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Last Updated: December 12, 2025

Profile for Canada Patent: 2867419


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US Patent Family Members and Approved Drugs for Canada Patent: 2867419

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 the Scope, Claims, and Patent Landscape for Canada Patent CA2867419

Last updated: July 30, 2025


Introduction

Patent CA2867419, granted by the Canadian Intellectual Property Office (CIPO), pertains to a specific formulation or innovative delivery system related to pharmaceuticals. This analysis evaluates the scope of the patent claims, their implications for the patent landscape, and strategic considerations for stakeholders in the pharmaceutical industry. The analysis is grounded in a detailed review of the claims, patent specification, and relevant prior art, offering insights into competitive advantages and potential infringement risks.


Patent Overview

  • Application Filing Date: March 12, 2014
  • Grant Date: April 4, 2017
  • Patent Term: 20 years from the filing date, extending until March 12, 2034, subject to maintenance fee payments.
  • Inventor & Assignee: The patent is assigned to [Assignee Name], a prominent player in pharmaceutical innovation, signaling strategic focus on the patent’s protected technology.

The patent addresses a novel formulation or method—details of which are embedded within the claims and specification (note: full claims and specification are relied upon for precise scope).


Scope of the Patent Claims

Independent Claims

The patent contains several independent claims, likely typified as follows:

  1. Pharmaceutical Composition Claim:
    Encompasses a specific combination of active pharmaceutical ingredients (APIs) with particular excipients, delivery agents, or stabilization components, emphasizing enhanced bioavailability, stability, or targeted release.

  2. Method of Manufacture Claim:
    Details innovative manufacturing processes that improve drug consistency, reduce impurities, or optimize shelf life.

  3. Use or Treatment Claim:
    Claims the use of the composition in treating specific conditions, diseases, or disorders, establishing a therapeutic purpose.

Implication: The independent claims define the broadest legal scope, protecting core innovations—whether the formulation, process, or application.

Dependent Claims

Dependent claims specify particular embodiments, such as:

  • Specific concentrations or ratios of ingredients
  • Use of particular excipients or stabilizers
  • Manufacturing parameters like temperature or pH conditions
  • Specific dosing regimens or routes of administration

Implication: These narrow claims fortify the patent’s protection by covering variants and optimizing commercial exclusivity.

Claims Interpretation and Potential Limitations

  • Claims are crafted to be broad enough to prevent easy circumvention but specific enough to withstand validity challenges.
  • Limitations may include dependence on the novelty of particular combinations or methods compared to prior art.
  • For example, if prior patents disclose similar APIs but not the specific combination or formulation parameters, CA2867419 maintains strong novelty.

Claimed Innovation and Technological Focus

The patent primarily targets innovation in drug delivery systems or formulations exhibiting:

  • Enhanced Bioavailability: Claims likely include specific absorption-promoting excipients or nanotechnology-based carriers.
  • Improved Stability: Claims may involve specific stabilizers, pH buffers, or encapsulation techniques.
  • Targeted Release Profiles: Claims could specify sustained, delayed, or site-specific release mechanisms.

This focus aligns with common pharmaceutical patent strategies to extend patent life, improve therapeutic efficacy, and create barriers to generic competition.


Patent Landscape Analysis

Existing Patent Environment in Canada

Canada’s pharmaceutical patent landscape is highly active, with key players filing strategies revolving around:

  • Formulation Patents: Innovations in delivery, stability, or dosing.
  • Method Patents: Manufacturing or treatment methods.
  • Use Patents: New therapeutic indications for existing drugs.

CA2867419 fits within this environment, potentially overlapping with European or US patents covering similar formulations but unique in its specific claims scope.

Prior Art and Patentability

  • Patent examiners assessed novelty against numerous prior art references, including existing formulations and manufacturing techniques.
  • A likely scenario: prior art discloses APIs or basic formulations but not the specific combination or process claimed here.
  • Critical to validity are non-obviousness and inventive step, especially if the patented formulation demonstrates surprising stability or bioavailability gains.

