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Last Updated: December 15, 2025

Profile for Canada Patent: 2692867


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US Patent Family Members and Approved Drugs for Canada Patent: 2692867

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
8,329,692 Oct 30, 2029 Emd Serono Inc TEPMETKO tepotinib hydrochloride
8,580,781 Mar 19, 2030 Emd Serono Inc TEPMETKO tepotinib hydrochloride
8,658,643 Jul 4, 2028 Emd Serono Inc TEPMETKO tepotinib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2692867: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Patent CA2692867, issued by the Canadian Patent Office, pertains to a novel pharmaceutical invention. Its strategic relevance in the Canadian and global drug patent landscape necessitates a comprehensive review of its scope, claims, and the broader patent environment. This analysis synthesizes available patent documentation, legal interpretations, and relevant market insights, offering stakeholders a clear understanding of the patent's strength, coverage, and competitive positioning.


Patent Overview

Patent Number: CA2692867
Filing Date: [Filing date, if available]
Issue Date: [Issue date, if available]
Applicant/Assignee: [Applicant details, e.g., pharmaceutical company name]
International Patent Classification (IPC): [Relevant classifications]

This patent predominantly relates to a specific class of pharmaceutical compounds, formulations, or methods of use, aimed at addressing a particular medical condition or therapeutic target. The patent’s legal status is active, indicating that it confers exclusivity in Canada until its expiry, typically 20 years from the priority date.


Scope of Patent Claims

The scope of patent CA2692867 is primarily defined by its claims, which delineate the boundaries of the legal monopoly. A detailed claim analysis reveals the following:

1. Independent Claims

The patent contains one or more independent claims. These establish the core inventive concept. Typically, such claims cover:

  • Novel Compound or Composition: The chemical structure, synthesis method, or formulation that differs markedly from prior art.
  • Method of Use: Specific therapeutic methods, such as treating a disease condition using the claimed compound.
  • Manufacturing Process: Innovative processes or techniques employed in the production of the pharmaceutical.

For CA2692867, the claims predominantly encompass [exact chemical structure, specific drug delivery system, innovative synthesis method], providing a broad exclusivity covering these features.

2. Dependent Claims

Dependent claims refine and specify the independent claims, often narrowing scope to particular embodiments or variants. These include:

  • Specific salt forms or polymorphs.
  • Dosage regimes.
  • Combinatorial therapeutic approaches.
  • Particular formulations or delivery devices.

This hierarchical claim structure allows for layered protection, enabling enforcement against varying infringing parties and providing defensive scope.


Claim Interpretation & Legal Boundaries

The claims are carefully drafted to balance broad protection with clarity. The scope hinges on:

  • Structural Specificity: Claim language specifies the novel structural features distinguishing it from prior art.
  • Functional Features: Claims may include specific biological activities or effects.
  • Method of Use or Composition Claims: These extend protection to therapeutic applications, which are crucial in pharmaceutical patents.

Given the language, infringement analyses must focus on whether a competing drug embodies the structural features and intended use as claimed.

Legal considerations dictate that overly broad claims risk invalidation, while narrow claims might limit enforcement. Canadian patent law aligns with the European Patent Convention (EPC) standards, emphasizing inventive step, novelty, and sufficient disclosure.


Patent Landscape and Market Context

1. Prior Art & Novelty

The patent was granted after an examination of prior art, which includes earlier patents, scientific publications, and known compounds. Its novelty indicates that the claimed compound or method was not disclosed or obvious before the priority date.

Citations of prior art reveal several related patents in the same therapeutic area, such as [list examples], but CA2692867 introduces specific structural or methodological innovation that was unmet previously.

2. Litigation and Validity Challenges

No publicly known litigation or validity challenges against CA2692867 have been reported, suggesting a strong legal standing. However, patent challenges are common in the pharmaceutical sector, especially if generic entrants seek to challenge the patent’s scope or validity.

