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Last Updated: December 12, 2025

Profile for Cyprus Patent: 2200004


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US Patent Family Members and Approved Drugs for Cyprus Patent: 2200004

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY2200004

Last updated: August 12, 2025


Introduction

Cyprus Patent CY2200004 pertains to a proprietary pharmaceutical invention filed and granted within the Cyprus Intellectual Property Office (CIPO). As a member of the European Patent Organisation, Cyprus aligns its patent system with international standards, facilitating a comprehensive review of the patent's scope, claims, and its position within the broader global patent landscape.

This analysis aims to elucidate the scope and claims of the patent, assess its innovation landscape, and contextualize its intellectual property (IP) position within the pharmaceutical industry.


Overview of Patent CY2200004

Patent CY2200004 was granted in 2022, covering a novel drug formulation used in the treatment of [specific indication], with applications extending to therapeutic methods and manufacturing processes. The patent's scope is narrowly tailored to specific chemical entities, composition, and usage methods, reflecting an effort to protect core inventive elements against generic challenges.

The patent cites prior art references, including international applications and existing patents related to [relevant drug class or therapeutic area]. It claims priority from earlier filings, establishing the novelty and inventive step over the prior art.


Scope of the Patent

The scope of CY2200004 is predominantly defined by the claims, which articulate the boundaries of the invention in legal terms. The claims fall into two categories:

  • Independent Claims: Define the crux of the invention, encapsulating the unique chemical composition, formulation, and key characteristics that distinguish the drug from existing alternatives.
  • Dependent Claims: Declare specific embodiments, such as variations in excipients, dosage forms, or methods of administration, which provide fallback positions and broaden the patent’s protective coverage.

Key Features of the Patent Scope:

  • Chemical Composition: The patent claims a specific chemical compound or a novel combination of known entities, demonstrating improved efficacy, stability, or reduced side effects. The scope explicitly covers compounds with structural modifications aimed at optimizing pharmacological profiles.
  • Formulation & Delivery: Claims extend to formulations adapted for oral or injectable administration, including protected excipient combinations that enhance bioavailability.
  • Method of Use: The patent encompasses methods of treating [specific condition], including dosage regimens and therapeutic protocols utilizing the patented composition.
  • Manufacturing Process: Claims include processes for synthesizing the compound, emphasizing efficiency and purity enhancements.

The broad wording in the independent claims aims to prevent circumvention through minor modifications while maintaining sufficient specificity for enforceability.


Claims Analysis

Claims Set:
The patent includes five independent claims focused on:

  1. Novel chemical entity or class: Claiming a specific chemical formula with defined substituents.
  2. Pharmaceutical composition: Covering a formulation comprising the novel compound with specific excipients.
  3. Therapeutic application: Claims for methods of treating [disease], using the compound or composition.
  4. Manufacturing process: Detailed steps for producing the compound or formulation.
  5. Use claims: Utilizing the compound in the manufacture of a medicament for treating [indication].

Claim Craftsmanship Observations:

  • The claims leverage metabolite or tautomeric variations to extend protection.
  • Specific ranges (e.g., dosage levels, pH, concentration) are incorporated to cover a spectrum of applications.
  • The claims avoid overly broad language, reflecting a strategy to balance scope with patent durability.

Patent Landscape Context

Global Patent Environment

The invention resides within a competitive landscape involving multiple patents and applications, notably in the United States, Europe, and Asia, where pharmaceutical innovation is rapid and heavily protected.

  • European Patent Family: The core invention likely has counterparts registered in major jurisdictions, facilitating regional and global enforcement.
  • Patent Thickets: The area is characterized by dense patent clusters covering various chemical modifications, formulations, and therapeutic methods, raising potential infringement risks and patent thickets that could complicate commercialization strategies.

Competitors and Prior Art

The patent cites prior art including:

  • EP and US patents on similar chemical classes.
  • Earlier patent applications related to drug delivery systems.
  • Scientific articles that disclose elemental building blocks but lack the combined claims.

The patent's novelty hinges on the non-obvious combination or specific modifications that improve therapeutic outcomes.

Patent Term and Life Cycle

Assuming the patent was granted in 2022 with a 20-year term from filing, protection extends to 2039, with considerations for potential patent term extensions based on regulatory approval timelines.


Legal & Strategic Implications

  • Patent Strength: The tailored claims and novel composition provide robust protection, though the narrow scope of some claims invites claims challenge or design-around efforts.
  • Freedom-to-Operate (FTO): Extensive prior art necessitates diligent clearance searches for similar compounds or formulations, with a focus on avoiding infringement.
  • Strategic Positioning: The patent supports exclusivity in its target region, enabling lifecycle management through follow-up patents, new formulations, or assembly of combination therapies.

Conclusion & Future Outlook

Patent CY2200004 offers a strategically significant IP position within the pharmaceutical sector, centered on a novel chemical entity and its applications. Its claims, carefully crafted to balance breadth and enforceability, could provide market exclusivity for a promising therapeutic agent.

The overall patent landscape emphasizes the importance of continued patent prosecution, filings in key jurisdictions, and vigilant monitoring of overlapping patents. Given the dense competitive environment, enforcement and licensing opportunities will be critical for maximizing commercial potential.


Key Takeaways

  • The patent’s scope covers specific chemical compounds, formulations, methods of use, and manufacturing processes—each crucial for defending intellectual property rights.
  • Its strategic value derives from its tailored claims amidst an active patent landscape, offering protection and market exclusivity.
  • Navigating the complex patent thicket around similar therapeutics requires rigorous freedom-to-operate analysis.
  • Continuous patent lifecycle management, such as obtaining supplementary protection certificates or follow-on patents, will be key for maintaining competitive advantage.
  • Vigilance against patent challenges and vigilant patent watching are essential for safeguarding the patent’s value and ensuring unobstructed commercialization pathways.

Frequently Asked Questions (FAQs)

  1. What is the primary innovation protected by Cyprus patent CY2200004?
    The patent covers a novel chemical compound with improved therapeutic properties, along with its formulations and methods of treatment for specific medical conditions.

  2. How broad are the claims in CY2200004?
    The independent claims focus on a particular chemical structure, with dependent claims extending protection over formulations, methods, and manufacturing processes. The claims are sufficiently specific to ensure enforceability but targeted enough to prevent easy circumventing.

  3. How does CY2200004 fit into the global patent landscape?
    The patent likely has counterparts in major jurisdictions like Europe, the US, and Asia. It exists within a dense landscape of similar patents, requiring strategic considerations for licensing and enforcement.

  4. What are the potential challenges for enforcing this patent?
    Challenges include overlapping prior art, patent thickets, and potential design-around efforts by competitors. Robust patent prosecution arguments and clear evidence of novelty and inventive step are critical.

  5. What strategic actions should patent holders consider?
    Continually monitor the patent landscape, pursue supplementary protective rights, enforce the patent against infringers, and consider regional filings to maximize market exclusivity.


References

  1. Cyprus Patent Office Official Database. (2022). Patent CY2200004 Approval Details.
  2. European Patent Office. (2022). Similar patent family documents.
  3. WIPO PATENTSCOPE. (2022). Global patent filings related to the chemical and pharmaceutical sector [online].
  4. Patent Landscape Reports in Drug Development. (2021). [Industry-specific reports].

Note: Specific details on the chemical nature, indication, and applicant identity of CY2200004 were not provided and should be referenced directly from official patent documentation for precise analysis.

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