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

Last Updated: December 28, 2025

Profile for Cyprus Patent: 1111689


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1111689

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
8,642,079 Jul 9, 2028 Duchesnay OSPHENA ospemifene
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1111689

Last updated: July 30, 2025

Introduction

Cyprus patent CY1111689 pertains to a novel pharmaceutical invention, believed to encompass a specific composition, method, or use related to a therapeutic agent. This analysis aims to dissect the scope and claims of CY1111689 comprehensively while contextualizing its patent landscape—covering prior art, similar patents, and its strategic positioning within the global pharmaceutical patent environment. Such insights are vital for stakeholders to evaluate patent strength, potential infringement risks, and licensing opportunities.

Patent Identification and Basic Details

  • Patent Number: CY1111689
  • Jurisdiction: Republic of Cyprus
  • Filing Date: [Specific date, if available]
  • Grant Date: [Specific date, if available]
  • Application Priority Date: [If applicable]
  • Assignee/Applicant: [Assignee's name or legal entity]
  • Inventors: [Inventors, if disclosed]

(Note: Exact dates and applicant details require referencing the official Cyprus Intellectual Property Office records or patent databases such as Espacenet or WIPO PATENTSCOPE.)


Scope of CY1111689: Patent Claims and Coverage

Types of Claims

A typical pharmaceutical patent like CY1111689 likely contains independent claims that define the broadest scope of the invention, complemented by dependent claims offering specific embodiments and variations.

  • Product Claims:
    May cover the active pharmaceutical ingredient (API), its salts, polymorphs, formulations, or combinations. These claims ensure the patent protects the specific compound(s) or their derivatives.

  • Method Claims:
    Encompass methods of synthesis, pharmaceutical use, or treatment methods utilizing the compound, including dosing regimens, administration routes, or targeted diseases.

  • Use Claims:
    Claiming the application of the compound for particular indications, which is common for pharmaceuticals intending to extend patent life via “second medical use” claims.

  • Formulation Claims:
    Covering specific dosage forms or delivery systems, such as controlled-release formulations, nanoparticles, or transdermal systems.

Claim Strategy and Language

The claims likely employ broad language to maximize scope:

  • Use of terms such as “comprising,” “consisting of,” and “adapted to” to define the claim boundaries.
  • Clauses specifying structural features, binding affinity, or pharmacological activity.
  • Inclusion of ranges (e.g., dosage, concentration) for flexibility.

This strategic claim drafting aims to balance broad protection with defensibility against prior art.

Key Aspects of Claim Scope

  • Novelty and Inventive Step:
    To be patentable, CY1111689 must demonstrate novelty over existing drugs and inventive step, meaning non-obviousness to someone skilled in the art based on prior art.

  • Scope Breadth vs. Validity:
    Broader claims increase market exclusivity but face higher invalidity risks if prior art shows overlaps. Specificity can improve robustness but limit coverage.

  • Post-Grant Amendments:
    The potential for claims to be amended or narrowed during prosecution is typical, especially if initial broad claims face rejections.


Patent Landscape Analysis

Global Patent Environment

Given that Cyprus is a member of the European Patent Convention (EPC), CY1111689’s strategic value extends into European markets through potential validation or extension. It’s vital to examine:

  • Prior Art:
    Review of existing patents, publications, or applications describing similar compounds or use cases is necessary. Major databases such as Espacenet, WIPO, and EPO provide comprehensive worldwide prior art.

  • Comparable Patents:
    Analyzing patents from established pharmaceutical players can reveal if CY1111689 is overlapping with existing patent families or if it introduces significant innovations.

  • Patent Families and Continuations:
    CY1111689 might be part of a broader patent family, including pending applications or divisional filings, which can extend its protection or signal ongoing R&D efforts.

Key Patent Classification

The patent likely falls under IPC classes related to:

  • A61K (Pharmaceutical preparations)
  • C07D (Heterocyclic compounds)
    Or specific classes depending on the chemical nature of the claimed compound(s).

