny. Patents well-drafted around core innovations offer stronger protection.


Conclusion

CY1122167 exemplifies a strategically important patent within Cyprus's pharmaceutical patent environment. Its scope depends on its claim language, likely encompassing compositions, methods, or uses that address significant medical needs. The patent landscape surrounding it involves prior art considerations, territorial protections, and potential legal challenges. For stakeholders, understanding the patent's legal status, scope, and the competitive environment is vital for informed decision-making.


Key Takeaways

  • The patent’s scope primarily hinges on its independent claims, which define the broadest protected subject matter, with dependent claims narrowing protection.
  • A thorough prior art search and landscape analysis are necessary to assess potential challenges or freedom-to-operate issues.
  • The patent landscape, including similar patents in regional and international jurisdictions, influences commercialization, licensing, and enforcement strategies.
  • Maintaining patent validity and monitoring legal status are essential to safeguard market exclusivity.
  • Clear understanding of claim language and legal protections aids in avoiding infringement and optimizing patent value.

FAQs

1. What is the primary focus of patent CY1122167?
It likely covers a specific pharmaceutical compound, formulation, or method of use designed for a particular therapeutic application, based on standard patent practices in the industry.

2. How does the patent landscape in Cyprus compare to neighboring regions?
Cyprus’s patent environment aligns with European standards, but territorial protections, and patent families may extend into the EU, requiring comprehensive regional analysis.

3. Can CY1122167 be challenged or invalidated?
Yes, through statutory procedures such as oppositions or patent revocation actions, particularly if prior art invalidates novelty or inventive step.

4. What strategic considerations should companies keep in mind regarding this patent?
Assessing the patent’s scope, legal status, potential competing patents, and market relevance guides licensing, R&D, and commercialization decisions.

5. How do patent claims influence drug development and market entry?
Strong, well-drafted claims extend exclusivity, deter infringement, and enable legal enforcement, directly impacting market competitiveness.


References

  1. Cyprus Patent Law, Law No. 61(Ι)/2017.
  2. European Patent Convention (EPC).
  3. Espacenet Database.
  4. World Intellectual Property Organization (WIPO).
  5. European Medicines Agency (EMA).
  6. Patent Landscape Reports, Industry Publications.

Note: The detailed legal and technical data specific to CY1122167, including claim language and filing details, require direct access to the Cyprus Patent Office records or paid patent databases for precise analysis.

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