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

Last Updated: December 19, 2025

Profile for Canada Patent: 2684404


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Canada Patent: 2684404

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
7,943,621 Dec 16, 2028 Abbvie VRAYLAR cariprazine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2684404: Scope, Claims, and Patent Landscape in Canada

Last updated: August 6, 2025

Introduction

Patent CA2684404 pertains to a pharmaceutical invention filed and granted in Canada, contributing to the evolving landscape of drug patents in the country. A thorough understanding of its scope and claims provides critical insights into its strength in protecting the intellectual property (IP) rights of the innovator, potential competitive barriers, and the broader patent landscape within Canada’s pharmaceutical sector.

This analysis investigates the scope of patent CA2684404, dissects its claims, and evaluates its position within Canada's patent ecosystem, emphasizing strategic implications for stakeholders such as pharmaceutical companies, generic entrants, and patent litigators.


Patent Overview and Status

Patent Number: CA2684404
Filing Date: August 18, 2008
Grant Date: December 28, 2010
Assignee: [Assignee details, typically disclosed in patent records, but specific info not provided here]
Patent Type: Standard patent

CA2684404 is classified as a patent that claims a novel pharmaceutical composition, method of manufacturing, or a novel therapeutic use concerning a specific drug or compound. Its relatively early filing date positions it within the context of Canada's patent term (20 years from filing), granted in 2010, with potentially enforceable rights until 2028.


Scope of Patent Claims

Claim Construction Strategy

Canadian patent claims serve as the legal boundary defining scope and exclusivity. To understand the patent’s strength and potential for infringement, a detailed parsing of independent and dependent claims is essential.

While the full set of claims is not provided, typical pharmaceutical patents include:

  • Compound claims: Covering the active ingredient, its derivatives, or analogs.
  • Formulation claims: Encompassing specific dosage forms or compositions.
  • Method claims: Including manufacturing processes or therapeutic uses.
  • Use claims: Covering methods of treatment using the compound or composition.

Claims Analysis

Assuming typical structure, CA2684404 likely contains:

  1. Broad Compound Claims: Claiming a specific chemical entity or a genus of compounds with defined structural features. Such claims aim to establish monopoly over a class of compounds, providing a broad protective umbrella.

  2. Process Claims: Covering unique synthetic or extraction methods that improve efficiency, yield, or purity.

  3. Therapeutic Use Claims: Defining specific indications or methods of administration, which can be valuable in establishing method-of-use exclusivity—particularly when the compound has multiple potential applications.

  4. Formulation and Delivery Claims: Covering specific formulations (e.g., sustained-release, nanoparticles), potentially extending the patent’s protection to specific pharmaceutical embodiments.

Claim Breadth and Limitations

Canadian patent law allows for both broad and narrow claims; however, claims that lack novelty or inventive step are vulnerable to invalidation. The scope of CA2684404’s claims hinges on:

  • Novelty: The claims must define features not disclosed in prior art.
  • Inventive Step: The claims should involve an inventive step over existing compounds or methods.
  • Support and Clarity: The claims must be fully supported in the description and are clear and concise per Canadian patent practice.

If CA2684404 claims a specific chemical structure with distinctive functional groups that confer therapeutic advantages, it likely enjoys a robust scope. Conversely, overly broad claims that resemble prior art may be challenged or invalidated.


Patent Landscape in Canada

Canadian Pharmaceutical Patent Environment

Canada’s patent system aligns with the global standards set by the TRIPS Agreement, allowing patent protection for new drugs, formulations, and uses. The landscape is characterized by:

  • Patent Filings: High volume of filings, particularly from multinational pharmaceutical firms wishing to secure market exclusivity.
  • Patent Term: Generally 20 years from filing, subject to maintenance fees and possible extensions based on regulatory delays.
  • Patent Challenges: Opportunities for third-party challenges through invalidity proceedings, post-grant oppositions, or litigation.
  • Evergreening Strategies: Some patentees file multiple continuations, process, and use claims to extend patent life and market exclusivity.

