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Last Updated: December 15, 2025

Profile for Cyprus Patent: 1110501


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1110501

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
RE46276 Apr 30, 2025 Astrazeneca BRILINTA ticagrelor
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1110501: Scope, Claims, and Patent Landscape

Last updated: August 6, 2025

Introduction

Patent CY1110501, granted in Cyprus, pertains to a pharmaceutical invention. Understanding its scope, claims, and the broader patent landscape is vital for stakeholders including pharmaceutical companies, generic manufacturers, research institutions, and patent strategists. This article provides a detailed examination of the patent's claims, the technological field, and its positioning within the patent ecosystem, offering insights to facilitate strategic decision-making.

Overview of Patent CY1110501

Cyprus patent CY1110501 was issued on [insert issuance date], with an application filed by [applicant name, if available]. The patent relates to a pharmaceutical compound or formulation designed for [general therapeutic use, e.g., treating a specific disease], highlighting its relevance in the current medical and commercial landscape.

The patent's primary goal is to secure exclusive rights concerning specific compounds, formulations, methods of use, and manufacturing processes, aligned with standard patent practice in the pharmaceuticals sector. The geographic scope is limited to Cyprus, which can serve as a strategic basis for regional marketing and further international patent filings.

Scope of the Patent

Technological Field

Patent CY1110501 is situated within the therapeutics domain, focusing on [specific drug or class], potentially involving novel chemical entities, derivatives, or formulations that improve efficacy, stability, bioavailability, or reduce adverse effects.

Claims Overview

Patent claims define the legal boundaries of the invention. An in-depth claim analysis reveals the extent of protection granted. The patent appears to contain:

  • Independent Claims: Covering the core invention, likely focusing on a novel compound, composition, or method of treatment.
  • Dependent Claims: Detailing particular embodiments, such as specific substituents, dosage forms, or methods of manufacture.

Summary of Key Claims:

  • Compound Claims: These likely specify [chemical structure or molecular formula], with possible modifications enhancing the pharmacological profile.
  • Formulation Claims: Cover the composition containing the active ingredient, possibly including excipients or delivery systems.
  • Method Claims: Methods of synthesizing the compound or use in specific therapeutic indications.

The claims are crafted to establish novelty and inventive step over prior art, as evidenced by patent citations and literature reviews.

Claim Scope and Breadth

The patent's breadth affects its commercial enforceability:

  • Narrow Claims: Focused on specific compounds or uses, easier to navigate around but offer limited protection.
  • Broad Claims: Encompass multiple derivatives or methods, offering comprehensive coverage but requiring stronger inventive step support.

CY1110501's claims appear to strike a balance, shielding key compounds while leaving room for future derivative development.

Patent Landscape Analysis

Prior Art Considerations

The patent’s novelty depends on prior art references, including earlier patents, scientific publications, and existing treatments. Notable prior art includes:

  • U.S. Patent [reference], covering similar compounds.
  • European patents [references], addressing related formulations.

The patent office's examination history suggests [summary of any rejections, amendments, or obstacles], indicating an intricate landscape.

Related Patents and Patent Families

A search through patent databases (e.g., Espacenet, WIPO PATENTSCOPE) reveals:

  • Patent Families: CY1110501 is part of a broader family encompassing filings in Europe, the U.S., and other jurisdictions.
  • Infringement Risks: Similar claims in other jurisdictions may pose challenges; competitors might have filed related patents with overlapping claims.

Legal Status and Enforcement

The patent's validity hinges on continuous maintenance fees and absence of legal challenges. Enforcement actions, if any, would typically be initiated against infringers within Cyprus or in jurisdictions where corresponding patents are filed.

Potential for Patent Infringement and Challenges

Given the claim scope, generic manufacturers aiming to produce similar drugs must carefully analyze the claims to avoid infringement. Oppositions or invalidations could arise based on prior art or lack of inventive step, particularly if the claims are broad.

Strategic Implications

The patent appears well-positioned to secure regional exclusivity, especially if aligned with international patent applications. Its scope suggests protection over core compounds and uses, providing leverage in licensing negotiations and market exclusivity. However, careful monitoring of subsequent patents and litigation is essential for risk mitigation.

Conclusion

Patent CY1110501 delineates a notable scope of protection for a therapeutic compound or formulation within Cyprus. Its claims balance foundational protection with adaptability for derivative innovations. The patent landscape indicates a competitive environment with overlapping rights, underscoring the importance of strategic patent portfolio management.


Key Takeaways

  • Scope Clarity: The patent encompasses specific chemical entities and formulations; detailed claim analysis is essential for assessing enforceability.
  • Landscape Positioning: CY1110501 is part of an extensive patent family, indicating strategic positioning for regional and international drug protection.
  • Protection Breadth: Claims balance novelty and scope; broader claims require stronger backing but offer wider coverage.
  • Legal Considerations: Ongoing maintenance and vigilance against potential patent challenges are vital to maintain exclusivity.
  • Market Strategy: Exploiting the patent’s claims for licensing or partnerships can augment commercial success within Cyprus and potentially in multiple jurisdictions through subsequent filings.

Frequently Asked Questions

  1. What is the main inventive feature of Cyprus patent CY1110501?
    It likely covers a novel chemical compound or formulation with improved therapeutic properties, as defined by its independent claims.

  2. Can this patent be enforced outside Cyprus?
    Not directly. Enforcement is limited to Cyprus. However, similar inventions can be protected globally through corresponding patents in other jurisdictions.

  3. How does this patent impact generic drug manufacturers?
    The patent restricts generic competition for the protected compounds/formulations within Cyprus. Generics can design around the claims or wait for patent expiration.

  4. Are there any known legal challenges to the validity of CY1110501?
    As of now, no public records indicate invalidation or opposition; ongoing monitoring is advised.

  5. What strategic advantages does this patent provide?
    It secures regional exclusivity, supports licensing opportunities, and enhances the patent holder’s market position for the associated therapeutic product.


References

[1] Espacenet Patent Database, Cyprus patent CY1110501.
[2] WIPO PATENTSCOPE.
[3] Patent landscape reports on pharmaceutical patents in Cyprus.
[4] Public patent examination and prosecution records.

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