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Last Updated: January 29, 2026

Profile for Cyprus Patent: 1123208


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1123208

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 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 8, 2031 Rempex VABOMERE meropenem; vaborbactam
⤷  Get Started Free Aug 29, 2031 Rempex VABOMERE meropenem; vaborbactam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1123208: Scope, Claims, and Patent Landscape

Last updated: August 28, 2025

Introduction

Cyprus Patent CY1123208 exemplifies the nation’s evolving pharmaceutical intellectual property (IP) environment. While Cyprus’s patent system aligns with European standards, its niche market requires nuanced understanding of patent scope, claims, and the broader patent landscape within Cyprus and globally. As a strategic asset, the patent's patentability, territorial coverage, claim breadth, and potential for infringement influence decision-making for stakeholders, including pharmaceutical innovators, generic manufacturers, and legal professionals. This analysis delves into the specifics of the scope and claims associated with CY1123208 and contextualizes its position within the patent landscape.


Overview of Cyprus Patent System in Pharmaceutical Patents

Cyprus, a member of the European Patent Organisation through the European Patent Convention (EPC), does not administer a unique national patent for pharmaceuticals but recognizes European patents validated locally. However, Cyprus provides a streamlined national patent system operating through the National Patent Office, which grants direct patents within Cyprus, often aligning with the EPC or PCT applications.

Given data availability, CY1123208 appears to be a national patent possibly derived from a European or PCT application, and the patent’s scope aligns with national rights. The specifics of the patent, particularly its claims and scope, are essential for determining litigation potential, licensing opportunities, and patentability of subsequent innovations.


Scope of Patent CY1123208

Territorial Scope

CY1123208, being a Cyprus national patent, confers exclusive rights within Cyprus territory. Its scope is geographically limited but strategically significant within the regional context, especially considering Cyprus's position as a gateway to the Eurasian and Middle Eastern markets.

Field of Application

The scope, as typical in pharmaceutical patents, spans:

  • Chemical composition or compound—the active ingredient(s).
  • Formulation and dosage form.
  • Manufacturing process.
  • Use or method of treatment.

The scope aims to protect the core innovation while shielding against similar infringing products or processes.


Analysis of Patent Claims

Types of Claims

Patent claims define the legal boundaries of the invention. They are crucial for establishing infringement and scope of protection.

  • Independent Claims: Broadly define the invention, establishing the core novelty.
  • Dependent Claims: Narrower, providing specific embodiments or preferred features.

Claim Structure of CY1123208

While the full patent document is accessible through local patent databases and the European Patent Register, a representative analysis indicates:

  • Chemical Composition Claims: Cover specific chemical structures or variants.
  • Method Claims: Cover particular methods of synthesis or therapeutic use.
  • Formulation Claims: Include novel pharmaceutical compositions with the active ingredient.
  • Use Claims: Cover specific medical indications or methods of administering the drug.

Claim Breadth and Novelty

  • The independent claims are likely positioned broadly to encompass various derivatives or formulations, which is common in pharmaceutical patents.
  • Novelty rests on unique chemical structures, surprising therapeutic effects, or innovative delivery methods.
  • Obviousness is assessed relative to existing prior art, including prior patents and scientific literature.

Potential Vulnerabilities and Challenges

Given that pharmaceutical patents often face challenges related to patent thickets or obviousness, the scope's resilience depends on:

  • Distinctive chemical features.
  • Evidence of inventive step.
  • Specific therapeutic indications.

In Cyprus, patent validity also hinges on compliance with novelty, inventive step, and industrial applicability.


Patent Landscape for Drugs in Cyprus

Regional and International Context

Cyprus's patent landscape for pharmaceuticals is predominantly complementary to European patent protection. The key considerations include:

  • European Patent System: Many relevant patents related to CY1123208 may originate from the European Patent Office (EPO).
  • PCT Applications: Applications filed via PCT routes are pivotal for broad territorial rights, including Cyprus.
  • National Patent Registrations: National filings, like CY1123208, serve as strategic tools for local enforcement.

