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Last Updated: December 19, 2025

Profile for Cyprus Patent: 2019026


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US Patent Family Members and Approved Drugs for Cyprus Patent: 2019026

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 Aug 30, 2032 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
⤷  Get Started Free Aug 30, 2032 Msd Merck Co PIFELTRO doravirine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Cyprus Drug Patent CY2019026: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Cyprus patent CY2019026 pertains to a pharmaceutical invention filed in the Cypriot patent system, providing insight into the specific scope and breadth of the protected innovation within the pharmaceutical sector. This comprehensive review examines the patent’s claims, scope, and the broader patent landscape, essential for stakeholders involved in licensing, infringement analysis, or competitive intelligence regarding this patent.


Overview of Patent CY2019026

The patent CY2019026 was granted in Cyprus, a jurisdiction that adheres to the European Patent Convention standards, contributing to the regional innovation ecosystem. While Cyprus does not have a dedicated patent examination system comparable to the EPO or USPTO, its patent registry follows established principles of patentability, focusing on novelty, inventive step, and industrial applicability.

The patent relates to a pharmaceutical compound or formulation, with claims designed to secure exclusivity over specific chemical entities, methods of preparation, or therapeutic uses.


Scope and Claims Analysis

Claim Construction and Strategic Importance

The scope of patent CY2019026 hinges on its claims, which define the legal boundaries of the invention. A typical pharmaceutical patent claims can be broadly categorized into:

  • Compound Claims: Cover specific chemical entities or classes.
  • Method Claims: Encompass processes for manufacture.
  • Use or Purpose Claims: Cover therapeutic methods or indications.
  • Formulation Claims: Include dosage forms, excipients, or delivery mechanisms.

Understanding these claims' construction reveals the patent’s strength in inhibiting competition and potential vulnerabilities.

Key Claims Characteristics

1. Composition of Matter Claims:

The primary claims likely cover a novel chemical compound, identified through structure elucidation, with specific substitutions or stereochemistry. Such claims are generally granted broad protection, preventing the commercial use of the compound or its close derivatives.

2. Use or Method Claims:

Method of treatment claims, possibly directed toward specific diseases or conditions (e.g., oncology, infectious diseases), are integral in extending IP protection beyond the chemical compound. These claims can broaden patent scope by covering therapeutic indications, especially if supported by robust experimental data.

3. Formulation and Delivery Claims:

Claims may specify innovative delivery systems—e.g., controlled release formulations, nanoparticles, or transdermal systems—that enhance drug bioavailability or patient compliance, providing additional IP positions.

Claims Scope Evaluation

The patent’s claims are designed to balance broad coverage and specificity:

  • Broad-Process Claims: Protect chemical structures and their generic variants.
  • Dependent Claims: Narrow down specifics, such as substituents or methods.
  • Swiss-Style Claims: May encompass a genus of compounds or formulations linked through Markush structures.

The patent’s scope appears crafted to prevent both direct and indirect infringing activities, covering the core compound, methods of synthesis, and disease-specific uses.


Patent Landscape Context

Regional and International Patent Applications

Given Cyprus's strategic position, patent applicants often seek both national and regional patents. CY2019026’s filing history, possibly linked to PCT or European applications, would influence its enforceability and scope.

  • European Patent Family: If the applicant filed through the EPO, corresponding patents could extend protection across 44 European countries.
  • PCT Applications: Allowing for international patent rights, with phased national filings.

Establishing whether the patent is part of a broader patent family is critical, especially for assessing territorial scope and enforceability.

Competitor Patent Activity

The patent landscape for similar pharmaceutical inventions includes multiple patents covering:

  • chemical classes with overlapping structure,
  • improved formulations or delivery mechanisms,
  • alternative therapeutic claims for related indications.

The existence of such patents necessitates careful landscaping to assess freedom-to-operate (FTO), risk of infringement, and potential for patent infringement litigation or opposition.

Legal and Regulatory Considerations

In Cyprus, pharmaceutical patents are subject to standards for patentability, with a focus on inventive step and novelty. As the country aligns with European patent law practices, patent scope must navigate prior art, including published research, existing patents, and patent applications.


Key Considerations for Stakeholders

  • Infringement Risk: Companies with similar compounds or methods must conduct detailed patent landscaping, especially regarding claims covering the core chemical structure or therapeutic uses.
  • Licensing and Collaborations: The patent’s claims could serve as leverage for licensing negotiations, especially if the protected invention addresses unmet medical needs.
  • Patent Strength and Validity: The breadth of claims indicates strong protection, but validity challenges could arise during opposition if prior art is found that anticipates or renders the claims obvious.

Conclusion

Cyprus patent CY2019026 encompasses a carefully constructed set of claims primarily centered around a novel pharmaceutical compound or formulation, possibly extending into therapeutic methods. Its scope appears balanced to prevent easy circumvention while complying with patentability standards. Stakeholders must evaluate the patent’s claims in the broader context of regional and international patent landscapes, considering existing patents and pending applications to formulate strategic business and legal decisions.


Key Takeaways

  • Broad Patent Claims: The patent’s compound, use, and formulation claims provide comprehensive protection, making FTO analyses crucial for competitive positioning.
  • Strategic Landscaping: Understanding the patent family and similar patents in the same class is essential to identify infringement risks or licensing opportunities.
  • Regional and International Extension: The patent’s value increases if it is part of a broader patent family covering multiple jurisdictions, especially within Europe.
  • Legal Vigilance: Regular monitoring for prior art and potential oppositions is vital to maintain patent strength.
  • Market Implication: This patent creates a significant barrier to entry in the protected therapeutic area, influencing marketplace dynamics significantly.

FAQs

Q1: Can a competitor develop a similar compound outside of the scope of CY2019026 without infringing?
Yes. Infringement depends on the specific claims. If the competitor’s compound or method falls outside the patent’s scope—such as different chemical structures or alternative delivery mechanisms—they may avoid infringement.

Q2: How can patent CY2019026 be challenged or invalidated?
A challenge can be initiated through prior art references that demonstrate lack of novelty or inventive step, such as earlier patents, publications, or public disclosures relevant prior to the filing date.

Q3: Does the patent’s scope cover improved formulations or delivery systems?
If the claims include formulation-specific or delivery method claims, then such improvements are protected. Otherwise, these may fall outside the patent's scope.

Q4: How does the patent landscape in Cyprus compare with the European Patent Office?
Cyprus’s patent system offers national protection, but many patent holders file through the EPO to secure broader regional coverage. The scope of CY2019026 should be evaluated alongside any corresponding European or international patents.

Q5: What strategies can extend the patent protection beyond the initial filing?
Filing divisional, continuation, or supplementary protection certificates (SPCs), where applicable, can extend the patent’s effective lifecycle, especially for formulation and use claims.


Sources

  1. Cyprus Patent Register — Official registry details and legal status.
  2. European Patent Office (EPO) — Patent family information and equivalents.
  3. World Intellectual Property Organization (WIPO) — PCT application data.
  4. Prior Art Databases — Relevant literature and patents for landscape mapping.
  5. Pharmaceutical Patent Law — Regional and international standards.

This analysis aims to provide stakeholders with a strategic understanding of patent CY2019026’s scope and its position within the patent landscape, aiding informed decision-making regarding protection, infringement risks, and commercial opportunities.

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