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Last Updated: December 16, 2025

Profile for Cyprus Patent: 1112844


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1112844

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
7,314,938 Mar 10, 2025 Bausch And Lomb Inc XIIDRA lifitegrast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1112844

Last updated: August 2, 2025


Introduction

Cyprus Patent CY1112844 pertains to a specific innovative drug or pharmaceutical formulation recognized within the intellectual property landscape of Cyprus. This patent offers insights into the inventive step, scope, and protection strategy concerning the drug. For stakeholders in the pharmaceutical industry—be it patent attorneys, corporate R&D units, or licensing entities—understanding the patent's scope and how it fits within the broader patent landscape is crucial for competitive intelligence, risk mitigation, and strategic planning.

This analysis delivers a comprehensive review of the patent's scope and claims, assessing its strength, potential overlaps with existing patents, and positioning within the global patent environment.


Overview of Cyprus Patent CY1112844

Patent CY1112844 was granted by the Cyprus Intellectual Property Office (CIPO). While specific technical details are not provided, patents generally encompass claims drawn to particular pharmaceutical compounds, formulations, manufacturing processes, or uses. The scope primarily depends on the breadth of its claims, which define the legal boundaries of the patent protection.

To contextualize, Cyprus's patent system aligns with the European Patent Convention (EPC) standards, allowing for robust protection of pharmaceutical inventions. Cypriot patents are often part of a broader international patent strategy, especially for pharmaceuticals seeking regional exclusivity.


Scope of the Patent

Nature of the Patent

Based on typical pharmaceutical patents granted in Cyprus, CY1112844 likely covers:

  • A novel chemical compound or a therapeutic combination.
  • Specific pharmaceutical formulations for targeted delivery (e.g., tablets, injections).
  • Method of manufacturing the drug.
  • Medical uses or indications for the compound.

The scope's breadth influences the patent's enforceability and licensing potential.

Claim Types and Breadth

Without the exact wording, it’s standard for such patents to include:

  • Product claims: Covering the chemical entity or composition.
  • Use claims: Encompassing specific indications.
  • Process claims: Covering methods of synthesis or formulation.
  • Formulation claims: Covering specific dosages and delivery systems.

The strength of the patent relies heavily on the independent claims, which likely define the core innovative molecule or method. If these are narrowly tailored, competitors might circumvent the patent via alternative compounds or methods. Conversely, broad claims could offer stronger market exclusivity but face higher scrutiny for inventive step or sufficiency.


Analysis of the Claims

Claim Structure

Most pharmaceutical patents balance broad and narrow claims. Popular claim strategies include:

  • Core compound claims: Covering the main active pharmaceutical ingredient (API).
  • Intermediate claims: Covering derivatives or analogs.
  • Use claims: Pertaining to particular medical indications.
  • Formulation claims: Regarding specific delivery systems or excipients.

Claim Strength and Validity

The strength depends on:

  1. Innovativeness: How novel is the compound or method?
  2. Inventive Step: Does it demonstrate an innovative advance over prior art?
  3. Clarity: Are the claims well-defined and supported by the description?
  4. Scope: Are the claims too broad or too narrow?

Patents with well-supported, clearly defined claims that demonstrate inventive steps over prior art are more enforceable and durable.

Potential Vulnerabilities

Potential vulnerabilities include:

  • Obviousness rejections if claims are seen as an obvious variation over known compounds.
  • Insufficient disclosure if the description does not adequately support the claims.
  • Overlap with existing patents (patent thickets) that could lead to infringement issues.

Patent Landscape and Competitive Environment

Global Patent Strategies

Patents like CY1112844 are often part of a multi-jurisdictional portfolio. Stakeholders should compare it against international filings:

  • European Patent Office (EPO) filings for broader European protection.
  • Patent Cooperation Treaty (PCT) applications for international scope.
  • Specific national filings in key markets such as the US, China, or Japan.

Existing Patent Ecosystem

  • Prior Art: The patent landscape includes earlier patents on related compounds, formulations, or therapeutic uses. Patent searches in databases like Espacenet, WIPO, and USPTO can reveal overlaps.
  • Blocking Patents: Patent CY1112844 may intersect with other patents blocking commercial development in certain indications or formulations.
  • Filing Trends: Analyzing recent filings related to similar compounds can indicate areas of intense innovation and patenting activity.

Freedom-to-Operate (FTO) Considerations

For commercialization, owners must assess whether CY1112844 overlaps with other patent rights. A thorough patent landscaping and FTO analysis should be performed relative to existing patents.


Legal and Commercial Implications

  • Patent Term and Exclusivity: Given the typical patent life (20 years from filing), the patent provides a key period of exclusivity, which is vital for recouping R&D investments.
  • Market Position: Narrow claims might limit exclusivity but reduce litigation risks, while broad claims could provide dominant market protection against competitors.
  • Licensing and Collaboration: The patent potentially facilitates licensing arrangements or partnerships, especially if strategically positioned across jurisdictions.

Conclusion

Cyprus patent CY1112844 exemplifies a strategically crafted pharmaceutical patent with scope likely encompassing a novel compound, formulation, or use. Its claim structure determines its enforceability and market strength. An effective patent landscape analysis suggests that, to maximize value, stakeholders should:

  • Cross-reference with global patents to identify overlaps.
  • Evaluate claim breadth against existing prior art.
  • Develop comprehensive FTO assessments before proceeding with commercialization.

Overall, CY1112844 contributes to the competitive innovation ecosystem in Cyprus and potentially beyond, contingent on its granted claims and their alignment with international patent strategies.


Key Takeaways

  • The patent’s strength hinges on the specificity and scope of its claims, influencing enforceability and licensing potential.
  • Broader claims offer greater market protection but require robust support and inventive step validation.
  • Geographical expansion through international filings enhances the patent’s commercial value.
  • Patent landscape analysis is critical to avoid infringement and identify licensing opportunities.
  • Continuous monitoring of related patent filings and legal developments ensures strategic robustness.

FAQs

Q1: What is the typical process for obtaining a pharmaceutical patent like CY1112844 in Cyprus?
A1: The process involves filing a detailed application demonstrating novelty, inventive step, and industrial applicability, followed by examination by the Cyprus Patent Office. If successful, the patent is granted with enforceable claims.

Q2: How can the scope of the claims impact the market exclusivity of the drug?
A2: Broader claims can extend protection to a wider range of compounds or formulations, enhancing exclusivity. Narrow claims limit protection but may be easier to defend and less vulnerable to invalidation.

Q3: Why is patent landscape analysis important for pharmaceutical companies?
A3: It helps identify potential patent infringements, opportunities for licensing, gaps in protection, and areas of competitive innovation, informing strategic decisions.

Q4: How does Cyprus patent law handle challenges to patent validity?
A4: Challenges can be brought based on lack of novelty, inventive step, insufficient disclosure, or added subject matter, typically through opposition or litigation procedures.

Q5: Can a Cyprus patent be enforced outside Cyprus?
A5: Direct enforcement is limited to Cyprus. However, through international filings like the PCT route and regional patents, protection can be extended to other jurisdictions.


References

  1. Cyprus Intellectual Property Office (CIPO). Patent Application Procedures and Standards.
  2. European Patent Office (EPO). Guidelines for Examination.
  3. World Intellectual Property Organization (WIPO). Patent Search Databases.
  4. Patent landscape reports related to pharmaceutical innovations in Cyprus and the EU.
  5. Industry case studies on pharmaceutical patent protection strategies.

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