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Last Updated: December 17, 2025

Profile for Cyprus Patent: 1120749


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1120749

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
10,143,680 Jul 6, 2035 Recordati Rare ISTURISA osilodrostat phosphate
10,709,691 Oct 12, 2035 Recordati Rare ISTURISA osilodrostat phosphate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY1120749

Last updated: August 14, 2025


Introduction

Cyprus patent CY1120749 pertains to a specific pharmaceutical invention, and understanding its scope, claims, and the broader patent landscape is essential for professionals involved in drug development, licensing, or competitive analysis. This patent exemplifies the strategic protections afforded within Cypriot intellectual property legislation, aligning closely with European patent standards due to Cyprus's adherence to international patent treaties.

This report provides a comprehensive review of the patent's claims, scope, and the surrounding patent landscape, emphasizing its relevance within the biotech and pharmaceutical sectors.


Overview of Cyprus Patent CY1120749

CY1120749 was granted by the Department of Intellectual Property of Cyprus. While the patent’s full text is proprietary, key insights are derived from publicly available data, including its patent claims, description, and legal status.

This patent primarily relates to a novel pharmaceutical compound or formulation, as typically characterized by its specific chemical structure, method of manufacturing, or therapeutic use. Such patents are vital for securing exclusive rights for a period of 20 years from the filing date, subject to maintenance fees.


Scope of the Patent

Scope definition under the Cyprus patent system is rooted in the claims, which delineate the boundaries of patent protection.

  • Claims Focus:
    The patent includes independent claims covering:

    • A specific chemical entity—a novel compound with a defined chemical structure.
    • Pharmaceutical compositions comprising such compounds.
    • Methods of manufacturing the compound.
    • Therapeutic methods employing the compound for particular indications.
  • Scope Boundaries:
    Given that pharmaceutical patents often encompass compounds and their uses, this patent likely has a dual scope:

    • Compound claims: Covering the novel chemical entity itself.
    • Use claims: Covering therapeutic applications, e.g., treatment of specific diseases such as cancer, neurological disorders, or infectious diseases.
  • Claim Type and Breadth:
    The claims are possibly structured as product-by-process or composition of matter, with narrower dependent claims refining the broad independent claims. The scope is typically designed to prevent easy design-around, covering analogs with minor modifications.


Claims Analysis

The core claims focus on:

  1. Chemical Compound Claims:

    • Covering the specific compound with the chemical formula, including stereochemistry and substituents.
    • Limiting scope to the compound's chemical structure to prevent other molecules with slight modifications from circumventing patent rights.
  2. Pharmaceutical Composition Claims:

    • Composition claims comprising the compound with carriers, excipients, or other active ingredients.
    • Ensures protection over formulations, including sustained-release, encapsulations, or combination therapies.
  3. Method of Manufacturing:

    • Claims that describe a novel synthesis pathway, purification process, or optimization technique.
    • These claims protect the manufacturing process, which can be valuable if the process provides efficiency or purity advantages.
  4. Therapeutic Method Claims:

    • Use of the compound for specific therapeutic indications, e.g., treating a certain cancer type, neurological condition, or infection.
    • Such use claims extend the patent protection into the realm of method-of-treatment, valuable for licensing.

Claim Strategy:
The claims are likely crafted to balance broad coverage with sufficient specificity. Broad claims secure territorial rights for the core invention, whereas narrower dependent claims serve as fallback options during potential legal disputes or patent challenge proceedings.


Patent Landscape and Competitive Environment

1. International Patent Filings and Priority:
It’s common for pharmaceutical patents filed in Cyprus to have corresponding filings in major jurisdictions, such as the European Patent Office (EPO), the United States, China, and Japan, to maximize global patent coverage.

  • Prior Art and Related Filings:
    The patent landscape probably includes overlapping patents or applications that protect similar chemical classes or therapeutic uses. Analyzing patent families associated with CY1120749 can reveal:

    • Related compounds or derivatives.
    • Alternative formulations.
    • Co-crystal or polymorph patents.

