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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1119028


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1119028

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 Sep 22, 2030 Horizon Therap Us RAVICTI glycerol phenylbutyrate
⤷  Get Started Free Sep 22, 2030 Horizon Therap Us RAVICTI glycerol phenylbutyrate
⤷  Get Started Free Sep 22, 2030 Horizon Therap Us RAVICTI glycerol phenylbutyrate
⤷  Get Started Free Sep 22, 2030 Horizon Therap Us RAVICTI glycerol phenylbutyrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Scope, Claims, and Patent Landscape for Cyprus Patent CY1119028

Last updated: July 27, 2025


Introduction

Patent CY1119028, granted by the Republic of Cyprus, pertains to a novel pharmaceutical invention. As a key document in the intellectual property landscape, this patent delineates specific rights over a drug formulation, process, or compound, playing a critical role in fostering innovation, market dominance, and licensing opportunities within Cyprus and potentially in broader jurisdictions via national or regional filings. This analysis examines the scope, claims, and the patent landscape surrounding CY1119028, offering insights to stakeholders such as pharmaceutical companies, patent strategists, and legal professionals.


Scope of Cyprus Patent CY1119028

The scope of Patent CY1119028 encompasses the protection conferred over a specific drug-related invention as described in its claims. Patents typically protect:

  1. Chemical Composition and Formulation: The unique chemical structure, its derivatives, or concentrations, particularly if the patent covers a novel compound or a synergistic combination used for therapeutic purposes.

  2. Method of Manufacturing: Processes for synthesizing, purifying, or formulating the drug can be protected if distinctly inventive.

  3. Therapeutic Use or Method of Treatment: Specific applications of the drug involving novel methods or indications.

  4. Delivery Systems: Innovative drug delivery methods, such as sustained-release formulations or targeted delivery mechanisms.

The detailed scope for CY1119028 hinges critically on its patent claims, which define the legal boundaries of the patent rights.


Claim Analysis

The claims are the most vital part of any patent, providing precise boundaries on what the patent covers. They are classified into independent claims, which stand alone, and dependent claims, which reference and narrow the scope.

Note: As the specific text of the claims is unavailable here, the analysis proceeds based on typical patterns observed in similar pharmaceutical patents and available public summaries.

Type and Breadth of Claims

  • Compound Claims: Likely includes the chemical entity or its salts, esters, or derivatives. These claims define the specific molecular structure, possibly with substitutions or modifications that confer improved pharmacokinetics, stability, or efficacy.

  • Formulation Claims: May claim a specific dosage form, excipient combination, or formulation process that enhances bioavailability, stability, or patient compliance.

  • Method Claims: Cover novel therapeutic methods, such as administering a defined dose for a specific condition or using a unique regimen.

  • Use Claims: Covering new therapeutic indications for established compounds, essential for extending patent life and market exclusivity.

Claim Strategy and Novelty

  • The patent likely emphasizes inventive aspects such as a new chemical moiety, a unique crystalline form, or an improved synthesis route.

  • Claims probably focus on narrow constraints to ensure enforceability, yet sufficiently broad to prevent workarounds by competitors.

  • The patent’s robustness depends on how well these claims withstand legal challenges, especially those asserting lack of novelty or inventive step, considering the prior art landscape.


Patent Landscape and Competitor Analysis

Regional and International Patent Landscape

Cyprus does not have a comprehensive pharmaceutical patent database independent of European or international databases. Thus, CY1119028's scope aligns with European Patent Convention (EPC) standards, and similar invention disclosures are likely filed within several jurisdictions.

  • European Patent Office (EPO): A critical comparator where corresponding filings could exist, offering broader geographic protection.

  • World Intellectual Property Organization (WIPO): International applications via Patent Cooperation Treaty (PCT) may have been pursued for wider protection.

  • National Patents: Countries with active pharmaceutical markets (e.g., Greece, UK, Germany, USA) may have filings covering similar compounds or uses, indicating potential patent thickets or freedom-to-operate concerns.

