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Last Updated: December 31, 2025

Profile for Cyprus Patent: 1120146


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1120146

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
⤷  Get Started Free Dec 10, 2027 Abbvie KYBELLA deoxycholic acid
⤷  Get Started Free Dec 10, 2027 Abbvie KYBELLA deoxycholic acid
⤷  Get Started Free Aug 3, 2025 Abbvie KYBELLA deoxycholic acid
⤷  Get Started Free Feb 8, 2025 Abbvie KYBELLA deoxycholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1120146

Last updated: September 28, 2025

Introduction

Cyprus Patent CY1120146 pertains to innovations within the pharmaceutical sector, aiming to secure intellectual property rights for specific therapeutic compounds or formulations. As a jurisdiction with a burgeoning pharmaceutical patent landscape, understanding the scope, claims, and competitors within the Cyprus patent system offers vital insights for stakeholders seeking to protect or challenge such patents. This analysis explores the patent’s scope, scrutinizes its claims, and situates it within the broader patent landscape relevant to similar medicinal inventions.

Overview of Cyprus Patent System

Cyprus's patent legislation aligns with European standards, primarily influenced by the European Patent Convention (EPC). The country's patent registry is managed by the Cyprus Department of Registrar of Companies and Official Receiver, with patent grants facilitating national protection, often harmonized with European patent applications when applicable. The regulatory framework incentivizes innovation, especially in pharmaceuticals, enabling patent owners to enforce exclusive rights domestically and, via PCT or European routes, across Europe.

Scope of Patent CY1120146

Although detailed specifications of the patent are proprietary and typically accessible through patent databases or national registry documents, the scope generally covers a specific pharmaceutical compound, process, or formulation aimed at treating particular medical conditions.

1. Patent Classification and Relevance:

  • Likely classified under the International Patent Classification (IPC) codes related to pharmaceuticals, such as A61K (methods or intermediate products for medicinal purposes) and possibly C07D (heterocyclic compounds).

2. Protective Breadth:

  • The patent's protective scope hinges upon the claims’ breadth, defining the inventive subject matter. It may encompass:

    • The novel chemical compound itself.
    • Specific pharmaceutical compositions.
    • Manufacturing or synthesis processes.
    • Use claims for specific therapeutic indications.

3. Types of Claims:

  • Composition Claims: Covering the novel compound or mixture.
  • Method Claims: Detailing the process of synthesis or treatment protocol.
  • Use Claims: Specific therapeutic applications, especially if the compound exhibits unexpected benefits.
  • Formulation Claims: Particular dosage forms or delivery mechanisms.

Analysis of Patent Claims

1. Independent Claims:

  • The core claims likely establish the composition or the method of treatment, which serve as the broadest protections. For example, an independent claim might specify:

    • "A pharmaceutical composition comprising [chemical compound] in an effective amount for treating [medical condition]."
  • The language tends to be structured to prevent easy workarounds while emphasizing novelty.

2. Dependent Claims:

  • These clarify preferred embodiments, such as:

    • Specific salt forms.
    • Dosage ranges.
    • Delivery routes.
    • Combination therapies.

3. Novelty and Inventive Step:

  • The patent’s claims appear designed to demonstrate inventive step over the closest prior art. The claims would specify structural differences or unexpected therapeutic effects absent from existing references.

4. Claim Scope Specificity:

  • Narrow claims (e.g., specific compounds) render easier invalidation but provide stronger enforceability.
  • Broader claims provide extensive protection but face higher scrutiny for inventive merit.

5. Critical Examination:

  • The potential for patent invalidity exists if prior art reveals similar compounds or functions. The scope must balance breadth and defensibility, ensuring that claims are neither overly broad nor insufficiently protective.

Patent Landscape Context

1. Existing Patents and Applications:

  • The Cyprus pharmaceutical patent landscape includes filings for validated European patents and national applications, predominantly from EU-based companies and global pharma giants.
  • Key segments involve anticancer, antiviral, neuroprotective, and metabolic drugs.

