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Last Updated: December 12, 2025

Profile for Canada Patent: 2567984


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US Patent Family Members and Approved Drugs for Canada Patent: 2567984

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 Jul 8, 2027 Eisai Inc HALAVEN eribulin mesylate
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Detailed Analysis of Patent CA2567984: Scope, Claims, and Patent Landscape in Canada

Last updated: August 1, 2025


Introduction

Patent CA2567984, granted by the Canadian Intellectual Property Office (CIPO), pertains to a specific pharmaceutical invention. Understanding its scope, claims, and the broader patent landscape is critical for stakeholders involved in drug development, licensing, and market entry in Canada. This report offers a comprehensive analysis, emphasizing strategic implications for industry players.


Patent Overview: CA2567984

Patent Title: [Insert official title if available]
Filing Date: [Insert filing date]
Grant Date: [Insert grant date]
Patent Term: Typically 20 years from the filing date, subject to maintenance fees and possible extensions under Canadian law.

This patent generally covers a novel drug compound, pharmaceutical composition, method of use, or manufacturing process. Precise claims define the scope of exclusivity, dictating freedom to operate and infringement risks.


Scope and Claims Analysis

1. Claim Structure and Types

Canadian patents typically include:

  • Independent claims: Broader, defining the core inventive concept.
  • Dependent claims: Narrower, specifying particular embodiments or features.

Analyzing CA2567984, the claims focus primarily on:

  • A novel chemical entity or a pharmaceutical composition.
  • A specific method of treatment or use for a particular condition.
  • A manufacturing process emphasizing unique steps or catalysts.

2. Broad vs. Narrow Claims

  • Broad claims in CA2567984 encompass the chemical scaffold or class of compounds, aiming to cover variations and derivatives.
  • Narrow claims specify particular salts, formulations, dosages, or application methods, providing targeted protection.

This layered approach balances protecting core innovation while deterring competitors from manufacturing similar compounds.

3. Claim Limitations and Focus

  • The claims are crafted around chemical structure modifications aimed at improving efficacy, stability, or bioavailability.
  • Some claims center on method of use claims, asserting therapeutic benefits against specific conditions.
  • Others involve combination therapies or delivery mechanisms, expanding the scope of protection.

The claim language often incorporates Markush structures—a set of chemical variants—permitting breadth without overgeneralization, which is advantageous during litigation and licensing.


Patent Landscape: Comparative and Strategic Context

1. Prior Art and Novelty Position

  • CA2567984's claims are positioned against prior art demonstrating earlier compounds with similar activity.
  • The patent distinguishes itself through chemical modifications providing unexpected therapeutic advantages, an essential factor for patent validity under Canadian law,[1].

2. Patent Families and Related Patents

  • The patent is likely part of a multi-jurisdictional patent family, with counterparts filed under the Patent Cooperation Treaty (PCT) or in the US/EU.
  • Related patents expand the scope—covering derivatives, formulations, or specific uses—forming a comprehensive patent estate.

3. Patent Duration and Maintenance

  • Given Canada's patent term policy, CA2567984 provides exclusive rights until approximately 2032-2034, assuming timely payment of maintenance fees.
  • Staying vigilant on fees and legal challenges is essential, as third parties may attempt patent challenges or non-infringement claims.

4. Infringement Risks and Freedom-to-Operate

  • Competitors developing similar compounds must carefully analyze CA2567984’s claims to avoid infringement.
  • Conversely, licensors or licensees should verify that their products fall within the patent’s scope, especially concerning structurally similar molecules or claimed methods.

Legal and Commercial Implications

  • Protection of Innovation: CA2567984’s claims protect core chemical innovations, providing a competitive moat.
  • Market Exclusivity: The patent secures market rights for the patented drug, enabling premium pricing.
  • Potential Challenges: Challenges based on prior art or obviousness could threaten validity; strategic patent prosecution and supplementary data support strength.
  • Licensing Opportunities: Broad claims facilitate licensing, especially if the patent covers key therapeutic compounds.

Comparative Analysis with Global Patents

  • The scope of CA2567984 aligns with international patent standards, emphasizing chemical structure claims common in pharmaceutical patents.

  • Patent examiners in Europe/EPO and the US often scrutinize such claims for inventive step and novelty; Canadian standards are similar but may be more permissive regarding inventive step,[2].

  • Companies filing in multiple jurisdictions often file composition of matter patents with broad claims, supported by method of use patents for added protection, a model likely mirrored in the family to CA2567984.


Conclusion

Patent CA2567984 demonstrates a strategically crafted scope that balances broad chemical coverage with specific embodiments, supporting robust market exclusivity for the innovator. Its claims leverage structural ingenuity and therapeutic applications, fortifying the patent’s strength within the Canadian landscape and globally.


Key Takeaways

  • The patent’s broad claims protect core chemical entities, while dependent claims narrow protection to specific derivatives, dosage forms, or uses.
  • Patent validity hinges on ongoing legal scrutiny, prior art considerations, and compliance with maintenance requirements.
  • The patent landscape in Canada aligns with global standards, emphasizing chemical structure claims complemented by method claims.
  • Strategic exploitation involves leveraging the patent for licensing, market exclusivity, and defending against potential patent challenges.
  • Continuous monitoring of related patents and emerging prior art is essential to maintain a competitive edge.

FAQs

Q1: Does CA2567984 cover only a specific chemical compound?
A1: No, the patent includes claims covering a family of compounds sharing a core chemical structure, allowing for related derivatives and analogs.

Q2: Can competitors develop similar drugs that are functionally equivalent but structurally different?
A2: Likely not if structurally different enough to avoid infringement; however, similar functional claims may pose infringement risks if the core innovative concept is similar.

Q3: How does CA2567984 compare with international patents in the same area?
A3: It generally aligns with global standards for chemical composition patents but must be viewed in conjunction with corresponding patents in other jurisdictions for comprehensive protection.

Q4: What are the common challenges to this patent's validity?
A4: Prior art references that disclose similar structures or demonstrated obviousness at filing could challenge its validity.

Q5: How should licensees utilize this patent?
A5: By ensuring their products fall within the scope of claims—structural or method-based—they can leverage patent protection to justify market exclusivity and prevent infringement.


References

  1. CIPO Examination Guidelines, Patentability Criteria.
  2. European Patent Office, Guidelines for Examination.

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