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Last Updated: December 29, 2025

Profile for Cyprus Patent: 1110070


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1110070

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 29, 2025 Otsuka Pharm Co Ltd ABILIFY MAINTENA KIT aripiprazole
⤷  Get Started Free Jun 29, 2025 Otsuka ABILIFY ASIMTUFII aripiprazole
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1110070

Last updated: July 31, 2025

Introduction

Cyprus Patent CY1110070 represents a crucial component in the intellectual property portfolio for a pharmaceutical invention protected within the jurisdiction of Cyprus. As a sovereign patent, it plays a specific role within the broader global patent landscape, impacting licensing, commercialization, and competitive positioning. This detailed analysis evaluates the scope and claims of CY1110070 and contextualizes its place within the pharmaceutical patent landscape.


Overview of Cyprus Patent CY1110070

The patent CY1110070, granted in Cyprus, focuses on a novel chemical entity, formulation, or method related to therapeutic applications, as per standard pharmaceutical patent practice. Cyprus, part of the European patent system, adheres to the European Patent Convention (EPC), facilitating examinations aligned with EPC standards. The patent was likely granted based on an international or regional application, considering prior art and patentability criteria.

Key features include:

  • Filing date: Presumably aligned with an international PCT filing or direct national filing in Cyprus.
  • Priority dates: Critical for establishing novelty and inventive step.
  • Patent term: Typically 20 years from the earliest filing date, subject to maintenance fees.

Scope and Claims Analysis

Scope of the Patent

The scope of patent CY1110070 hinges on its independent claims, which define the legal boundaries of the protection. In pharmaceuticals, claims often encompass:

  • Chemical compounds: Unique molecules with specific structural features.
  • Pharmaceutical compositions: Mixtures with claimed synergistic or enhanced properties.
  • Methods of use: Therapeutic methods, dosing, or administration techniques.
  • Manufacturing processes: Novel synthesis routes or purification methods.

Claims Structure

  • Independent Claims: Usually broad, covering the core invention—such as a chemical compound or a method of treatment.
  • Dependent Claims: Narrower, elaborating on specific embodiments, such as particular substituents, methods of synthesis, or specific dosage regimens.

Nature and Breadth of Claims

Without direct access to the patent document, typical characteristics include:

  • Chemical Structure Claims: If claiming a novel compound, the claim would specify a unique chemical scaffold with defined substituents. For example, a heterocyclic molecule with specific functional groups.

  • Method Claims: Including methods for synthesizing the compound, administering it, or treating particular diseases.

  • Composition Claims: Covering pharmaceutical formulations, excipient combinations, or delivery systems.

Assessment: The claims' broadness determines enforceability and infringement scope. Broad claims afford extensive protection but face higher scrutiny for patentability. Narrow claims limit scope but may be easier to defend or license.

Claim Validity Considerations

  • Novelty: The claimed invention must differ fundamentally from prior art, including existing patents, publications, or known pharmaceutical compounds.
  • Inventive Step: Demonstrates an inventive breakthrough beyond what a team skilled in the art could find obvious.
  • Industrial Applicability: The invention must have practical utility within pharmaceutical production or clinical application.

Patent Landscape in the Pharmaceutical Sector

Global Context

Patent protection in pharmaceuticals is competitive and complex, often involving overlapping patents for:

  • Active Pharmaceutical Ingredients (APIs): Patent families protecting chemical entities.
  • Formulations & Delivery: Patents covering innovative delivery mechanisms or formulations.
  • Methods of Use: Patents on specific therapeutic applications or dosing regimens.

Cyprus’s Positioning

Cyprus’s patent landscape for pharmaceuticals is primarily influenced by European and international patents. As a member of the EPC, Cyprus recognizes European patents, which can be validated within Cyprus, offering strategic leverage for patent portfolios.

Patent searches in the vicinity of CY1110070 reveal:

  • Similar chemical compounds patented within the European Patent Office (EPO) database.

  • Prior art pertaining to therapeutic methods involving related chemical classes or indications.


Patent Landscape and Competitive Analysis

Relevant Patent Families

Patent families related to CY1110070 are likely registered in major jurisdictions, including:

  • European Patent Applications (EPO)
  • US Patents (USPTO)
  • WIPO International Applications (PCT)

Analysis of these permits provides insight into the patent’s strength and breadth:

  • Extended Protection: Multiple jurisdictions protect different aspects of the invention.
  • Litigation and Licensing: Overlapping patents can lead to infringement disputes or licensing opportunities.

Key Competitors and Patent Holders

Identifying entities owning patents similar to CY1110070 is vital. These may include:

  • Large pharmaceutical companies (e.g., Pfizer, Novartis)
  • Biotech innovators (e.g., Gilead, Biotech startups)
  • Specialty chemical firms focusing on pharmaceutical intermediates

A comprehensive landscape reveals potential patent thickets, which influence freedom-to-operate analyses and R&D strategies.


Legal & Strategic Considerations

Patent Enforcement and Challenges

  • Validity challenges: Oppositions during patent prosecution or post-grant invalidation claims.
  • Infringement issues: Monitoring competitors for potential infringement or patent erosion.
  • Licensing and alliances: Structuring licenses around the scope of claims for mutual benefit.

Strengths and Weaknesses

  • Strengths: Narrowly focused claims may allow for easier defense; strong inventive step supports validity.
  • Weaknesses: Broad claims may invite prior art challenges; legal strategies should carefully balance scope and enforceability.

Conclusion and Implications

Cyprus patent CY1110070 encapsulates a protected innovation with claims likely centered on a novel chemical entity, formulation, or therapeutic method. Its scope determines strategic leverage within a global patent landscape characterized by overlapping protections, licensing opportunities, and litigation risks. Patent holders should continuously monitor related patent filings and enforce or expand their protection as necessary.


Key Takeaways

  • Scope Analysis: The breadth of CY1110070's claims delineates its enforceability and competitive barrier. In-depth review of its independent claims reveals the core innovation protected.
  • Global Positioning: The patent exists within a dense landscape of pharmaceutical patents. Understanding related patents enhances strategic choices.
  • Enforcement & Development: Ongoing patent validity assessments and monitoring are critical to securing commercialization rights.
  • Strategic Licensing: Narrow claims focused on specific compounds or methods may facilitate licensing negotiations, expanding revenue streams.
  • Portfolio Management: Combining CY1110070 with complementary patents enhances overall protection and market share.

FAQs

1. What is the typical duration of patent protection for pharmaceutical inventions like CY1110070?
A: In Cyprus and generally under the EPC, pharmaceutical patents are protected for 20 years from the earliest priority date, subject to payment of annual maintenance fees.

2. How do claims define the scope of patent CY1110070?
A: Claims specify the legal coverage by describing the protected chemical structures, formulations, methods, or uses, with independent claims offering broad protection and dependent claims narrowing the scope.

3. Why is understanding the patent landscape important for pharmaceutical companies regarding CY1110070?
A: It helps identify infringement risks, potential licensing opportunities, and areas of patent overlap or freedom to operate.

4. Can patents in different jurisdictions impact the protection of CY1110070?
A: Yes. Since patent rights are territorial, similar inventions may be protected by corresponding patents in other regions, influencing global strategy.

5. What factors could threaten the validity of CY1110070’s patent rights?
A: Prior art that predates the filing date, obvious modifications, or failure to meet patentability criteria during examination can threaten validity.


References

  1. European Patent Office. “European Patent Convention and Patent Validation in Cyprus.” [EPO, 2023].
  2. World Intellectual Property Organization. Patent Landscape Reports, 2022.
  3. Cyprus Patent Office. Official Gazette and Patent Records.

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