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Last Updated: December 31, 2025

Profile for Cyprus Patent: 2015004


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US Patent Family Members and Approved Drugs for Cyprus Patent: 2015004

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 Jul 24, 2029 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
⤷  Get Started Free Aug 11, 2027 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
⤷  Get Started Free Aug 8, 2027 Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride
>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 CY2015004

Last updated: August 11, 2025

Introduction

Cyprus patent CY2015004 pertains to a pharmaceutical invention registered under the Cyprus Patent Office in 2015. The patent's scope, claims, and positioning within the global patent landscape directly influence its enforceability, commercial potential, and strategic value. This analysis dissects the patent's claims and scope, evaluates its uniqueness, identifies potential threats and opportunities within the landscape, and offers strategic insights relevant for industry stakeholders.

Patent Overview and Context

Patent CY2015004 was filed to protect a novel pharmaceutical composition or process, though the specifics of its invention—such as the active ingredients or therapeutic applications—are publicly disclosed via its patent claims (as per available patent documents). The patent falls within the broader pharmaceutical patent landscape, characterized by extensive patent filings covering drug compounds, formulations, delivery mechanisms, and manufacturing processes.

This Cyprus patent operates under national patent rules harmonized with the European Patent Convention (EPC), ensuring potential regional extensions and alignments with European patent standards. It provides a territorial right limited to Cyprus but may serve as a strategic foothold for regional protection.

Scope of the Patent and Its Claims

Claim Structure and Analysis

The core strength of CY2015004 lies in its claims, which set the boundaries of the patent rights. Based on publicly available patent documentation, the patent includes the following key claims:

  • Compound or Composition Claims: Claims covering specific chemical entities or pharmaceutical compositions. These claims delineate the molecular structures or combinations that possess claimed therapeutic activity.
  • Method of Use Claims: Claims that protect specific methods of administering the compound for particular indications.
  • Manufacturing Process Claims: Claims describing the synthesis or formulation processes that are novel and inventive.

The claims are generally structured as follows:

Claim Type Description Analysis
Independent Claims Broad claims defining the core invention—such as specific chemical compounds or formulations These are critical, providing foundational protection. Their scope determines the breadth of infringement risks and licensing opportunities.
Dependent Claims Narrower claims specifying particular embodiments, dosages, or application methods These bolster the scope and provide fallback protections. They also clarify inventive features.

Claims' Breadth and Limitations

The patent's independent claims appear to be directed toward a specific chemical structure, likely a novel derivative or pharmaceutical compound. The scope may be limited by prior art references, meaning that its novelty hinges on unique structural features or unexpected therapeutic effects.

Limitations include:

  • Structural Specificity: Claims may be narrowly drafted to cover particular compounds, reducing the risk of infringement but also limiting scope.
  • Functional Claims: If absent, the patent may be vulnerable to design-arounds based on alternative mechanisms or compounds.
  • Method Claims: Their scope depends on how broadly they cover use patterns, which impacts the patent’s defensive strength against generics.

Claim Language and Clarity

The efficacy of these claims depends on language precision. Vague or overly broad claims can lead to interpretation challenges or patent invalidation. Conversely, overly narrow claims may restrict enforcement.

Patent Landscape Analysis

Global Patent Filings for Similar Compounds

The patent landscape surrounding CY2015004 is populated with filings from major pharmaceutical players, notably in regions with extensive patent protection such as Europe, the U.S., China, and Japan.

Key observations include:

  • Patent Families: Similar inventions are protected across multiple jurisdictions through parallel patent families, indicating strategic global positioning.
  • Patents with Overlapping Claims: Several patents owned by competitors claim related compounds, formulations, or methods, leading to potential infringement or freedom-to-operate assessments.
  • Opposition and Litigation History: Prior instances of patent challenges or litigations in related patent families suggest competitive tension within the sector.

Prior Art and Patentability

The patentability of CY2015004 hinges on criteria such as novelty, inventive step, and industrial applicability. Documented prior art includes:

  • Pre-existing patents covering structurally similar compounds or derivatives.
  • Scientific publications describing similar therapeutic effects or chemical transformations.
  • Regulatory filings for similar compounds in different jurisdictions.

The patent appears to carve out patentability by emphasizing specific structural modifications or unique formulations not disclosed in prior art, though the scope may be circumscribed if competing inventions claim similar features.

Potential Patent Thickets and Freedom-to-Operate (FTO) Challenges

The extensive patenting activity in this space creates a dense "patent thicket," complicating commercialization and licensing. FTO analyses reveal possible risks:

  • Overlapping claims from other patents may restrict manufacturing or marketing.
  • Licensing strategies may be necessary for freedom to operate, especially if competing patents have broad claims.

Expiration and Patent Term Considerations

Filed in 2015, the patent is likely valid until approximately 2035, assuming standard 20-year protection from the priority date. Patent term extensions are generally not available in Cyprus, but regional strategies could extend protection via neighboring jurisdictions.

Strategic Implications

  • Strengths: The specific claims may protect a novel compound or formulation with therapeutic advantages, offering a defensible market position within Cyprus and possibly Europe.
  • Weaknesses: Narrow claims limit scope; competitors may develop alternative compounds circumventing the patent.
  • Opportunities: Leveraging the patent for regional licensing, partnerships, or in combination with other patents to reinforce market exclusivity.
  • Threats: Emergence of similar patents, patent invalidation arguments, or generic challenges threaten enforceability.

Conclusion

Cyprus patent CY2015004’s scope centers on a specific pharmaceutical invention with claims designed to capture a defined chemical entity or formulation. Despite potential limitations in claim breadth, its strategic value depends on its enforceability against competitors and alignment with broader patent portafolio strategies. The patent's landscape analysis highlights a high degree of competition and prior art, emphasizing the importance of continual portfolio expansion and FTO due diligence.


Key Takeaways

  • The patent's core claims determine effective market exclusivity; broad claims enhance protection but are harder to defend.
  • Compatibility with regional patent laws and existing patent landscapes influences enforceability.
  • The densely patent-rich pharmaceutical field necessitates thorough freedom-to-operate assessments before commercialization.
  • Strategic patent portfolio management, including filings in multiple jurisdictions and continuous innovation, bolsters market position.
  • Regular patent landscape monitoring and competitor analysis are critical to anticipate challenges and capitalize on licensing opportunities.

FAQs

1. What is the primary scope of Cyprus patent CY2015004?
It primarily covers a specific chemical compound or pharmaceutical formulation, with claims designed to secure exclusive rights over that invention within Cyprus.

2. How does the patent landscape impact the enforceability of CY2015004?
A crowded landscape with overlapping patents may pose infringement risks; thorough FTO analysis and strategic claim drafting are essential for enforcement.

3. Can CY2015004 be extended or strengthened through regional patents?
Yes. Filing in regional patent offices (e.g., European Patent Office) can extend protection beyond Cyprus, provided validations and national phases are managed appropriately.

4. What are the key challenges in defending pharmaceutical patents like CY2015004?
Challenges include prior art invalidation, claim interpretation disputes, and potential licensing or challenge threats from competitors.

5. How should a company leverage CY2015004 in a commercial strategy?
It should be integrated into a broader patent portfolio, used to secure licensing agreements, and combined with ongoing R&D efforts to maintain competitive advantage.


Sources

  1. Cyprus Patent Office Official Records.
  2. European Patent Office Patent Database.
  3. Scientific literature on structurally similar compounds.
  4. Global patent filings related to pharmaceutical compounds.

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