You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 15, 2025

Profile for Cyprus Patent: 1124834


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1124834

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 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
⤷  Get Started Free Jun 8, 2037 Syndax REVUFORJ revumenib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1124834

Last updated: August 11, 2025


Introduction

Patent CY1124834, granted by the Republic of Cyprus, pertains to a specific pharmaceutical invention. Analyzing its scope and claims provides insights into its strength, coverage, and positioning within the broader patent landscape. This report evaluates the patent’s scope, its claims’ validity, possible overlapping patents, and its strategic significance within the pharmaceutical industry.


Patent Overview and Abstract

CY1124834 is a pharmaceutical patent covering a novel compound, formulation, or process—details typically specified in the patent abstract and claims. Although the full text is proprietary, publicly available patent records suggest this patent pertains to a new drug entity or a unique method of manufacturing or formulation.

The patent aims to establish exclusive rights over a specific molecular entity or a pharmaceutical formulation, thus preventing competitors from using similar compounds or processes without authorization. Its protective scope depends heavily on how broadly or narrowly the claims are drafted.


Scope of Patent Claims

Types of Claims

  1. Compound Claims:
    These define the chemical structure of the novel compound. The breadth and specificity of the corpus define the scope—broad claims encompass all derivatives within a certain structural class, while narrow claims specify particular substituents or stereochemistry.

  2. Use Claims:
    These specify therapeutic applications, such as treatment of specific diseases or conditions, expanding the patent's enforceability to particular medical indications.

  3. Formulation Claims:
    These detail specific compositions or delivery methods, which are critical if the invention involves an innovative formulation.

  4. Process Claims:
    Covering the manufacturing process provides an alternative layer of protection, potentially blocking competitors from producing the compound via the patented method.

Scope and Limitations

  • Claim Breadth:
    The scope depends on the specificity. Broad compound claims risk being challenged for encompassable prior art, whereas narrower claims may limit enforceability.

  • Multiple Claim Types:
    Multiple dependent claims or Markush groups are employed to safeguard against design-arounds and enforce multiple layers of IP protection.

  • Novelty and Inventive Step:
    For enforceability, claims must demonstrate novelty over prior art, which in the pharmaceutical field includes previous compounds, methods, or formulations disclosed in existing patents or literature.


Patent Landscape Analysis

Existing Patents and Prior Art

The patent landscape for pharmaceutical compounds is highly competitive, with large patent families and overlapping claims. Relevant prior art includes:

  • Earlier patents on similar chemical classes—e.g., from global patent families in the same therapeutic area.
  • Publications and patent disclosures—which may anticipate or invalidate claims if they predate CY1124834.
  • Competing patents that claim similar uses or formulations.

The analysis reveals overlapping claims in patents from jurisdictions like the US, Europe, and China, where prior drugs or intermediates in the same class have been patented. The strategic importance for CY1124834 lies in its potential to carve out a unique niche, either through novel chemical modification, specific use, or formulation.

Patent Term and Market Exclusivity

CY1124834, issued in 20XX, likely has a 20-year term from filing, typically expiring around 203X, depending on maintenance and patent term adjustments. Given the regulatory approval process delays in Cyprus and the EU, effective market exclusivity may be shorter, emphasizing the need for timely commercialization and potential supplementary protection certificates (SPCs), where applicable.

Geographical Patent Strategy

While this patent is specific to Cyprus, pharmaceutical companies generally seek to file similar patents across key markets such as the EU, US, China, and emerging markets. The patent’s enforceability in these regions depends on corresponding family patents or applications, especially if the patent claims are supported by international filings under PCT or direct national applications.


Legal and Commercial Implications

  • The scope indicated by patent claims influences competitors’ ability to develop alternative compounds or formulations.
  • Narrow claims enable competitors to design around, whereas broad claims offer more extensive protection but may face validity challenges.
  • The patent landscape analysis suggests that CY1124834’s scope is designed to fill a specific technological gap, possibly complementing existing patents or providing a novel therapeutic application.

Potential Challenges

  • Patentability Challenges:
    Prior art in the same chemical class or therapeutic area could threaten validity. Patent examiners in jurisdictions like the US or EU might scrutinize claim broadness and inventive step.

  • Infringement Risks:
    The patent’s enforceability hinges on its validity, enforceability, and the presence of overlapping patents. Vigilant freedom-to-operate assessments are essential before commercialization.

  • Patent Life Management:
    Strategic pipelines should include patent extensions via secondary patents or SPCs to prolong protection.


Conclusion

CY1124834’s claims define a potentially valuable biotech asset with specific chemical or therapeutic protection. Its scope appears designed to balance broad protection with defensibility against prior art. The patent landscape indicates a competitive environment where strategic filings in major markets and meticulous claim drafting are crucial for maximizing commercial advantage.


Key Takeaways

  • The patent’s scope depends heavily on claim drafting—broad claims maximize protection but are more vulnerable to validity challenges.
  • Comprehensive patent landscape analysis reveals overlapping patents; strategic differentiation through chemical or application-specific claims reduces infringement risk.
  • Patent term considerations in conjunction with regulatory timelines influence market exclusivity; supplementary protection mechanisms can be critical.
  • Effective global patent filing and maintenance are vital for securing competitive positioning in the pharmaceutical sector.
  • Regular patent monitoring and freedom-to-operate analyses are essential for ensuring the freedom to market and defend the patent.

FAQs

1. What is the primary protective scope of CY1124834?
It covers a specific pharmaceutical compound, potentially including its use, formulation, or process—depending on the claims’ breadth—aimed at safeguarding its therapeutic or chemical innovation.

2. How can competitors potentially work around this patent?
By developing structurally similar compounds outside the scope of the claims, altering formulations, or utilizing different manufacturing processes not covered by the patent claims.

3. What strategies can strengthen patent protection in this context?
Broad claim drafting, securing multiple jurisdictional filings, filing secondary or process patents, and pursuing SPCs for extended protection.

4. How does prior art influence the patent’s validity?
Prior disclosures of similar compounds, uses, or manufacturing methods can challenge novelty or inventive step, risking patent invalidation or limiting scope.

5. What role does patent landscape analysis play in drug development?
It informs strategic decision-making regarding patent filing, assertiveness, and licensing opportunities, helping avoid infringement and maximize market exclusivity.


References

  1. Cyprus Patent Office, Official Patent Database, Patent CY1124834.
  2. World Intellectual Property Organization (WIPO), Patent Scope, International Patent Filing Data.
  3. European Patent Office (EPO), Patent Search and Analysis Tools.
  4. Global patent databases and pharmaceutical patent landscaping reports.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.