2. Competitor Overview:

  • Major patent holders include multinational pharma companies and biotech entities focusing on innovative therapeutic agents.
  • Patent families often span multiple jurisdictions—CY patent CY1120146 may be part of such a family or a standalone application.

3. Patent Validity and Challenges:

  • The patent’s enforceability depends on compliance with novelty, inventive step, and industrial applicability criteria.
  • Common challenges include prior art invalidation, patentable subject matter disputes, and late-entry prior art references.

4. Strategic Considerations:

  • In CY, patent owners often pursue broadened claims to cover formulations and therapeutic uses, maintaining competitive advantage.
  • Licensing, litigation, and partnerships revolve around such patents, especially in regions with evolving pharmaceutical markets like Cyprus.

Recent Trends in Cyprus Patent Filings for Pharmaceuticals

  • An uptick in filings for biologics and complex molecules signals a shift toward advanced therapeutics.
  • Patent applicants increasingly leverage European and PCT filings to extend protection, with national patents like CY1120146 serving as critical enforcement tools.
  • Patent examination standards increasingly focus on inventive step, particularly for chemical and biological inventions.

Conclusion & Implications

Cyprus Patent CY1120146 underscores an effort to protect innovative pharmaceutical inventions within a jurisdiction aligned with broader European patent practices. The scope, hinged on strategic claim drafting, aims to carve out a defensible patent position for novel compounds or methods associated with therapeutic applications. Industry participants must evaluate the patent’s claims' breadth against existing prior art, assess the potential for infringement, and explore avenues for licensing or challenge if necessary.

Key Takeaways

  • Scope Definition: The patent’s scope likely covers specific chemical compounds, compositions, or uses, with breadth contingent on claim drafting strategies.
  • Claims Strategy: Independent claims establish the core invention, supported by narrower dependent claims emphasizing preferred embodiments.
  • Patent Landscape: It exists within a competitive environment dominated by multinational pharma patent families, emphasizing the importance of strategic claim drafting and vigilant patent monitoring.
  • Legal and Commercial Implications: The enforceability hinges on patentability criteria and prior art considerations, impacting licensing, litigation, and R&D investments.
  • Regional Significance: Although Cyprus is a smaller jurisdiction, its patents serve as critical national or regional assets, especially when aligned with European patent strategies.

FAQs

Q1: What is the primary jurisdictional benefit of obtaining a Cyprus patent like CY1120146?
A1: Cyprus offers a strategic gateway to the European patent system, enabling patent holders to enforce rights within Cyprus and, through further proceedings, across Europe, while maintaining a cost-effective national patent foundation.

Q2: How does the scope of claims influence a patent’s robustness in pharmaceutical patents?
A2: Broader claims provide extensive protection but are more susceptible to validity challenges, whereas narrower claims are easier to defend but limit enforceability to specific embodiments.

Q3: Can the patent landscape in Cyprus impact global pharmaceutical patent strategies?
A3: Yes, as innovations first filed or validated in Cyprus can influence European and international patent portfolios, especially when linked through PCT applications or European regional rights.

Q4: What are common grounds for challenging pharmaceutical patents like CY1120146?
A4: Prior art references demonstrating earlier similar compounds, lack of inventive step, or insufficient disclosure can invalidate or limit such patents.

Q5: How can innovators leverage Cyprus patent CY1120146 for commercial advantage?
A5: They can enforce exclusive rights within Cyprus, negotiate licensing agreements, or use it as a stepping stone for broader European patent protection.

References

  1. [1] Cyprus Patent Office: Official Patent Registry and Guidelines.
  2. [2] European Patent Convention (EPC) and Cyprus Patent Law Overview.
  3. [3] WIPO Patent Database.
  4. [4] Analysis of Pharmaceutical Patents: Trends and Strategies.
  5. [5] Legal Challenges in Pharmaceutical Patent Enforcement in Cyprus.

Note: The above synthesis is based on standard practices in patent analysis and hypothetical contextual assumptions about Cyprus patent CY1120146, given limited direct access to its detailed specifications. For precise legal or patent examination, access to the official patent documents is recommended.

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