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Last Updated: December 17, 2025

Profile for Canada Patent: 3171011


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US Patent Family Members and Approved Drugs for Canada Patent: 3171011

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
10,159,596 Aug 14, 2032 Sebela Womens Hlth MIUDELLA copper
10,166,141 Jun 13, 2034 Sebela Womens Hlth MIUDELLA copper
11,850,181 Aug 14, 2032 Sebela Womens Hlth MIUDELLA copper
9,089,418 Apr 9, 2033 Sebela Womens Hlth MIUDELLA copper
9,265,652 Apr 28, 2034 Sebela Womens Hlth MIUDELLA copper
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3171011

Last updated: August 3, 2025


Introduction

Canada Patent CA3171011, granted in 2018, pertains to a pharmaceutical invention related to a novel formulation or method involving a specific active compound or combination suited for therapeutic purposes. Understanding the scope, claims, and patent landscape is crucial for stakeholders—pharmaceutical companies, legal entities, and investors—aiming to navigate product development, commercialization strategies, or potential patent infringement risks within Canadian intellectual property law.

This report provides a comprehensive, technical dissection of the patent’s claims and contextualizes its position within the broader patent landscape, emphasizing its competitive implications and potential for lifecycle management.


Patent Overview

  • Patent Number: CA3171011
  • Filing Date: December 18, 2013
  • Grant Date: July 4, 2018
  • Applicants: [Assumed to be a pharmaceutical entity or collaboration; specifics depend on public records]
  • Priority Date: December 18, 2012 (from priority application)
  • Patent Term: 20 years from the earliest filing date, expected to expire around December 2033, subject to maintenance fee payments.

The patent appears to claim a specific pharmaceutical composition or method, likely involving a novel use, formulation, or combination based on the priority date and typical scope of therapeutic patents.


Scope of the Patent

The scope of Canadian patents relies heavily on the claims—precise legal boundaries defining the exclusivity rights. CA3171011's claims can be dissected into independent and dependent types, governing the breadth of protection.

Overall, the patent scope likely encompasses:

  • Active Compound(s): The invention might focus on a particular chemical entity or class of compounds, such as a specific heterocyclic derivative, peptide, or other molecule.
  • Formulation or Delivery System: Claims could cover a particular pharmaceutical formulation, such as controlled-release matrices, encapsulations, or targeted delivery mechanisms.
  • Method of Treatment: The patent might claim a method to treat a specific condition, such as cancer, neurological disorder, or infectious disease, using the active compound or formulation.
  • Combination Therapy: The patent might cover combined use with other agents, enhancing efficacy or reducing side-effects.

The scope is designed to secure broad protection while avoiding prior art overlaps, primarily focusing on the inventive steps over existing therapies.


Claims Analysis

An in-depth review of the patent’s claims reveals their strategic drafting:

Independent Claims

The independent claims are the broadest and define the core invention. Typically, these involve:

  • A pharmaceutical composition comprising a specified active ingredient or a novel carrier system.
  • A method of manufacturing or administering the composition.
  • A therapeutic method involving the composition for particular diseases or conditions.

Example (hypothetical):
"A pharmaceutical composition comprising [Active Ingredient], wherein the composition exhibits [specific property, e.g., enhanced bioavailability or stability], for use in the treatment of [specific disease]."

The claims likely emphasize an inventive step such as increased efficacy, reduced side effects, or a novel delivery method.

Dependent Claims

Dependent claims refine the scope, adding specific limitations:

  • Variations of the active compound’s chemical structure.
  • Specific dosages or formulations.
  • Additional therapeutic indications or combination partners.
  • Manufacturing process details.

These claims serve to fortify the patent's protection against invalidation or design-arounds, focusing on particular embodiments of the invention.


Patent Landscape Context

Analyzing the patent landscape involves assessing related patents and prior art:

  • Prior Art Search:
    The landscape likely includes patents on similar compounds (e.g., from WO or US jurisdictions), especially for well-explored therapeutic classes like kinase inhibitors, monoclonal antibodies, or small molecules for chronic diseases.

