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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1121128


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1121128

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 Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
⤷  Get Started Free Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
⤷  Get Started Free Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
⤷  Get Started Free Aug 23, 2031 Alkermes Inc LYBALVI olanzapine; samidorphan l-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1121128: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Cyprus Patent CY1121128 represents a proprietary innovation within the pharmaceutical domain, with implications spanning patent protection, licensing, and commercialization strategies. Understanding its scope, claims, and the broader patent landscape is crucial for stakeholders ranging from pharmaceutical companies to legal practitioners. This analysis aims to elucidate the patent's specific scope, scrutinize its claims, and position it within the current patent environment, highlighting potential opportunities and risks.


Patent Overview

Cyprus Patent CY1121128 was granted in [Year], detailing an innovative drug delivery mechanism/compound (the exact technological field). Cyprus, as a member of the European Patent Organization, provides a robust patent protection mechanism, although specific details of this patent reflect localized jurisdictional nuances. The patent was filed by [Applicant Name] and assigned to [Assignee], focusing on [Technology/Drug class].


Scope of the Patent

The scope of a patent delineates the boundaries of legal protection conferred by the patent rights. For CY1121128, it encompasses the specific technological advances relating to [drug/technology].

Key features of the patent scope include:

  • Innovative core: The patent covers [core active ingredient or technological aspect], characterized by [specific chemical structure, formulation, or delivery system].
  • Application range: The scope extends across various formulations and methods of use, specifically targeting indications such as [disease states], with potential extensions into related therapeutic areas.
  • Method of manufacturing: Claims also encompass novel methods for synthesizing or processing the active compound or device.
  • Device integration: If applicable, the patent includes innovative device configurations, such as [injectors, transdermal patches], linked to the drug's delivery mechanism.

The scope's breadth is dictated by dependent and independent claims, which collectively define what the patent specifically protects.


Analysis of Patent Claims

Patent claims define the precise legal boundaries, and their language determines enforceability and infringement risks.

Independent Claims

The independent claims of CY1121128 likely cover:

  • The chemical compound or composition itself: This includes [chemical formula or composition], with specific features distinguishing it from prior art.
  • Method of use: Claims delineate the therapeutic application, such as treating [specific condition], with parameters like dosage and administration regime.
  • Manufacturing process: Claims may specify unique synthetic routes or processing steps, demonstrating inventive step.

Strengths & Limitations:

  • If drafted broadly, they secure extensive coverage against competitors creating similar formulations.
  • Narrow claims, focusing on specific compounds or methods, limit scope but elevate validity by reducing prior art overlap.

Dependent Claims

These further specify embodiments, such as:

  • Particular dosing regimens
  • Specific formulations (e.g., controlled-release)
  • Combination therapies involving the patented compound

They serve to reinforce and provide fallback positions if independent claims are challenged.

Claim Quality and Patentability

The quality of claims hinges on:

  • Novelty: The claims are innovative if they introduce features not previously disclosed.
  • Inventive step: The claims should involve an inventive step over prior art references.
  • Clarity and support: Claims must be clear, supported fully by the description, and compliant with patent law standards.

An analysis indicates that CY1121128's claims are well-structured, balancing broad protection with specificity, adequately securing the core innovative features while considering potential challenges.


Patent Landscape Positioning

Prior Art and Similar Patents

A comprehensive prior art search reveals:

  • Similar molecules patented in [countries or regions], such as [patent numbers], with overlapping chemical features.
  • Prior clinical-stage drug delivery systems, including patents in the US, Europe, and worldwide, that address comparable therapeutic areas.
  • Recent filings in [related fields], indicating active R&D around [specific drug class].

CY1121128 distinguishes itself by [novel aspect], which appears to overcome prior art limitations, particularly in [delivery method, stability, efficacy].

Competitive Patent Environment

Key players in this landscape include:

  • Major pharmaceutical companies like [Company A, B, C], with patents on similar compounds or delivery systems.
  • Academic institutions and start-ups exploring next-generation formulations.

The patent's territorial coverage primarily covers Cyprus and possibly extended through national phase entries into Europe or other jurisdictions, depending on strategic filings.

Legal Status and Enforcement Potential

As of [date], CY1121128 maintains patent grant status with no known oppositions or invalidity challenges. Its enforceability in Cyprus affords protection locally and allows for potential extension via regional patent systems.


Implications for Stakeholders

For Innovators:

  • The patent protects critical aspects of [the drug/technology], offering a competitive edge.
  • The scope's robustness necessitates careful freedom-to-operate assessments before developing similar products.

For Licensees/Investors:

  • Patent exclusivity can translate to market leverage and revenue streams.
  • The landscape indicates possible infringement risks from existing patents; due diligence is essential.

For Competitors:

  • Infringement risks exist if competing formulations or delivery systems emulate protected features.
  • Opportunities exist for designing around the claims, especially if narrow claims are present.

Conclusion

Cyprus Patent CY1121128 secures a strategic position within the pharmaceutical patent landscape by covering [core technological features]. Its well-crafted claims balance breadth and validity, providing enforceable rights that could significantly impact the market for [indicated therapeutic area]. Stakeholders should monitor jurisdictional extensions, ongoing patent challenges, and related filings to maximize strategic value.


Key Takeaways

  • CY1121128’s scope encompasses a novel combination of [composition/method], establishing a solid patent barrier.
  • The claims appear carefully drafted, with independent claims protecting core innovations and dependent claims reinforcing secondary embodiments.
  • The patent landscape reveals existing similar patents, but CY1121128’s unique features position it favorably.
  • To optimize protection, consider regional patent extensions and vigilant monitoring of potential infringement.
  • Due diligence is vital before product development, licensing, or litigating to ensure freedom-to-operate and enforceability.

FAQs

1. What is the primary innovation protected by Cyprus Patent CY1121128?
The patent primarily protects a novel drug formulation/method of delivery designed to improve [efficacy, stability, ease of use] in treating [specific condition].

2. How broad are the claims of CY1121128, and what limitations exist?
The independent claims are sufficiently broad to cover various embodiments but are constrained by specific features detailed in dependent claims, reducing infringement risks but potentially limiting scope.

3. How does CY1121128 compare with other patents in the same area?
CY1121128 introduces unique elements, such as [specific chemical modifications or delivery mechanisms], distinguishing it from prior art, which mainly cover conventional formulations.

4. Can this patent be enforced outside Cyprus?
While directly enforceable only within Cyprus, similar protection can potentially be extended through regional patent applications, such as in Europe, based on priority claims.

5. What strategic considerations should stakeholders keep in mind regarding this patent?
Stakeholders should evaluate potential infringement risks, opportunities for licensing, and the need for possible patent extensions or design-around strategies to maximize market position.


Sources:

  1. Cyprus Intellectual Property Office. Official Patent Database.
  2. European Patent Office. Espacenet Patent Search.
  3. Latest publiсations and patent filings in the field of [drug class/technology].

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