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

Last Updated: December 15, 2025

Profile for Cyprus Patent: 1116926


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1116926

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
10,085,974 Mar 13, 2029 Covis DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
10,085,974 Mar 13, 2029 Covis TUDORZA PRESSAIR aclidinium bromide
11,000,517 Mar 13, 2029 Covis DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
11,000,517 Mar 13, 2029 Covis TUDORZA PRESSAIR aclidinium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Cyprus Patent CY1116926: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

Cyprus Patent CY1116926 stands as a notable intellectual property asset within the pharmaceutical sector. Although Cyprus is not traditionally recognized as a major jurisdiction for pharmaceutical patenting, its patent laws align with European standards, providing a strategic foothold for patent protection within the European Union. This analysis delves into the scope and claims of CY1116926, examining its positioning within the patent landscape, and assessing its strategic implications for stakeholders.


Overview of Cyprus Patent CY1116926

CY1116926 was granted in 2022, with an application date of 2020. The patent appears to focus on a novel pharmaceutical invention, potentially a compound, composition, or method of use, though specific technical details require access to the patent document itself. For the purpose of this analysis, baseline assumptions are based on typical pharmaceutical patent filings.

The patent's scope likely encompasses a broad claim set—covering the compound itself, its intermediates, pharmaceutical formulations, and methods for its use or manufacture. Its patent life remains standard, with protection lasting until approximately 2040, contingent on maintenance fee payments.


Scope of the Patent: Claims Analysis

1. Types of Claims

Patent claims generally divide into:

  • Product claims: Covering the chemical entity itself.
  • Process claims: Methods of synthesis or manufacturing.
  • Use claims: Specific therapeutic indications or methods.
  • Formulation claims: Pharmaceutical compositions enhancing stability or efficacy.

Given the typical strategy in pharmaceutical patents, CY1116926 likely encompasses multiple claim categories to maximize scope coverage.

2. Claim Construction and Breadth

  • Independent Claims: Expected to define a novel compound, perhaps with specific structural features, or a unique combination of known entities.
  • Dependent Claims: Narrowed claims refining the scope, such as specific substituents, dosage forms, or manufacturing conditions.

The scope determination hinges on the breadth of the structural definitions. For example, if the patent claims a compound with a core structure and a wide range of substituents, it could produce a broad patent scope, potentially blocking competitors across multiple therapeutics.

3. Novelty and Inventive Step

  • Novelty: For the patent to be valid, the claims must be novel over prior art. Given that many similar compounds are documented, the claim set likely emphasizes unique structural modifications, specific stereochemistry, or unexpected pharmacological effects.
  • Inventive Step: The patent probably leverages unexpected properties, such as increased bioavailability or reduced toxicity, to justify inventive step over prior art compounds.

Patent Landscape Context

1. Comparative Patent Environment

The patent landscape for similar compounds is highly competitive in the EU and worldwide:

  • European patents: Numerous filings exist, often aligned or overlapping with CY1116926, with major pharmaceutical players filing composition and use patents.
  • US and Asian filings: Similar compounds usually have concurrent filings, with variations tailored to regional patent strategies.

CY1116926's positioning within this landscape is crucial. If it claims a broad novel compound with specific advantageous properties, it strengthens its strategic value.

2. Patent Family and Coadministration/IP Strategies

  • Family members: Likely extended coverage in European Patent Office (EPO) jurisdictions and possibly in US and China.
  • Design-around potential: Competitors might design around the patent by modifying substituents or synthesis routes. The scope's narrowness influences its enforceability.

Legal and Strategic Implications

  • Validity and Enforcement: The strength of CY1116926 depends on robustness of claims, prior art considerations, and prosecutorial history.
  • Litigation and Licensing: A broad, well-supported patent can serve as leverage for licensing, partnerships, or litigation.

Additionally, given the patent's recent grant date, enforcement actions or licensing negotiations are likely in early stages, relying heavily on the claim drafting and scope.


Emerging Trends and Future Outlook

The pharmaceutical patent landscape continues to evolve, influenced by:

  • Patent cliffs: Companies seek stronger, broader patents to extend lifecycle.
  • Patent thickets: Overlapping patents create complex landscapes requiring detailed freedom-to-operate analyses.
  • Incremental innovation: Focusing on specific modifications for extended exclusivity.

CY1116926's strategic relevance hinges on its claims' strength and the competitive environment.


Conclusion

Cyprus patent CY1116926 showcases a typical pharmaceutical patent's nuanced scope—aiming to protect a novel compound or method with broad implications. Its claims likely define multiple layers of protection, from the specific chemical entity to usage claims, securing competitive advantage within a crowded patent landscape.

However, the ultimate enforceability and commercial utility depend on the clarity and novelty of the claims relative to prior art, as well as ongoing strategic patent management practices.


Key Takeaways

  • CY1116926's patent scope encompasses multiple claim types, potentially offering broad protection.
  • Its validity depends on claim constructiveness, novelty, and inventive step amid existing prior art.
  • The patent landscape for similar drugs is dense; strategic claim drafting critical for market advantage.
  • Maintaining patent strength requires vigilant monitoring of potential challenges and designing around existing patents.
  • Licensing and enforcement strategies should leverage the patent's scope to maximize commercial returns.

FAQs

Q1: What is the typical scope of a pharmaceutical patent like CY1116926?
A1: It usually covers the chemical compound itself, manufacturing processes, formulations, and therapeutic uses, with claims designed to maximize protection and prevent easy design-arounds.

Q2: How does the patent landscape impact the value of CY1116926?
A2: A crowded landscape with overlapping patents can limit enforceability and market exclusivity, making strong claim construction essential for maximizing value.

Q3: Can existing prior art challenge the validity of CY1116926?
A3: Yes. Prior art that discloses similar compounds or methods can be grounds for invalidating claims unless the patent demonstrates inventive step and novelty.

Q4: What role does claim breadth play in patent enforceability?
A4: Broader claims can uphold wider protection but are more vulnerable to validity challenges; narrower claims are easier to defend but may limit enforceability.

Q5: How can companies extend the protection of CY1116926?
A5: Through filing related patents (patent families), developing new uses, formulations, or process improvements to create a robust patent portfolio around the core invention.


Sources:

[1] European Patent Office (EPO) public databases.
[2] World Intellectual Property Organization (WIPO) PATENTSCOPE.
[3] Patent documentation and prosecution history (assumed for analysis).

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.