Identifying relevant classifications assists in targeting patent searches, litigation risks, and licensing strategies.

Patent Valuation and Freedom-to-Operate (FTO) Analysis

  • The patent’s validity depends on distinctiveness over prior art.
  • An FTO analysis examines existing patents in relevant jurisdictions to assess risks of infringement when commercializing the drug.
  • Weak claims might necessitate supplementary patent filings or development strategies to extend exclusivity.

Legal and Commercial Implications

The strength of CY1111689 hinges on claim breadth, prior art overlap, and jurisdictional coverage. A robust patent landscape provides:

  • Market Exclusivity:
    Protecting the proprietary compound and use methods within the validated territories.

  • Partnership Opportunities:
    Licensing or co-development deals hinge upon clear patent rights.

  • Infringement Risks:
    Ensuring freedom to operate involves detailed analysis of existing patents to avoid costly litigations.


Challenges and Opportunities

Challenges

  • Patent Invalidity Risks:
    If prior art closely resembles CY1111689, claims may be challenged, leading to narrower patent scope or invalidation.

  • Patent Lean Periods:
    Lifecycle management strategies, including pediatric or second medical use patents, are critical as initial claims expire.

  • Crisis of Overlap:
    Entry into crowded pharmaceutical patent landscapes requires careful navigation around existing patents.

Opportunities

  • Patent Term Extensions:
    Exploiting pediatric or supplementary protection certificates can prolong exclusivity.

  • Strategic Claim Drafting:
    Focused claims on novel formulations or specific indications may yield defensible patent rights.

  • Global Patent Filings:
    Expanding into jurisdictions like the European Patent Office or USPTO enhances market reach.


Conclusion

The Cyprus patent CY1111689 embodies a strategic piece within the pharmaceutical patent landscape. Its scope—centered on chemically or clinically novel aspects—must be validated against rigorous prior art searches. The claims likely combine broad protection with specific embodiments to maximize enforceability and commercial utility.

Careful management of its patent strategy involves continual landscape monitoring, considering jurisdictional extensions, and leveraging the patent's strength to secure market exclusivity. This landscape analysis underscores the importance of comprehensive patent drafting, diligent prior art research, and strategic global patent portfolio development to optimize R&D investments.


Key Takeaways

  • CY1111689’s scope appears to encompass core therapeutic compounds and methods, with claims tailored for broad yet defensible pharmaceutical protection.
  • Effective patent landscape management requires ongoing review of similar patents, especially in major markets, to maintain market exclusivity.
  • Broader claims increase commercial leverage but may face invalidity challenges; precision and strategic claim drafting are critical.
  • The patent’s success depends on robust prosecution, ongoing innovation, and international patent protections aligned with business goals.
  • Regular FTO and validity analyses mitigate infringement risks and inform licensing or partnership negotiations.

FAQs

  1. What is the significance of claim scope in pharmaceutical patents?
    It defines the breadth of protection; broader claims cover more variations but are more vulnerable to invalidity, whereas narrower claims are easier to defend but limit market scope.

  2. How does prior art impact CY1111689’s enforceability?
    Prior art that overlaps with claimed features can invalidate the patent or require narrowing claims, reducing enforceability and market exclusivity.

  3. Can CY1111689 be extended beyond Cyprus?
    Yes, through filings in the European Patent Office, PCT applications, or national patents in key markets, expanding its geographic scope.

  4. What strategies enhance the value of pharmaceutical patents like CY1111689?
    Focusing on claim breadth, filing for secondary uses, extending patent life via supplementary protections, and continuous innovation.

  5. How important is patent landscape analysis for pharmaceutical R&D?
    It is critical for avoiding infringement, identifying licensing opportunities, and shaping patent strategies to maximize commercial advantage.


Sources:

  1. Cyprus Intellectual Property Office Patent Database.
  2. Espacenet Patent Search.
  3. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  4. European Patent Office (EPO) Public Patent Data.
  5. Relevant scientific and patent literature on pharmaceutical patents.

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.