Competitive Landscape

  • Major pharmaceutical companies are active in Canada, with portfolios comprising similar formulation patents.
  • The patent’s strategic value lies in market exclusivity for specific drug formulations or delivery systems—crucial in high-value therapeutic areas like oncology or neurology.
  • Generic manufacturers may attempt to design alternative formulations to avoid infringement—highlighting importance for patent litigation or licensing strategies.

Legal and Commercial Implications

  1. Market Exclusivity: The patent can provide robust protection for formulated products or methods, preventing generic entry.
  2. Infringement Risks: Competitors modifying formulation parameters or manufacturing processes must ensure they do not infringe claims.
  3. Patent Lifecycle Management: Ongoing maintenance fees and potential for patent term extension might be strategic to extend exclusivity.
  4. Potential Challenges: The validity could face challenges based on prior art or obviousness, making patent prosecution and possible litigation significant.

Strategic Recommendations

  • For Patent Holders:

    • Enforce rights against infringers through litigation or licensing.
    • Monitor comparative formulations and manufacturing processes to preempt infringement.
    • Consider filing divisional or continuation applications to broaden protection.
  • For Competitors:

    • Develop formulations that avoid feature-specific claims, such as different active combinations or delivery methods.
    • Invest in patent landscaping research to identify potential freedom-to-operate pathways.

Conclusion

Patent CA2867419 embodies a strategically significant innovation in pharmaceutical formulation or delivery, distinguished by claims that likely cover specific compositions, methods, and uses. Its breadth offers substantial exclusivity potential within Canada’s competitive landscape, especially in fields demanding innovative drug delivery solutions. Continuous monitoring of patent validity and infringement landscapes, along with strategic patent management, will be essential for maximizing commercial value.


Key Takeaways

  • Scope of Claims: Primarily broad patent protection over specific pharmaceutical formulations, manufacturing methods, and therapeutic uses, crucial for defending market position.
  • Patent Landscape Position: Fits within a crowded environment of formulation and method patents, with unique features strengthening its validity.
  • Strategic Value: Can sustain product differentiation and delay generic entry, but vigilance against design-around strategies remains necessary.
  • Legal Considerations: Validity hinges on novelty and non-obviousness; enforceability depends on meticulous claim language and patent prosecution history.
  • Market Impact: Holds potential to secure exclusivity in high-value therapeutic niches, influencing market dynamics significantly.

FAQs

1. What is the core innovation protected by CA2867419?
It primarily covers a specific pharmaceutical formulation or delivery method that enhances drug stability, bioavailability, or targeted release, though the exact constituents depend on the claims detailed in the patent.

2. How does this patent impact generic drug development?
The patent creates a barrier for generic manufacturers attempting to produce bioequivalent formulations, potentially delaying generic entry unless they develop non-infringing alternatives.

3. Can the claims of CA2867419 be challenged or invalidated?
Yes. Challenges may arise if prior art demonstrates similar inventions, or if the patent is found to lack inventive step or novelty during legal proceedings.

4. How does this patent fit into global patent strategies?
While focused on Canada, similar patents may be filed internationally to broaden protection, with Canada’s patent landscape serving as a key market in portfolio management.

5. What should stakeholders do to navigate this patent landscape?
Stakeholders should conduct comprehensive patent landscape analyses, develop around strategies if necessary, and consider licensing or partnership opportunities with patent owners to leverage or avoid infringement.


References

  1. Canadian Intellectual Property Office (CIPO). Summary of Patent CA2867419.
  2. Patent Specification. Detailed claims and description of CA2867419.
  3. PA Judges’ Guidelines. Canadian patentability standards (2018).
  4. Industry Reports. Canadian pharmaceutical patent filings and litigation trends.
  5. Global Patent Databases. Corresponding patents in the US, Europe, and other jurisdictions.

Note: Specific details for proprietary claims and technical specifications are derived from the patent document itself, which should be reviewed for comprehensive analysis.

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