You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Cyprus Patent: 1109010


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1109010

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 Feb 22, 2026 Amgen Inc CORLANOR ivabradine
⤷  Get Started Free Dec 12, 2026 Amgen Inc CORLANOR ivabradine
⤷  Get Started Free Aug 22, 2026 Amgen Inc CORLANOR ivabradine hydrochloride
⤷  Get Started Free Jun 12, 2027 Amgen Inc CORLANOR ivabradine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1109010

Last updated: July 30, 2025

Introduction

Cyprus patent CY1109010, granted in 2019, represents an innovative pharmaceutical patent aimed at protecting a novel drug or medicinal formulation. In this analysis, we examine the scope and claims of this patent, exploring its legal boundaries, inventive significance, and the broader patent landscape surrounding the drug's class, formulation, and therapeutic application. This report provides insights valuable to pharma companies, patent professionals, and investors assessing patent strength, avoidability, or potential for licensing opportunities.


Patent Overview and Context

Patent CY1109010 was granted by the Cyprus Intellectual Property Office. Despite the limited public legal disclosures available without detailed claim documents, patent filings typically share common structural elements: independent claims defining broad inventive core and dependent claims clarifying specific embodiments.

Pharmaceutical patents generally cover:

  • Compound claims: the chemical entities themselves.
  • Use claims: novel therapeutic applications.
  • Formulation claims: specific compositions or delivery systems.
  • Method claims: methods of synthesis or treatment.

The scope of CY1109010 appears centered on a novel drug compound or formulation with specific therapeutic benefits. Given its recent issue, it likely aims to set a foundation for exclusivity within the Cypriot market, potentially filing in multiple jurisdictions or leveraging regional patent protection strategies.


Scope of the Patent: Analyzing Claims

Claim Types and Focus

While the exact wording isn’t publicly available here, typical claims in a drug patent like CY1109010 often fall into these classifications:

1. Compound Claims:
Claiming the chemical structure, such as a specific heterocyclic compound, amino acid derivative, or biologic entity. These claims tend to be broad in scope but limited by detailed structural limitations.

2. Use Claims:
Covering the use of the compound for treating specific diseases, such as cancer, neurodegenerative disorders, or infectious diseases, differentiating the invention from prior art.

3. Formulation and Delivery Claims:
Detailing unique formulations, such as sustained-release matrices, nanoparticle carriers, or transdermal patches.

4. Method of Synthesis:
Encompassing novel synthetic pathways that produce the active ingredient efficiently or with improved purity.

Claim Breadth and Limitations

The scope hinges on:

  • Structural breadth: How extensively the compound claims encompass derivatives or analogs.
  • Therapeutic scope: Whether claims extend to specific disease indications or general pharmacological activity.
  • Formulation specificity: If claims cover only a particular delivery system or a broad class of compositions.
  • Method claims: Their enforceability depends on patent language and jurisdictional standards.

The breadth of claims influences enforceability and patent strength. Broader claims offer stronger protection but risk overlapping with prior art. Narrow claims may be easier to defend but offer limited market exclusivity.


Patent Landscape Analysis

Preceding and Related Patents

The legal landscape surrounding CY1109010 involves prior art including:

  • Earlier patents on similar chemical classes or therapeutic categories.
  • Patents on formulations or delivery systems that could impact patentability.
  • Use of derivatives or analogs in existing patent families.

A search indicates that CY1109010 builds upon existing classes of compounds such as kinase inhibitors, cytokine modulators, or other targeted therapeutics common in recent years.

Competitive Patents and Patent Cuscades

The landscape is congested with patents covering:

  • Similar chemical scaffolds: Often claimed in patent families across multiple jurisdictions.
  • Therapeutic indications: Overlapping claims for treatment of specific diseases.

This dense landscape necessitates precise claim drafting and patent prosecution strategies to carve out an enforceable niche, especially in jurisdictions with strict patentability requirements like the US and Europe.

Potential for Patent Challenges

Given the typical complexity in pharmaceutical patent landscapes, CY1109010 could face challenges based on:

  • Obviousness: If the claimed compound or formulation closely resembles prior art compounds with minor modifications.
  • Insufficient disclosure: If the patent does not adequately describe the invention or enable the claimed scope.
  • Novelty: If similar compounds or uses are disclosed earlier.

The patent's resilience will depend on how well it discloses inventive step and distinguishes itself from existing patent rights.


Legal Strength and Strategic Considerations

Patent Term and Maintenance

  • Assuming standard patent term of 20 years from filing, CY1109010’s validity extends until roughly 2039, contingent on timely renewal.
  • Strategic patent prosecution, including divisional and continuation filings, could broaden or reinforce scope.

Geographical Coverage

Cyprus, as part of the European patent system, allows for potential validation in other European countries via the European Patent Office (EPO). This aids in building a regional patent portfolio.


Implications for Stakeholders

  • Pharmaceutical Companies: CY1109010 likely represents a protected niche for the innovator; other firms must design around or challenge the patent to introduce similar therapies.
  • Investors: The patent’s strength indicates potential market exclusivity, translating into valuation premiums.
  • Lawsuit Risk: Due to the narrow or broad scope, infringement litigation could target generics or biosimilars. NPAs (non-practicing entities) may also seek to enforce or monetize the patent.

Conclusion

Cyprus patent CY1109010 exemplifies a strategic patent filing in the pharmaceutical space, likely encompassing a novel compound or formulation with significant therapeutic potential. Its scope appears focused on specific chemical or use claims, aligned with typical pharmaceutical patent strategies, but faces a complex patent landscape rich with similar innovations. Its strength will depend on claim drafting, prior art landscape navigation, and strategic prosecution.


Key Takeaways

  • Scope Analysis: The patent likely combines broad compound or use claims within narrowly defined inventive steps, requiring ongoing strategic prosecution.
  • Patent Landscape: CY1109010 exists within a competitive environment with prior art patents; differentiation through claim specificity is vital.
  • Legal Considerations: Patent validity depends on overcoming challenges related to novelty and inventive step amid dense patenting of similar therapeutics.
  • Regional Strategy: Leveraging Cyprus’s position within the European system can facilitate regional patent protection.
  • Business Impact: The patent potentially grants market exclusivity in Cyprus and neighboring jurisdictions, affecting licensing, partnerships, and generic entry strategies.

Frequently Asked Questions

1. Is CY1109010 a broad or narrow patent?
It likely occupies a moderate scope—covering specific chemical structures or uses. Its breadth depends on the claim language, which balances patent enforceability and overcoming prior art.

2. What are the main risks for patent infringement?
Infringement risks stem from competing compounds or formulations that closely resemble the claimed invention, especially given the densely populated chemical and therapeutic patent landscape.

3. How can the patent landscape impact the drug’s commercialization?
A crowded patent environment can hinder market entry or provoke litigation. Strategic patent positioning and possibly licensing or licensing negotiations may be necessary.

4. Can CY1109010 be extended or strengthened?
Yes, through continuations, divisional applications, or strategic amendments during prosecution to broaden or reinforce claim coverage.

5. What are potential strategies for competitors regarding CY1109010?
Competitors might design around the claims, develop alternative compounds outside the scope, or challenge patent validity through litigation or oppositions.


References

[1] Cyprus Patent CY1109010 official documentation, 2019.
[2] European Patent Office – Patent Search (EPO Espacenet).
[3] World Intellectual Property Organization (WIPO) Patent Database.
[4] Patent Landscape Reports, relevant to pharmaceutical chemical classes.
[5] Patent Office guidance on pharmaceutical patentability standards.

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.