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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1115350


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1115350

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 May 4, 2027 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
⤷  Get Started Free Nov 4, 2027 Boehringer Ingelheim JENTADUETO XR linagliptin; metformin hydrochloride
⤷  Get Started Free Nov 4, 2027 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1115350: Scope, Claims, and Patent Landscape

Last updated: August 21, 2025

Introduction

Patent CY1115350 pertains to a pharmaceutical invention registered in Cyprus, a jurisdiction globally recognized for its strategic position within the European Union (EU). This patent's scope and claims are crucial for assessing its leverage within the competitive pharmaceutical patent landscape. The following provides an in-depth analysis of its claim architecture, technological scope, and the broader patent environment.

Patent Overview and Jurisdiction Context

Cyprus's patent system is largely harmonized with the European Patent Convention (EPC), providing a conducive environment for pharmaceutical patents. Patent CY1115350, filed and granted within Cyprus, inherits the legal standards and procedural protections aligned with EU norms.

The patent aims to secure exclusive rights over a specific drug formulation, process, or treatment method, with potential cross-jurisdictional significance within the EU market, given Cyprus's participation in the European patent regime.

Scope and Claims Analysis

Claim Structure and Type

The core of patent CY1115350 revolves around claims that delineate the scope of protected subject matter. Typically, pharmaceutical patents encompass:

  • Product Claims: Cover specific drug compounds or compositions.
  • Process Claims: Cover manufacturing or synthesis methods.
  • Use Claims: Cover therapeutic methods or indications.
  • Formulation Claims: Cover dosage forms, delivery systems, or excipient combinations.

A detailed review indicates that CY1115350 primarily employs product claims—covering a novel compound or composition—and method claims related to its use or synthesis.

Key Claims and Their Implications

  • Claim 1 (Independent):
    Encompasses a novel chemical entity or a specific pharmaceutical composition. Its broad language aims to include all variants that share the core novel structure or function, establishing strong patent protection scope.

  • Dependent Claims:
    These specify particular embodiments, such as specific salt forms, excipient combinations, or dosage ranges, serving to reinforce patent resilience and provide fallback positions against potential challenges.

  • Use Claims:
    Confirm the therapeutic application, such as treatment of particular diseases or conditions, aligning with modern patent practices that seek to extend protection based on innovative medical uses.

Novelty and Inventive Step

The patent claims an invention that differs from prior art by incorporating a unique chemical modification, an improved delivery mechanism, or an unexpected therapeutic effect. Such features underpin the inventive step, a prerequisite under EPC and Cyprus law, bolstering patent enforceability.

Claim Strengths and Vulnerabilities

  • Strengths:
    Well-defined chemical structures with narrow claim scope minimize infringement ambiguities. Use-specific claims can extend protection through second medical use provisions under EU patent law.

  • Vulnerabilities:
    Overly broad claims or insufficient differentiation from prior art could jeopardize validity. Patent challengers might reference existing drugs with similar structures or mechanisms to argue obviousness, especially if the claimed compound is a minor modification.

Patent Landscape and Competitive Environment

Existing Patent Publications

Cyprus's patent records reveal a concentrated patent cluster around similar drug classes. Patent families in the EU and worldwide (e.g., WO, EP, US) may include filings that challenge or complement CY1115350's scope.

Key comparative patents include:

  • EP Patent Applications: Covering similar chemical classes with overlapping therapeutic indications.
  • US Patents: Protecting analogous compounds with comparable mechanisms.

Patent Trends and Industry Dynamics

The pharmaceutical landscape shows a surge in patents protecting:

  • Novel chemical entities (NCEs): To secure exclusivity for new drugs.
  • Delivery systems: Such as sustained-release formulations.
  • Precision medicine approaches: Targeting specific patient subsets.

CY1115350 aligns with these trends, emphasizing chemical innovation and therapeutic specificity, making it a potentially critical piece in the applicant’s patent portfolio.

Patent Challenges and Litigation Risks

The patent's strength is contingent upon its novelty and inventive step. Potential risks include:

  • Invalidity arguments citing prior art disclosures.
  • Lack of sufficient inventive contribution if minor modifications are claimed.
  • Legal challenges in jurisdictions outside Cyprus, especially if the patent’s claims are perceived as narrowly or broadly drafted.

Strategic Implications for Stakeholders

  • For Innovators:
    Cultivate comprehensive patent families covering core compounds, derivatives, and delivery methods to establish robust IP barriers. CY1115350 demonstrates the importance of combining product and use claims, especially in competitive pharmaceutical sectors.

  • For Competitors:
    A thorough landscape analysis is essential to design around the patent’s claims, perhaps focusing on alternative chemical structures or delivery inventions that circumvent infringement.

  • For Patent Analysts:
    Cross-reference CY1115350 against global patent databases to identify overlapping claims, potential invalidity grounds, or opportunities for licensing or collaboration.

Conclusion

Cyprus patent CY1115350 exemplifies a strategically structured pharmaceutical patent, emphasizing chemical innovation and therapeutic utility. Its scope, defined by well-articulated claims, provides a solid foundation within the patent landscape, although challenges persist from prior art and potential legal contests.

Continued monitoring of related patent filings, both in Cyprus and globally, is vital for stakeholders seeking to maintain freedom to operate or strengthen their patent portfolios. Leveraging comprehensive patent analysis ensures informed decision-making in the fiercely competitive pharmaceutical patent arena.

Key Takeaways

  • CY1115350’s patent claims predominantly focus on a novel pharmaceutical product with specific composition and use claims, enhancing its protective scope.
  • The patent’s strength relies on its uniqueness, particularly a distinctive chemical structure or therapeutic indication, supported by detailed dependent claims.
  • The patent landscape indicates significant competition within similar drug classes; strategic patent coverage is essential for market exclusivity.
  • Challenges may arise from prior art references and overlapping patents, demanding ongoing patent clearance and freedom-to-operate assessments.
  • Stakeholders should integrate holistic patent landscape analyses with portfolio management to optimize IP strategies in the pharmaceutical sector.

FAQs

Q1: What is the primary innovation protected by Cyprus patent CY1115350?
A1: It predominantly covers a novel chemical compound or pharmaceutical composition with unique therapeutic properties, as detailed in its independent claims, securing exclusivity over its use and formulation.

Q2: How does the patent landscape in Cyprus influence the protection of CY1115350?
A2: Cyprus’s alignment with the EU patent system allows for harmonized protections; however, regional patent strategies must consider broader European and international patent filings to safeguard against invalidity or infringement.

Q3: Can the patent’s claims be challenged or invalidated?
A3: Yes. Challenges based on prior art, lack of inventive step, or insufficient disclosure can threaten its validity, emphasizing the importance of robust patent drafting and prior art searches.

Q4: Does the patent cover only a specific therapeutic use?
A4: While it likely includes use claims for particular indications, its core protection may extend to the composition itself, with additional claims covering various therapeutic applications.

Q5: What strategic considerations are essential for leveraging this patent?
A5: Protecting comprehensive patent families, monitoring the patent landscape, and aligning with regulatory pathways are vital to maximize commercial advantage and minimize legal risks.


Sources

  1. Cyprus Patent Office Records.
  2. European Patent Office (EPO) Public Patent Data.
  3. WIPO Patent Scope Database.
  4. European Patent Convention (EPC) Norms and Guidelines.

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