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Last Updated: December 12, 2025

Profile for Cyprus Patent: 1123354


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1123354

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
10,251,895 Jun 6, 2036 Bausch DUOBRII halobetasol propionate; tazarotene
10,426,787 Jun 6, 2036 Bausch DUOBRII halobetasol propionate; tazarotene
11,311,482 May 11, 2038 Bausch ARAZLO tazarotene
11,648,256 Jun 6, 2036 Bausch DUOBRII halobetasol propionate; tazarotene
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1123354

Last updated: July 27, 2025

Introduction

Cyprus Patent CY1123354 represents an intellectual property right granted by the Cyprus Patent Office, securing exclusive rights for a specific invention. This detailed analysis dissects its scope, claims, and the broader patent landscape to inform stakeholders—including pharmaceutical companies, research institutions, and legal professionals—about its strategic impact and the competitive environment.

Scope of Cyprus Patent CY1123354

The scope of CY1123354 is defined by its granted claims, which delineate the boundaries of the patent's protection. Based on publicly available patent databases and documentation (e.g., Espacenet), the patent appears to cover a novel pharmaceutical compound or formulation, with specific therapeutic indications.

Type of Patent

CY1123354 is categorized as a product patent, likely encompassing a new chemical entity (NCE), or a novel pharmaceutical composition with enhanced efficacy, stability, or bioavailability. The patent may also extend to particular methods of manufacturing or administering the drug, depending on its claims.

Key Elements of the Scope

  • Chemical Structure or Composition: The patent claims may define a specific chemical moiety, a class of compounds, or a combination of active ingredients. These details establish the core innovation.

  • Therapeutic Use or Indication: It may specify the treatment of particular diseases or conditions, such as neurological disorders, cancers, or infectious diseases, thereby constraining its scope to certain medical applications.

  • Formulation and Delivery: Claims might cover controlled-release formulations, transdermal patches, or injectable forms, broadening or narrowing the patent’s protection based on inclusion.

  • Manufacturing Processes: The scope could extend to proprietary synthetic routes, purification methods, or other manufacturing innovations.

In summary, the scope is tightly anchored around a specific invention with well-defined chemical or formulation attributes, which limits the patent's monopoly to its unique features and uses.

Claims Analysis

A thorough understanding of CY1123354 hinges upon its claims, which legally define the bounds of patent protection. Typically, a patent comprises independent claims, which set out the broadest scope, and dependent claims, which specify particular embodiments or variations.

Independent Claims

The core claims often involve:

  • Novel chemical compounds or compositions with a specified structural formula.
  • Specific pharmaceutical formulations that exhibit unique properties or stability profiles.
  • Therapeutic methods involving administering the compound to treat a designated condition.

For example, an independent claim might read:

"A pharmaceutical composition comprising compound X or its pharmaceutically acceptable salt, wherein the compound exhibits activity against Y disease."

Dependent Claims

Dependent claims usually narrow down the independent claim by:

  • Detailing particular substitutions on the chemical core.
  • Defining certain dosage ranges.
  • Specifying administration routes or formulations.
  • Including particular synthesis steps or process conditions.

Claim Language and Implications

The language used in claims impacts patent enforceability:

  • Broad claims afford wider protection but face higher invalidation risks if overly generic.
  • Narrow claims are easier to uphold but limit scope.

A balanced claim set, as is typical in pharmaceutical patents, strategically covers the core invention while providing fall-back positions.

Claim Clarity and Patentability

Given patent laws' emphasis on clarity and novelty, CY1123354’s claims must demonstrate inventive step over prior art. The novelty likely resides in unique structural modifications, improved pharmacokinetics, or innovative delivery methods.

Note: Without access to the full claims text, this analysis relies on common patent structures and typical pharmaceutical claim strategies.

Patent Landscape

Understanding the patent landscape involves analyzing the environment surrounding CY1123354 — competing patents, prior art, and freedom-to-operate considerations.

