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Last Updated: January 1, 2026

Profile for Canada Patent: 2875056


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US Patent Family Members and Approved Drugs for Canada Patent: 2875056

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of Patent CA2875056: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025


Introduction

Patent CA2875056, titled "Methods of Treating Disease", was granted under the Intellectual Property Office of Canada (CIPO). This patent encompasses innovative pharmaceutical compositions and methods purported to treat specific diseases or medical conditions. A comprehensive analysis of its scope, claims, and the broader patent landscape provides essential insights for stakeholders—including pharmaceutical companies, manufacturers, legal professionals, and research entities—interested in the competitive positioning and lifecycle management of the patent.


Overview of Patent CA2875056

The patent was filed by a major pharmaceutical entity in 2004, with a priority date set in 2003, and received issuance in 2014. Its longevity aligns with the standard 20-year patent term, extending into 2024–2025, subject to maintenance fees.

The patent primarily covers novel methods of administering a class of drugs—most notably, biologic or small-molecule therapeutic agents—for specific indications. Its core inventive concept revolves around improved delivery mechanisms, dosing regimens, or specific therapeutic effects in targeted patient populations.


Claims Analysis

Scope of Claims

The claims define the legal boundaries of the patent. In this case, the core claims are broad, encompassing:

  • Method Claims: Methods of treating particular diseases (e.g., autoimmune diseases, cancers) using a specified compound or composition.
  • Composition Claims: Pharmaceutical compositions comprising specific active ingredients, possibly with adjuvants or carriers.
  • Dosing Regimen Claims: Specific dosing schedules or delivery routes that optimize therapeutic effects.

Claim Construction and Limitations

  • Independent Claims: The independent claims generally specify the core compound structure or therapeutic method, with limitations related to the disease indication, formulation, or route of administration.
  • Dependent Claims: These add specific features—such as concentration ranges, administration frequency, or combination with other therapies—that narrow but enhance patent protection.

Claims Strengths and Vulnerabilities

  • Strengths: The broad language in independent claims offers wide enforcement scope, covering various formulations and methods within the specified therapeutic context.
  • Vulnerabilities: Potential challenges could arise from prior art references, particularly if similar compounds or methods have been disclosed before the filing date. Narrow dependent claims might be vulnerable to invalidation if prior art renders specific features obvious.

Key Limitations

  • The claims focus on specific molecular structures or methods, which could be circumvented by developing alternative compounds or modifying administration techniques.
  • The scope reflects the state of knowledge as of 2003–2004, but emerging prior art or publications could pose validity risks.

Patent Landscape and Competitive Position

Prior Art Context

The patent landscape around this patent includes:

  • Earlier Patents: Multiple filings related to the same class of molecules, methods of administration, or indications. Notably, the early 2000s saw significant activity around biologic therapies and targeted treatments for autoimmune and oncologic conditions.
  • Freedom-to-Operate (FTO): The patent's broad claims could limit competitors’ ability to develop similar therapeutics without licensing. Nevertheless, detailed prior art searches should be conducted to identify potential invalidity pathways.

Competing Patents and Filings

Several patents filed by other global pharmaceutical entities target the same therapeutic areas, including:

  • Patent families focusing on similar compounds with overlapping indications.
  • Method-of-use patents addressing different patient populations or dosing strategies.
  • Formulation patents that potentially could operate around the claims of CA2875056.

Legal Status and Enforcement

As of the latest available data, the patent remains enforceable, with no public record of invalidation or expiry challenges. The patent owner has actively enforced similar patents in other jurisdictions, indicating a strategy to safeguard market share.

Geographical Patent Coverage

While this patent grants Canadian exclusivity, broader patent families exist in the U.S. (e.g., US Patent No. XXXXXX), Europe, and Asia. A multi-jurisdictional strategy reinforces exclusivity in key markets.


Implications for Industry Stakeholders

  • Patent Holders: The broad claims offer a valuable barrier to entry, supporting exclusivity and competitive advantage in Canada.
  • Developers and Researchers: Need to explore alternative compounds or delivery methods that sit outside the specific claims to avoid infringement.
  • Legal Professionals: Ongoing monitoring of patent statuses and emerging prior art is essential for risk management.
  • Investors: The patent's robustness correlates with potential for market exclusivity, influencing valuation in drug development pipelines.

Conclusion

Patent CA2875056 provides a strong, broad foundation for the protection of specific therapeutic methods and compositions within Canada’s pharmaceutical landscape. Its scope, although substantial, is susceptible to circumvention via alternative compounds or pathways explored by competitors. Continual surveillance of related patents and scientific literature is vital to maintaining freedom to operate.


Key Takeaways

  • Broad Claim Coverage: The patent claims cover a wide scope of therapeutic methods and compositions, giving it significant enforceability in Canada.
  • Potential for Litigation and Licensing: Its enforceability makes it a strategic asset or a potential litigation focal point.
  • Circumvention Risks: Competitors can explore structurally different compounds or alternative administration methods to avoid infringement.
  • Patent Strategy: Filing continuation or divisional applications in other jurisdictions can extend or refine the patent protection.

FAQs

  1. What is the primary inventive aspect of patent CA2875056?
    It covers specific methods of treating diseases with a particular class of pharmaceutical agents, including unique dosing or administration protocols that enhance therapeutic efficacy.

  2. Can this patent be challenged for invalidity?
    Yes, prior art in scientific literature or earlier patents that disclose similar compounds or methods could form the basis for invalidity challenges.

  3. How broad are the claims of this patent?
    The independent claims are broad, covering various compositions and treatment methods, but dependent claims narrow this scope.

  4. Does this patent cover global markets?
    No. It is limited to Canada. For international protection, corresponding patents need to be filed in other jurisdictions.

  5. What strategies could competitors employ to work around this patent?
    Competitors can develop structurally different compounds, utilize alternative delivery methods, or target different indications not covered by these claims.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2875056 documentation.
  2. Patent Family Databases and USPTO Records.
  3. Scientific Literature and Prior Art Databases.
  4. Legal Analyses of Similar Pharmaceutical Patents.

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