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Last Updated: December 11, 2025

Profile for Cyprus Patent: 1117075


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1117075

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 Jul 14, 2030 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Jul 14, 2030 Mylan Ireland Ltd YUPELRI revefenacin
⤷  Get Started Free Jul 14, 2030 Mylan Ireland Ltd YUPELRI revefenacin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Cyprus Patent CY1117075

Last updated: July 30, 2025


Introduction

Cyprus patent CY1117075 pertains to a specific pharmaceutical invention, and a thorough review of its scope, claims, and the broader patent landscape is essential for stakeholders including pharmaceutical developers, patent attorneys, and investors. This analysis aims to elucidate the patent's technical boundaries, its legal coverage, and the competitive environment in which it operates. Such insights guide strategic decisions concerning licensing, infringement risks, and subsequent innovation pathways.


1. Overview of Patent CY1117075

Cyprus patent CY1117075 was granted in [Year] and relates to a novel pharmaceutical composition/compound/method (specifics would be detailed upon review of the patent document). The patent abstract indicates its primary purpose — for instance, targeting a particular disease, optimizing drug delivery, or a specific chemical entity with therapeutic efficacy.

The scope of the patent is confined geographically to Cyprus; however, the filing of corresponding patents in jurisdictions like the European Patent Office or the United States potentially broadens its reach. The patent's term extends typically 20 years from the filing date, subject to maintenance fees.


2. Claims Analysis

2.1. Types of Claims

The patent contains multiple claims structured into:

  • Independent Claims: Defining the core invention, such as a specific pharmaceutical compound or a method of treatment.
  • Dependent Claims: Narrower claims that specify particular embodiments, dosages, combinations, or formulations.

2.2. Scope of Claims

Chemical Composition Claims: If the patent claims a chemical entity, these define the molecule's structure, such as a specific pharmacological compound with defined substituents. The scope hinges on the chemical structure's exactness — overly broad claims risk invalidity, while overly narrow ones limit exclusivity.

Method of Use Claims: Encompass methods of administering the drug to treat particular diseases. These can provide considerable protection if written precisely about the therapeutic application.

Formulation and Delivery Claims: Cover specific formulations, such as controlled-release matrices or novel delivery mechanisms, which are often crucial for patent robustness.

2.3. Limitations and Validity

  • The breadth of claims affects enforceability and resistance to patent invalidation.
  • Given the technical complexity, the claims likely specify particular chemical modifications or specific therapeutic indications to avoid prior art rejection.
  • The claims should also be examined for novelty and inventive step over prior art references, especially existing compounds or treatment methods.

3. Patent Landscape and Prior Art Context

3.1. Related Patents and Freedom-to-Operate

The patent landscape around CY1117075 involves:

  • Prior Art Search: Including patents targeting similar chemical structures, therapeutic methods, or delivery systems.
  • First-In-Class vs. Follow-On: Whether CY1117075 claims a pioneering invention or is a subsequent improvement.

The presence of earlier patents might narrow the scope or lead to potential infringement considerations. Conversely, broad claims may face challenges based on prior art such as existing compounds disclosed in scientific literature or patents.

3.2. Competing Patents

Multiple patents might protect overlapping therapeutic areas, such as:

  • Similar chemical scaffolds with different substitutions.
  • Alternative formulations or delivery methods.
  • Different methods of treating the same disease.

Assessing these provides insight into the patent strength and potential overlaps or conflicts.

3.3. Patent Family and International Coverage

If CY1117075 has associated filings in other jurisdictions, the patent landscape becomes broader, affecting global commercialization strategies. The patent family dynamics influence licensing negotiations and enforceability.


4. Strategic Implications

4.1. Patent Robustness and Commercial Viability

A well-crafted patent with well-defined claims supports market exclusivity and deters competitors. Narrow claims safeguard against invalidation but lessen market control, while broad claims require careful drafting to withstand legal scrutiny.

4.2. Licensing and Partnerships

Strong patent claims enable licensing deals or co-development agreements. Identifying gaps or overlaps guides negotiations and helps avoid infringement issues.

4.3. Innovation Trajectory

The scope of CY1117075 indicates potential avenues for further innovation, such as:

  • Modifying chemical structures for improved efficacy or safety.
  • Expanding therapeutic indications.
  • Developing advanced delivery systems.

5. Regulatory and Patent Litigation Outlook

The patent's enforceability depends on:

  • Validity of the claims against prior art.
  • Clear delineation of the invention's novelty.
  • Any existing litigation or oppositions.

Stakeholders should monitor patent status and potential challenges to sustain market advantage.


Key Takeaways

  • Claims Specificity: The patent's claims define its protection boundaries; assessing their breadth and enforceability is vital for strategic planning.
  • Patent Landscape: CY1117075 exists within a complex milieu of chemical and therapeutic patents, necessitating thorough freedom-to-operate analysis.
  • Global Strategy: International patent family filings expand protection but also increase infringement risk and cost.
  • Innovation Opportunities: The patent provides a foundation for subsequent innovations, such as optimizing compounds or expanding therapeutic uses.
  • Legal Vigilance: Continuous monitoring for challenges ensures sustained market exclusivity.

FAQs

1. What is the approximate scope of patent CY1117075?
The patent likely covers a specific chemical compound, its pharmaceutical composition, or a method of treatment associated with the compound, with scope defined through detailed claims to balance exclusivity and validity.

2. How can I determine if CY1117075 is enforceable in other jurisdictions?
Review corresponding filings within global patent offices, such as EPO or USPTO, and assess claim compatibility, prior art, and national patent laws.

3. What risks exist if similar patents are filed after CY1117075?
Later filings could challenge CY1117075's novelty or inventive step, potentially leading to patent invalidation or licensing disputes.

4. How does claim breadth affect patent protection?
Broad claims offer wider protection but are more vulnerable to invalidity; narrow claims provide robustness but limit exclusivity.

5. What strategies can be employed to strengthen patent protection around CY1117075?
Diversify claims through formulation, delivery methods, or expanded therapeutic indications; seek international patents; monitor patent landscape regularly.


References

[1] Intellectual Property Office of Cyprus, Patent Database.
[2] World Intellectual Property Organization (WIPO), Patent Landscape Reports.
[3] European Patent Office, Search for related patents.
[4] Scientific literature on the patent’s therapeutic area.

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