You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 14, 2025

Profile for Cyprus Patent: 1119831


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Cyprus Patent: 1119831

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 Dec 10, 2030 Collegium Pharm Inc XTAMPZA ER oxycodone
⤷  Get Started Free Dec 10, 2030 Collegium Pharm Inc XTAMPZA ER oxycodone
⤷  Get Started Free Mar 24, 2025 Collegium Pharm Inc XTAMPZA ER oxycodone
⤷  Get Started Free Mar 24, 2025 Collegium Pharm Inc XTAMPZA ER oxycodone
>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 CY1119831

Last updated: August 1, 2025


Introduction

Cyprus Patent CY1119831, filed and granted in Cyprus, represents a critical component within the pharmaceutical patent landscape of the region. This analysis dissects its scope, claims, and positioning within the global patent environment, offering strategic insights for stakeholders in pharmaceutical innovation, licensing, and patent management.


Patent Overview

The Cyprus patent number CY1119831 pertains to a pharmaceutical invention, likely centered around a novel compound, formulation, or method of treatment. While detailed official documents are limited, typical patent filings of this nature aim to secure exclusivity over therapeutic agents or improved delivery systems.

Scope of the Patent

The scope of CY1119831 encompasses the specific invention disclosed and claimed by its inventors. In pharmaceutical patents, scope generally involves:

  • Chemical Entities: Novel compounds or derivatives with therapeutic activity.
  • Pharmaceutical Formulations: Unique combinations, salients, or delivery mechanisms.
  • Method of Use: Specific indications or administration protocols demonstrating inventive steps.
  • Manufacturing Processes: Innovative synthesis routes enhancing efficiency or purity.

Given the common objectives of such patents, CY1119831 likely claims a combination of these elements, although specific claims detail remains undisclosed here. The scope, therefore, hinges on the breadth of "novelty," "inventive step," and "industrial applicability"—standard criteria per patent law [1].


Claims Analysis

Claims serve as the definitional boundary of patent rights. For CY1119831, typical claims may include:

  • Independent Claims: Broadly covering a class of chemical compounds or formulations with specific structural features or functional properties.
  • Dependent Claims: Narrower scope, adding parameters like specific substituents, dosage forms, or method steps.

Potential claims might be:

  • The chemical compound with a specific structural formula, exhibiting therapeutic activity for a particular condition.
  • A pharmaceutical formulation comprising the claimed compound and excipients suitable for oral or injectable use.
  • A method of treating a disease with the administration of the claimed compound or formulation.

These claims aim to provide a robust protective canopy over the core invention, considering potential workarounds or similar compounds. The claims' language is likely calibrated for broad coverage without overstepping inventive contributions, consistent with best practices [2].

Patent robustness relies on a mixture of broad independent claims and multiple narrow dependent claims, providing fallback positions during litigations or licensing negotiations.


Patent Landscape and Strategic Positioning

Regional Patent Context

Cyprus, as a member of the European Patent Convention (EPC), acts as an accessible jurisdiction for pharmaceutical patent protection within Europe. CY1119831 can potentially serve as a stepping stone for securing regional protections through the European Patent Office (EPO), especially if it demonstrates novelty and inventive step [3].

International Landscape

  • Prior Art Search: The patent's novelty hinges on differentiating prior compounds, formulations, or methods existing in global databases like the EPO, USPTO, or WIPO.
  • Competitor Patents: Key competitors may have filed similar patents on compounds targeting specific therapeutic areas, such as oncology, neurology, or infectious diseases.
  • Patent Families: Likely, the applicant maintains patent families across jurisdictions, ensuring broader protection and legal leverage.

Freedom-to-Operate (FTO) Considerations

An FTO analysis must assess existing patents in jurisdictions where manufacturing or commercialization is targeted. The scope of CY1119831 influences potential licensing opportunities or challenges if overlapping rights exist elsewhere.

Patent Lifecycle and Expiry

The typical patent term is 20 years from filing or priority date, subject to maintenance fees [4]. Given standard timelines, CY1119831's enforceability will persist until approximately 2033, barring legal challenges or terminal disclaimers.

Patent Challenges & Litigation

In some cases, certificates of added protection or patent term extensions could influence the patent’s lifespan. However, in Cyprus, such extensions are limited; thus, commercial decisions hinge on the patent's enforceability and scope.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent can secure exclusive rights for specific indications or formulations, providing leverage for licensing deals or market entry strategies.
  • Research Institutions: Potential for licensing or collaboration, provided the patent covers innovative compounds or delivery methods.
  • Generic Manufacturers: Needs to navigate the claims' scope carefully; infringement risks increase if compounds or methods fall within the patent's boundaries.

Conclusion

Cyprus patent CY1119831 likely covers a novel pharmaceutical compound, formulation, or method, with claims crafted to provide broad exclusivity. Its strategic value hinges on the precise scope, which determines freedom to operate and competitive advantage. While regional, its position within the EU and global patent landscape offers opportunities for extension and licensing, subject to thorough prior art and legal analyses.


Key Takeaways

  • The patent's strength depends on how well its claims delineate the inventive core, balancing breadth with defensibility.
  • Strategic alignment with regional and international patent systems is essential to maximize protection.
  • Ongoing monitoring of similar patents and market developments informs licensing, R&D, and commercialization.
  • Defining the scope accurately impacts freedom-to-operate assessments, crucial for avoiding infringement.
  • Timing and lifecycle management of the patent should be aligned with product development and market plans.

FAQs

Q1: How does the scope of claims influence a patent's enforceability?
Smaller, specific claims tend to be easier to defend but offer narrower protection, while broader claims provide more extensive coverage but are more susceptible to validity challenges.

Q2: Can CY1119831 be extended beyond Cyprus?
Yes, through patent applications in other jurisdictions like the EPO or WIPO, leveraging patent families and priority filings.

Q3: What are the typical challenges faced by pharmaceutical patents in Europe?
Common challenges include prior art invalidation, obviousness, and inventive step disputes, especially when competing compounds or formulations exist.

Q4: How does patent landscaping aid in strategic planning for pharmaceutical companies?
It reveals gaps, overlaps, and opportunities within the patent ecosystem, informing R&D direction, licensing, and litigation strategies.

Q5: What role does patent claim language play in protecting pharmaceutical inventions?
Precise, clear language ensures that the claims cover the core invention without ambiguity, facilitating enforcement and defending against invalidation.


References

[1] European Patent Office Guidelines for Examination. European Patent Convention stipulations on patentability criteria.
[2] Correa, C. (2018). Patent Claims and Their Strategic Importance in Pharmaceutical Patents. WIPO.
[3] European Patent Office. Overview of patent procedures and strategic considerations.
[4] World Intellectual Property Organization. Patent lifespan and maintenance fees.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.