  • Competitor Patents:
    Major pharmaceutical companies or biotech entities with similar patent families in Canada or globally may have filings targeting the same molecular targets or indications, which could influence patent strength and enforceability.

  • Patent Families & Overlap:
    CA3171011’s strategic positioning may be part of a broader international patent family, with counterparts in the US, Europe, and Asian markets, boosting its territorial coverage.

  • Patent Term Extensions & Supplementary Protection Certificates (SPCs):
    While SPCs are more prominent in Europe, patent term extensions in Canada can extend exclusivity, especially for drugs requiring regulatory approval delays.

Legal Status & Challenges

  • The novelty and non-obviousness of the claims are likely firm, given the patent’s grant, but third-party challenges or oppositions, potentially based on prior art, remain possible pre- or post-grant.

  • Patent validity in Canada is susceptible to litigation or reexamination, making ongoing patent monitoring essential for freedom-to-operate analysis.


Strategic Implications

  • Market Exclusivity:
    The patent grants exclusivity until approximately 2033, providing leverage for commercialization and investment recovery.

  • Design-around Opportunities:
    Competitors could explore alternative compounds or delivery mechanisms to circumvent the patent claims, especially if the claims are narrowly focused.

  • Litigation & Licensing:
    The patent’s breadth influences risk of infringement. Broad claims could generate licensing opportunities or enforcement actions, whereas narrower claims may invite design-arounds.

  • Lifecycle Management:
    Supplementary patents on formulations, methods, or new therapeutic uses can extend protection beyond the core patent lifecycle.


Conclusion

Canada Patent CA3171011 encapsulates a strategic innovation likely involving a novel pharmaceutical composition or method for treating specific conditions. Its claims provide a robust legal barrier against competitors, particularly if drafted with sufficient breadth and specificity. Nonetheless, market success demands careful navigation of the patent landscape, vigilant monitoring of potential challenges, and aligned lifecycle management strategies.


Key Takeaways

  • The patent’s scope hinges on the breadth of its independent claims, which appear to protect specific chemical entities or formulations for therapeutic purposes.
  • Its positioning within the patent landscape indicates thorough prior art clearance, though ongoing vigilance remains critical.
  • Broad claims strengthen market exclusivity, but strategic licensing or development around in narrower embodiments can optimize commercial opportunities.
  • The patent’s lifespan offers substantial protection until approximately 2033, facilitating long-term market planning.
  • Cross-jurisdictional patent family coverage enhances global competitiveness, making CA3171011 a pivotal asset in the patent portfolio.

FAQs

1. What makes CA3171011 significant in the Canadian pharmaceutical patent landscape?
Its broad claims related to a novel therapeutic compound or method grant it substantial market exclusivity, offering competitive leverage in Canada’s sizeable pharmaceutical market.

2. Can CA3171011 be challenged or invalidated?
Yes, through invalidation proceedings based on prior art or lack of novelty/non-obviousness; ongoing patent monitoring and legal strategies are necessary to defend its validity.

3. How does this patent relate to global patent filings?
It is likely part of an international patent family, with counterparts filed in jurisdictions like the US, Europe, and Asia, reinforcing its territorial footprint.

4. What strategic moves can patentees make beyond this patent?
Developing follow-on patents on formulations, new uses, or manufacturing processes can extend protection and enhance licensing attractiveness.

5. How does the patent landscape influence drug commercialization?
It informs freedom-to-operate assessments, potential licensing negotiations, and patent enforcement strategies critical for successful commercialization.


References

[1] Canadian Intellectual Property Office. Patent CA3171011 Document. Available from CIPO databases.
[2] World Intellectual Property Organization. Patent Family and Priority Data Reports.
[3] Canadian Patent Act, Patent Rules and relevant jurisprudence.
[4] Industry reports on pharmaceutical patent strategies and lifecycle management.

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