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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1108656


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1108656

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 6, 2029 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
⤷  Get Started Free Jul 6, 2029 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Cyprus Patent CY1108656: Scope, Claims, and Patent Landscape

Last updated: August 11, 2025


Introduction

Patent CY1108656, filed and granted within the Cyprus jurisdiction, pertains to a specific pharmaceutical invention. While Cyprus’s patent system is part of the European Union framework, it does not independently issue patents but grants patents based on applications filed through the European Patent Office (EPO) or national filings. This analysis scrutinizes CY1108656’s scope, claims, and position within the broader patent landscape, assisting stakeholders in innovation strategy, licensing, or marketing.


Understanding the Patent: Fundamental Details

CY1108656 was granted to a pharmaceutical entity on a specified date (exact dates require access to Cyprus Patent Office records). Due to the similarity of Cypriot patents with European patents, this patent most likely reflects a biotechnology or medicinal chemistry innovation with specific claims designed to protect a novel drug or method of use. The patent’s scope hinges critically on its claims, which define the legal boundaries of the invention.


Scope of Patent CY1108656

Broadly, the patent’s scope encompasses:

  • Chemical entities or molecules: Possibly a novel compound, a pharmaceutical salts, or derivatives with claimed medicinal properties.
  • Preparation processes: Methods for synthesizing the claimed compounds.
  • Therapeutic applications: Specific medical indications, such as treating a disease or condition.
  • Formulation or delivery methods: Innovations in how the compound is administered or formulated to enhance efficacy or stability.
  • Combination therapies: Use alongside other drugs for synergistic effects.

The scope’s breadth depends on how the claims are drafted—ranging from independent claims that broadly cover compounds or methods, to narrower dependent claims detailing specific embodiments.


Claims Analysis

1. Independent Claims

The core independent claims delineate the fundamental invention. Examples may include:

  • Compound Claims: A chemical structure with a defined core scaffold and specific substituents, such as a novel heterocyclic ring or a specific stereochemistry.
  • Method of Use: A claim describing treating a particular disease (e.g., cancer, neurological disorder) using the compound.
  • Manufacturing Process: A novel synthesis pathway to produce the compound with improved yield or purity.

2. Dependent Claims

These specify particular embodiments, such as:

  • Specific substituent variations.
  • Particular formulations (e.g., oral tablet, injection).
  • Dosage regimens or administration routes.

3. Claim strategy implications

A well-crafted patent balances breadth with enforceability. Overly broad claims risk invalidation, while narrow claims limit enforcement scope.


Patent Landscape and Competitor Analysis

1. Prior Art Review

Patent scope interprets the prior art landscape, which includes:

  • Existing drug patents for related molecules.
  • Earlier synthesis methods.
  • Known therapeutic compounds in the same class.

2. Related Patent Families

Investigation into related patents filed internationally—via PCT applications or European filings—may reveal:

  • Priority data from earlier filings.
  • Family members covering different jurisdictions.
  • Patent disputes or litigations.

3. NPL (Non-Patent Literature)

Scientific publications may disclose similar compounds or methods, providing insight into the novelty aspect.

4. Competitive Analysis

Major players in the same therapeutic area could hold overlapping patents, influencing freedom-to-operate (FTO) considerations.

5. Patent Term and Market Implications

Considering patent life, exclusivity periods, and potential patent extensions or supplementary protection certificates (SPCs) is crucial for commercial planning.


Legal and Strategic Considerations

  • Validity and Enforceability: Determined by the breadth of claims vis-à-vis prior art.
  • Potential Infringements: Competitors with similar molecules or methods might infringe, offering licensing or litigation opportunities.
  • Patent Maintenance: Ensuring timely maintenance fees and considering lifecycle extensions.
  • Patent Challenges: Invoking opposition procedures or third-party challenges, common in EU jurisdictions, can threaten patent scope.

Conclusion: Positioning and Recommendations

CY1108656 appears to secure a targeted yet potentially broad scope within its claim set, covering critical aspects of a novel pharmaceutical invention. Strategic considerations involve:

  • Monitoring related patents for freedom-to-operate.
  • Exploiting narrower dependent claims for market segmentation.
  • Evaluating opportunities for patent term extension.
  • Considering licensing arrangements or collaborations depending on competitive landscape.

Key Takeaways

  • Patent claims define the innovation’s scope; careful analysis of independent versus dependent claims indicates versatility of patent protection.
  • The patent landscape must be analyzed in conjunction with prior art and related patent families to assess infringement risks and opportunity windows.
  • In pharmaceuticals, strategic patent positioning involves balancing broad claims for protection and narrow claims for enforceability.
  • Legal nuances such as potential patent challenges and lifecycle management are critical for maximizing commercial value.
  • A comprehensive freedom-to-operate (FTO) analysis in jurisdictions beyond Cyprus—such as Europe, the US, and other key markets—is advisable for global commercialization strategies.

FAQs

1. What is the primary focus of patent CY1108656?
It likely covers a novel pharmaceutical compound or its method of use, formulation, or manufacturing process, aimed at treating specific medical conditions.

2. How does the scope of claims impact patent enforceability?
Broader claims offer wider protection but are more susceptible to invalidation, while narrower claims provide more robust enforcement for specific embodiments.

3. Can CY1108656 be challenged or invalidated?
Yes, through prior art references, oppositions, or other legal procedures in Cyprus or within the European patent system if it’s part of a broader application family.

4. How does this patent fit within the global patent landscape?
It may have corresponding filings or patent families internationally, affecting global market rights and competition.

5. What are the strategic considerations for a company holding this patent?
Focusing on licensing opportunities, defending against infringers, expanding claim scope via continuations, and geographic patent protection are key strategies.


References

  1. Cyprus Patent Office. (2023). Patent Search Database.
  2. European Patent Office. (2023). Patent Landscape Reports on Pharmaceuticals.
  3. World Intellectual Property Organization. (2023). Patent Cooperation Treaty (PCT) filings related to pharmaceutical inventions.
  4. Patent law manuals and guidelines relevant to EU and Cyprus jurisdictions.

(Note: Specific details such as filing and grant dates, inventors, and exact claims require access to official patent documentation.)

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