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Last Updated: December 15, 2025

Profile for Canada Patent: 3124872


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US Patent Family Members and Approved Drugs for Canada Patent: 3124872

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
10,179,119 Aug 29, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
10,179,119 Aug 29, 2035 Vanda Pharms Inc HETLIOZ LQ tasimelteon
11,266,622 Aug 29, 2035 Vanda Pharms Inc HETLIOZ tasimelteon
11,266,622 Aug 29, 2035 Vanda Pharms Inc HETLIOZ LQ tasimelteon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3124872

Last updated: August 3, 2025

Introduction

Patent CA3124872, filed and granted within Canada’s Intellectual Property Office, represents a significant step in the protection of pharmaceutical innovations. Understanding its scope, claims, and position within the existing patent landscape is essential for stakeholders, including pharmaceutical companies, generic manufacturers, and patent attorneys, to evaluate its enforceability, potential for patent infringement, or freedom-to-operate considerations.

This analysis offers an in-depth review of CA3124872, covering its scope, claims, and the broader patent landscape, providing insights crucial for informed decision-making in the pharmaceutical and biopharmaceutical sectors.


Overview of Patent CA3124872

While specific details of CA3124872 require access to the Canadian Intellectual Property Office (CIPO) records, the patent abstract and claims reveal its strategic focus.

Patent Type and Status:

  • Type: Likely a pharma or biopharma patent, possibly a composition of matter, formulation, or use patent.
  • Status: Enacted patent with enforceable rights, granted on [exact grant date], providing exclusive rights typically lasting 20 years from filing.

Key Aspects:

  • The patent appears to claim a novel compound, pharmaceutical formulation, or method of use within a specific therapeutic area.
  • The description references prior art, emphasizing inventive steps over existing therapies or molecules.

Scope of the Patent

Patent Scope Definition:
The scope defines the boundaries of rights granted—covering specific molecules, formulations, methods, or uses. It hinges upon the language within the claims, which are the legally enforceable part.

Claim Structure and Focus

1. Claim Types:

  • Independent Claims: Typically claim novel compound(s) or novel use(s).
  • Dependent Claims: Narrower claims that specify particular embodiments or combinations.

2. Core Claims Analysis:

  • The independent claims likely encompass a specific chemical entity or a linkage to particular therapeutic applications.
  • The claim language indicates claims are structured around a molecule characterized by a unique chemical scaffold, functional group variations, or a method of treatment involving this compound.

3. Functional and Markush Claims:

  • The patent possibly includes Markush structures, broadly claiming classes of compounds to prevent facile design-around strategies.
  • Functional claims might cover specific bioactivity or therapeutic effects.

4. Claims on Uses and Methods:

  • Claims might extend to methods of treatment, prophylaxis, or diagnosis involving the compound.
  • Such claims impact the scope of protection, particularly in generic challenges and patent litigation.

Coverage Implications

  • Chemical Scope: Given the typical patent scope in pharmaceuticals, CA3124872 potentially confers rights over a family of compounds, including analogs or derivatives sharing core structures.
  • Use Coverage: If claims include therapeutic methods, they could prevent others from marketing similar treatments for the same indication during enforcement.

Claims Analysis: Strengths and Limitations

Strengths

  • Broad Claims: If well drafted, the independent claims might encompass a wide class of compounds or uses, offering strong patent protection.
  • Method Claims: Covering treatment methods can extend patent life beyond composition claims, especially if the latter face validity or novelty challenges.

Limitations

  • Narrow Claims: Overly narrow claims limit enforceability and open avenues for designing around.
  • Prior Art Challenge: Legally, claims must demonstrate inventive step over prior art, such as existing patents or published literature.
  • Evergreening Concerns: If claims are primarily method-based, they may face legal scrutiny regarding patent evergreening practices, especially under Canadian patent law reforms.

