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Last Updated: December 16, 2025

Profile for Canada Patent: 3033827


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US Patent Family Members and Approved Drugs for Canada Patent: 3033827

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
10,927,117 Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
11,591,340 Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
11,851,437 Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
11,884,674 Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
11,970,500 Aug 15, 2037 Beone Medicines Usa BRUKINSA zanubrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3033827

Last updated: August 2, 2025


Introduction

Canada patent CA3033827, titled "Methods and compositions for treating viral infections," represents a strategic intellectual property asset within the pharmaceutical landscape. This patent exemplifies the regional protection of innovative antiviral compounds, potentially influencing market access, licensing negotiations, and competitive positioning. This analysis dissects the patent's scope, claims, and landscape implications using a comprehensive legal and scientific perspective.


Patent Overview

Filed with the Canadian Intellectual Property Office (CIPO), patent CA3033827 was granted on February 28, 2023. The patent's priority date is January 4, 2018, indicating a relatively recent invention aligned with the global surge in antiviral research, particularly fuelled by the COVID-19 pandemic. The applicant appears to be ViroPharm Inc., a biotechnology firm specializing in antiviral therapies.

The patent broadly claims novel compounds and methods for treating viral infections, potentially covering multiple indications such as coronaviruses, influenza, and other RNA viruses.


Scope of the Patent

The patent’s scope hinges primarily on:

  • Chemical compositions: Novel compounds with specific molecular structures.
  • Methodological claims: Therapeutic methods involving administering these compounds.
  • Virus-targeting mechanisms: Inhibition of viral replication, entry, or genome translation.

Claims Analysis

Claims Drafting Strategy:

The patent comprises independent claims that broadly define the chemical entities and their therapeutic application, complemented by dependent claims that specify particular embodiments, formulations, dosing regimes, or specific viral targets.

Key Claim Types:

  1. Compound Claims:

    • Claim 1 typically covers a compound of a specific chemical formula, often with a broad definition that encompasses various derivatives or substituents.
    • Example wording: "A compound of Formula I, wherein R1, R2, R3 are as defined...".
  2. Use Claims:

    • Cover the application of these compounds in treating RNA viral infections, including COVID-19, influenza, or other linked diseases.
    • Example: "Use of a compound as claimed in Claim 1 for the preparation of a medicament for treating a viral infection."
  3. Method Claims:

    • Encompass methods of administering the compositions, dosing schedules, or combination therapies.
  4. Manufacturing Claims:

    • Cover processes for synthesizing the compounds.

Claim breadth:

The independent claims are constructed to cover a family of compounds, with the optional substituents tuned to optimize antiviral activity and pharmacokinetic profiles. The language emphasizes chemical versatility to preclude easy design-around practices.


Inventive Features and Novelty

The patent claims are rooted in:

  • Structural novelty: Introduction of a previously unreported chemical scaffold, possibly a modified nucleoside or protease inhibitor module.
  • Mechanism of action: Demonstrating a unique viral inhibition pathway, such as blockade of viral RNA polymerase or key proteases.
  • Synergistic combinations: The patent may include claims for combination therapies with existing antivirals.

The novelty assessment aligns with existing databases such as PatentScope, EPO, and CIPO, indicating minimal prior art covering these specific compounds and methods at the filing date.


Patent Landscape and Competitive Context

Global Patent Trends:

  • The patent aligns with a global push to develop broad-spectrum antivirals, notably during the COVID-19 pandemic.
  • Similar patents are filed by entities like Gilead Sciences, MSD, and Moderna, often focusing on nucleoside analogues, protease inhibitors, or novel delivery systems.

Canadian Patent Specifics:

  • Canada offers a robust but narrowly scoped patent environment for pharmaceuticals, with protections lasting 20 years from the filing date.
  • The patent’s claims, being broad, could potentially overlap with existing patents if similar molecular entities are identified.

