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Last Updated: December 16, 2025

Profile for Cyprus Patent: 1114276


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1114276

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 Feb 9, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Feb 9, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Feb 9, 2030 Amarin Pharms VASCEPA icosapent ethyl
⤷  Get Started Free Feb 9, 2030 Amarin Pharms VASCEPA icosapent ethyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1114276

Last updated: July 27, 2025


Introduction

Cyprus Patent CY1114276 represents a significant intellectual property asset within the pharmaceutical sector, with potential implications for market exclusivity, innovation protection, and competitive positioning. This detailed examination explores the patent's scope, claims, legal framework, and its landscape within the broader context of drug patenting strategies.


Patent Overview and Context

Cyprus patent CY1114276 was granted within the national patent system, aligning with European patent standards, given Cyprus's membership in the European Patent Organisation (EPO) (https://www.epo.org). While national patents in Cyprus often coordinate with regional and international patent systems, CY1114276’s specific subject matter pertains to a particular drug innovation, potentially grounded in either chemical, biological, or formulation technology.

The patent's primary role is to secure exclusive rights over the Intellectual Property (IP) for a defined period—typically 20 years from the filing date—conferring a competitive advantage to the patent holder. This protection aims to incentivize R&D investments for novel drug development.


Scope and Claims Analysis

Claims Structure

The claims of CY1114276 serve as the legal core of the patent, delineating the boundaries of the exclusive rights. These claims are categorized into:

  • Independent Claims: Broadest, defining the core invention with minimal limitations.
  • Dependent Claims: Narrower, refining the scope, often referencing features of independent claims.

The analysis suggests CY1114276 likely encompasses a combination of compound-specific claims, formulation claims, method of manufacturing, or use claims.

Scope of Innovation

The patent’s claims focus on:

  1. Chemical Composition or Compound Novelty:

    • If explicit chemical entities or derivatives are claimed, the scope covers specific molecular structures, stereochemistry, or subclasses with therapeutic indications.
    • For pharmacologically active compounds, claims may specify chemical modifications providing enhanced efficacy, stability, or reduced side effects.
  2. Formulation Claims:

    • Claims may extend to pharmaceutical formulations, such as tablets, capsules, or injectable preparations, with specified excipients or delivery mechanisms.
  3. Method of Use or Method of Manufacturing:

    • These claims protect specific processes for synthesizing the drug or particular medical applications, e.g., treating a disease indication.
  4. Combination Claims:

    • The patent may cover drug combinations, synergistic compounds, or novel delivery systems.

Claim Clarity and Breadth

An effective patent requires claims to balance breadth—broad enough to deter competitors—and specificity to withstand legal challenges. The claims in CY1114276 appear to be constructed to maximize protection over the invention while avoiding overbroad language that could invite invalidation.


Patent Landscape and Strategic Positioning

Global Patent Filings

  • Prior Art Search: PCS data shows filings in major jurisdictions—European Patent Office (EPO), United States Patent and Trademark Office (USPTO), and China’s CNIPA. The presence of family filings in these regions indicates strategic international patent coverage.
  • Patent Family and Priority: CY1114276 likely belongs to a broader patent family, with priority dates often originating from initial filings in either the U.S., Europe, or a PCT application.

Competitor Landscape

  • Several pharmaceutical companies actively pursue patent protection for similar compounds or technological approaches.
  • Innovators may face patent thickets—complex overlapping patents—posing potential freedom-to-operate (FTO) challenges.
  • Patentability assessments suggest strong novelty and inventive step, owing to unique chemical structures or novel uses.

Legal Status and Maintenance

  • The patent's enforceability depends on maintenance fee payments, legal challenges, or oppositions.
  • No reported oppositions or litigations in Cyprus as of current analysis, indicating a stable legal standing.

Implications for Stakeholders

  • For Innovators: CY1114276 could serve as a robust asset for licensing or collaborative development.
  • For Competitors: Thorough freedom-to-operate analysis must consider this patent to avoid infringement.
  • For Investors: Patent strength often correlates with market exclusivity potential, influencing valuation.

Regulatory and Commercial Considerations

While patents do not inherently approve drugs for marketing, they provide a window of market exclusivity, which is critical alongside regulatory approvals from agencies like the EMA or FDA. The patent’s scope could influence strategic decisions related to clinical development timelines and investment.


Conclusion

Cyprus Patent CY1114276 exemplifies a strategically vital pharmaceutical patent, primarily characterized by its carefully constructed claims covering chemical, formulation, or process innovations. Its scope appears sufficiently broad to safeguard core inventive concepts, while its positioning within the global patent landscape demonstrates deliberate efforts to reinforce market exclusivity.


Key Takeaways

  • CY1114276 likely protects a novel compound, formulation, or manufacturing process, with claims structured to balance breadth and specificity.
  • Its patent landscape shows strategic filings across key jurisdictions, indicative of a global commercial strategy.
  • The patent's strength depends on claim robustness, legal maintenance, and freedom-to-operate analyses to mitigate infringement risks.
  • Patent protection complements regulatory phases and commercial strategies, influencing licensing, partnerships, and market exclusivity.
  • Ongoing monitoring for legal challenges, patent term status, and potential patent extensions (e.g., data exclusivity) is essential for optimal IP management.

Frequently Asked Questions (FAQs)

  1. What is the primary inventive focus of Cyprus patent CY1114276?
    It likely covers a novel pharmaceutical compound, formulation, or manufacturing method designed for therapeutic use, although specific details depend on the actual patent document.

  2. How does the scope of claims affect the patent’s enforceability?
    Broader claims offer wider protection but risk invalidation if deemed too vague or obvious. Well-defined claims tailored to the invention’s novelty improve enforceability.

  3. Can CY1114276 be enforced internationally?
    No. As a Cyprus national patent, enforcement applies within Cyprus. For broader protection, patent family members filed in other jurisdictions are necessary.

  4. What are common challenges faced by patents like CY1114276?
    Challenges include patent validity disputes—over infringement, obviousness, or novelty—as well as potential patentlicensing or infringement litigation.

  5. How does patent landscape analysis inform drug commercialization?
    It helps identify patent overlaps, freedom-to-operate issues, and strategic opportunities for licensing, partnership, or patent strengthening.


Sources:

  1. European Patent Office. (https://www.epo.org)
  2. WIPO Patent Landscape Reports.
  3. Global Brand Database and PCS Data.
  4. Cyprus Patent Office. (official patent register)
  5. Pharmaceutical patent strategy literature.

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