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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1124056


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1124056

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 Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
⤷  Get Started Free Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
⤷  Get Started Free Apr 13, 2036 Pfizer DAURISMO glasdegib maleate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1124056

Last updated: July 31, 2025

Introduction

Cyprus patent CY1124056 pertains to a pharmaceutical invention filed and granted within the jurisdiction of Cyprus. As a member of the European Patent Office (EPO), Cyprus's patent system facilitates regional patent protection, providing insight into global patent strategies. This analysis dissects the scope of the patent's claims, evaluates its structural and legal breadth, and examines its position within the broader patent landscape, focusing on the patent's innovation, enforceability, and strategic significance in the pharmaceutical field.

Overview of Patent CY1124056

CY1124056 was granted on [Insert granting date], with the applicant listed as [Applicant Name], and the assignee primarily engaged in [Therapeutic Area/Field]. The patent's priority claims date back to [Priority date], indicating its filing history and potential patent term length extending into [Year].

The patent claims a specific pharmaceutical composition, method of treatment, or compound, designed for therapeutic use. Given the complexity typical of pharmaceutical patents, the claim set likely comprises independent claims defining the core invention and multiple dependent claims describing specific embodiments or variations.


Scope of Patent Claims

Claim Structure and Breadth

A typical pharmaceutical patent such as CY1124056 often includes:

  • Compound claims: Covering particular chemical entities or classes.
  • Method claims: Encompassing methods of using or manufacturing the compound(s).
  • Composition claims: Detailing formulations with specific excipients, dosages, or delivery mechanisms.
  • Use claims: Claiming the application of the compound for specific therapeutic indications.

The scope determination hinges on the breadth of these claims:

  • Independent claims: Likely focused on a chemical compound or a specific therapeutic method, with wording aiming to achieve broad coverage, provided structural features are adequately disclosed.
  • Dependent claims: Narrower, embedding specific variations, such as dosage forms, combination therapies, or targeted patient populations.

Analysis: The scope of CY1124056 is expected to be a balance between broad protection—covering a new chemical class or therapeutic method—and narrower claims that delineate particular embodiments to withstand clearance or validity challenges.

Legal and Strategic Implications

  • Breadth versus Validity: Broader claims increase market exclusivity but risk validity challenges if not supported by sufficient disclosure.
  • Claim Language: Phrases such as “comprising,” “consisting of,” and “wherein” influence scope. “Comprising” tends to be open-ended, expanding protection, whereas “consisting of” narrows coverage.
  • Claim Dependencies: Multiple dependent claims reinforce the patent's enforceability across different embodiments and scenarios.

Patent Landscape Context

Related Patents and Prior Art

The landscape for pharmaceuticals similar to CY1124056 involves:

  • Prior Art Search: Existing patents and publications prior to the filing date that disclose similar compounds or methods. The strength of CY1124056 hardens if it claims a novel, non-obvious compound or indication.
  • Novelty and Inventive Step: The patent must satisfy these criteria over prior art, establishing uniqueness in chemical structure, formulation, or therapeutic application.

Competitor Patents and Overlap

  • Patent Clusters: The existence of multiple patents in the same class indicates a competitive landscape. CY1124056's scope must differentiate itself sufficiently to avoid infringement or validity issues.
  • Freedom to Operate (FTO): Companies considering commercialization need to establish that CY1124056 does not infringe other patents, and vice versa, to safeguard market position.

Geographical Protection and Filing Strategy

  • European Extension: Given Cyprus's inclusion in the European Patent Convention, similar patents probably extend into the EPO framework, providing broader regional protection.
  • Global Patent Strategy: To maximize commercial value, patent families may have been filed in key jurisdictions such as the US, China, and Japan, aligned with the imatinib or other competitive therapeutic markets.

Legal Status and Maintenance

  • Patent Validity: Maintaining CY1124056 during its full term involves paying renewal fees and defending against oppositions or invalidity challenges.
  • Potential Challenges: Third-party observations citing prior art or patentability issues could influence the patent's enforceability or scope.

Implications for Stakeholders

  • Pharmaceutical Innovators: The patent's scope indicates a strategic edge if it covers a novel therapeutic mechanism or compound.
  • Generic Manufacturers: The scope and remaining life of CY1124056 influence their ability to introduce generic versions, particularly if the patent faces legal challenges.
  • Investors and Licensees: Patent strength and landscape positioning impact valuation and partnership prospects.

Key Takeaways

  • Claims Analysis: CY1124056 most likely employs a balanced claim set, with broad compound or method claims supported by narrower dependent claims to ensure enforceability and robustness.
  • Strategic Positioning: The patent's geographic and patent family breadth suggests a focus on regional, then potentially global, patent protection aligned with commercial ambitions.
  • Legal Landscape: The pharmaceutical patent space in Cyprus and Europe remains highly competitive, with continued innovation requiring vigilant patent monitoring and strategic filings.
  • Protection Robustness: The validity of CY1124056 depends on supporting disclosure, claim drafting, and ongoing legal defenses against potential invalidity or infringement assertions.

FAQs

1. What is the primary focus of patent CY1124056?
CY1124056 primarily covers a specific pharmaceutical compound or composition designed for a therapeutic application, likely targeting a particular disease or condition.

2. How broad are the claims in CY1124056?
While specifics require detailed claim analysis, pharmaceutical patents generally balance broad chemical structure claims with narrower use or formulation claims to maximize protection while maintaining validity.

3. How does the patent landscape impact CY1124056’s enforceability?
The surrounding patent landscape, including prior art and similar patents, influences the patent's validity and scope. A well-drafted claim set supports enforceability, but conflicts can arise in overlapping patent territories.

4. Can CY1124056 be extended or fortified through international filings?
Yes. Patents filed under the PCT or directly in other jurisdictions like the US, China, and Japan can extend protection, creating a patent family that broadens commercial exclusivity globally.

5. What should stakeholders monitor regarding CY1124056?
Stakeholders should monitor legal status updates, potential oppositions, and subsequent filings that may narrow or strengthen the patent's scope, alongside market developments and competitor patent activities.


References

  1. European Patent Office (EPO) patent database, CY1124056 record.
  2. WIPO Patentscope database, related patent family applications.
  3. Relevant patent prosecution and legal analysis reports.
  4. Industry reports on pharmaceutical patent strategies in Cyprus and Europe.

This detailed examination provides critical insights for decision-makers in pharmaceuticals, licensing, and strategic patent management, emphasizing the importance of comprehensive patent claim drafting and landscape awareness for maximizing patent value.

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