Major Patent Filings and Competitors

  • Large pharmaceutical players tend to file family patents covering their innovations across jurisdictions.
  • Patent families for blockbuster drugs often include CY1123208 as part of their regional protection strategy.
  • Generic manufacturers monitor such patents to assess the viability of market entry upon patent expiry.

Patent Litigation and Generic Entry

  • Patent validity is often challenged via opposition procedures or patent invalidation actions.
  • Cyprus's legal framework, aligned with EU standards, provides mechanisms for patent enforcement and litigation.
  • The scope of claims directly influences the ability to prevent generic entry effectively.

Implications for Stakeholders

For Patent Holders

  • Broad claims provide stronger territorial protection but must withstand validity challenges.
  • Strategic claim drafting is essential to encompass various formulations and uses.
  • Regular patent landscaping helps anticipate challenges and monitor patent thickets.

For Generics

  • Analyzing claim scope reveals potential design-around opportunities.
  • Patent expiry timelines influence market entry strategies.

For Legal Professionals

  • Understanding the scope and claims supports effective patent prosecution and litigation.
  • Recognizing regional nuances (e.g., Cyprus-specific rules) is crucial for enforcement.

Conclusion

Cyprus Patent CY1123208 exemplifies a tailored protection strategy for pharmaceutical innovation within Cyprus, operating within the broader European patent landscape. Its scope, predominantly defined by chemical, formulation, and use claims, aims to shield core innovations, with claim breadth directly influencing its enforceability. The patent landscape for drugs in Cyprus is characterized by a synergy of national and European patents, emphasizing the importance of strategic patent drafting, vigilant monitoring, and understanding regional legal nuances.


Key Takeaways

  • Scope Consideration: The patent’s territorial scope is limited to Cyprus but is part of a broader European IP strategy. Claim broadness enhances protection but must balance against validity challenges.
  • Claims Analysis: Effective patent protection hinges on a combination of broad independent claims and detailed dependent claims, covering chemical structures, formulations, and uses.
  • Landscape Integration: Patent portfolios in Cyprus often coincide with European and PCT filings. Monitoring global patent trends is essential for market positioning.
  • Legal and Commercial Relevance: The strength of CY1123208 influences market exclusivity, potential infringement risks, and licensing opportunities. Regular landscape assessments optimize these strategies.
  • Legal Framework: Cyprus aligns with EU standards, offering robust mechanisms for patent enforcement, but patent validity must be diligently maintained through innovative claim drafting and proactive monitoring.

FAQs

Q1: How does the scope of patent claim language influence enforcement strategies in Cyprus?
A1: Broader language in claims enhances legal protection, enabling enforcement against a wider range of infringing products. Precise, clear language reduces ambiguity, making enforcement more straightforward.

Q2: Can CY1123208 be challenged post-grant, and what are common grounds?
A2: Yes, patent validity can be challenged based on lack of novelty, inventive step, or industrial applicability. Opposition procedures or invalidation actions are typical avenues.

Q3: How does Cyprus’s patent landscape impact global pharmaceutical patent strategies?
A3: Cyprus's strategic location and its IP alignment influence regional patent filings, allowing companies to extend their European protection with national patents, facilitating market exclusivity.

Q4: What role do patent landscaping tools play for patent owners of CY1123208?
A4: They help identify potential infringements, monitor new prior art, evaluate patent validity, and develop strategic licensing or litigation plans.

Q5: How does patent claim drafting vary in pharmaceutical patents based on regional IP laws?
A5: In Cyprus, claim drafting must consider local legal standards for clarity and scope, with an emphasis on inventive step and industrial applicability, aligning often with European practices.


References

  1. European Patent Office. (2022). European Patent Convention.
  2. Cyprus Department of Intellectual Property. Patent laws and guidelines.
  3. WIPO. (2022). Patent Cooperation Treaty (PCT) systems.
  4. European Union Intellectual Property Office. Pharmaceutical Patent Strategies.
  5. Patent databases and official registers of Cyprus.

More… ↓

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