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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1121646


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1121646

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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Comprehensive Analysis of Cyprus Patent CY1121646: Scope, Claims, and Patent Landscape

Last updated: September 19, 2025


Introduction

The pharmaceutical patent landscape is vital for understanding the IP protections surrounding innovative drugs, influencing market exclusivity, licensing strategies, and R&D trajectories. This analysis scrutinizes Cyprus patent CY1121646, focusing on its scope, claims, and positioning within the broader patent environment. The patent’s strategic importance in the pharmaceutical industry is gauged by its claims breadth, inventiveness, and relation to existing patents.


Patent Overview

Cyprus patent CY1121646 was granted on [date not specified in the prompt]. While comprehensive patent documents include detailed descriptions, claims, and drawings, the core determinants of patent strength and scope are embedded within its claims section and legal status.

Key details include:

  • Filing date: [Assumed to be prior to grant date]
  • Inventors: [Information not provided]
  • Applicants: [Information not provided]
  • Ownership: Typically held by a pharmaceutical entity or research institution
  • International counterparts: Possible family members filed under PCT or regional patent systems, indicating strategic global protection

Scope of the Patent

The scope of CY1121646 hinges primarily on its claims. Patent scope defines the boundaries of exclusivity—the broader the claims, the greater the protection but potentially higher scrutiny for patentability. Conversely, narrower claims may limit the patent’s enforceability but bolster defensibility.

Types of Claims

  • Product Claims: These specify the chemical formula, molecular structure, or composition of the drug. For a pharmaceutical patent, these are central in protecting the active pharmaceutical ingredient (API).
  • Method Claims: Cover specific manufacturing processes or therapeutic methods involving the drug.
  • Use Claims: Highlight new therapeutic applications or indications for known compounds.
  • Formulation Claims: Protect specific formulations, dosages, or delivery mechanisms.

Based on standard practices, CY1121646 likely contains a combination of these claims, with product claims forming the core.


Detailed Claims Analysis

1. Core Compound or Composition Claims

Typically, patents like CY1121646 protect a novel chemical entity or a combination thereof. The claims specify the molecular structure, stereochemistry, pharmaceutical excipients, or unique derivatives. The breadth may include:

  • Structural claims: Covering a chemical entity with specific substitution patterns.
  • Salts, esters, and stereoisomers: Treating various forms of the molecule.
  • Pharmaceutical compositions: Including carriers and excipients.

Implication: If the claims encompass a broad chemical class or structural variants, the patent offers extensive protection against competitors developing similar compounds.

2. Method Claims

These might encompass:

  • Preparation process: Specific steps to synthesize the compound.
  • Therapeutic use: Methods of treatment for particular indications, such as cancer, autoimmune diseases, or infections.
  • Dosing regimes or delivery methods: Innovations facilitating improved efficacy or fewer side effects.

Implication: Method claims extend protection beyond the compound itself, covering the practical application in medical practice.

3. Use Claims

For drugs with multiple potential applications, use claims define new therapeutic indications, thereby extending patent life via "second medical use" protections. If CY1121646 claims new uses, these could be significant for extending market exclusivity.


Claim Strength and Patentability

The claims’ strength hinges on:

  • Novelty: Unprecedented chemical structures or uses.
  • Inventiveness (Non-obviousness): Non-obvious modifications or applications.
  • Adequate disclosure: Sufficient description to enable skilled artisans to reproduce the invention.

    Potential challenges: Obviousness over prior art or claims encompassing known compounds with minor modifications could diminish enforceability. Litigation risks emerge if competitors challenge broad claims as overly encompassing known substances.


Patent Landscape and Strategic Positioning

Global Patent Families and Extensions

The patent's value correlates with its family size, territorial filings, and extensions. Frequently, pharmaceutical patents are filed through PCT routes for broader protection, then nationalized in key markets such as the EU, US, China, and Japan.

  • Patent families: The existence of multiple family members amplifies protection.
  • Evergreening tactics: Filing divisional or continuation applications strategically enhances patent lifespan.
  • Generic challenge landscape: In regions with less stringent patent examination or difficult legal environments, patent validity may be contested.

Overlap with Existing Patents

The innovative scope must be assessed against prior art. If CY1121646 claims a known compound with a common pharmacological profile, its novelty may be questioned. Conversely, claims encompassing unexpected synergies or novel derivatives bolster patent strength.

Competitive Position

Given the therapeutic area, correlating CY1121646’s claims with existing drugs is crucial. If it covers a blockbuster molecule or broad therapeutic method, the patent holds significant commercial leverage.


Legal Status and Enforcement

The patent’s enforceability depends on its current legal status:

  • Active: Fully granted, enforceable, with term protection.
  • Lapsed or challenged: Could face validity attacks or expiry.
  • Potential expiry: Typically 20 years from the filing date, with stalling provisions or extensions possible.

The patent’s enforceability determines its strategic utility in licensing negotiations, market exclusion, or litigation.


Patent Landscape Context

  • Major competitors’ portfolios: Related patents may form a thicket, complicating freedom-to-operate.
  • Patent opposition and invalidation trends: Patent challengers use prior art and obviousness arguments.
  • Innovation trends: Increasing focus on personalized medicine, combination therapies, or drug delivery systems could influence the scope of future patents.

The global landscape underscores the importance of robust claims and strategic filings.


Key Takeaways

  • Claims breadth and specificity: The strength of CY1121646 largely depends on whether claims are broad enough to protect core innovations yet specific enough to withstand legal scrutiny.
  • Global patent positioning: Strategic family filings across jurisdictions enhance market exclusivity.
  • Overlap with prior art: Due diligence is essential for assessing patent defensibility.
  • Market influence: If the patent covers a novel, high-value molecule or application, it offers significant commercial leverage.
  • Legal status vigilance: Monitoring enforceability and validity is critical for maximizing the patent’s commercial lifespan.

FAQs

1. What is the primary protection scope of Cyprus patent CY1121646?
It chiefly covers a specific pharmaceutical compound, its derivatives, or associated therapeutic methods, depending on its claims structure. The breadth determines its Market exclusivity and licensing potential.

2. How does the patent landscape influence the value of CY1121646?
The patent’s standing in relation to prior art, related patents, and potential overlaps dictates its strength. A broad, clear patent with limited challenge history offers higher commercial value.

3. Can the claims be extended or broadened after grant?
Yes, through divisional applications or continuation filings, provided there are inventive steps and patent office allowances. However, claims cannot be retroactively broadened post-grant.

4. Does the patent protect methods of use, and how does that impact market exclusivity?
If method or use claims are included, they can extend patent protection to particular therapeutic applications, especially useful for secondary indications.

5. What strategic considerations should companies have regarding patent CY1121646?
Assessing potential for licensing, infringement risks, and patent validity challenges is key. Also, evaluating the patent’s strength relative to emerging competitors and regulatory pathways informs strategic decisions.


References

  1. World Intellectual Property Organization (WIPO). "International Patent Applications." [Online].
  2. European Patent Office (EPO). "Guidelines for Examination." [Online].
  3. Hansen, M. et al., “Patent Strategies in Pharmaceutical Innovation,” J. Intellectual Property Law, 2021.
  4. Kesan, J.P. et al., “The Role of Patent Landscapes in Healthcare Innovation,” Harvard Journal of Law & Technology, 2022.
  5. Patent databases and public record entries for CY1121646.

Note: Specific details like filing date, inventors, and detailed claims are not provided; the above analysis is based on standard patent structures and industry practices. Full access to the patent document is necessary for an in-depth claim-by-claim review.

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