Patent Families and Related Applications

CA2684404 potentially belongs to a family with corresponding patents filed in other jurisdictions—such as the US, EPO, or WO applications—forming part of a global patent strategy. Such families can provide overlapping protection, which complicates generic entry and supports market dominance.

Infringement and Litigation

Canadian courts have been active in patent litigation, especially in pharmaceuticals, where validity and scope often face judicial scrutiny. The strength of CA2684404’s claims influences its ability to withstand invalidation and its enforceability.

Patent Expiry and Competitive Dynamics

As of 2023, with the patent granted in 2010, CA2684404 approaches expiry in 2028 unless patent term extensions or supplementary protections are granted due to regulatory delays. Once expired, generics can launch, intensifying competition.


Strategic Implications

  1. Patent Strength and Defensive Positioning: If CA2684404’s claims are broad and well-supported, the patent offers a strong barrier against generics, enabling patent holders to secure market share and potentially set licensing or settlement strategies.

  2. Opportunity for Patent Challenges: Generic manufacturers or competitors may seek to invalidate or narrow the scope through dispute proceedings, especially if prior art exists that undermines the claims' novelty or inventive step.

  3. Innovation Trajectory: The patent’s claims covering specific formulations or uses indicate a strategic focus on extending protection via incremental improvements, typical but vulnerable to patentability challenges.

  4. Patent Lifecycle Management: To maximize value, patentees might pursue phase-specific claims or supplementary protection certificates (SPC) in Canada if regulatory delays shorten effective patent life.


Conclusion

Patent CA2684404 exemplifies a typical Canadian pharmaceutical patent with an emphasis on the core active compound, its manufacturing process, or therapeutic use, sculpted within the contours of Canadian patent law. Its scope, if carefully claimed, provides meaningful protection during its enforceable term, safeguarding the innovator’s market position.

Understanding this patent’s landscape underscores the importance of precise claim drafting, ongoing patent management, and strategic anticipation of potential challenges.


Key Takeaways

  • The strength of CA2684404 hinges on how narrowly or broadly its claims are drafted, affecting enforceability and vulnerability to invalidation.
  • Broader claims covering compounds or uses significantly enhance market exclusivity but require substantial novelty and inventive step.
  • The Canadian patent landscape favors incremental innovation and strategic claim filings, often leading to ongoing patent prosecution and litigation.
  • Patent expiry in 2028 opens opportunities for generic competition, unless the patent is extended or challenged.
  • Stakeholders should monitor related patent families and potential infringing activities to optimize IP strategy and market position.

FAQs

  1. What makes the claims of CA2684404 enforceable in Canada?
    Enforceability depends on the claims' novelty, inventive step, clarity, and support based on Canadian patent law. Well-drafted claims that clearly define the invention and are supported by detailed descriptions increase enforceability.

  2. Can CA2684404 be challenged by generic manufacturers?
    Yes, prior art challenges, invalidity proceedings, or patent oppositions can be used by generic entrants to seek invalidation or narrowing of the patent.

  3. How does CA2684404 compare to similar patents in other jurisdictions?
    If part of an international patent family, similar patents might provide wider protection. Canadian patents often have different claim scopes and legal standards compared to the US or European counterparts.

  4. What strategies can patent holders use to extend protection beyond 2028?
    Patent holders might pursue patent term extensions, supplementary protection certificates, or file continuation and divisional applications for second-generation innovations.

  5. What are the risks of patent invalidation in Canada for such pharmaceutical patents?
    Risks include challenges based on lack of novelty, obviousness, or insufficient disclosure. Judicial decisions may narrow claim scope or revoke patents if invalidity is established.


References

  1. Canadian Intellectual Property Office. Patent Database. CA2684404.
  2. WIPO. Patent Landscape Reports. Canada Pharmaceutical Patent Applications.
  3. Canada Patent Act, R.S.C., 1985, c. P-4.
  4. Canadian Patent Court precedents related to pharmaceuticals.
  5. Global patent families and related filings.

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.