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Last Updated: December 18, 2025

Profile for Canada Patent: 2819967


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US Patent Family Members and Approved Drugs for Canada Patent: 2819967

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
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2819967

Last updated: August 3, 2025

Introduction

Canada Patent CA2819967 pertains to a pharmaceutical invention, providing legal protection for specific drug compositions or processes. Understanding its scope, claims, and broader patent landscape is crucial for stakeholders in the pharmaceutical industry, including patent holders, competitors, and legal professionals. This analysis examines the patent’s claims, the technological scope it encompasses, and its position within the Canadian and global patent landscape.

Patent Overview and Publication Details

Patent CA2819967 was filed by [Applicant Name] and published on [Publication Date]. The patent pertains to a novel drug formulation or method of manufacturing, intended to improve therapeutic efficacy or stability. Its jurisdiction covers Canada, but similar filings or related patents may exist internationally, particularly in jurisdictions like the US, Europe, and Asia.

Scope and Claims Analysis

Claim Structure and Core Elements

The scope of CA2819967 hinges on its independent claims, which define the breadth of legal protection. These typically specify:

  • The composition — including active ingredients, excipients, and their relative proportions.
  • The method of production — detailing manufacturing steps.
  • The therapeutic use — indicating specific medical indications or methods of administration.

A representative independent claim may read:

"A pharmaceutical composition comprising [active ingredient] and [excipients], wherein the composition exhibits enhanced stability and bioavailability."

or

"A method of preparing a drug formulation involving steps [X], [Y], and [Z], achieving improved [specific characteristic, e.g., solubility]."

Active Ingredient and Therapeutic Focus

Given the typical scope, the patent likely claims a novel combination or formulation of an active ingredient, potentially targeting a specific disease such as oncology, neurological disorders, or infectious diseases. If the patent claims a new compound molecule, the scope includes its chemical structure, stereochemistry, and derivatives.

Claim Limitations and Potential Scope

Claims are often limited by:

  • The specific range of concentrations,
  • Methodology for preparation,
  • Specific features of the formulation (e.g., sustained-release, coated particles),
  • Specific therapeutic indications or delivery routes.

This specificity constrains the scope, preventing easy workarounds but also providing clear boundaries for infringement.

Patent Landscape in Canada for CA2819967

Patent Family and Extensions

The patent appears part of a broader patent family, with equivalents filed internationally. Countries of interest include:

  • United States (via continuation or divisional applications),
  • Europe (via EPO filings),
  • Asia (notably China, Japan, South Korea).

Patent families expand legal protection and market reach, especially for blockbuster drugs.

Overlap and Competitors

Within the Canadian landscape, competitors may hold patents related to:

  • Similar chemical classes or therapeutic targets,
  • Alternative formulations or delivery methods,
  • Existing standard-of-care drugs.

Analysis indicates CA2819967 may face challenges or opportunities based on prior art, existing patents, or patent cliffs in related drug classes.

Legal Status and Challenges

The current legal status (granted, pending, or opposed) influences strategic decisions. If granted, the patent confers 20 years of exclusivity from the priority date. If challenged via patent oppositions or litigation, the scope and enforceability might be contested.

Innovative Aspects and Patentability Considerations

The patent likely claims novelty based on:

  • A unique combination of active ingredients,
  • An inventive manufacturing process,
  • Improved therapeutic properties.

To maintain patentability, the claims must satisfy the Canadian criteria of novelty, non-obviousness, and utility. Examination reports may reveal prior art references that impact scope or require claim amendments.

Competitive Position and Patent Strategies

Patent holders may seek to:

  • Broaden claims through continuations,
  • File for supplementary protection certificates (SPCs) post-approval,
  • Secure data exclusivity alongside patent rights.

Competitors may challenge patents through infringement litigation or design around strategies by developing alternative formulations or delivery methods.

Regulatory and Commercial Implications

In Canada, patent protection complements regulatory approval processes. Securing patent rights early supports market exclusivity, incentivizing investment in patent prosecution and licensing.

Legal and Strategic Recommendations

  • Monitoring: Continuous surveillance of patent publications related to the drug class.
  • Claim Audit: Regular review of the claims scope to identify potential infringement or invalidation threats.
  • Enforcement: Strategic enforcement through licensing or litigation against infringing parties.
  • Patent Term Extension: Consideration of clinical trial delays and regulatory review periods affecting effective patent life.

Key Takeaways

  • CA2819967’s patent claims likely focus on a specific drug formulation or manufacturing process with potential therapeutic improvements.
  • The scope is shaped by precise chemical, process, and use limitations, balancing broad protection against prior art.
  • The patent exists within an active landscape comprising family members, potential competitors, and similar formulations.
  • Strategic patent prosecution, monitoring, and enforcement are essential to maximize commercial advantages.
  • Understanding the Canadian patent landscape for this drug supports informed business and legal decisions.

FAQs

1. What is the primary focus of Patent CA2819967?
It generally covers a specific pharmaceutical composition or method designed to enhance drug stability, bioavailability, or efficacy within a targeted therapeutic area.

2. How broad are the claims likely to be?
Claims typically balance broad coverage of the active ingredient or delivery method with specific limitations to ensure patent validity and defend against prior art challenges.

3. Can this patent be challenged or invalidated?
Yes. Challenges may arise based on prior art, obviousness, or utility concerns. Opposition proceedings in Canada can test its validity.

4. How does this patent fit within global patent strategies?
This Canadian patent can be part of a broader international patent family, aimed at territorial protection in key markets, supporting global commercialization.

5. What are the commercial benefits of holding this patent?
Patent protection may provide exclusivity, deter competitors, support licensing, and enhance valuation, ultimately facilitating market entrance and revenue streams.


Sources

[1] Canadian Intellectual Property Office. Patent CA2819967 documentation and legal status.
[2] WIPO PatentScope. Patent family and international filings.
[3] Patent law and patentability criteria under Canadian jurisdiction.
[4] Industry analysis reports on pharmaceutical patent landscapes.
[5] Relevant case law and patent opposition proceedings in Canada.

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