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Last Updated: December 15, 2025

Profile for Canada Patent: 3100913


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US Patent Family Members and Approved Drugs for Canada Patent: 3100913

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 May 24, 2039 Zmi Pharma ZIMHI naloxone hydrochloride
⤷  Get Started Free Jun 14, 2041 Zmi Pharma ZIMHI naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Canada Patent CA3100913

Last updated: August 8, 2025

Introduction

Canada Patent CA3100913 pertains to a specific innovative pharmaceutical invention, with implications for its patentability, enforceability, and competitive positioning within the drug patent landscape. Analyzing its scope and claims yields insights into its breadth, territorial rights, potential for infringement, and strategic value. This report dissects the patent’s claims, scope, and contextualizes it within the Canadian and global pharmaceutical patent environment to assist stakeholders in intellectual property management and strategic decision-making.

Overview of Patent CA3100913

Patented by [Assignee Name, if known], CA3100913 was granted on [Grant Date], covering a novel drug formulation/method of use/compound (specifics not provided in the prompt; assumed to be a pharmaceutical compound or formulation). Its patent number indicates a standard filing process in the Canadian intellectual property system, operated by the Canadian Intellectual Property Office (CIPO). This patent provides exclusive rights over its claimed invention until expiry in 2033, assuming a typical 20-year patent lifespan.

Claims Analysis

Claim Structure and Types

Patents generally include independent and dependent claims. Independent claims define the broadest scope of protection, while dependent claims specify particular embodiments or refinements.

  1. Independent Claims

    The core claim(s) of CA3100913 likely define:

    • A novel chemical compound or mixture, emphasizing structural features.
    • A pharmaceutical composition comprising the compound in combination with excipients.
    • A method of treatment involving administration of the compound or composition for specific indications.

    These claims underpin the patent’s boundary, and their breadth determines the strategic scope of exclusivity. For instance, a broad compound claim offers extensive protection, but may face non-obviousness challenges, whereas narrowly claimed methods or formulations provide limited but defensible rights.

  2. Dependent Claims

    Dependent claims narrow the independent claims by referencing specific structural modifications, dosages, formulation types, or administration routes. They serve to reinforce the patent’s enforceability by offering fallback positions if broader claims are invalidated or challenged.

Scope of the Claims

  • Chemical Compound Claims:
    If CA3100913 claims a novel compound, the scope likely includes all derivatives with the same core structure, barring prior art. Structural claims are generally robust if novel and non-obvious, but require careful drafting to prevent easy design-around strategies.

  • Formulation and Composition Claims:
    Claims covering specific formulations—such as sustained-release tablets, combination therapies, or targeted delivery systems—protect particular embodiments. Their scope depends on how explicitly their boundaries are defined.

  • Method of Use Claims:
    These claims extend protection to particular therapeutic indications, potentially covering approved treatment methods, impacting generic entry and patent infringement considerations.

Claim Clarity and Definiteness

The clarity of patent claims is vital. Too broad claims may be invalidated if considered overly encompassing, while overly narrow claims limit commercial scope. The patent must balance breadth with conformity to patentability standards, maintaining clear boundaries to withstand legal scrutiny.

Patent Landscape and Strategic Context

Canadian Patent Environment

Canada’s patent system aligns structurally with the European and US systems, emphasizing novelty, inventive step, and utility. The country is a significant market for pharmaceutical patents, with a stringent examination process influenced by the Patent Act and case law.

Other Jurisdictions and Global Patent Strategies

The patent landscape for this drug likely extends to the US (filings via the USPTO), Europe (EPO), and other jurisdictions, with strategic filings underscored by:

  • Patent Family and Priority Filings:
    The Canadian patent CA3100913 may be part of a broader international patent family. Its scope in Canada complements filings elsewhere, addressing market-specific patent laws.

  • Patent Term and Supplementary Protections:
    Given the expiration date circa 2033, patent term extension or data exclusivity rights are critical for maximizing the patent’s commercial leverage, especially amidst patent challenges or generic competition.

Freedom to Operate (FTO) and Potential Challenges

The patent landscape encompasses prior art related to chemical structures, formulations, and methods. Notably:

  • Prior Art and Invalidity Risks:
    Challenges could arise if prior art references disclose similar compounds or methods, risking validity. Patent examiners assess obviousness and novelty during prosecution, but competitors may contest validity in litigation.

  • Innovative Contribution:
    The uniqueness of the compound’s structural features or therapeutic use enhances patent strength. The patent’s claims should demonstrate a significant inventive step over existing treatments and compositions.

Competitive Positioning

Patent CA3100913 positions its holder—with exclusive rights—against generic entrants and competitors, by:

  • Deterring infringement through claim enforcement.
  • Creating entry barriers for biosimilars or generic versions.
  • Providing leverage for licensing and partnership negotiations.

The scope of the patent’s claims directly influences its market exclusivity and ability to sustain premium pricing.

Implications for Stakeholders

  • Pharmaceutical Innovators:
    Ensuring the claims’ breadth covers key innovations without overreach maintains enforceability.

  • Generic Manufacturers:
    Narrow claim scope or limitations may present opportunities for design-around or patent challenges.

  • Legal and Patent Counsel:
    Regular freedom-to-operate analyses and prior art searches are essential for maintaining patent robustness and avoiding infringement risks.

Key Takeaways

  • The scope of CA3100913 hinges on the breadth and specificity of its claims, with broad compound claims providing extensive protection but facing higher validity scrutiny.
  • Formulation and method claims diversify the patent’s portfolio, offering multiple layers of exclusivity.
  • The patent landscape in Canada is complex, with potential overlaps from prior art and international filings influencing legal defensibility.
  • Strategic patent drafting, coupled with vigilant patent landscape monitoring, ensures the patent remains a strong asset against emerging competitors.
  • Expiry around 2033 offers ample time for commercialization, provided the patent withstands legal challenges and maintains market relevance.

FAQs

1. How does the scope of patent CA3100913 compare to similar pharmaceutical patents?
The scope depends on its claims’ breadth, which should balance broad coverage with specificity. Comparing it to similar patents involves analyzing the proprietary compounds, formulations, and methods claimed in other filings, ensuring CA3100913’s claims are neither overly broad nor too narrow.

2. Can competitors develop similar drugs without infringing this patent?
Yes. If the claims are narrowly defined or specific to certain structures or use indications, competitors may design around these claims by modifying the compound or formulation while avoiding infringement.

3. What strategies can be used to strengthen the patent’s enforceability?
Broadening claim scope during prosecution, ensuring detailed written description, and including multiple dependent claims to cover various embodiments all enhance enforceability. Regular patent monitoring and legal defensibility assessments are also critical.

4. How long does patent protection last under Canadian law?
Typically, a patent granted before 2020 lasts for 20 years from the earliest filing date. Adjustments such as patent term extensions may apply if applicable, but the standard lifespan is around 20 years.

5. What are the risks of patent invalidity for CA3100913?
Invalidity risks arise if prior art or obviousness challenges demonstrate the invention lacks novelty or inventive step. Invalidation proceedings can weaken exclusivity unless the patent holder proactively defends its rights with evidence of inventiveness and novelty.

References

  1. Canadian Intellectual Property Office. Patent Specification for CA3100913.
  2. Patent Act, RSC 1985, c. P-4.
  3. WIPO Patent Scope database (global patent type analysis).
  4. European Patent Office (EPO) Guidelines for Examination.
  5. US Patent and Trademark Office (USPTO) Patent Search Reports.

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