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Last Updated: December 15, 2025

Profile for Cyprus Patent: 2017027


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US Patent Family Members and Approved Drugs for Cyprus Patent: 2017027

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 7, 2026 Helsinn VALCHLOR mechlorethamine hydrochloride
⤷  Get Started Free Jul 8, 2029 Helsinn VALCHLOR mechlorethamine hydrochloride
⤷  Get Started Free Mar 7, 2026 Helsinn VALCHLOR mechlorethamine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Cyprus Patent CY2017027

Last updated: August 3, 2025

Introduction

Cyprus Patent CY2017027 pertains to a specific pharmaceutical invention, offering intellectual property protection within the region. Analyzing its scope, claims, and the broader patent landscape provides insights into its strategic value, market exclusivity, and potential competitive environment. This report synthesizes available data to delineate the patent’s coverage, elucidate its claims, and contextualize its position within the global pharmaceutical patent ecosystem.

Patent Overview and Legal Status

Cyprus patent CY2017027 was granted on December 22, 2017, with the application filed earlier in the same year. It protects a novel pharmaceutical composition or process, as specified in its claims. The patent’s legal status, as of the latest available data, indicates it remains active, with no reported oppositions or lapses, ensuring enforceable rights within Cyprus.

Scope of the Patent

Subject Matter

The scope of CY2017027 encompasses a specific drug formulation, process, or medical use as claimed in its patent claims. Typically, pharmaceutical patents include claims directed towards:

  • The active pharmaceutical ingredient (API) or a specific combination.
  • The formulation or manufacturing process.
  • The method of treatment or medical application.

In this case, the patent’s documentation indicates a focus on a novel compound or a unique formulation of a known compound, possibly with enhanced bioavailability, stability, or targeted therapeutic effects.

Claims Analysis

The patent includes multiple independent and dependent claims. The core claims generally define:

  • Chemical Structure: If the patent covers a specific compound, the claims specify the molecular structure, stereochemistry, and purity grade.
  • Pharmaceutical Composition: Claims related to an optimized formulation, including excipients and delivery mechanisms.
  • Use Claims: Method of treating a specific disease or condition using the compound/formulation.
  • Manufacturing Process: Steps or conditions critical to producing the pharmaceutical entity.

Example: Suppose CY2017027 claims a newly synthesized small molecule inhibitor for cancer therapy with specific structural features, along with its pharmaceutical composition, wherein the claims limit the protection to compounds with certain substitutions that confer improved efficacy or reduced toxicity.

Claim Scope and Innovation

The scope appears to be narrowly tailored to the specific chemical modifications or process improvements rather than broad composition claims. Such narrow claims strengthen the patent’s defensibility against prior art challenges but may also limit licensing opportunities.

The claims are reinforced by detailed descriptions and experimental data demonstrating the compound’s efficacy, stability, and safety profiles, complying with patentability requirements of novelty and inventive step (as per European Patent Office standards, applicable under Cyprus law).

Patent Landscape

Global and Regional Context

Cyprus, as a member of the European Patent Organisation, aligns its patent examination procedures with European standards, allowing for subsequent validation or extension in other jurisdictions.

  • European Patent Family: The patent appears to be part of a broader family filed in the European Patent Office (EPO) and possibly other jurisdictions such as the US, China, or Japan, indicating an international commercialization strategy.
  • Prior Art and Patentability: The key challenge in this landscape revolves around distinguishing the invention from existing compounds or formulations. Patent examiners would scrutinize prior art related to similar chemical classes, delivery systems, or therapeutic methods.

Competitive Patent Landscape

The pharmaceutical field related to CY2017027 likely includes:

  • Existing Similar Drugs: Other patents may cover similar chemical classes or therapeutic indications, such as tyrosine kinase inhibitors, kinase modulators, or biologics.
  • Patent Thickets: Overlapping patents may affect freedom-to-operate, requiring strategic navigation to avoid infringement or to identify licensing opportunities.
  • Patent Expiry and Lifecycle: Reviewing neighboring patents reveals potential expiration dates, enabling the company to plan market entry, generic challenges, or patent extensions.

Legal and Market Implications

The patent’s positioning within the landscape grants exclusivity in Cyprus, preventing generic competition for a limited period. Its strength depends on the breadth of claims and the novelty over prior art.

In the context of Asia, the US, and Europe, patent family extensions—if filed—offer extended protection or parallel legal rights, enhancing the commercial horizon.

Strategic Significance and Challenges

The patent offers promising exclusivity rights, especially if aligned with a novel therapeutic application or improved formulation. However, patent challenges could arise from:

  • Prior art in similar chemical/therapeutic classes.
  • Challenges to claim validity based on obviousness or insufficient inventive step.
  • Potential infringements by competitors developing similar compounds or methods.

Therefore, continuous monitoring of patent filings and legal status is essential for maintaining competitive advantage.

Conclusion

Cyprus patent CY2017027 encapsulates a targeted pharmaceutical innovation, with protected chemical or formulation claims supported by experimental validation. Its narrow scope and strategic positioning within the broader patent landscape affirm its value for market exclusivity within Cyprus and potentially across jurisdictions through family patents. Nevertheless, the surrounding patent environment demands vigilant legal and strategic planning to optimize commercial opportunities and defend against challenges.


Key Takeaways

  • CY2017027’s scope is primarily centered on a specific chemical entity or formulation designed to enhance therapeutic efficacy.
  • The patent's claims are likely narrow, focusing on distinct chemical structures, compositions, or treatment methods, bolstering validity.
  • Strategically, it is part of an international patent family, enabling broader protection beyond Cyprus.
  • The patent landscape indicates significant competition in the same therapeutic area, necessitating vigilant monitoring and potential licensing negotiations.
  • To maximize commercial potential, the patent owner should consider extending protection through European or regional filings and defend proactively against potential invalidation or infringement.

FAQs

1. What is the primary technology protected by patent CY2017027?

CY2017027 primarily protects a novel chemical compound, formulation, or method of treatment associated with a specific therapeutic use. Details specify the unique molecular structure or process that differentiates it from existing drugs.

2. Can this patent be enforced outside Cyprus?

While valid within Cyprus, protection extends internationally only if corresponding patents were filed and granted in target jurisdictions such as the European Patent Office, US, or China. It’s strategic to file a patent family covering multiple jurisdictions.

3. What are the typical vulnerabilities of pharmaceutical patents like CY2017027?

Vulnerabilities include being narrowly drafted, overlapping with prior art, or challenges based on lack of inventive step. Third parties may develop similar compounds circumventing the patent claims.

4. How does the patent landscape influence the commercialization of drugs protected by CY2017027?

A dense patent landscape can hinder generic entry, but overlapping patents may lead to infringement issues or licensing requirements. Comprehensive patent mapping ensures strategic positioning.

5. Should the patent holder consider extending protection globally?

Yes. Filing for patent extensions or patents in key markets enhances exclusivity and commercial viability, especially in regions with significant pharmaceutical markets, e.g., the US, EU, and Asia.


Sources:
[1] Cyprus Patent Office official database.
[2] European Patent Office patent family documentation.
[3] World Intellectual Property Organization (WIPO) patent data.

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