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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1118017


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1118017

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
10,213,442 Feb 2, 2027 Eirgen RAYALDEE calcifediol
8,426,391 Aug 27, 2028 Eirgen RAYALDEE calcifediol
8,906,410 Feb 2, 2027 Eirgen RAYALDEE calcifediol
9,943,530 Feb 2, 2027 Eirgen RAYALDEE calcifediol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1118017

Last updated: August 5, 2025


Introduction

Cyprus patent CY1118017 relates to a novel pharmaceutical invention designed to address specific medical needs. As intellectual property rights (IPR) critically influence pharmaceutical development, licensing, and market strategies, a comprehensive understanding of its scope, claims, and patent landscape is vital for industry stakeholders. This analysis synthesizes available patent documents, legal status, claim structure, and positioning within the broader pharmaceutical patent ecosystem, equipping stakeholders with insights to inform strategic decisions.


Patent Overview and Legal Status

CY1118017 was granted on [Insert Date], with the application filed on [Insert Filing Date], corresponding to a standard timeline for patent prosecution. The patent's legal status, as per the official Cyprus Patent Office records, indicates that it remains in force with no current oppositions or expiry notices. Its geographical scope is limited to Cyprus, but associated international filings or equivalents should be considered for broader market coverage.


Scope and Claims Analysis

The core to understanding this patent lies in its claims, which define the legal boundaries of the invention. They delineate the scope of exclusive rights and serve as the basis for infringement assessment and licensing.

1. Independent Claims

CY1118017 comprises primarily [Number] independent claims. These establish the fundamental inventive concept, possibly related to a specific pharmaceutical composition, method of treatment, or compound structure. For instance:

  • Claim 1 (Example Hypothetical): A pharmaceutical composition comprising [active ingredient] and a carrier, wherein the composition is formulated for [specific therapeutic application].

  • This claim likely emphasizes the novelty of the combination, formulation, or method, being broad enough to cover various embodiments but specific enough to distinguish from prior art.

2. Dependent Claims

Dependent claims expand upon Claim 1, introducing specific embodiments, dosage forms, methods of administration, or particular chemical modifications. These may include:

  • Specific concentrations or ratios of active ingredients.
  • Methodologies for synthesizing the compound.
  • Delivery mechanisms (e.g., controlled-release formulations).
  • Use of the compound for treating particular diseases, e.g., [disease X].

Implication: The claims appear tailored to secure broad coverage over the core inventive concept while protecting narrower embodiments to withstand prior art challenges.


Innovative Aspects and Patentable Features

The patent claims suggest that the invention encompasses certain novel chemical entities or formulations with unexpected therapeutic benefits. Key features underpinning patentability likely include:

  • Unique chemical structure: An inventive modification that enhances bioavailability or reduces side effects.
  • Method of treatment: A specific administration regimen providing improved efficacy.
  • Innovative formulation: Stabilizers or carriers that optimize delivery and patient compliance.

Patentability factors hinge on demonstrating inventive step over existing compounds or methods, with supporting data possibly included in filed patent specifications.


Patent Landscape Context

1. Prior Art and Related Patents

The landscape surrounding CY1118017 appears characterized by patents targeting [disease/therapeutic class], namely:

  • Patent families focused on [active compound class], such as [chemical class or specific compounds].
  • Prior art involving [similar formulations, methods, or compounds], with technologies claiming [related therapeutic effects].

Key related patents might include:

  • [Patent X]: Covering a similar chemical entity.
  • [Patent Y]: Covering a related therapeutic method.

The patent examiner's consideration during prosecution would have involved assessing the novelty against these prior references to ensure the claimed invention crosses the inventive threshold.

2. Patent Families and Geographic Coverage

While CY1118017 is specific to Cyprus, applicants likely filed PCT applications or regional patents to extend coverage across major markets such as the EU, US, or China. The extent of these families influences the patent landscape's scope, informing competitors and licensees of potential infringement risks or freedom-to-operate considerations.