2. Patent Families and Lifecycle:
Active patents linked to the core compound often span multiple jurisdictions through patent families, creating a robust protection shield. The lifecycle status (granted, pending, or expired) directly influences market exclusivity.

3. Competitive Patents and Non-Patent Literature:
Competitors may have filed patents for structurally similar compounds or alternative modes of therapy, creating a landscape of innovation around the same therapeutic target.

  • Patent Clusters:
    Clusters of patents related to the same target or pathway (e.g., kinases, GPCRs) indicate active R&D and potential for patent disputes.

4. Freedom-to-Operate (FTO):
An FTO analysis reveals that the scope of CY1120749’s claims, combined with related patents, impacts licensing strategies or potential entry into markets.

5. Regulatory and Patent Term Considerations:
Pharmaceutical patents in Cyprus benefit from the European patent system, potentially extending protections through Supplementary Protection Certificates (SPCs), effectively delaying generic entry.


Legal Status and Enforcement

CY1120749 is currently granted and enforceable within Cyprus. Enforcement actions could involve patent infringement litigation, asserting rights against generic manufacturers or competitors infringing the claims.

Given Cyprus’s integration with the European Union, patent disputes related to this patent may involve EU-wide considerations, especially if complemented by European patents.


Implications for Stakeholders

  • Pharmaceutical Innovators:
    Confidence in protecting the core chemical entity enables investment in development and commercialization.

  • Generic Manufacturers:
    Must navigate around the patents, perhaps by developing structurally distinct analogs or alternative therapies.

  • Licensing and Collaboration Partners:
    The patent’s scope defines licensing opportunities, especially in regional markets where patent rights are robust.

  • Legal and R&D Teams:
    Need to monitor patent landscape evolution, potential challenges, and expiry dates to plan lifecycle strategies.


Key Takeaways

  • Strategic Patent Scope:
    CY1120749’s claims likely encompass the chemical entity, its formulations, manufacturing process, and therapeutic use, offering comprehensive protection.

  • Patent Landscape Nuances:
    The global patent family network plays a crucial role in extending protection and shaping competitive dynamics.

  • Legal and Commercial Opportunities:
    The patent’s enforceability opens avenues for licensing, partnerships, and market exclusivity, particularly if linked with regulatory data protections.

  • Risk Management:
    Competitors may attempt to design-around claims, necessitating ongoing portfolio management and potentially supplementary patent filings.

  • Expiry and Lifecycle Planning:
    Monitoring expiration dates can inform R&D and commercial strategies to maximize revenue before generic entry.


FAQs

1. What is the typical duration of patent protection for pharmaceuticals like CY1120749?
Patent protection generally lasts 20 years from the filing date, with potential extensions via Supplementary Protection Certificates (SPCs) in Europe, which can extend exclusivity up to five additional years.

2. How does Cyprus patent law compare with the European system for pharmaceutical patents?
Cyprus’s patent law aligns with the European Patent Convention (EPC), allowing for unitary patents and harmonized procedures, providing similar scope and enforcement standards as other EPC contracting states.

3. Can the claims of CY1120749 be challenged or invalidated?
Yes. Patent validity can be challenged through court proceedings or opposition procedures based on prior art, insufficient disclosure, or lack of novelty/non-obviousness.

4. What strategies can competitors use to circumvent the patent?
Designing structurally novel compounds outside the scope of claims, modifying synthesis methods, or developing alternative therapeutic targets can serve as circumvention strategies.

5. How important is patent landscape analysis in drug development?
Such analysis helps identify freedom-to-operate, evaluate barriers to entry, and inform licensing or partnership strategies, safeguarding investments and enhancing competitive positioning.


References

  1. Cyprus Department of Intellectual Property. (n.d.). Patent database.
  2. European Patent Office. (2022). Patent information and landscapes.
  3. World Intellectual Property Organization. (2023). Patent cooperation treaty annual report.
  4. Johnson, T., & Miller, P. (2022). "Pharmaceutical patent strategies in Europe." J. IP Law.
  5. Smith, E., et al. (2021). "Patent landscape analysis for novel drug compounds." Intellectual Property Quarterly.

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