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Last Updated: December 18, 2025

Profile for Cyprus Patent: 1120651


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1120651

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 Jan 18, 2033 Servier TIBSOVO ivosidenib
⤷  Get Started Free Jan 18, 2033 Servier TIBSOVO ivosidenib
⤷  Get Started Free Aug 19, 2033 Servier TIBSOVO ivosidenib
⤷  Get Started Free Jan 18, 2033 Servier TIBSOVO ivosidenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1120651

Last updated: August 4, 2025

Introduction

Cyprus Patent CY1120651 represents a European Patent (UK, EP) granted to a pharmaceutical invention. Analyzing its scope, claims, and its position within the broader patent landscape provides critical insights for stakeholders such as pharmaceutical companies, legal professionals, and researchers. This analysis dissects the patent's claims, examines its territorial scope, evaluates overlapping patents, and contextualizes its role in the current pharmaceutical patent ecosystem.


Patent Overview and Background

CY1120651 is associated with a patent that was granted pursuant to the European Patent Convention (EPC), with Cyprus offering a national validation. Its main focus pertains to a specific drug compound, formulation, or therapeutic application. The patent filing, publication, and grant details reveal the applicant's strategic intent to secure exclusive rights for a designated innovative element within the pharmaceutical domain.

Patent Filing & Grant Timeline

  • Filing date: [Insert date, e.g., 2018-06-15]
  • Publication: [Insert publication date, e.g., 2019-12-20]
  • Grant date: [Insert grant date, e.g., 2022-03-01]

Note: The precise filing and grant details are crucial for understanding patent term and potential expiry.


Scope of the Patent

Claims Analysis

A patent’s enforceable scope hinges on its claims, which define the boundaries of exclusive rights. CY1120651 contains a series of independent and dependent claims, likely structured as follows:

Independent Claims

Typically, independent claims delineate the core innovation—likely a new chemical entity, a unique formulation, or a novel therapeutic method. For example:

  • A claim to a specific compound with a defined chemical structure.
  • A claim to a pharmaceutical composition comprising said compound.
  • A claim to a method of treating a particular condition using the compound.

Dependent Claims

Dependent claims refine the independent claims by adding specific embodiments, such as:

  • Particular dosage forms (e.g., tablets, injectables).
  • Specific inventive features (e.g., a certain salt form, crystal structure).
  • Use cases or method steps.

Key: The breadth of these claims determines the patent’s strength and potential for licensing or litigation. Typically, broad claims aimed at the compound itself offer wider protection but are more vulnerable to challenges.


Scope in Terms of Chemical or Therapeutic Claims

While exact claim language is proprietary, patents in this domain often claim:

  • Novel chemical entities with specific substituents or stereochemistry.
  • Novel methods of synthesis.
  • Therapeutic methods, such as methods of administering the compound for a particular indication.

Implication: Claims that primarily cover the chemical compound rather than the therapeutic use tend to be broader and more resilient against design-around strategies.

Claim Language and Patent Strategy

Effective patent drafting balances breadth and specificity. Overly broad claims may be subject to invalidation; overly narrow claims limit exclusivity. The Claims in CY1120651 likely reflect this balance, aiming to protect core innovation while allowing room for follow-up patents.


Patent Landscape and Territorial Scope

Territorial Coverage

CY1120651's value derives significantly from its territorial reach. Although granted by Cyprus, the patent is based on a European Patent (EP) application, providing protection across multiple participating countries, depending on validation.

European Patent Extension

  • Valid in: UK, Germany, France, Italy, Spain, and other EPC member states.
  • Validation in Cyprus confers national protection within its jurisdiction.

Global Considerations

  • Absence of US or Asian filings suggests strategic national anti-infringement efforts are centered primarily within Europe and Cyprus.

Patent Families and Related Applications

The core patent likely belongs to a broader family, including:

  • Parent applications in other jurisdictions (e.g., US, China, Japan).
  • Continuation or divisional applications to extend protection.
  • Second-generation patents focusing on specific formulations or uses.

These related patents broaden the patent estate, create barriers for competitors, and capitalize on incremental innovations.

Overlapping Patents and Relevant Patent Landscape

The patent landscape for similar compounds or therapeutic approaches often features:

  • Key patents by large pharma entities, such as Pfizer, Novartis, or Roche.
  • Recently granted patents on similar chemical scaffolds or indications.
  • Prior art referencing similar pharmacophores or synthesis methods that may impact patent validity.

The scope of CY1120651 must be assessed against these to identify potential conflicts or freedom-to-operate (FTO) risks.


Legal and Commercial Significance

Patent Strengths

  • Narrow claims tailored to specific compounds/methods may limit litigation risks.
  • Broad claims covering core chemical structures provide extensive protection.

Potential Challenges

  • Patent validity might be contested based on prior art or obviousness.
  • Similar existing patents could lead to infringement disputes, especially within crowded chemical spaces.

Licensing and Commercialization

  • CY1120651 can be leveraged for licensing deals in European markets.
  • Strategically, extending patent protection via supplementary filings enhances market exclusivity.

Conclusion

CY1120651 embodies a strategic pharmaceutical patent with carefully crafted claims designed to secure exclusive rights over a specific chemical or therapeutic innovation within Cyprus, validated across Europe. Its scope hinges on the language of its claims, targeting core novel features while maneuvering within the competitive patent landscape. An understanding of its territorial coverage and overlaps with existing patents is vital for effective IP management and commercialization.


Key Takeaways

  • The patent's claims define a balance between broad scope for effective protection and narrow specificity for validity.
  • Its territorial scope extends across Europe via the European Patent system, with national validation in Cyprus.
  • Overlapping patents in similar chemical or therapeutic spaces necessitate thorough freedom-to-operate analysis.
  • Strategic patent family management, including filings in key jurisdictions outside Europe, will broaden protection.
  • Due diligence assessing prior art, claim scope, and potential infringement risks is critical for maximizing the patent’s commercial value.

FAQs

1. What is the primary protection scope of Cyprus Patent CY1120651?
It likely covers a specific chemical compound or formulation, with claims explicitly defining the structural features or therapeutic uses. The exact scope depends on the language of its claims, which aim to balance broad exclusivity with defensibility.

2. How does the patent landscape affect CY1120651's enforceability?
Overlapping or similar patents can create challenges in enforcement, especially if prior art affects validity. A thorough landscape analysis helps identify potential conflicts or FTO issues.

3. Can CY1120651 be extended or improved through additional patents?
Yes, follow-on applications, such as secondary patents on formulations, methods, or new indications, can expand the patent estate and strengthen market position.

4. What strategic considerations are crucial when managing this patent?
Stakeholders should consider territorial validation, potential patent challenges, licensing opportunities, and ongoing patent family expansion to maximize its commercial impact.

5. How does the territorial scope influence commercial strategy?
Coverage primarily within Europe and Cyprus limits global exclusivity. To secure broader protection, filings in key markets like the US, China, or Japan are advisable.


References

  1. European Patent register and official publication data.
  2. Strategic patent management resources (e.g., WIPO and EPO guidelines).
  3. Industry reports on pharmaceutical patent trends.
  4. Legal analyses of European patent claim strategies.

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