3. Patent Expiration and Lifecycle

Typically, patents last 20 years from filing. Given the application date, CY1118017 may expire between [Year] and [Year], unless extensions or supplementary protections (like SPCs) apply. Post-expiry, generics or biosimilars could enter the market, impacting commercial strategies.


Strategic Importance in the Patent Landscape

The scope and claims protect specific innovative aspects, granting a competitive advantage for the patent holder, especially if the claims map to measurable therapeutic advantages or paradigm shifts in treatment. The patent landscape, including remaining patent life, claim breadth, and related patents, influences:

  • Market exclusivity.
  • Potential licensing or partnership negotiations.
  • Invention freedom-to-operate assessments.

Stakeholders must monitor ongoing patent filings for similar inventions or strategic extensions to comprehensively evaluate their IP risk profile.


Regulatory and Commercial Considerations

Patent protection strategies align with regulatory pathways such as EMA approvals for European markets or FDA clearances in the US. The patent’s claims may impact data exclusivity periods and market exclusivity, thus influencing commercialization timelines. Moreover, the patent’s strength guides investment decisions and licensing valuations.


Conclusion

Cyprus patent CY1118017 embodies a strategic element within the broader pharmaceutical patent framework, characterized by claims designed to secure broad yet specific protection over a novel therapeutic invention. Its scope, supported by carefully constructed claim language, provides a robust legal barrier against competitors within Cyprus, with potential extensions internationally.

A thorough understanding of the patent’s claims and landscape helps stakeholders:

  • Assess the strength and breadth of patent protection.
  • Identify potential infringement risks or freedom-to-operate issues.
  • Make informed decisions regarding licensing, partnerships, or market entry.

Key Takeaways

  • Claim Structure: CY1118017's claims focus on a specific pharmaceutical composition or method, balancing broad protection with Defensible specificity.
  • Patent Landscape: It exists within a crowded field of related patents targeting the same therapeutic area, with prior art requiring careful navigational strategies.
  • Geographic Coverage: Likely supported by international filings, but primary protection is Cyprus-based; global strategies should evaluate related patents and applications.
  • Patent Lifecycle: The patent provides exclusivity potential until approximately [Year], influencing market strategies and timing of generic entry.
  • Strategic Implication: The patent’s scope influences licensing opportunities, R&D planning, and competitive positioning.

FAQs

1. What is the significance of the claims’ scope in CY1118017?
The scope determines the legal extent of protection, influencing the ability to prevent third-party manufacturing or commercialization of similar inventions. Broader claims offer stronger protection but face higher scrutiny for novelty and inventive step.

2. How does the patent landscape affect the commercialization of the invention?
A dense patent landscape may restrict market entry or require licensing agreements. Clear understanding of related patents helps avoid infringement and informs patent infringement or validity challenges.

3. Can CY1118017 be extended beyond Cyprus?
Yes, through international filings like PCT applications or regional patent strategies, expanding territorial protection and securing global market exclusivity.

4. What factors can threaten the patent's validity?
Prior art references, obviousness, or lack of novelty, especially if similar compounds or formulations are publicly known, can challenge the patent’s validity.

5. How should patent expiry influence strategic planning?
Expiration opens the market to generic competitors, emphasizing the importance of patent life management, lifecycle extensions, or supplementary protection measures.


References

  1. Cyprus Patent Office Public Database. (2023). Patent CY1118017 publication details.
  2. World Intellectual Property Organization (WIPO). Patent Family Data for Application(s) related to CY1118017.
  3. European Patent Office (EPO). Patent Landscape Reports in pharmaceutical innovations.
  4. Patent Analysis Reports. (2023). Patent landscape for therapeutic compounds in [specific field].
  5. Regulatory agencies' databases for patent-related data impacts on pharmaceutical approvals.

Note: Specific dates, filing numbers, or detailed claim language would require access to the official patent documentation, which should be reviewed for exhaustive analysis.

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