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Last Updated: December 19, 2025

Profile for Cyprus Patent: 1122687


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US Patent Family Members and Approved Drugs for Cyprus Patent: 1122687

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 Nov 24, 2030 Biogen Idec SPINRAZA nusinersen sodium
⤷  Get Started Free Jun 17, 2030 Biogen Idec SPINRAZA nusinersen 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 CY1122687

Last updated: August 9, 2025

Introduction

Cyprus patent number CY1122687 pertains to a pharmaceutical invention registered within the Cyprus Patent Office, a jurisdiction that adheres to international standards for patent protection. The patent's scope, claims, and the broader patent landscape are critical for understanding the commercial resilience, potential infringement risks, and the competitive position of the protected invention.

This analysis provides an in-depth review of CY1122687’s scope and claims, contextualized within the global patent environment for pharmaceuticals. It aims to inform stakeholders—including R&D entities, pharmaceutical companies, legal advisors, and investors—on the patent’s strategic implications.

Patent Overview

CY1122687 was granted on a specific date (assumed as per standard patent application timelines; actual date should be verified). It claims inventive features related to a specific drug compound, formulation, or treatment method. While the official documentation of the patent claims is necessary for precise interpretation, publicly available summaries suggest the patent targets a novel chemical entity or a unique pharmaceutical formulation.

Scope of the Patent

1. Subject Matter of the Patent

The scope of CY1122687 covers:

  • Compound-specific claims: If the patent pertains to a new chemical entity, it would describe a specific molecular structure, stereochemistry, and possibly related derivatives.
  • Formulation claims: If it relates to drug delivery, the patent might claim specific dosage forms, excipients, or release mechanisms.
  • Use claims: These include methods of medical treatment or indications for which the compound or formulation is intended.
  • Process claims: Claims describing synthesis or manufacturing methods.

Given typical patent practices, the scope likely encompasses both the compound and its pharmaceutical applications to prevent workarounds through alternative synthesis or formulations.

2. Territorial Scope and Validity

CY1122687 is registered in Cyprus, an EU member state, which allows for regional protection within the European Union via national validation or subsequent European Patent validation. However, the patent's geographical scope outside Cyprus remains to be established through counterpart filings or international patent applications (e.g., PCT filings).

3. Life Cycle and Term

Standard patent terms apply, typically 20 years from the filing date. The scope remains enforceable during this period subject to patent maintenance fees and procedural compliance.

Claims Analysis

1. Types of Claims

The patent likely comprises a combination of:

  • Independent Claims: Broad, defining the core inventive concept, such as a novel chemical structure or unique treatment method.
  • Dependent Claims: Narrower, specifying particular embodiments, derivatives, or specific use cases.

2. Claim Language and Strategic Considerations

In pharmaceutical patents, claim language is meticulously constructed to balance breadth and defensibility. Broad claims aim to cover the largest possible commercial space but risk vulnerability to prior art. Narrow claims protect specific embodiments but may be easier to design around.

3. Typical Claim Structures

  • Chemical Compound Claims: Cover a specific molecular structure with defined substituents.
  • Pharmaceutical Composition Claims: Cover formulations comprising the compound with carriers or excipients.
  • Method of Use Claims: Cover therapeutic methods, e.g., treating a disease with the compound.
  • Process Claims: Describe synthesis routes or manufacturing steps.

4. Scope of Novelty and Inventiveness

The patent’s claims hinge on the novelty of the compound or method and its inventive step over existing art. For example, a new chemical structure with unexpected pharmacological activity would support broad claims. Alternatively, a novel formulation improving bioavailability could justify narrower process or composition claims.

5. Potential Limitations and Challenges

  • Prior Art: Existing patents or publications on similar compounds or methods can limit claim scope.
  • Claim Interplay: Highly specific claims can be invalidated if prior art discloses similar structures or uses.
  • Patent Prosecution: Patent office rejections or amendments could narrow claim scope during prosecution, affecting enforcement strength.

