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Last Updated: December 28, 2025

Profile for Cyprus Patent: 1111927


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1111927

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 Mar 14, 2025 Abbvie VIBERZI eluxadoline
⤷  Get Started Free May 27, 2029 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Mar 14, 2025 Abbvie VIBERZI eluxadoline
⤷  Get Started Free Mar 14, 2025 Abbvie VIBERZI eluxadoline
>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 CY1111927

Last updated: October 7, 2025

Overview of Patent CY1111927

Cyprus drug patent CY1111927 pertains to a pharmaceutical invention filed and granted within the jurisdiction of Cyprus, a member state of the European Union (EU). While the detailed technical disclosures are often proprietary, examining the patent’s scope and claims provides insight into its strategic positioning in the pharmaceutical patent landscape.


Scope of Patent CY1111927

The scope of a patent determines the extent of exclusive rights granted to the inventor, defined primarily by its claims. For CY1111927, the scope is likely centered around a novel chemical compound, a formulation, a manufacturing process, or a therapeutic use associated with a specific drug candidate.

Based on typical patent drafting standards in the pharmaceutical field, the patent’s scope can include:

  • Chemical Composition: Specific molecular entities, including salt forms, stereoisomers, or derivatives.
  • Pharmacological Use: Therapeutic indications or methods of use in particular diseases.
  • Manufacturing Process: Specific methods of synthesis or formulation techniques.
  • Combination Therapies: Use of the compound in combination with other agents.

Understanding the scope is crucial for assessing patent strength and potential infringement risks, particularly considering the overlapping rights within the EU.


Claims Analysis of CY1111927

The claims define the legal boundaries of the patent and are usually divided into:

  • Independent Claims: Broadest rights, establishing the core invention.
  • Dependent Claims: Narrower claims that add specific features or embodiments.

1. Independent Claims

These generally encompass:

  • The novel chemical entity with a defined structural formula.
  • The compound prepared via a specific synthetic route.
  • A method for treating a particular disease using the compound.
  • Pharmaceutical compositions containing the compound.

The independence of these claims implies they aim to cover a wide scope, which can influence the patent’s strength and enforceability.

2. Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific stereochemistry (e.g., enantiomerically pure forms).
  • Particular formulations (e.g., controlled-release tablets).
  • Specific dosage ranges.
  • Use in specific diseases (e.g., cancer, autoimmune disorders).

The claims’ language directly impacts how competitors may design around the patent. Narrower dependent claims can provide additional layers of protection but may be more vulnerable to design-around strategies.


Patent Landscape and Strategic Positioning

Examining the broader patent landscape involves assessing filings within relevant jurisdictions and patent families surrounding CY1111927. Considerations include:

1. Patent Family and Priority Attempts

  • Likely part of a broader patent family filing via the Patent Cooperation Treaty (PCT) or within the EU, aiming for international coverage.
  • Priority dates, if applicable, are crucial in establishing novelty over prior arts.

2. Competitive Patent Filings

  • Other filings may cover similar chemical classes or therapeutic uses.
  • Established pharmaceutical companies likely have overlapping patents, necessitating freedom-to-operate analyses.

3. Patent Challenges and Litigation Trends

  • The pharmaceutical field faces frequent patent litigations over similar compounds or indications.
  • The patent’s strength depends on novelty, inventive step, and written description.

4. Regional and International Filing Strategy

  • The patent’s coverage in major markets like the EU, US, China, and Japan influences commercial viability and licensing potential.
  • Given Cyprus’s status within the EU, the patent may serve as a strategic foothold for European market access.

5. Patent Term and Market Exclusivity

  • Patent expiry timelines directly affect market exclusivity periods.
  • Supplementary protections or data exclusivity provisions could extend commercial benefits.

Legal Status and Patent Validity

  • The patent’s current legal status (granted, pending, or opposed) impacts strategic decisions.
  • Validity assessments involve examining prior art, obviousness, and inventive step challenges.
  • Any prior art references or oppositions in Cyprus or EU patent offices could influence enforceability.

Implications for Stakeholders

  • Pharmaceutical Companies: CY1111927 signifies a protected innovation, offering a competitive advantage in targeted therapeutic areas.
  • Generic Manufacturers: Must evaluate the scope to avoid infringement or consider licensing negotiations.
  • Investors: The patent’s breadth and strength influence valuation and commercialization timelines.
  • Legal Practitioners: Ongoing patent prosecution or potential disputes require close monitoring.

Key Takeaways

  • Scope of CY1111927 likely covers a specific chemical entity, therapeutic use, and formulations, with claims tailored to defend broad and narrow rights.
  • Claims strategy involves a mix of independent claims covering core invention and dependent claims adding specific embodiments, balancing scope with enforceability.
  • Patent landscape positioning in Cyprus and broader EU markets underscores importance for strategic protections, licensing, and competitive defense.
  • Patent validity and enforceability depend on ongoing patent prosecution, prior art considerations, and potential oppositions.
  • Commercial relevance hinges on the patent’s expiration, scope, and coverage in major jurisdictions, influencing business valuation and R&D investments.

FAQs

1. What is the significance of the patent claims’ language in CY1111927?
Claims’ language determines the scope of protection; broad claims offer wider coverage but may face higher invalidity risks, while narrow claims provide focused rights but are easier to design around.

2. How does CY1111927 compare with other patents in the same therapeutic area?
Without direct access to patent family data, it’s typical to compare claim scope, filing dates, and jurisdictional coverage to assess overlaps and gaps with other patents in similar drug classes.

3. What strategic considerations arise from the patent’s jurisdictional scope?
Coverage within Cyprus and the EU facilitates market exclusivity in Europe; extending patent protections through international filings enhances global competitiveness.

4. How can competitors circumvent CY1111927’s patent rights?
Design-around strategies include developing structurally or functionally different compounds, modifying formulations, or exploiting limitations in claim scope.

5. What future steps should patent holders consider to maintain their market position?
Regular patent lifecycle management, filing for secondary patents (e.g., method of use, formulations), and monitoring patent challenges ensure sustained exclusivity.


References

[1] European Patent Office (EPO) Patent Search and Analysis Tools.
[2] World Intellectual Property Organization (WIPO) PatentScope Database.
[3] Patent documentation and official publications related to Cyprus Patent CY1111927.
[4] Industry reports on pharmaceutical patent strategies in Europe.
[5] Legal case studies involving pharmaceutical patent litigations.

Note: Specific technical details, such as chemical structures and claim language, are not publicly available here. For precise legal and technical analysis, review of the patent document itself is recommended.

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