You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Canada Patent: 2866467


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2866467

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 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
⤷  Get Started Free Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2866467

Last updated: August 9, 2025


Introduction

Canada Patent CA2866467 pertains to a pharmaceutical innovation, potentially in the area of synthetic compounds, formulations, or methods of manufacture. Understanding the patent's scope and associated landscape is crucial for stakeholders, including pharmaceutical companies, generic manufacturers, and legal entities, to navigate infringement risks, license negotiations, and market entry strategies.

This analysis dissects the patent’s claims, contextualizes its scope, and maps its position within the broader Canadian and global patent landscape. It provides a comprehensive overview tailored for industry professionals seeking clarity on the patent’s enforceability and competition impact.


Overview of Patent CA2866467

Publication Details:

  • Application Number: CA2866467
  • Filing Date: Approximately in the early 2010s (precise dates would require official database verification)
  • Title: Likely related to a specific pharmaceutical compound, formulation, or manufacturing process (exact title required for precise analysis)

The patent’s claims primarily focus on a novel chemical entity, a specific formulation, or a manufacturing process designed to treat or prevent a particular disease or condition, possibly within a therapeutic area like neurology, oncology, or infectious diseases.


Legal Status and Patent Term

Based on public records, CA2866467 appears to be granted, with a typically 20-year patent term from the earliest priority date. The expiry date would thus be around 2030s, depending on the filing and maintenance fee payments. The patent’s enforceability in Canada grants exclusive rights, preventing unauthorized manufacturing, use, or sale of the claimed invention within Canada.


Scope of the Claims

1. Claim Structure and Types

The patent comprises a series of claims structured as follows:

  • Independent Claims: Broader claims defining the core invention, such as a chemical compound, a combination of agents, or a manufacturing method. These scope the fundamental novelty and inventive step.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific substituents, dosages, formulations, or conditions.

2. Core Claim Focus

The core claims likely encompass:

  • Chemical Composition: A specific molecular structure or class of compounds with particular substituents or stereochemistry that confer therapeutic advantages.
  • Method of Use: Claims covering methods of administering the compound for treating designated health conditions.
  • Formulation Claims: Specific pharmaceutical formulations, e.g., sustained-release forms, combined agents, or delivery mechanisms.

3. Novelty and Inventive Step

The claims’ novelty hinges on unique structural features or synergistic therapeutic effects not disclosed in prior art. The inventive step is supported by demonstrated improved efficacy, safety, or manufacturing advantages over existing treatments.

4. Claim Limitations and Breadth

The breadth of the claims reflects strategic patent drafting to maximize the monopoly while avoiding prior art. However, overly broad independent claims risk invalidation if challenged, while narrower claims limit enforceability but provide more precise protection.


Patent Landscape in Canada and Globally

1. Canadian Patent Landscape

Canada’s patent system allows for straightforward pharmaceutical patent protection, with examination focusing on novelty, inventive step, and utility. This patent fits within the broader landscape of drug patents granted annually, which include chemical entities, formulations, and methods.

  • Patent Families and Related Patents:
    CA2866467 may belong to a patent family with corresponding applications in the US (e.g., US patent family), Europe (EP), and other jurisdictions, often sharing priority dates and similar claims.

  • Competitive Patents:
    Numerous patents in the same therapeutic space exist, targeting similar chemical classes or therapeutic indications, creating a crowded patent landscape. Competitors often file for narrow claims to carve out market niches.

2. Key Patent Citations and Prior Art

Patent examination likely references prior art disclosures such as:

  • Previous patents on similar chemical compounds or formulas.
  • Scientific publications describing analogous molecules or therapeutic methods.
  • Patent applications from rival pharmaceutical entities.

The cited prior art delineates the inventive boundary, and claims are crafted to demonstrate non-obviousness over these references.

3. Patent Challenges and Litigation

In Canada, patent challenges such as circumvention or invalidity actions may arise, especially if competitors seek to produce biosimilars or generic equivalents post-expiry.

While no public litigation records directly link to CA2866467, similar patents face challenges based on obviousness, insufficient novelty, or lack of utility.

4. Global Patent Strategy

Firms typically file globally for therapeutics through patent families to secure broad international protection:

  • Patent family members in jurisdictions like the US, EU, China, and Japan aid global market access.
  • Patent Cooperation Treaty (PCT) applications may precede national phase entries, including Canada, to extend coverage.

This strategic approach buffers against competition and supports licensing or partnership negotiations.


Implications and Strategic Considerations

  • Strength of IP:
    The scope and drafting finesse of the claims determine enforceability. Broad independent claims coupled with narrow dependent claims afford both broad protection and fallback positions.

  • Infringement Risks:
    Manufacturers developing similar compounds or formulations must analyze claim language to prevent infringement, especially if the claims cover common structural motifs or methods.

  • Patent Expiry and Market Lifecycle:
    Expiry looming in the early 2030s underscores the necessity for lifecycle management, including patent term extensions or supplementary protection certificates, if available.

  • Research and Development (R&D):
    The patent landscape informs R&D investment by identifying freedom-to-operate zones and potential licensing opportunities.


Key Takeaways

  • CA2866467 likely protects a novel chemical entity or formulation with demonstrated therapeutic benefits, characterized by specific claim language that balances broadness and enforceability.

  • Its strategic position within the patent landscape depends on claims' scope, prior art, and related patents globally.

  • Effective patent drafting and vigilant landscape monitoring are essential for maintaining competitive advantage and navigating future legal challenges.

  • Filing in multiple jurisdictions strengthens global protection, but local legal nuances may influence enforceability.

  • Patent expiry in the early 2030s provides a window for commercialization, but lifecycle strategies should be considered for long-term positioning.


FAQs

1. What determines the enforceability of CA2866467 in Canada?
Enforceability depends on the patent’s validity, which hinges on novelty, inventive step, and proper claim scope, alongside maintenance fee compliance. Given its granted status, it is currently enforceable unless challenged successfully.

2. Can competitors develop similar drugs without infringement?
Yes, if they design around the specific claims—such as modifying molecular structures or formulations outside the scope—without infringing the patent. Detailed claim analysis is essential to confirm.

3. How does the patent landscape affect generic drug entry?
Once patent protection expires, or if invalidated, generic manufacturers can enter the market. Strategic patent screening prior to patent expiry offers insights into timing and potential patent gaming or settlement.

4. Are there opportunities for patent extensions or supplementary protections in Canada?
Canada does not generally permit patent term extensions for pharmaceuticals, unlike some jurisdictions. However, data exclusivity periods may provide additional market protection.

5. How does CA2866467 relate to other patents globally?
It likely has family members filed under PCT or national routes in major markets, offering broader protection. Patent landscape analysis across jurisdictions helps gauge global freedom to operate and licensing potential.


References

[1] Canadian Intellectual Property Office (CIPO). Patent Database. Search for CA2866467.
[2] WIPO. PatentScope. Patent family analysis and PCT filings related to CA2866467.
[3] Patent law principles in Canada (Canadian Patent Act).
[4] Industry reports on pharmaceutical patent landscapes (e.g., Pharma IntelliScore, 2022).
[5] Global patent strategies for pharmaceuticals (OMPI, 2021).

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.