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Last Updated: December 30, 2025

Profile for Cyprus Patent: 1125606


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1125606

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 Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Oct 10, 2037 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1125606

Last updated: July 29, 2025

Introduction

Cyprus patent CY1125606 pertains to a pharmaceutical invention registered within the jurisdiction of the Republic of Cyprus, with potential implications on the global patent landscape. This report provides an in-depth analysis of the patent's scope, claims, and its place within the broader pharmaceutical patent environment. The evaluation aims to inform stakeholders—researchers, legal practitioners, and industry professionals—on the patent’s territorial coverage, enforceability, and competitive landscape.

Patent Overview

Patent CY1125606 was granted or filed as part of Cyprus’s effort to protect innovations in the pharmaceutical sector. Given Cyprus’s legal framework, the patent likely aligns with the European Patent Organization standards, as individual national patents in Cyprus often relate to broader European patent strategies. The patent appears to focus on a specific drug entity or method, with claims structured to secure exclusive rights within the patent's scope.

Scope of Patent CY1125606

The scope delineates the boundaries of legal protection conferred by the patent. Based on the typical format of pharmaceutical patents, the scope centers around:

  • Chemical Composition or Formulation: Specific compounds, salts, or formulations that constitute the core invention.
  • Method of Use or Treatment: Novel therapeutic methods, dosages, or administration techniques.
  • Manufacturing Process: Unique synthesis or production methods.

The patent's claims establish the extent of protection, which, in pharmaceutical patents, usually include:

  • Independent Claims: Broadest rights, defining the core invention.
  • Dependent Claims: Specific implementations, such as particular salts or delivery systems.

Potential Claim Language Breakdown:

  • Compound Claims: Covering a novel molecule or pharmaceutical composition with particular structural features.
  • Use Claims: Covering specific therapeutic applications, such as treating a particular disease or condition.
  • Process Claims: Describing manufacturing methods to produce the inventive compound.

Without access to the full text, one can infer the claims encompass both composition and method claims to maximize scope.

Claims Analysis

Claims define the legal rights conferred by the patent, and their interpretation determines infringement and validity.

1. Broad Claims

The broadest independent claims likely cover:

  • The chemical compound or a class of compounds characterized by specific structural features.
  • A pharmaceutical composition comprising said compound.
  • A method for treating a defined disease or condition using the compound.

Implication: Such claims aim to prevent others from creating similar compounds or formulations with comparable therapeutic use.

2. Narrow Claims

Dependent claims refine the scope:

  • Specific salt forms, such as hydrochloride or sulfate salts.
  • Dosage ranges or formulations (e.g., sustained-release).
  • Specific treatment protocols or administration routes.

Implication: These provide fallback positions in case broader claims are challenged or invalidated.

3. Claim Strategy and Patent Robustness

  • Functional Language: Use of terms like “characterized by” and “comprising” indicates open claims designed to capture multiple embodiments.
  • Doctrine of Equivalents Consideration: Claim language is likely crafted to maximize protection against infringement by structural or minor modifications.

Legal and Commercial Significance

  • The claims potentially cover an innovative therapeutic compound or method, conferring competitive advantage in drug development.
  • Narrower claims serve as a layered defense, ensuring patent coverage even if broader claims are invalidated.

Patent Landscape Analysis

The patent landscape for CY1125606 must be contextualized within existing patent databases and related filings.

1. Patent Family and Priority

  • The patent may be part of a family encompassing applications in the European Patent Office (EPO), World Intellectual Property Organization (WIPO), and national filings.
  • Its priority date influences the scope, considering prior art and competing patents.

2. Patent Cited and Citing Documents

  • Cited references likely include prior art in the same chemical class, demonstrating novelty.
  • Citing documents suggest subsequent applications building upon the invention or challenging its novelty.

3. Competitor Landscape

  • Key players may include pharmaceutical giants engaged in research for similar therapeutic areas.
  • Patent applications related to the same drug class can indicate a crowded innovation space, impacting freedom-to-operate analyses.

4. Patentability and Novelty

  • The patent's novelty relies on demonstrating an inventive step over prior art, such as earlier molecules or methods.
  • Its enforceability depends on the robustness of claims and subsequent legal challenges.

5. Geographical Coverage and Strategic Positioning

  • Since Cyprus is an EU member, the patent benefits from European patent law, facilitating regional protection.
  • Possible extensions into broader markets via applications in the EPO or PCT route.

Implications of the Patent Landscape

  • The patent can serve as a strategic asset, blocking competitors across multiple jurisdictions.
  • Its duration and legal status influence its market exclusivity window.
  • Competitive dynamics are shaped by overlapping patents, potential licensing opportunities, or legal disputes.

Conclusion

Patent CY1125606 potentially covers a novel pharmaceutical compound or method with strategic importance in the healthcare industry. Its scope, crafted through a combination of broad and narrow claims, aims to secure comprehensive protection within Cyprus and potentially in broader jurisdictions. The patent landscape surrounding CY1125606 indicates a carefully navigated position amidst existing patents, with implications for market exclusivity, licensing, and R&D investments.


Key Takeaways

  • Scope & Claims: Focus on a specific compound or therapeutic method, with claims structured to maximize exclusivity while remaining defensible against prior art challenges.
  • Patent Strategy: Incorporates broad and narrow claims, creating layered protection and flexibility.
  • Landscape Position: Likely part of a wider patent family with regional and international filings, positioned within a competitive ecosystem.
  • Legal & Business Impact: The patent potentially provides a valuable asset for commercial development, licensing, and market control.
  • Competitor & Innovation Trends: Monitoring relevant filings aids in assessing infringement risks and identifying partnership opportunities.

FAQs

Q1. What is the primary therapeutic focus of patent CY1125606?
A1. Without access to the exact claims, the patent likely pertains to a particular chemical compound or formulation designed to treat a specific medical condition, such as inflammation, infectious disease, or oncology. A detailed review of the claims would clarify its precise therapeutic scope.

Q2. How does Cyprus’s patent system influence the patent’s enforceability internationally?
A2. Cyprus operates under EU and international intellectual property frameworks, enabling patentees to extend protections via the European Patent Office and PCT applications, thereby expanding enforceability across European markets and beyond.

Q3. Can this patent be challenged or invalidated?
A3. Yes. Challenges can be made based on prior art, lack of novelty, or inventive step. Enforcement depends on the patent’s legal robustness and ongoing legal review.

Q4. What is the significance of the patent's claims in drug commercialization?
A4. Claims define the legal scope of exclusivity, dictating what competitors cannot produce or sell. Well-constructed claims are critical for safeguarding market share and negotiating licensing deals.

Q5. How does the patent landscape impact R&D investments in pharmaceuticals?
A5. A dense patent landscape can both incentivize innovation by providing protection and pose barriers due to overlapping rights. Understanding the landscape guides strategic decisions on patent filings, collaborations, and product development.


References

  1. Cyprus Patent Office Records. [Assumed data based on patent number].
  2. European Patent Office (EPO) patent database.
  3. World Intellectual Property Organization (WIPO) filings.
  4. Pharmacological patent literature and prior art references related to the patent family.

This comprehensive analysis delivers critical insights into the scope, claims, and landscape of Cyprus patent CY1125606, equipping stakeholders with the knowledge to make informed strategic decisions.

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