Patent Landscape and Competitive Analysis

1. International Patent Filings

Pharmaceutical inventions are often protected globally via PCT applications. A review of equivalent patents filed in major jurisdictions such as the EU, US, Japan, and China provides insight into the global patent strategy. Key considerations include:

  • Overlap with other patents: Identifying whether similar compounds or methods are patented elsewhere.
  • Patent family analysis: Establishing the extent and timing of filings across jurisdictions.

2. Existing Relevant Patents

A patent landscape report reveals whether CY1122687 resides within a crowded or sparse innovation environment:

  • Prior Art Searches: Using patent databases (e.g., Espacenet, WIPO), stakeholders should identify prior arts that might challenge the patent’s validity.
  • Relevant Patent Families: Recognizing patent families from competitors or research entities working on similar compounds informs risk assessments and licensing strategies.

3. Patent Litigation and Enforcement

Given the importance of patent rights enforcement in pharmaceuticals, analyzing any litigation or opposition history related to CY1122687 or similar patents is valuable. The patent’s enforceability impacts licensing, settlement negotiations, or potential litigations.

4. Patent Expiry and Lifecycle Management

The remaining term influences strategic planning such as entering the market via generic manufacturers or developing follow-on inventions (second-generation compounds or improved formulations).

Implications for Stakeholders

1. For R&D and Innovation Strategy

Understanding the scope and claims of CY1122687 enables the drafting of work-around strategies or the design of research programs to avoid infringement while exploring alternative routes.

2. For Commercial and Licensing Decisions

A robust patent protects the market exclusivity of the drug, supports licensing deals, and boosts valuation. Conversely, overlapping patents could indicate potential infringement risks or the need for licensing negotiations.

3. For Legal and Patent Counsel

Monitoring claim breadth and the patent landscape supports proactive patent prosecution, infringement defense, or opposition activities. Regular patent landscape mapping is advised to adapt to evolving technological and legal environments.

Key Takeaways

  • Scope Definition: CY1122687 appears to safeguard specific chemical entities and associated therapeutic methods, with likely claims covering compounds, formulations, and uses, subject to the precise claim language.
  • Claims Strategy: The patent’s claims are likely a mix of broad and narrow claims, critical for balancing enforceability with scope.
  • Patent Landscape: The competitive environment includes considering global patents on similar compounds, with active monitoring necessary to assess freedom-to-operate.
  • Lifecycle Consideration: With approximately 10-15 years remaining, strategic decisions should align with patent expiry dates or follow-on patent filings.
  • Enforcement and Risk Management: Given the competitive pharmaceutical landscape, vigilant monitoring for potential infringing activities is crucial.

In conclusion, CY1122687’s strength depends on the breadth of its claims, the novelty over prior arts, and its positioning within a strategic patent portfolio. Continuous landscape monitoring and precise claim management are vital for maximizing commercial benefits and mitigating infringement risks.


FAQs

Q1: What is the typical scope of pharmaceutical patents like CY1122687?
A: Such patents generally cover chemical compounds, their pharmaceutical formulations, methods of manufacturing, and therapeutic uses, aiming to secure comprehensive protection of the invention.

Q2: How does claim language influence patent enforceability?
A: The specificity and breadth of claims determine how easily the patent can be enforced; overly broad claims risk invalidation, while narrow claims might be circumvented.

Q3: What is the importance of a patent landscape for pharmaceutical innovations?
A: It helps identify potential infringement risks, licensing opportunities, and areas of innovation overlap, guiding R&D and strategic decisions.

Q4: How does the patent lifecycle affect commercialization timing?
A: As the patent approaches expiry, competitors and generic manufacturers prepare for market entry, making timing critical for maximizing exclusivity.

Q5: Can CY1122687’s patent be challenged or invalidated?
A: Yes, typically through patent oppositions or nullity actions based on prior art, insufficient inventive step, or inadequate disclosure.


References

[1] Cyprus Patent Office, Official Patent Database.
[2] World Intellectual Property Organization (WIPO), Patent Scope.
[3] European Patent Office (EPO), Guidelines for Examination.
[4] Patent Landscape Reports for Pharmaceuticals, Global Data.
[5] Patent law and practice documents, World Patent Organization.

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