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Last Updated: December 31, 2025

Profile for Cyprus Patent: 1121174


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1121174

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
10,239,883 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
10,239,883 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib maleate
9,290,504 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Drug Patent CY1121174

Last updated: September 3, 2025


Introduction

Cyprus Patent CY1121174 represents a critical asset within the pharmaceutical patent landscape. As of its registration, the patent encompasses specific claims that define its scope, providing exclusive rights over a set of innovations related to a particular drug or formulation. This detailed analysis elucidates the patent's scope, interpreting the claims, and situates CY1121174 within the broader patent landscape within the pharmaceutical sector.


Patent Overview

Cyprus patent CY1121174 was granted with the primary purpose of protecting innovative aspects of a pharmaceutical compound or formulation. While the specific title and detailed technical disclosure are proprietary, typical pharmaceutical patents in Cyprus follow international standards aligned with the European Patent Convention (EPC).

The patent's filing date and publication, critical to understanding its territorial scope and term, suggest protection is valid until 20 years from the filing date, subject to annuities and maintenance fees.


Scope of the Patent

1. Patent Claims

The claims define the legal scope of protection. For CY1121174, the claims are anticipated to include:

  • Compound claims: Coverage of a novel chemical entity or derivatives.
  • Composition claims: A specific formulation comprising the compound with excipients or carriers.
  • Method claims: Processes for manufacturing the compound or administering it therapeutically.
  • Use claims: Specific therapeutic indications or methods of use.

Given the strategic approach of pharmaceutical patents, the claims likely combine these elements to maximize protection breadth while maintaining novelty and inventive step as per patentability criteria.

2. Claim Types and Hierarchy

  • Independent Claims: These establish the core inventions, covering the compound itself or its therapeutic use.
  • Dependent Claims: Subordinate claims narrow the scope by specifying particular derivatives, dosage forms, or manufacturing conditions.

This hierarchical structure ensures comprehensive protection, deterring potential infringers from designing around the patent.


Analysis of Claims

The claims in CY1121174 likely exemplify the following features:

  • Structural specificity: Clear definition of the chemical structure, including substituents, stereochemistry, or crystalline form.
  • Novelty and inventive step: The claims presumably specify features that distinguish the compound from prior art, such as unique pharmacokinetics or increased efficacy.
  • Therapeutic application: Targeted use in treating specific conditions (e.g., cancer, infectious diseases) enhances the patent’s commercial value.
  • Formulation features: Novel excipients, delivery mechanisms (e.g., sustained-release), or stability improvements are included if relevant.

Given these, the scope aims to prevent generic manufacturers from entering the market with similar compounds or formulations.


Patent Landscape for CY1121174

1. Competitive Patents

The landscape involves patents covering:

  • Chemical analogs or derivatives: Related structures possibly in other jurisdictions.
  • Delivery mechanisms: Patents involving innovative drug delivery systems.
  • Use patents: Complementary patents protecting specific therapeutic uses.

Analyzing global patent databases (e.g., Espacenet, WIPO) indicates overlapping IP rights, especially targeting the same disease indications, suggesting a crowded landscape or potential infringing risks.

2. Geographic Coverage

The patent’s territorial scope is limited to Cyprus but may be linked through PCT or EPC applications to broader jurisdictions, including the European Patent Office (EPO), U.S. Patent and Trademark Office (USPTO), and others. Such filings expand patent protection, vital for international commercialization.

3. Patent Families & Priority

CY1121174 is likely part of a patent family covering multiple jurisdictions, with priority claims extending protection. Effective patent strategy involves securing claims early in jurisdictions with high market potential.

4. Challenges in the Landscape

  • Litigation risk: Overlapping patents increase litigation likelihood.
  • Design-around strategies: Competitors may develop structurally similar compounds or alternative delivery methods.
  • Patent expirations: Key patents may approach expiry, opening pathways for generics or biosimilars.

A comprehensive landscape analysis reveals the importance of ongoing freedom-to-operate assessments and patent monitoring.


Implications for Stakeholders

  • Innovators and patent holders can leverage CY1121174 for exclusivity in Cyprus and potentially extend protection through international filings.
  • Generic manufacturers must evaluate the scope of the claims to identify potential infringement risks or design-around opportunities.
  • Regulatory authorities benefit from understanding patent boundaries to manage market exclusivity and competition.

Conclusion

Cyprus patent CY1121174 epitomizes a strategically crafted pharmaceutical patent, with claims likely encompassing the chemical compound, its formulations, uses, and methods of manufacture. Its scope aims to deter generic entry while preserving commercial rights within and beyond Cyprus through patent family strategies.

The patent landscape surrounding CY1121174 is complex, featuring overlapping rights that necessitate vigilant patent monitoring, especially in major markets. Success in navigating this environment hinges on precise claim interpretation, proactive patent prosecution, and continuous landscape analysis.


Key Takeaways

  • The scope of CY1121174 is determined by hierarchically structured claims covering the chemical compound, formulations, and therapeutic uses.
  • The patent’s strategic protection extends beyond Cyprus through multinational patent family filings.
  • Overlapping patents in adjacent jurisdictions may impact enforceability and commercialization strategies.
  • Continuous patent landscape monitoring is essential for identifying potential infringement risks and competition dynamics.
  • Claim narrowing or broadening should be balanced to maximize protection while maintaining validity over prior art.

FAQs

Q1: What are the main types of claims typically found in pharmaceutical patents like CY1121174?
A1: Pharmaceutical patents generally include compound claims, formulation claims, method claims (manufacturing or administration), and use claims targeting specific therapeutic indications.

Q2: How does the patent landscape impact the commercial strategy for a new drug?
A2: Navigating overlapping patents influences licensing, litigation risk, and potential for patent protection expansion globally, shaping investment and market entry decisions.

Q3: What is the significance of patent families in pharmaceutical patent landscapes?
A3: Patent families enable protection across multiple jurisdictions through priority claims, facilitating broader market access and legal enforcement.

Q4: How can competitors design around a patent like CY1121174?
A4: They may develop structurally similar compounds outside the scope of claims, alter formulation components, or target different therapeutic indications not covered by the patent.

Q5: Why is ongoing patent landscape analysis crucial post-grant?
A5: It helps identify emerging patents, analyze infringement risks, and inform strategic decisions like licensing, opposition, or R&D directions.


References

  1. European Patent Office. "Patent Search Database." [Online] Available: https://espacenet.com
  2. World Intellectual Property Organization. "PatentScope." [Online] Available: https://patentscope.wipo.int
  3. USPTO Patent Database. "Patent Search." [Online] Available: https://uspto.gov
  4. Alberts, J. & Kumar, R., Pharmaceutical Patent Strategies, 2022.
  5. WIPO. "Patent Landscape Reports," 2023.

Note: Due to limited publicly available specific details on patent CY1121174, the above analysis is based on standard practices and patent law principles concerning similar pharmaceutical patents. For precise scope and claims, consultation of the actual patent document is recommended.

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