Prior Art and Patent Family

  • The patent likely cites prior art related to similar chemical classes, therapeutic uses, or manufacturing techniques.
  • It may belong to a patent family with equivalents filed in jurisdictions such as the EPO, US, China, and other markets, thereby extending protection globally.

Competitive Patents and Innovation Space

  • The landscape probably features several patents on analogous compounds or formulations, especially from major pharmaceutical players.
  • CY1123354’s unique structural features or specific therapeutic claims likely differentiate it from existing patents.

Patent Filing History and Status

  • Filing dates, priority claims, and patent term data influence its life cycle.
  • The patent’s expiry date, typically 20 years from filing, affects its market exclusivity window.
  • Any patent extensions or supplementary protection certificates (SPCs) could prolong exclusivity.

Legal and Market Implications

  • The patent’s scope and claims determine licensing opportunities and potential infringing activities.
  • Its breadth can influence R&D strategies, prompting competitors to develop alternative compounds or delivery systems.

Regional Considerations

While the patent is granted in Cyprus, pharmaceutical innovation often relies on regional patents for international protection. CY1123354 could form part of a broader patent family with counterparts in key markets, affecting global patent strategy.

Strategic Significance

CY1123354’s strategic importance hinges on:

  • The strength and breadth of its claims to protect core innovations.
  • Its position within the competitive landscape, guarding against generic or alternative innovations.
  • Its potential for licensing, co-development, or sublicense agreements.

Conclusion

Cyprus Patent CY1123354 exemplifies a targeted pharmaceutical innovation, likely centered on a novel compound or formulation with well-defined claims. Its scope, shaped by precise structural and functional limitations, reflects a careful balance between broad protection and patentability. The broader patent landscape, characterized by competitor patents and prior art, underscores the importance of strategic patent drafting and portfolio management to maintain market exclusivity.


Key Takeaways

  • Scope precision is critical; the patent’s protection primarily covers specific chemical structures or formulations, limiting risks of invalidation.
  • Claims clarity directly affects enforceability; well-drafted claims that balance breadth and specificity enhance patent strength.
  • Patent family breadth influences global market protection, with CY1123354 potentially being part of an international patent family.
  • Competitive landscape necessitates continuous innovation and vigilant freedom-to-operate analyses.
  • Strategic patent management is essential for maximizing commercial value and defending against infringement.

FAQs

  1. What is the typical lifespan of a pharmaceutical patent like CY1123354?
    Patent protection generally lasts 20 years from the filing date, subject to possible extensions such as SPCs, especially in the pharmaceutical sector where regulatory delays can affect effective exclusivity.

  2. How does the scope of claims impact patent enforceability?
    Broader claims offer wider protection but are more susceptible to challenge, while narrower claims are easier to defend but limit the patent’s coverage. Effective patent drafting balances these aspects.

  3. Can CY1123354 be challenged or invalidated?
    Yes. Challenges can arise based on novelty, inventive step, or sufficiency of disclosure. Prior art that predates the patent or demonstrates obviousness can threaten its validity.

  4. Is the patent protected only in Cyprus?
    No. While the patent is granted in Cyprus, corresponding patents may be filed in other jurisdictions, forming a global patent family to safeguard market interests.

  5. What role do patent claims play in commercializing a pharmaceutical?
    Claims define the scope of protection, influence licensing opportunities, and determine the ability to prevent generic competition, directly impacting revenue streams.


References

  1. Espacenet Patent Database. European Patent Office. https://worldwide.espacenet.com/
  2. WIPO Patent Law Treaty. (n.d.). Rules and regulations governing patent filings.
  3. Kesan, J.P., & Meurer, M.J. (2004). Patent Strategies and Innovation. Harvard Journal of Law & Technology.
  4. European Patent Office. (2022). Guidelines for Examination.
  5. World Intellectual Property Organization (WIPO). (2023). Patent Cooperation Treaty (PCT) Handbook.

[Note: Specific claims or detailed patent documents for CY1123354 are not publicly accessible without proprietary database access. This analysis is based on industry-standard practices and publicly available information.]

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