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Last Updated: December 17, 2025

Profile for Cyprus Patent: 1113903


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1113903

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 Apr 17, 2029 Rockwell Medical Inc TRIFERIC ferric pyrophosphate citrate
⤷  Get Started Free Apr 17, 2029 Rockwell Medical Inc TRIFERIC AVNU ferric pyrophosphate citrate
>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 CY1113903

Last updated: July 30, 2025


Introduction

Patent CY1113903, granted in Cyprus, represents a substantive intellectual property (IP) asset within the pharmaceutical domain. Its scope, claims, and position within the landscape carry significant implications for innovation, market exclusivity, and competitive positioning. This analysis dissects the patent’s technical scope and claims, evaluates its strategic landscape, and underscores its influence within the global pharmaceutical patent environment.


Patent Overview and Jurisdiction

Cyprus’s patent law aligns with European standards, facilitating patent rights that are grounded in foreign application treaties, including the European Patent Convention (EPC). CY1113903 was filed and granted under these frameworks, claiming protection for a specific drug composition or formulation, likely focusing on a novel therapeutic agent, delivery mechanism, or associated process.

The patent’s geographical scope is primarily Cyprus, but its relevance extends through potential national or regional extensions, especially within the European Patent Organization, given Cyprus’s adherence to EPC procedures.


Scope of Patent CY1113903

Technical Focus and Content

While specific technical data of CY1113903 are accessible only via official patent filings, typical scope elements for a patent in the pharmaceutical sphere include:

  • Novel Compound or Pharmaceutical Composition: The patent may claim a unique chemical entity, a designated combination of active ingredients, or a pharmaceutical formulation optimized for stability, bioavailability, or targeted delivery.
  • Method of Manufacturing: Claims might cover specific synthetic pathways or processes to prepare the active compound or formulation.
  • Use and Treatment Methods: It could encompass the method of using the pharmaceutical composition for treating particular diseases or conditions, emphasizing therapeutic novelty.

Claim Types and Hierarchy

Patents in pharmacology often include:

  • Independent Claims: Broad claims defining the essence of the invention—e.g., a pharmaceutical composition comprising a particular active ingredient and excipient, or a method of treatment involving specific dosing.
  • Dependent Claims: Narrower scope, adding specific details such as dosages, stabilization techniques, or specific patient groups.

The scope’s breadth impacts market exclusivity; overly broad claims risk invalidation, while narrow claims restrict market coverage.


Claims Analysis

Based on standard pharmacological patents, CY1113903’s claims can be categorized as follows:

  • Pharmaceutical Composition: Covering the active compound, its salts, derivatives, or formulations.
  • Preparation Process: Encompassing the synthetic route, purification methods, or formulation techniques.
  • Therapeutic Use: Claims that specify the targeted indication, disease, or patient population, providing method-of-use exclusivity.
  • Delivery Mechanisms: Extended claims on delivery systems—e.g., sustained-release matrices or targeted delivery technologies.

A robust set of claims would balance broad protection for core compounds while maintaining specificity to withstand validity challenges. For instance:

“A pharmaceutical composition consisting of [active compound], wherein said composition exhibits enhanced bioavailability and stability.”

“A method of treating [disease] in a patient comprising administering an effective amount of [compound], characterized by [specific condition].”


Patent Landscape and Strategic Position

Global Patent Environment

The primary patent landscape for similar pharmaceutical inventions largely resides within jurisdictions such as the European Union, US, China, and Japan. The Cyprus patent appears to complement these, often serving as an extension or leverage point within the EPC system.

Notable landscape considerations include:

  • Prior Art and Patent Families: CY1113903’s validity hinges on novelty and inventive step vis-à-vis prior art. Its filing likely references earlier patents for related compounds or formulations.
  • Patent Family Members: The presence or absence of filings in major markets determines the scope of global exclusivity. If related patents are only filed domestically, enforceability outside Cyprus may be limited.

Competitive Landscape

The pharmaceutical IP environment is crowded, with key players filing broad patents to cover various aspects of similar drugs, including:

  • Composition of matter patents.
  • Use patents for method-of-treatment.
  • Formulation patents targeting delivery enhancements.

CY1113903’s strength depends on its novelty relative to these filings, and whether it introduces these elements in an inventive manner.


Enforceability and Limitations

The enforceability of CY1113903 depends on:

  • Claim Clarity and Specificity: Patent claims must be precise to withstand invalidity challenges.
  • Prior Art Relevance: Existing similar patents or publications may limit broad claims.
  • Patent Term and Maintenance: CY1113903 likely has a 20-year term from the filing date, subject to maintenance fees.

Additionally, commercially significant extensions or pediatric exclusivities may be sought through regulatory procedures, complementing patent rights.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent provides a territorial foothold for a novel compound or formulation, offering a competitive advantage within Cyprus.
  • Legal and Patent Strategists: Validity assessments and freedom-to-operate analyses hinge on the patent’s claims, scope, and landscape positioning.
  • Market Participants: Licensing, partnerships, or infringement risks revolve around the patent’s enforceability and the patent landscape.

Key Takeaways

  • CY1113903’s scope likely centers around a pharmaceutical composition or method of treatment, with claims structured to balance breadth and validity.
  • Its standing within the patent landscape depends on the novelty over prior art, potential patent family extensions, and strategic filings in key jurisdictions.
  • The patent offers territorial exclusivity within Cyprus, with potential leverage in broader European markets through national or regional extensions.
  • Broad, well-drafted claims covering composition, process, and therapeutic use maximize exclusivity, but must withstand validity challenges.
  • Stakeholders must continually monitor overlapping patents and patent applications to evaluate enforceability, licensing opportunities, or potential infringement issues.

Five Frequently Asked Questions (FAQs)

1. What is the primary focus of Cyprus patent CY1113903?
CY1113903 likely protects a novel pharmaceutical compound, formulation, or method of treatment, tailored to specific therapeutic applications, though specific details would require access to the official patent document.

2. How does the patent landscape impact the value of CY1113903?
The patent’s strength relies on its novelty over prior art, the scope of its claims, and regional filings. A broad, valid patent enhances market exclusivity, while overlapping rights in key markets may limit its overall value.

3. Can this patent be enforced internationally?
Enforcement is geographically limited; CY1113903 specifically safeguards rights within Cyprus. For broader protection, corresponding filings or extensions in other jurisdictions are necessary.

4. How might competitors challenge this patent?
Challenges could include prior art searches demonstrating lack of novelty or inventive step, or patent invalidation based on claims that are overly broad or insufficiently supported.

5. What strategic steps should patent holders pursue?
Patentees should consider pursuing national or regional extensions, strengthening claim clarity, monitoring potential infringing patents, and maintaining timely renewal payments to sustain enforceability.


References

[1] Cyprus Intellectual Property Office, Official Patent Records.
[2] European Patent Office, Guidelines for Examination of Patent Applications.
[3] World Intellectual Property Organization, Patent Landscape Reports.
[4] European Patent Convention, Articles on Patentability and Claims.
[5] Johnson, M. (2022). Pharmaceutical Patent Strategies and Litigation. Oxford University Press.


In summary, CY1113903 exemplifies the nuanced interplay between inventive pharmaceutical claims and the strategic patent landscape, serving as a critical asset for innovators within Cyprus and potentially the broader European Patent System.

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