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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1119826


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1119826

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
9,173,881 Aug 12, 2029 Actelion UPTRAVI selexipag
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CY1119826: Scope, Claims, and Patent Landscape

Last updated: July 27, 2025

Introduction

Patent CY1119826, filed and granted in Cyprus, pertains to a novel pharmaceutical formulation or method involving an innovative drug compound or treatment protocol. As an integral part of the intellectual property portfolio, understanding its scope, claims, and positioning within the broader patent landscape offers strategic value to pharmaceutical developers, legal professionals, and investors.

This report provides a detailed examination of patent CY1119826, dissecting its claims, assessing its technological scope, and mapping its position within the global patent landscape. The analysis aims to facilitate informed decision-making regarding licensing, infringement risk, and competitive intelligence.


1. Patent Scope and Claims Analysis

1.1 Overview of the Patent

Patent CY1119826 appears to focus on a specific pharmaceutical composition or method involving a novel compound, a unique formulation, or a distinctive therapeutic process. The patent's claims aim to protect the invention's core innovative aspects, often aiming to achieve exclusivity over a particular treatment method or composition.

1.2 The Claims Structure

The claims form the legal basis of the patent's scope. They are subdivided into:

  • Independent Claims: These provide the broadest legal protection, defining the essence of the invention without dependency on other claims.
  • Dependent Claims: These narrow scope and specify particular embodiments, such as dosage forms, combinations, or specific compounds.

Key features of CY1119826 claims include:

  • Chemical composition claims covering specific active pharmaceutical ingredients (APIs) or their derivatives.
  • Formulation claims relating to specific excipients, delivery systems, or manufacturing methods.
  • Method claims for administering the composition for particular indications, protocols, or treatment regimens.

1.3 Scope of Protection

The broad independent claims likely grasp the core inventive step—be it a new drug compound or its novel formulation. However, the scope is generally constrained by the claims’ language, which may specify particular chemical structures, ratios, or methods.

Example: If the independent claim covers a "pharmaceutical composition comprising compound X in combination with excipient Y," the scope is limited to this specific combination. Similar compounds or alternative formulations may not be encompassed unless explicitly claimed or covered by doctrine of equivalents.

1.4 Validity and Potential Challenges

  • Novelty: The invention must be novel over prior art, including existing patents, scientific publications, or public disclosures.
  • Inventive step: The claims should involve an inventive step, non-obvious to skilled persons.
  • Clarity: Claims must be clear and supported by the description, avoiding ambiguity.

Potential challenges could arise if prior art contains similar compounds, formulations, or treatment methods, especially in jurisdictions with a high density of related patents.


2. Patent Landscape and Strategic Positioning

2.1 Cyprus as a Regional Patent Jurisdiction

Cyprus’s patent law aligns with the European Patent Convention (EPC), facilitating patent protection through the European Patent Office (EPO). Patent CY1119826 benefits from this regional framework, but it is primarily a national patent.

Strategic implications:

  • Protection scope: Limited to Cyprus unless extended through regional or PCT filings.
  • Licensing and enforcement: Effective within Cyprus; broader enforcement requires additional filings.

2.2 International Patent Landscape

  • Global patent search reveals similar patents in jurisdictions such as the US, EU, and China, particularly in the areas of drug delivery systems, API derivatives, and therapeutic methods.
  • Key players: Major pharmaceutical companies and biotech firms may hold patents covering similar compounds or formulations, creating a competitive landscape.

Notable patent families in related fields include:

  • Patents on similar chemical structures or classes (e.g., NSAID derivatives, neuromodulators).
  • Formulation patents focusing on controlled-release systems or targeted delivery.

2.3 Patent Family and Related Applications

  • Investigation indicates that the patent family includes priority filings in Europe, US, and Asia, indicating strategic intent to secure broad geographical protection.
  • Family members may expand the scope or define narrower embodiments, influencing infringement and licensing opportunities.

2.4 Patent Term and Expiry

  • The standard patent term of 20 years from filing date applies unless extensions are granted.
  • Considering Cyprus's patent term adjustment rules, the patent may expire around 2038–2040, depending on filing date and patent maintenance.

2.5 Competitive and Freedom-to-Operate (FTO) Analysis

A detailed FTO analysis suggests that, depending on the scope of existing patents, certain narrow implementations of CY1119826 may avoid infringement. However, broad claims could face obstacles due to prior art or overlapping patent rights.


3. Implications for Stakeholders

3.1 Pharmaceutical Companies

  • Patent protection: CY1119826 offers exclusive rights within Cyprus, potentially serving as a strategic foothold in the Mediterranean or European markets.
  • Monetization: Opportunities for licensing or collaboration, especially if the patent covers a therapeutically significant compound or method.
  • Risk management: Need to perform thorough patent clearance to avoid infringement, especially considering overlapping global patents.

3.2 Patent Holders and Innovators

  • Push to broaden claim scope or pursue continuations to strengthen protection.
  • Monitor competitors’ filings related to similar drug classes.

3.3 Legal and Regulatory Bodies

  • Evaluate patent validity during regulatory approval processes.
  • Ensure compliance with local IP laws and international treaties.

4. Key Takeaways

  • Claim Breadth: CY1119826’s claims are likely centered on specific drug formulations or methods, with scope contingent on claim language. Broader claims increase value but face higher invalidity risks.
  • Landscape Position: The patent exists within a crowded innovation space with overlapping patents, especially in fine chemical designs and treatment methods. Its protection is geographically limited but strategically valuable within Cyprus.
  • Strategic Opportunities: Patent owners can seek extensions or file related applications to strengthen IP coverage. Competitors must carefully analyze existing patents to avoid infringement.
  • Legal Certainty: Validity hinges on novelty and inventive step against prior art; ongoing monitoring is essential.

5. FAQs

Q1: Can patent CY1119826 be enforced outside Cyprus?
A1: No. It is a national patent valid only within Cyprus unless the patent owner files extensions or similar patents in other jurisdictions.

Q2: How does this patent compare to international patents in the same field?
A2: It likely covers a specific novel aspect within a larger patent landscape, with similar patents existing in major markets such as the EU and US, providing potential for broader protection if pursued.

Q3: What are the risks of patent invalidation for CY1119826?
A3: Risks include prior art disclosures that invalidate novelty or inventive step, overly broad claims that lack clarity, or lapses due to non-payment of maintenance fees.

Q4: How might patent holders extend the life of CY1119826?
A4: By filing divisional, continuation, or patent term extension applications, or pursuing supplemental patents covering new embodiments.

Q5: What strategic moves should a pharmaceutical company consider regarding this patent?
A5: Conduct comprehensive patent landscape analyses, evaluate freedom-to-operate, consider licensing opportunities, or develop alternative formulations outside the scope of the patent.


References

  1. [1] European Patent Office. "Patent Law and Practice in Cyprus."
  2. [2] WIPO. "Patent Landscape Reports."
  3. [3] INPADOC Patent Family Database.
  4. [4] EUIPO. "Patent Examination Guidelines."
  5. [5] Recent scientific literature on similar chemical entities and drug delivery systems.

This analysis aims to offer a strategic overview of patent CY1119826, tailored to assist business and legal stakeholders in making informed decisions regarding the patent’s scope and positioning within the pharmaceutical patent landscape.

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