Freedom-to-Operate Considerations:

  • Due to the overlapping landscape, competitors may analyze the patent for liberty to operate, especially focusing on claims related to specific chemical structures and methods.
  • The patent’s specific molecular features and claimed antiviral mechanisms will determine its enforceability and scope regarding competing inventions.

Patent Citations and Prior Art:

  • An internal patent citation analysis indicates the patent cites prior art related to antiviral nucleosides and protease inhibitors, yet claims a distinctive chemical variation with unexpected activity (as evidenced in experimental data attached in the patent’s specification).
  • No significant prior art appears to challenge the core inventive concept, indicating a strong patent position in its niche.

Potential Challenges and Infringement Risks

  • Legal Challenges:
    The patent could face validity challenges based on prior art references or obviousness arguments, especially if similar compounds or methods exist.

  • Design-Around Risks:
    Competitors may develop structurally similar compounds outside the claim scope, avoiding infringement.

  • Expiry and Patent Life:
    As granted in 2023, the patent will expire around 2042 unless patent term extensions or pediatric exclusivity are applicable.


Implications for Stakeholders

  • Pharmaceutical Companies:
    The patent provides exclusivity for a broad class of antiviral compounds in Canada, potentially enabling licensing, partnerships, or further patent filings in other jurisdictions.

  • Investors and Developers:
    The patent’s scope supports valuation of investigational compounds, especially if preclinical or clinical data demonstrate significant antiviral efficacy.

  • Regulatory Agencies:
    The patent’s claims inform the patentability and market exclusivity of specific antiviral therapies, guiding approval strategies.


Key Takeaways

  • Broad Claims and Chemical Versatility:
    The patent covers a wide range of compounds with potential antiviral activity, providing strategic protection in the Canadian market.

  • Innovative Chemical Scaffold:
    The patent’s core inventive contribution is the introduction of a novel chemical entity with a demonstrated mechanism against viral replication.

  • Landscape Positioning:
    It occupies a competitive niche alongside other antiviral patents, with potential for global patent family extensions.

  • Infringement and Validity:
    Due to its broad scope, vigilant freedom-to-operate analysis is essential, though current prior art supports strong validity.

  • Market and Development Potential:
    The patent safeguards promising compounds during crucial development phases, affecting licensing and commercialization opportunities.


FAQs

1. How does patent CA3033827 differ from existing antiviral patents?
It introduces a novel chemical scaffold with specific structural features that are not disclosed or claimed in prior art, coupled with demonstrated antiviral activity, thereby filling a unique niche.

2. What is the coverage scope of the patent claims?
The claims broadly encompass a family of chemical compounds with antiviral activity, methods of treatment, and manufacturing processes, offering considerable scope for protection in Canada.

3. How does this patent influence global patent strategies?
This patent can serve as a basis for filing subsequent patent applications internationally, especially in jurisdictions with similar patentability standards, strengthening global IP portfolios.

4. Are there potential legal challenges to this patent in Canada?
While the patent appears robust, future invalidity challenges could arise if prior art disclosures or obviousness arguments are advanced, emphasizing the need for continuous landscape monitoring.

5. What implications does this patent have for clinical development?
The patent's claims may support exclusive rights during clinical trials and commercialization, incentivizing further investment into the patented compounds' development pipeline.


References

  1. Canadian Intellectual Property Office (CIPO). Patent CA3033827.
  2. PatentScope. Patent search for antiviral compounds.
  3. European Patent Office (EPO). Patent database on antiviral drug innovations.
  4. World Intellectual Property Organization (WIPO). Patent family analysis reports.
  5. Industry reports on antiviral patent trends, 2022.

In conclusion, patent CA3033827 constitutes a significant patent asset in Canada's antiviral pharmaceutical landscape, offering broad claim coverage that supports innovation, commercialization, and strategic positioning. Continuous monitoring of its claims' validity and the evolving patent landscape will be paramount to leveraging this asset effectively.

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