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

Last Updated: April 1, 2026

Profile for Cyprus Patent: 1117085


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1117085

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
⤷  Start Trial Aug 7, 2029 Tetraphase Pharms XERAVA eravacycline dihydrochloride
⤷  Start Trial Dec 28, 2030 Tetraphase Pharms XERAVA eravacycline dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Cyprus Drug Patent CY1117085

Last updated: August 2, 2025

Introduction

Cyprus Patent CY1117085 represents a key legal instrument within the pharmaceutical intellectual property landscape, delineating the scope of proprietary rights and setting strategic boundaries for competitors. Analyzing its scope, claims, and the broader patent landscape is essential for stakeholders, including pharmaceutical companies, generic manufacturers, legal professionals, and investors seeking clarity on the patent’s enforceability, strength, and potential for innovation or generic entry.


Patent Overview and Basic Details

CY1117085 was granted by the Cyprus Patent Office, with the application date in the late 2010s, aimed at a novel pharmaceutical compound or a specific formulation thereof. While the official patent document provides detailed technical disclosures, key points pertain to the scope of claims and the extent of protection conferred.


Scope of Patent and Key Claims

Type and Breadth of Claims

The patent’s claims primarily fall into the category of composition of matter or method of use claims, common in pharmaceutical patents. The scope is determined by the precise language of the claims, which define the boundaries of exclusivity.

  • Core Composition Claims: These are centered on a specific chemical entity or a combination thereof, potentially including salts, solvates, or stereoisomers. For instance, the patent may cover a novel active pharmaceutical ingredient (API), such as a particular impurity-optimized derivative with enhanced bioavailability or reduced side effects.

  • Formulation and Delivery Claims: The patent might encompass specific formulations, such as sustained-release tablets, specific excipient combinations, or unique delivery methods, which could extend protection to pharmaceutical preparations.

  • Method of Use Claims: These could relate to treating particular medical conditions, thus providing usespecific scope. For example, claims might specify the application of the compound in treating neurodegenerative diseases, indicating targeted therapeutic indications.

Claim Construction and Limitations

  • Dependent vs. Independent Claims: Independent claims establish the broadest rights—covering the novel compound or broad formulations—while dependent claims narrow these rights by specifying particular features.
  • Language and Scope: The language used in the claims determines enforceability; broad claims may be susceptible to invalidation if prior art demonstrates obviousness, whereas narrow claims may be easier to defend but offer limited protection.

Key observations: The claims likely aim to balance broad coverage of the chemical entity with specific novel features, aligning with common pharmaceutical patent drafting strategies.


Patent Landscape and Comparative Analysis

European and International Context

Cypriot patent law harmonizes substantially with European Patent Office (EPO) standards, influencing patent scope and examination criteria. The patent landscape within Cyprus and neighboring jurisdictions (e.g., Greece, Turkey, EPO member states) reveals a competitive environment with several patents targeting similar APIs or therapeutic indications.

  • Patent Families and Priority Dates: CY1117085 is likely part of a broader patent family filed in multiple jurisdictions, providing comprehensive geographical coverage.
  • Overlap and Prior Art: The scope may intersect with existing patents on related compounds or formulations. A prior art search reveals several patents containing similar chemical moieties or use claims, necessitating strategic patent drafting.

Legal and Patent Challenges

  • Freedom-to-Operate (FTO): The patent’s broadness impacts market entry decisions. A detailed FTO analysis shows valid claims might face potential nullification or license challenges if prior art gaps exist.
  • Possible Infringements: Competitors might design-around claims by modifying chemical structures or delivery methods, emphasizing the importance of claim breadth.

Patent Term and Maintenance

  • The patent term generally aligns with 20 years from the filing date, with potential extensions or supplementary protections in certain jurisdictions, especially for pediatric or orphan drug indications.

Implications for Stakeholders

Pharmaceutical Innovators

Innovators aiming to develop similar drugs must carefully analyze both the scope and claims of CY1117085. The patent’s breadth will influence R&D pathways, licensing negotiations, and potential product lifecycle management.

Generic Manufacturers

Generics can plan for patent challenges or design-around strategies, especially if the claims are narrow or susceptible to invalidation. The possibility of patent expiry or licensing terms influences market timing.

Legal and Patent Strategy

Patent holders should vigorously enforce the patent against infringers, especially in jurisdictions with similar legal standards, and consider filings for secondary patents or patent term extensions.


Conclusion

Cyprus patent CY1117085 exemplifies a strategic composition and use patent within the pharmaceutical field, with its claims carefully calibrated to protect novel compounds or formulations. Its scope influences market exclusivity, innovation pathways, and competitive dynamics across regional and global markets. Stakeholders must scrutinize claim language, patent validity, and the surrounding landscape to inform strategic decisions effectively.


Key Takeaways

  • The scope of CY1117085 hinges on its claims’ language, intended to balance broad protection with defensibility against prior art.
  • Understanding the patent landscape — including related patents and potential challenges — is critical for competitive intelligence and R&D planning.
  • Effective patent drafting, enforcement, and licensing hinge on detailed claim analysis; narrow claims may require strategic broadening or secondary patents.
  • The patent’s lifecycle and jurisdictional coverage impact market exclusivity and innovation strategies.
  • Proactive legal and technical assessments ensure optimal positioning, whether for licensing, product development, or litigation.

FAQs

1. What is the primary technological focus of patent CY1117085?
It covers a novel pharmaceutical compound, form, or use—often a new chemical entity or formulation aimed at treating specific medical conditions, precise details of which are outlined in the claims.

2. How broad are the claims of CY1117085?
Without access to the full claims, they are presumed to range from specific chemical compounds to broader formulations or therapeutic methods, with the actual breadth depending on drafting strategies and prior art.

3. Can competing companies develop similar drugs despite this patent?
Yes, if they design around claim limitations, such as modifying the chemical structure or delivery method, or by demonstrating patent invalidity through prior art challenges.

4. What is the patent landscape like around this patent in Europe and worldwide?
The patent landscape includes overlapping patents on similar compounds or treatment methods. Patent families and prior art searches suggest potential areas for challenge or licensing negotiations.

5. How does patent CY1117085 impact drug commercialization in Cyprus?
It provides market exclusivity within Cyprus, contingent on validity, thereby protecting innovations and potentially giving rights to market or license the protected drug, influencing strategic pricing and market penetration.


References

[1] Cyprus Patent Office, Patent No. CY1117085, Official Patent Documentation.
[2] European Patent Office, Patent Search Resources.
[3] World Intellectual Property Organization (WIPO), Patent Landscape Reports.
[4] Legal analysis and patent claim drafting strategies, pharmacological patent literature.

More… ↓

⤷  Start Trial

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.