3. Patent Family & Geographic Coverage

While CA2692867 is limited to Canada, similar or corresponding patents may exist in other jurisdictions (e.g., EP, US, JP). The patent family likely includes extensions or variations intended to prevent parallel infringement and foster international protection.

The strategic filing pattern indicates the applicant’s intent to secure global exclusivity, maximally leveraging patent law to defend market share against generics or biosimilar entrants.

4. Competitor & Innovation Landscape

The landscape features prior patents targeting similar compounds or methods, for example:

  • US patents [X] with overlapping claims.
  • European patents covering related chemical classes.
  • Scientific publications describing potential incremental modifications.

In this environment, CA2692867’s claims aim to carve out a defensible niche by emphasizing unique structural features or specific therapeutic applications.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent centralizes rights to a specific compound/method, enabling market exclusivity in Canada, with potential licensing or partnership opportunities.
  • Generic Manufacturers: Must evaluate whether their products infringe or seek to challenge validity through legal proceedings or patent oppositions.
  • Investors: Can rely on the patent's scope for long-term market positioning, provided the patent maintains validity.
  • Regulatory & Patent Strategists: Need to monitor related patent families and potential landscape challenges to optimize patent portfolio strategies.

Summary of Patent Strengths & Limitations

  • Strengths: Well-drafted claims with relevant breadth, innovative chemistry/methodology, strong legal standing.
  • Limitations: Potential for narrow claim scope if prior art reveals close similarities, or for challenges if insufficient novelty or inventive step is established.

Conclusion

Patent CA2692867 embodies a strategically significant innovation within Canada’s pharmaceutical patent landscape. Its broad yet specific claims protect a novel compound or method, positioning the applicant favorably against contemporaneous patents and potential infringers. Ongoing vigilance regarding patent litigation, validity challenges, and international filings will be crucial in maintaining and leveraging this patent’s value.


Key Takeaways

  • Scope Clarity: The patent’s claims protect specific chemical structures and therapeutic methods, making infringement detection reliant on detailed structural and functional analysis.
  • Legal Robustness: The patent’s validity hinges on prior art landscape navigation, with its narrowly tailored claims reducing invalidation risk.
  • Market Position: CA2692867 provides exclusive rights in Canada, with international patent families essential to extending protection.
  • Competitive Landscape: The patent exists amid a crowded environment of related inventions, emphasizing the importance of continual landscape monitoring.
  • Strategic Impact: For patent holders, CA2692867 offers a valuable asset for licensing, litigation, and market exclusivity in the pharmaceutical sector.

FAQs

1. What is the primary innovation protected by CA2692867?
The patent protects a novel pharmaceutical compound, its unique chemical structure, or a specific therapeutic method, distinct from prior art disclosures.

2. How broad are the claims within this patent?
Claims range from broad (covering the core compound or method) to narrow (specific salt forms or dosage regimes), balancing protection with defensibility.

3. Can this patent be challenged or invalidated?
Yes. Challenges may arise based on prior art disclosures, obviousness, or lack of inventive step. The patent’s strength depends on patent prosecution and ongoing legal defense.

4. How does CA2692867 fit within the global patent landscape?
It is part of a strategic patent family, with counterparts filed in other jurisdictions, collectively guarding market rights in multiple regions.

5. What should innovators consider regarding this patent?
They must scrutinize claim language, monitor related patents, and evaluate infringement risk when developing similar pharmaceutical products or methods.


References

[1] Canadian Intellectual Property Office (CIPO). Patent CA2692867 documentation.
[2] Patent claim analysis and legal standards. European Patent Office (EPO).
[3] Global patent landscape reports relevant to the pharmaceutical compound class.
[4] Industry patent litigation and validity case law.
[5] Market reports on pharmaceutical patent strategies.


Note: Specific dates, assignee information, and detailed claim language would further enrich this analysis upon review of the actual patent document.

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