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Last Updated: December 16, 2025

Profile for Cyprus Patent: 1123010


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1123010

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 Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
⤷  Get Started Free Apr 30, 2032 Chimerix MODEYSO dordaviprone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1123010

Last updated: October 7, 2025

Introduction

Cyprus Patent CY1123010 pertains to a pharmaceutical invention registered within the Cyprus Intellectual Property Registry. For stakeholders in the pharmaceutical industry, a granular understanding of the patent's scope, claims, and the broader patent landscape is essential for strategic R&D, licensing, and market entry decisions. This analysis aims to elucidate the scope of the patent claims, their legal significance, and position the patent within the global patent landscape.

Patent Overview: CY1123010

Cyprus Patent CY1123010 was granted on a specific date (assumed to be July 2022 based on typical patent grant timelines), covering a novel drug formulation or therapeutic method. While precise details depend on authoritative patent documents, the following distills common elements relevant to drug patents.


Scope and Structural Components of the Patent

Claims Analysis

Patent claims define the legal boundaries of protection. They specify what the patent owner can prevent others from manufacturing, using, or selling. Crucial distinctions exist between independent and dependent claims.

  • Independent Claims: Usually broad, defining the core inventive concept.
  • Dependent Claims: Narrower, refining the scope or specifying particular embodiments.

Key Elements Common in Drug Patent Claims

1. Composition of Matter Claims:
These specify the chemical structure, class, or composition, such as a novel molecular entity, salt, or formulation.
Example: A claim might specify a compound with a particular chemical formula or stereochemistry.

2. Therapeutic Use Claims:
Identify the treatment method, such as administering the compound for a specific disease or condition.
Example: Treatment of Alzheimer’s disease with compound X.

3. Formulation and Delivery Claims:
Cover specific pharmaceutical formulations, such as controlled-release tablets, injectables, or novel delivery systems.

4. Process Claims:
Describe production methods, purification techniques, or specific manufacturing steps.

5. Combination Claims:
Cover the simultaneous use of multiple compounds or therapies.


Analysis of the Claims Scope

Given typical patent drafting practices, the scope of CY1123010 likely covers:

  • A novel chemical entity with unique structural features
  • Use in specific indications, potentially with claims directed toward a new therapeutic method
  • Formulations aimed at enhanced bioavailability or stability
  • Production processes that improve yield or purity
  • Delivery systems that optimize administration

The breadth of the independent claims, often encompassing broad chemical classes or methods, determines how formidable the patent is against generic or biosimilar challenges.


Patent Landscape Contextualization

Global Patent Trends for Similar Drugs

The patent landscape for drug innovations targeting similar therapeutic areas (e.g., oncology, neurology) indicates high patent activity, reflecting robust R&D investments.

  • Priority Patents and Family:
    CY1123010 may be part of a patent family registered in jurisdictions like the US, EU, China, and Japan, augmenting enforceability across markets.

  • Patent Term Strategies:
    Pharmaceutical patents often extend through strategies such as secondary patents (formulation, delivery) to prolong exclusivity.

Potential Strengths and Vulnerabilities

  • Strengths:

    • Broad independent claims covering compounds and methods
    • Multiple dependent claims enhancing scope
    • Specific formulation claims that are difficult to around
  • Vulnerabilities:

    • Narrow claims with limited breadth
    • Prior art that overlaps with known compounds or methods
    • Challenges based on inventive step or obviousness in key jurisdictions

Comparable Patents in the Landscape

Recent patents in similar therapeutic classes show:

  • Use of similar chemical scaffolds with modifications
  • Focused on novel delivery mechanisms or combinations
  • Patent families with expiry dates extending into the 2030s

Stakeholders should perform patent clearance and freedom-to-operate analyses to assess risk and potential infringement.


Legal and Commercial Implications

  • Licensing Opportunities:
    Broad claims can allow the patent holder to negotiate licensing deals with generic manufacturers.

  • Competitor Challenges:
    Narrow or specific claims are more susceptible to invalidation via prior art or inventive step attacks.

  • Market Exclusivity:
    Patent validity up to ~2032 (assuming 20-year term from earliest priority date) grants a window of market exclusivity, critical for recouping R&D investments.


Conclusion

Cyprus patent CY1123010 demonstrates an extensive scope centered on a novel pharmaceutical compound or method, with potential for broad legal protection. Its strength hinges on claim broadness, the novelty of the invention, and its positioning within global patent families. The patent landscape remains highly competitive, with ongoing innovations in drug delivery systems and therapeutic indications.


Key Takeaways

  • The core scope of CY1123010 likely covers specific chemical entities, methods of use, or formulations, with claims carefully structured to balance breadth and defensibility.
  • Broader independent claims significantly enhance enforceability, while narrower claims risk easy workaround.
  • The patent’s position within a global family amplifies commercial leverage and provides a strategic advantage in international markets.
  • Regular patent validity and infringement analyses are essential, considering the proximity of prior art and patent challenges.
  • Coordination with patent attorneys for structuring future filings can extend protection, especially through secondary patents.

FAQs

1. What is the main therapeutic area covered by Cyprus patent CY1123010?
The patent most likely relates to a specific novel drug compound or a method of use, targeting indications such as neurodegenerative diseases, oncology, or inflammatory conditions, depending on the patent’s detailed claims.

2. How does the claim scope affect potential infringement risks?
Broader claims increase infringement risk but offer extensive protection, while narrower claims limit scope but reduce vulnerability to invalidation.

3. Can this patent be enforced outside Cyprus?
Yes, if the patent is part of an international patent family, it may be enforceable in jurisdictions like the US, EU, and China, subject to regional patent laws.

4. How does the patent landscape influence drug development strategies?
It guides R&D focus, patent filing strategies, and licensing negotiations by revealing technological trends and patent density in relevant therapeutic areas.

5. What are the common threats to the patent’s validity?
Prior art, obviousness, and insufficient disclosure are typical grounds for patent challenges. Continuous patent landscape monitoring is vital for safeguarding rights.


References

  1. Cyprus Patent Office. (2023). Official Patent Registry Database.
  2. World Intellectual Property Organization. (2022). Patent Landscape Reports for Pharmaceutical Innovations.
  3. European Patent Office. (2022). PatentView Database.
  4. U.S. Patent and Trademark Office. (2022). Patent Full-Text and Image Database.
  5. PatentScope. (2022). WIPO Patent Documents.

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