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Last Updated: December 28, 2025

Profile for Cyprus Patent: 1123398


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1123398

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 Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>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 CY1123398

Last updated: July 30, 2025


Introduction

Patent CY1123398, filed under Cyprus intellectual property regulations, pertains to a pharmaceutical invention with potential implications across therapeutic, manufacturing, and market domains. This analysis deciphers the patent's scope, claims, and its position within the broader global patent landscape, emphasizing strategic insights for stakeholders in the pharmaceutical industry.


Patent Overview and Technical Field

CY1123398 centers on a novel compound, formulation, or method intended for medical application, possibly in areas such as oncology, neurology, or infectious diseases, as is common for contemporary patent filings. While the exact details of the patent abstract are not provided here, patent landscapes suggest that the invention aims to improve treatment efficacy, minimize side effects, or optimize manufacturing processes. Its scope likely encompasses both the chemical compound(s) and their pharmaceutical use, including methods of synthesis, formulation techniques, and administration routes.


Scope of the Patent

1. Core Innovation and Core Claims

The scope generally aligns with the core inventive concept—be it a new chemical entity (NCE), a novel dosage form, or a combination therapy. The patent claims often include:

  • Chemical Composition Claims: Covering the structure, derivatives, and salts of the novel compound(s).
  • Method-of-Use Claims: Protected methods for treating specific medical conditions employing the compound.
  • Manufacturing Claims: Techniques or processes for synthesizing the active ingredient or formulating it into therapeutic products.
  • Formulation and Delivery Claims: Specific dosage forms such as controlled-release systems, injectables, or transdermal patches.

2. Claim Types and Hierarchies

  • Independent Claims: Establish the broadest scope, defining the novel compound or method in a general sense.
  • Dependent Claims: Add specificity, such as particular substituents, dosages, or formulations, effectively narrowing the scope but strengthening patent defensibility.

3. Comparative Scope Analysis

Compared to international filings (e.g., PCT applications), Cyprus patent CY1123398's claims likely mirror broader regional patent strategies, targeting the European Patent Office (EPO) via the national phase. This alignment ensures regional protection, especially within the European Union, where Cyprus is a member state.


Claims Analysis

1. Claim Breadth and Clarity

Efficient claims are precisely worded to maximize scope while ensuring clarity and validity. Claim structure probably follows standard formats:

  • The primary claim: broad, covering the core compound/method.
  • Secondary claims: covering variations, specific embodiments, or secondary uses.

2. Potential for Patentable Novelty

The inventive step resides in unique chemical modifications or innovative therapeutic applications. For example, modifications that enhance bioavailability or reduce toxicity are patentable if they demonstrate technical improvement over prior art.

3. Challenges and Limitations

  • Overlap with Prior Art: Established compounds or known formulations could threaten novelty unless sufficiently differentiated.
  • Scope vs. Patentability: Extremely broad claims risk being invalidated for encompassing known technology; overly narrow claims might restrict commercial utility.

4. Claim Strategy

An effective patent strategy likely includes a hierarchy of claims—covering a broad concept with broader claims, supplemented by narrower, more detailed claims to withstand legal challenges and enforceability.


Patent Landscape and Strategic Context

1. Global Patent Context

  • Key Jurisdictions: The invention appears aligned with patent protection strategies in the European Patent Office (EPO), the United States Patent and Trademark Office (USPTO), and China, among others.
  • Patent Families: CY1123398 is potentially part of a global family, including patent applications in the US (e.g., USXXXXXX), European Patent applications, and PCT filings, ensuring broad geographical coverage.

2. Competitive Landscape

  • Major Players: Patent filings by large pharmaceutical companies or biotech firms indicate competitive positioning for similar therapeutic classes. Alternatively, specialty biotech firms could be developing similar compounds, creating landscape complexity.
  • Patent Thickets: The pharmaceutical space for innovative compounds often involves dense patent thickets—multiple overlapping patents—making freedom-to-operate assessments critical.

3. Patent Expiry and Market Implications

Most pharmaceutical patents last 20 years from the filing date. Given the typical patent lifecycle, early-stage patents like CY1123398 serve as foundational filings, with potential for follow-up extensions or supplementary patents covering new indications, formulations, or manufacturing methods, extending commercial exclusivity.

4. Regulatory and Commercial Significance

Patent protection enhances commercial valuation and facilitates investment during clinical development phases. Patent landscape analysis also reveals potential licensing opportunities, partnerships, or patent challenges that may emerge in later stages.


Legal and Commercial Considerations

1. Patent Validity Risks

  • Prior Art Challenges: Existing literature, databases, and earlier patents may threaten patent novelty or non-obviousness.
  • Patent Examination & Office Actions: Patents filed in Cyprus are subject to examination by local authorities, which may issue rejections if claims are not sufficiently novel or inventive.

2. Enforceability and Defensive Strategies

  • Patent enforcement hinges on clear claim scope and the robustness of prosecution history.
  • Supplementary filings or continuation applications can bolster patent life and breadth, addressing emerging competitor innovations.

3. Market and Licensing Potential

  • Given the strategic importance of the claimed invention, licensing deals, or collaborations with larger pharma companies, can derive value.
  • Opposition or patent validity disputes are potential future hurdles requiring vigilant IP management.

Key Takeaways

  • Patent Scope Analysis: CY1123398 encapsulates a targeted innovation, likely emphasizing a specific chemical entity or method. Its claims are structured to balance broad coverage with enforceability, supporting therapeutic and manufacturing claims.

  • Landscape Position: It resides within a competitive intellectual property ecosystem, with potential overlaps with international patent families. Its strength derives from strategic claim drafting and geographic coverage.

  • Strategic Implications: Protecting this patent is critical for maintaining market exclusivity in Cyprus and potentially in broader European markets. Aligning filing strategies with international counterparts maximizes global protection.

  • Risk Management: Vigilant patent prosecution, freedom-to-operate assessments, and ongoing landscape monitoring are essential to mitigate legal challenges and capitalize on market opportunities.


FAQs

Q1: What is the primary inventive aspect of patent CY1123398?
A1: While specifics are unpublished here, such patents typically focus on novel chemical structures, unique methods of synthesis, or innovative therapeutic applications, emphasizing technical enhancements over prior art.

Q2: How does this patent impact global market exclusivity?
A2: As a Cyprus patent, it grants territorial protection within Cyprus. Through national filings and PCT routes, it can extend protection across Europe and other jurisdictions, building a broader patent portfolio.

Q3: What are the key challenges in defending this patent?
A3: Challenges include prior art invalidation, claim interpretation issues, and potential patent infringement disputes. Robust prosecution and detailed claim drafting mitigate these risks.

Q4: How does patent CY1123398 fit into a broader research and development strategy?
A4: It serves as a foundation for further innovation, allowing the patent holder to explore additional claims, new indications, or formulations, and defend market position during clinical and commercialization phases.

Q5: What should stakeholders consider regarding future legal developments?
A5: Continual monitoring for overlapping patents, potential oppositions, or licensing opportunities is crucial. Moreover, periodic patent maintenance and strategic continuations extend lifecycle benefits.


References

  1. European Patent Office (EPO) Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Relevant patent databases: Espacenet, USPTO, and national registry filings.
  4. Industry reports on pharmaceutical patent strategies.
  5. Cyprus Intellectual Property Office records.

End of Analysis

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