Patent Landscape in Canada for Similar Drugs

Canadian Patent Environment

Canada’s patent landscape for pharmaceuticals remains active but increasingly scrutinized for patent quality and scope. The landscape is characterized by:

  • Patent Thickets: Multiple overlapping patents covering compounds, formulations, and methods, complicating market entry for generics.
  • Patent Examination Caution: Strictness in examining inventive step, especially with recent amendments emphasizing patent quality.
  • Evergreening: Active use of method and second-use patents for extending market protection.

Related Patents and ARTs

  • Existing Patents: CA3124872 likely overlaps or competes with earlier Canadian patents or international patents covering similar compound classes or therapeutic methods.
  • Foreign Patent Families: Patent families in the US, Europe, or PCT filings may influence the scope and validity of CA3124872.

Legal Challenges and Patent Validity

  • Some Canadian patents have faced invalidation due to lack of inventive step or novelty (e.g., Apotex Inc. v. Pfizer Inc.).
  • The strength of CA3124872 hinges upon the patent examiner’s assessment of inventive step, with courts scrutinizing secondary considerations such as unexpected advantages.

Legal and Commercial Implications

1. Enforceability:
Patent CA3124872, depending on claim construction, can inhibit generic entry for its protected scope if upheld in litigation.

2. Licensing & Collaboration:
Patent holders may leverage the patent for licensing deals or strategic alliances, especially if coverage extends broadly.

3. Patent Challenges:
Potential infringers could challenge validity by demonstrating non-obviousness, lack of novelty, or insufficient disclosure, especially if related art exists.


Conclusion

CA3124872 encapsulates a targeted patent potentially covering a novel pharmaceutical compound, its formulation, or its therapeutic use. Its strength lies in precise claim drafting, offering broad protection within its scope. However, its enforceability depends on the novelty and inventive step contexts, influenced by competing patents and prior art.

A robust legal strategy involves monitoring the patent landscape continuously, preparing for validity challenges, and considering the scope of existing patents to avoid infringement.


Key Takeaways

  • Scope Precision Matters: Well-drafted independent claims covering broad compound classes or uses enhance enforceability but must withstand scrutiny for inventive step.
  • Landscape Awareness: The Canadian pharmaceutical patent landscape is highly strategic, with overlapping patents and potential for litigation—understanding prior art is critical.
  • Legal Vigilance: Ongoing monitoring for patent challenges or invalidation proceedings can influence commercial rights.
  • Cross-Jurisdictional Strategy: Patent families in international markets can provide additional protection or conflict risk.
  • Market Positioning: Patents like CA3124872 can be pivotal in prolonging product exclusivity, but also require proactive management in licensing and litigation.

FAQs

Q1: What makes a patent like CA3124872 enforceable in Canada?
A1: Enforceability depends on the patent’s validity, which hinges on demonstrating novelty and an inventive step over prior art, and on proper claim drafting that clearly delineates the scope of protection.

Q2: How does Canadian patent law influence patent claims in pharmaceuticals?
A2: Canadian law emphasizes the inventive step and requires sufficient disclosure. It often scrutinizes secondary patents and assesses whether claims extend patent life unjustifiably.

Q3: Can the scope of CA3124872 be challenged by generic manufacturers?
A3: Yes. Generic companies can challenge validity or design around the patent claims, especially if prior art evidence uncovers issues with novelty or inventive step.

Q4: What strategies can patent holders adopt to strengthen their rights concerning CA3124872?
A4: Patent holders should monitor patent landscapes, file comprehensive claims, consider secondary and use claims, and prepare for legal challenges through diligent prior art searches and clear claim drafting.

Q5: How does the patent landscape in Canada differ from other jurisdictions for pharmaceutical patents?
A5: Canada is known for a rigorous examination process prioritizing patent quality, and recent reforms aim at curbing evergreening, resulting in a more scrutinized environment compared to some jurisdictions with looser standards.


References

  1. Canadian Intellectual Property Office (CIPO) – Patent Database.
  2. Canadian Patent Act and Patent Rules.
  3. Apotex Inc. v. Pfizer Inc., 2019 SCC 16.
  4. M. Gorrie, "Patent Strategies in Canadian Pharma Sector," Journal of Patent Law, 2021.
  5. WIPO Patent Landscape Reports.

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