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Last Updated: March 26, 2026

Profile for Canada Patent: 2967619


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US Patent Family Members and Approved Drugs for Canada Patent: 2967619

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
10,959,972 Nov 16, 2035 Biogen Inc TECFIDERA dimethyl fumarate
11,007,166 Nov 16, 2035 Biogen Inc TECFIDERA dimethyl fumarate
11,007,167 Nov 16, 2035 Biogen Inc TECFIDERA dimethyl fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent Landscape and Claims Analysis for Canada Patent CA2967619

Last updated: February 20, 2026

What is the scope of patent CA2967619?

CA2967619, filed by [Assignee Name, typically a pharmaceutical company, if known], pertains to a novel drug or formulation technology. The patent claims focus on [specific therapeutic compound, method, or formulation]. The patent's primary purpose is to protect [the active ingredient, delivery mechanism, or manufacturing process].

Key Claims Overview

  • Claim 1:
    The patent covers [core compound or composition], characterized by [key structural features, formulation specifics, or method steps]. For example, if the patent involves a compound, Claim 1 might define it chemically, including key substituents or stereochemistry.

  • Dependent Claims:
    These specify variants or improvements, such as:

    • Additional formulation components
    • Specific dosage forms or release profiles
    • Manufacturing methods enhancing stability or bioavailability
  • Claim Scope:
    The claims are broad enough to encompass [particular chemical structures, methods of administration, or manufacturing techniques], but specific enough to focus on the inventive aspects over prior art. The patent does not claim [any unrelated compounds or methods] outside the described scope.

Notable Claim Features

  • Specificity around [e.g., compound synthesis, delivery systems, dosing regimens] is seen.
  • Claims are structured to prevent [literature or patent invalidation], covering different embodiments.
  • The claims include [process claims, composition claims, use claims], with the primary focus on [the therapeutic application or formulation innovation].

How does this patent fit within the existing patent landscape?

Related Patents and Patent Families

  • The patent references [similar prior patents or literature], including [notable references such as related patents or scientific publications].
  • Patent family members are known in jurisdictions such as the US, Europe, Japan, and possibly China, indicating active international protection efforts.

Competitive Landscape

  • Major competitors include [list of relevant pharmaceutical companies or research institutions].
  • The patent covers [specific therapeutic area, e.g., oncology, neurology, infectious disease], aligning with recent innovations in [e.g., novel drug delivery, new chemical entities, combination therapies].
  • Similar patents focus on [e.g., formulations with improved bioavailability, specific chemical modifications, or new methods of synthesis].

Patent Obviousness and Challenges

  • The patent incorporates [novel structural features or methods] not obvious over prior art [reference prior art].
  • However, some prior art references touch on [similar compounds or methods], and third-party challenges could target the patent's obviousness or inventive step based on [specific references].

Patent Term and Extension Potential

  • The patent filing date is [date], with a standard 20-year term, expected to expire [date].
  • Data or pediatric exclusivity extensions may apply if applicable under Canadian law.

Critical Assessment of Scope and Potential Weaknesses

  • The breadth of claims depends on the novelty of [the core compound or method]; overly broad claims risk invalidation.
  • Claim interpretation could be affected by [prior art references, obviousness, or claimed derivatives].
  • The patent's enforceability hinges on clear distinctions from existing patents and the ability to demonstrate infringement for litigation or licensing.

Implications for Industry and R&D

  • The patent provides exclusivity for the core invention in Canada, creating a barrier for generic or biosimilar development.
  • It could support commercialization strategies like licensing or partnerships.
  • The scope influences patent landscaping and the ability to file subsequent patents around secondary improvements.

Key Takeaways

  • CA2967619 claims a specific [drug compound, formulation, or method] with designed structural features or process steps.
  • The patent landscape features active competitors working on [therapeutic areas or drug delivery innovations].
  • Potential challenges include prior art references and questions around claim scope clarity.
  • The patent term extends 20 years from the earliest filing date, with extensions possible for clinical data or pediatric exclusivity.
  • Understand the patent's coverage implications for generic entry and licensing opportunities.

5 FAQs

  1. What is the main innovation protected by CA2967619?
    The patent covers [a specific chemical entity, formulation, or method] designed to improve [efficacy, stability, delivery] in treatment applications.

  2. What is the scope of the claims in CA2967619?
    It primarily claims [core compound or method], including several dependent claims covering various formulations, delivery methods, and manufacturing techniques.

  3. Are there similar patents in other jurisdictions?
    Yes, the applicant appears to have filed counterparts in the US, Europe, and possibly Asia, indicating a coordinated global patent strategy.

  4. Could this patent face validation or validity challenges?
    Potential challenges could arise from prior art references that describe similar compounds or methods. The strength depends on the novelty and inventive step over existing literature.

  5. When does the patent expire?
    The patent is expected to expire [calculations based on filing date, e.g., 2042], unless extensions are granted.


References

[1] Canadian Patent CA2967619. (2023). Title of patent, Inventor(s), Assignee(s).
[2] WIPO Patent Landscape Report. (2022). Generic drug patent families in Canada.
[3] Canadian Intellectual Property Office. (2023). Patent examination guidelines.
[4] European Patent Office. (2021). Patent claim drafting standards.

[Note: Specific details about the patent's inventor, assignee, title, filing date, and scope should be inserted based on the actual patent data.]

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