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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1115292


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1115292

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
8,278,292 Jul 6, 2027 Leo Labs PICATO ingenol mebutate
8,372,827 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,372,828 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,377,919 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,536,163 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,716,271 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,735,375 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
>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 CY1115292

Last updated: August 14, 2025

Introduction

Patent CY1115292, filed in Cyprus, pertains to a specific pharmaceutical invention. This patent's scope, claims, and the overall patent landscape are critical for understanding its commercial impact, potential for licensing, or enforcement actions. This analysis dissects the patent's claims, elucidates its scope, examines the landscape context, and evaluates its strategic importance within the pharmaceutical sector.


Patent Overview

CY1115292 was granted or filed based on a novel chemical entity, formulation, or therapeutic method. While specific filing details are segmentally unavailable in the prompt, typical patent documents encompass:

  • A detailed description of the invention.
  • Claims that delineate the legal scope.
  • Drawings or descriptions illustrating the molecule, formulation, or method.

For this analysis, the primary focus remains on the claims and scope and how they position CY1115292 within the broader patent landscape.


Scope and Claims Analysis

Claims Structure

Patent claims define the legal boundary of the invention, highlighting the aspects deemed new and inventive. They are typically divided into:

  • Independent Claims: Broadest scope, outlining core inventive features.
  • Dependent Claims: Narrower, adding specific features or embodiments.

Analysis of Key Claims

Without the explicit text, the following is a hypothetical framework based on standard pharmaceutical patents:

  • Chemical Compound Claims: Likely define the active pharmaceutical ingredient (API) structure, including specific chemical moieties, stereochemical configurations, or derivatives.
  • Method of Use Claims: Cover specific therapeutic applications, such as indications for neurological, oncological, or infectious diseases.
  • Formulation Claims: Encompass particular formulations such as tablets, injectables, or controlled-release systems.
  • Manufacturing Claims: Address specific synthesis routes, purification methods, or stability improvements.

The breadth of core claims determines the patent’s strength:

  • If the independent claim broadly covers a chemical class with minimal limitations, it affords significant protection.
  • Narrow claims, targeting specific compounds or methods, limit the scope but may be easier to defend.

Novelty and Inventiveness

Key to patentability are the novelty and inventive step:

  • Novelty: CY1115292 must differ significantly from prior art, such as existing patents, scientific literature, or known compounds.
  • Inventive Step: Demonstrates an unexpected technical benefit over prior art, such as improved efficacy, safety, stability, or synthetic route efficiency.

Scope Considerations

  • Broad independent claims maximize market protection but are more vulnerable to invalidation.
  • Narrow claims provide robust defensibility but reduce market exclusivity scope.

Patent Landscape Context

Global Patent Filing Strategy

Pharmaceutical patents typically gain protection across jurisdictions, with key markets including the US, EU, China, and emerging markets. The landscape surrounding CY1115292 involves:

  • Prior Art Search: Encompasses prior patents, literature, and known compounds in the same chemical space.
  • Related Patents: Other patents may cover derivatives, formulations, or methods related to CY1115292's active ingredient.
  • Competitive Portfolio: Companies often file multiple family members, covering various formulations, methods, or indications.

Key Competitors and Patent Families

Identifying competitors' patent filings helps:

  • Assess potential infringement risks.
  • Understand licensing or litigation threats.
  • Gauge the duration of exclusivity before generic challenges.

Patent Term and Life Cycle

  • The duration of patent rights typically extends 20 years from filing.
  • SPAs (Supplementary Protection Certificates) or extensions might apply, especially in Europe, further prolonging exclusivity.
  • Patent expiry impacts market entry and generics competition.

Legal Status in Cyprus and International

In Cyprus, patent protection aligns with the European Patent Convention guidelines. The patent may also have counterparts in major jurisdictions, with the landscape evaluating synchronization or divergence across regions.


Strategic Patent Considerations

Strengths

  • If claims cover a broad chemical class with specific therapeutic use, the patent holds significant strategic value.
  • A well-crafted set of dependent claims can safeguard against validity challenges.

Weaknesses and Risks

  • Narrow claims might be circumvented with minor modifications.
  • Prior art could threaten the patent's validity if claims are overly broad.
  • Patent cliffs approaching after 20 years necessitate robust continuation and diversification strategies.

Potential for Litigation or Licensing

  • Strong claims and broad coverage increase likelihood of licensing revenues.
  • Infringement risks depend on competitor portfolios and existing patents.

Conclusion

Patent CY1115292's scope hinges on the claims' breadth and the novelty over prior art. The strategic positioning is influenced by related patents, the strength of claims, and the regional patent landscape. A comprehensive understanding of these facets guides licensing, enforcement, and infringement risks, impacting the commercial trajectory of the underlying pharmaceutical invention.


Key Takeaways

  • The scope of CY1115292 hinges on its independent claims, which should balance broad protection with defensibility.
  • A strong patent landscape involves diligent prior art searches, encompassing both existing patents and scientific literature.
  • Regional differences, especially within European jurisdictions, influence patent enforceability and length of protection.
  • Narrow claims, while easier to defend, may limit market exclusivity; broad claims increase risk but extend protection.
  • Continuous portfolio development, including filing in multiple jurisdictions, is vital to safeguard innovation and uphold market position.

FAQs

1. How does the scope of CY1115292's patent claims affect its market protection?
A broader scope claims more extensive protection, deterring competitors from developing similar products. Narrow claims limit protection but are often more defensible against invalidation.

2. What are common challenges in defending pharmaceutical patents like CY1115292?
Challenges often relate to prior art invalidation, claim interpretation, and proving inventive step. Patent examiners or competitors may argue lack of novelty or obviousness.

3. How does the patent landscape influence licensing opportunities for CY1115292?
A well-defined patent estate with broad claims enhances licensing appeal by offering exclusivity. Overlapping patents or prior art can complicate licensing negotiations.

4. Why is regional patent strategy important for a pharmaceutical invention like CY1115292?
Different jurisdictions have varying patent laws, examination standards, and market dynamics. Tailored filings maximize global protection and commercial value.

5. When does a patent similar to CY1115292 generally expire, and how can lifecycle management strategies extend protection?
Typically after 20 years from filing, though extensions or supplementary protections can add value. Lifecycle management includes filing divisional applications, new use claims, or formulation patents.


References

  1. European Patent Office, "Guidelines for Examination," 2022.
  2. World Intellectual Property Organization, "Patentability Requirements," 2022.
  3. Pharma Intelligence, "Global Patent Landscape Trends," 2022.
  4. European Patent Convention, "Legal Framework and Rules," 2022.
  5. Smith & Johnson IP Law, "Strategic Patent Portfolio Management," 2022.

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