Legal and Market Position

  • The patent’s stake lies in its novelty, inventive step, and industrial applicability. Its strength depends on how well it differentiates from prior art, especially existing drugs with similar mechanisms or formulations.

  • Competitors might have analogous patents or applications for similar compounds, which need to be assessed through freedom-to-operate (FTO) studies before commercialization.

  • The lifecycle management, including patent term extension (if applicable), and potential patent opposition dynamics in jurisdictions with rigorous patent examination processes, influence strategic planning.

Relevant Patent Families and Collaborations

  • The patent probably belongs to a patent family targeting a specific therapeutic area, that is, oncology, cardiology, CNS disorders, etc.

  • Its relationship with ongoing research collaborations or licensing agreements could signal industry interest and patent value.


Legal Status and Enforcement

  • Validity and Maintenance: Regular renewal fees are essential in Cyprus for maintaining patent rights. Any lapses could open opportunities for generic competition.

  • Enforceability: The scope of claims and legal strategies employed by patent holders significantly influence enforcement outcomes in cases of infringement.

  • Opposition and Litigation: While Cyprus has less frequent patent opposition procedures, similar challenges at the European or international level could impact the patent’s strength.


Implications for Stakeholders

  • Pharmaceutical Developers: Should analyze CY1119028's claims against existing portfolios to avoid infringement and identify potential licensing opportunities.

  • Investors and Licensing Partners: Need detailed claim scope analysis to assess risks and valuations.

  • Legal Professionals: Should monitor patent maintenance, potential oppositions, and jurisdictional extensions.


Key Takeaways

  • The patent covers a specific drug formulation or compound with potential therapeutic utility, with claims tailored to its novelty, formulation, or use.

  • Its strength depends on claim breadth, prior art landscape, and ongoing regional or international filings.

  • Strategic patent planning, including potential extensions and vigilant enforcement, can sustain commercial dominance.

  • Competitors must perform comprehensive FTO analyses considering potential overlaps with CY1119028 and similar patent families.

  • Continuous monitoring post-grant, encompassing oppositions or challenges, is essential for protecting market position.


Frequently Asked Questions (FAQs)

1. What is the typical scope of pharmaceutical patents like CY1119028?
Pharmaceutical patents often cover chemical compounds, formulations, manufacturing processes, and therapeutic methods. The scope is defined by claims specifying the molecular structure, delivery mechanism, or use, ensuring exclusive rights over the protected invention.

2. How does patent claim scope influence market exclusivity?
Broader claims can extend market exclusivity but risk invalidation if too encompassing compared to prior art. Narrow claims offer stronger defensibility but limit exclusivity, influencing strategic patent and commercialization planning.

3. Can CY1119028 be enforced outside of Cyprus?
Protection is limited to jurisdictions where corresponding filings exist. Enforcing rights in other markets requires filing patents or applications aligned with international treaties such as the EPC or PCT.

4. What are common challenges faced by patents like CY1119028?
Challenges include prior art invalidity claims, patent oppositions, and freedom-to-operate issues stemming from similar existing patents. Continuous monitoring and strategic patent drafting are vital.

5. How can stakeholders leverage patent landscape analysis?
It facilitates risk assessment, licensing negotiations, and R&D direction, ensuring competitive advantage and strategic alignment with patent rights.


References

  1. European Patent Office. "Patent Searching and Reporting Resources."
  2. WIPO PatentScope Database. "International Patent Applications and Family Data."
  3. Cyprus Patent Office. "Patent Filing and Maintenance Procedures."
  4. Patent landscape reports for pharmaceuticals in Europe and Cyprus jurisdictions.
  5. Industry analysis reports on patent strategies in pharmaceutical innovation.

In conclusion, Patent CY1119028 consolidates a specific drug-related innovation within Cyprus and possibly broader regions. Its claims define the valuable rights protecting the invention against infringement, while its position within the global patent landscape influences strategic decisions for industry stakeholders. A thorough understanding of its scope, claims, and competitive landscape is essential for maximizing its commercial value and safeguarding innovation.

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