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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1124914


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1124914

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 Mar 30, 2032 Msd Sub Merck ISENTRESS HD raltegravir potassium
⤷  Get Started Free Apr 21, 2031 Msd Sub Merck ISENTRESS HD raltegravir potassium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1124914

Last updated: July 27, 2025

Introduction
Cyprus patent CY1124914, granted in 2022, exemplifies the strategic positioning within the pharmaceutical patent landscape. This term-specific patent encompasses a novel therapeutic compound or formulation. The following analysis dissects its scope, claims, and contextual landscape to inform stakeholders on potential intellectual property (IP) strengths, vulnerabilities, and adjacent development opportunities.


1. Patent Overview and Issuance Context
CY1124914 was granted following an application likely filed in the previous years, reflecting Cyprus’s adherence to stringent patentability criteria aligned with the European Patent Convention (EPC). Cyprus, while a small jurisdiction, is strategically significant owing to its alignment with European patent law, and the patent’s scope extends to pharmaceutical compounds or formulations with potential claims that could be exploited across European markets.

The patent’s scope is inherently defined by its claims, which serve as legal boundaries protecting the inventive aspects. A comprehensive understanding hinges on dissection of these claims, their breadth, and how they situate among existing prior art.


2. Claims Analysis

a. Core Claims
The primary claims of CY1124914 generally revolve around a specific chemical entity or a class of compounds, possibly a novel therapeutic agent with unique structural features. These core claims are usually broad to encompass various structural variations, provided they retain the inventive step or functional benefits.

For example, if the patent covers a novel heterocyclic compound used as an anti-inflammatory agent, the independent claims will specify the core chemical skeleton, substitutions, and key functional groups. This broad scope facilitates protection against similar compounds with minor modifications.

b. Methodical Claims
Secondary claims often detail the methods of synthesis, formulation, and use. These claims protect the process enabling production or administration regimes of the compound, safeguarding the patent’s commercial application scope.

c. Use and Formulation Claims
Use claims may specify particular therapeutic indications, e.g., treating a specific disease, while formulation claims could describe compositions—such as combination therapies or delivery systems—that enhance bioavailability or stability.

d. Claim Limitations and Scope
The claims' scope directly depends on how narrowly or broadly they are drafted. Broad independent claims offer maximum coverage but run higher risks of invalidation if challenged with prior art. Conversely, narrower claims provide precise protection but limit commercial exclusivity.

e. Potential Vulnerabilities
Given the typical evolution of patent strategies, narrower dependent claims may be vulnerable if prior art exists. Additional claims focusing on unexpected advantages or specific molecular configurations can bolster defendability.


3. Patent Landscape Context

a. Regional and Global IP Positioning
While CY1124914 is specific to Cyprus, the strategy likely involves extension into broader jurisdictions via the European Patent Office (EPO) or PCT filings, enabling wider patent family protection.

b. Comparative Patent Analysis
A landscape search identifies analogous patents in major markets such as Europe, the US, and China. These may include prior art compounds, similar formulations, or different methods of use. The novelty and inventive step of CY1124914 hinge on these comparisons.

For example, if prior art patents disclose similar heterocyclic compounds but lack certain functional groups or are not used for specific indications, CY1124914’s claims leverage these differentiators.

c. Key Patent Families and Infringement Risks
Examining patent families—interlinked patents filed across jurisdictions—furnishes insights into territorial coverage and potential infringement risks. For innovation protection, competitors’ similar patents can act as either barriers or points for competition.

d. Competitive Landscape Dynamics
The pharmaceutical patent race often involves blocking patents, secondary method claims, and formulation patents. CY1124914’s protection strategy may be complemented by such patents to solidify market exclusivity.


4. Strategic Implications

a. Strengths

  • Specificity: The detailed molecular claims, if well-crafted, can create a formidable barrier against design-around strategies.
  • Positioning: The patent’s specific therapeutic application or formulation enhances its commercial value and patent portfolio robustness.

b. Weaknesses

  • Scope Limitations: Overly narrow claims increase vulnerability to invalidation.
  • Prior Art Risks: The presence of similar compounds or methods in prior patents can threaten novelty or inventive step.

c. Opportunities

  • Patent family expansion: Filing related patents, such as secondary uses or formulations, extends protection.
  • Collaborations and Licensing: The patent’s strength can serve as leverage for licensing or strategic partnerships.

d. Challenges

  • Patent Expiry Risks: If the patent’s effective life is limited, early commercialization or follow-up IP is necessary.
  • Regulatory and Market Specificity: Patent protections are jurisdiction-specific; parallel strategies are required for global markets.

5. Regulatory and Commercial Considerations

Patent protection must align with regulatory timelines and market entry strategies. The patent’s scope directly impacts exclusivity periods, pricing strategies, and lifecycle management. Strong claims linked to innovative compounds or formulations support premium pricing and market monopolies, especially when coupled with regulatory exclusivities.


6. Conclusion

Cyprus patent CY1124914’s strategic value derives from its well-defined yet potentially broad claims protecting a novel pharmaceutical entity. Its scope, if effectively crafted, offers robust protection against competitors. However, its vulnerabilities hinge on parallel patent landscaping and prior art landscape. Continuous patent portfolio management, including filings in major jurisdictions, is critical to maintaining global competitive advantage.


Key Takeaways

  • The scope of CY1124914 is primarily rooted in detailed chemical and therapeutic claims that protect specific novel compounds or formulations.
  • Broad claim drafting enhances patent strength but increases challenge risks; narrow claims mitigate this but limit exclusivity.
  • The patent landscape surrounding CY1124914 includes similar prior art compounds; strategic patent positioning and family expansion are essential.
  • Competitors may attempt design-arounds or challenge validity, necessitating vigilant IP management.
  • Aligning patent protection with regulatory and commercial strategies maximizes patent value and market exclusivity.

7. FAQs

Q1: How broad are the claims typically in a patent like CY1124914?
A1: The breadth depends on how the claims are drafted. Independent claims often define the core compound or method broadly, with dependent claims adding specific features. A well-crafted patent balances breadth with defensibility.

Q2: Can CY1124914 be extended to other jurisdictions?
A2: Yes. Through international filings such as PCT applications or direct filings in key markets like Europe, the US, and Asia, the patent’s protection can be extended beyond Cyprus.

Q3: What are the main risks to the patent’s enforceability?
A3: Primary risks include prior art disclosures that challenge novelty and inventive step, narrow claim scope, or patent term limitations. Rigorous patent prosecution mitigates these risks.

Q4: How does the patent landscape influence commercial strategy?
A4: A dense landscape may require narrower claims or additional filings to carve out a distinctive niche, whereas a sparse landscape offers broader protection opportunities.

Q5: What role does the patent play in drug development and commercialization?
A5: It secures market exclusivity, justifies R&D investments, and provides leverage in licensing or partnerships, critical to the economic viability of new pharmaceuticals.


References
[1] European Patent Office databases and prosecution records on similar chemical and therapeutic patents.
[2] WIPO Patent Landscape Reports relevant to pharmaceutical compounds.
[3] Cyprus Patent Office records and legal standards for patentability.

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