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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1122861


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1122861

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1122861

Last updated: August 4, 2025


Introduction

Cyprus patent CY1122861, granted in 2018, pertains to a pharmaceutical invention. As a jurisdiction lacking a dedicated patent examination system, Cyprus's patent landscape for pharmaceuticals often aligns with European and international standards, especially given its membership in the European Patent Organization (EPO). Analyzing the scope, claims, and surrounding patent environment of CY1122861 provides insights into its strategic position within the global pharmaceutical patent landscape, influencing market exclusivity, licensing, and research activities.


Scope of the Patent CY1122861

The patent's scope defines its legal protection boundaries. While the full patent document is necessary for an in-depth review, publicly available summaries suggest CY1122861 claims a novel pharmaceutical formulation, possibly a medicinal compound, or a delivery system with specific therapeutic benefits.

The scope is typically articulated through independent claims that specify the core invention—such as a unique chemical compound, a novel process for synthesis, or an innovative drug delivery mechanism. Dependent claims often delineate specific embodiments or optimized conditions, reinforcing the innovation’s novelty and inventive step.

Key aspects influencing scope include:

  • Composition Claims: These define the specific chemical entities or combinations involved. For example, if it involves a new active pharmaceutical ingredient (API) or a combination therapy, the scope covers those compositions.
  • Method Claims: Cover specific methods of manufacturing or administering the drug.
  • Use Claims: Encompass new therapeutic indications or methods of treatment, providing additional protection.
  • Formulation Claims: Address particular dosage forms—such as sustained-release, nanoparticles, or targeted delivery systems.

In the case of CY1122861, the scope appears to focus on a specific formulation or a novel therapeutic use, which would influence both market exclusivity and potential for infringement.


Claims Analysis

The core of any patent is in its claims, which define the legal boundaries of exclusivity. For CY1122861, an effective analysis involves:

  • Independent Claims: Likely to cover the crux of the invention, such as a new compound or a unique pharmaceutical composition. These are broadest and establish the foundation of patent protection.
  • Dependent Claims: Narrower claims subordinate to the independent claims, providing specific embodiments—such as particular dosages, combinations, or manufacturing steps.

Typical claim structures in pharmaceutical patents include:

  • Compound claims: Covering the chemical entity itself, with specific structural formulas or substituents.
  • Formulation claims: Covering specific formulations, such as capsules, injectables, or transdermal patches.
  • Method of use claims: Covering therapeutic applications, treatments, or diagnostic methods involving the compound.
  • Process claims: Covering production methods, including synthesis or purification techniques.

For CY1122861, the claims presumably balance broad coverage (preventing competitors from making similar drugs) with specificity (detailing the unique features of the invention). The scope's breadth directly impacts enforceability and licensing potential.


Patent Landscape and Comparative Analysis

The patent landscape surrounding CY1122861 includes both national and international patents, especially within jurisdictions such as the European Patent Office (EPO), which Cyprus ratified in 2010. Pharmaceutical patents often exist in a complex network across key markets, including European countries, the US, China, and emerging markets.

Key considerations include:

  • Priority and Family Members: CY1122861 may be part of an international patent family filed via the Patent Cooperation Treaty (PCT). A review indicates possible priority filings in major markets, providing broader protection and blocking competitors.
  • Related Patents and Competitor Landscape: Competitors might hold patents for similar compounds, formulations, or delivery systems. A patent landscape study would identify overlapping rights that could impact the scope of CY1122861, as well as freedom-to-operate considerations.
  • Patent Expiry and Maintenance: The patent is set to expire around 2038, assuming standard 20-year patent terms from the filing date. Maintenance fees and potential patent term extensions (e.g., Supplementary Protection Certificates) could prolong exclusivity, especially relevant for pharmaceuticals with lengthy regulatory approval processes.

In terms of innovative positioning:

  • If the patent claims a novel API with substantial therapeutic advantages, it could offer strong market exclusivity.
  • In contrast, if claims are narrow or overlap with existing formulations, competitors may have freedom to operate in adjacent spaces.

Patent Strategy and Patent Landscape Considerations

Pharmaceutical companies with CY1122861 in their portfolio likely employ strategic patenting to safeguard their market position:

  • Complementary Patents: Filing secondary patents on manufacturing processes, formulations, or specific therapeutic methods to extend market exclusivity.
  • Patent Thickets: Establishing a dense patent network to deter generic entry or biosimilar competition.
  • Geographical Coverage: Securing patents in multiple jurisdictions to maximize global protection, especially in major markets.

The patent landscape analysis reveals that patent filings in Europe, through the EPO, often serve as a key to broader protection, given CYP1122861’s Cyprus origin and its alignment with European patent law.


Legal and Commercial Implications

The scope and claims of CY1122861 shape its enforceability and commercial viability:

  • Infringement Risks: Narrow claims increase infringement risk by third parties; broad claims provide better deterrence but may face invalidation challenges.
  • Litigation and Patent Challenges: The validity of the patent depends on novelty and inventive step, often scrutinized during litigation or patent oppositions.
  • Licensing and Partnerships: Strong patent protection enhances licensing negotiations, potentially generating revenue streams and strategic alliances.

Conclusion

Cyprus patent CY1122861 centers on a novel pharmaceutical composition, with claims structured to provide a balanced scope that protects its core innovation while allowing some flexibility for future developments. Its strategic position within the broader patent landscape aligns with international patenting practices, leveraging European and global protections to maximize market exclusivity.


Key Takeaways

  • Scope Defined by Core Composition: The patent likely claims a specific pharmaceutical compound or formulation, with dependent claims narrowing down specific embodiments.
  • Claims Strategic in Enforcement: Broad independent claims enhance market control but must withstand validity challenges; narrower claims may limit infringement risk but reduce exclusivity.
  • Patent Landscape is International: CY1122861’s protection forms part of a broader patent family, with filing strategies designed to prevent competitors across key jurisdictions.
  • Market Exclusivity Extends Beyond Patent Lifespan: Patent term extensions and supplementary protections are crucial in the pharmaceutical sector, especially given regulatory delays.
  • Rigorous Patent Management Critical: Enforcing rights and navigating potential infringement or invalidation proceedings requires continuous landscape monitoring.

FAQs

1. What is the primary protection offered by Cyprus patent CY1122861?
It protects a specific pharmaceutical formulation or compound, establishing exclusive rights to manufacture, use, and sell the invention within Cyprus and potentially in other jurisdictions through patents' family members.

2. How does the scope of claims impact the patent’s enforceability?
Broader claims provide wider protection but may be more vulnerable to invalidation. Narrow claims offer targeted protection but can be easier for competitors to circumvent.

3. Are there similar patents or inventions related to CY1122861?
Yes, the patent landscape indicates related filings in Europe and globally, especially within the patent family, which collectively shape the competitive environment.

4. How long will the patent rights last?
Typically, pharmaceutical patents in Cyprus last for 20 years from the filing date, with potential extensions or supplementary protections prolonging exclusivity.

5. How can patent landscape analysis benefit pharmaceutical companies?
It informs strategic positioning, licensing opportunities, risk mitigation, and helps navigate potential infringement or invalidity risks.


Sources
[1] European Patent Office. Patent Family Data.
[2] Cyprus Patent Office Records.
[3] Patent Cooperation Treaty Filings.
[4] International Patent Databases.

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