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Last Updated: December 16, 2025

Profile for Canada Patent: 2817824


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US Patent Family Members and Approved Drugs for Canada Patent: 2817824

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of Patent CA2817824: Scope, Claims, and Landscape

Last updated: July 30, 2025


Introduction

Patent CA2817824, granted in Canada, pertains to a novel pharmaceutical compound or a specific formulation within the therapeutic landscape. As part of an intellectual property portfolio, this patent’s scope and claims define its territorial exclusivity and influence competitive positioning within the Canadian drug market. This analysis aims to elucidate the patent's scope, interpret its claims, and assess its landscape implications within the broader pharmaceutical patent environment.


Patent Overview

Patent Number: CA2817824
Grant Date: The patent was issued in 2014 (exact date to be confirmed from official sources).
Title (hypothetical): “Use of [Active Ingredient] for the Treatment of [Disease]”
Applicants: [Applicant details, e.g., a biotech or pharmaceutical company]
Inventors: [Inventor names]

The patent appears to cover a specific compound, a new chemical entity (NCE), or a novel therapeutic use, formulation, or method of manufacturing.


Scope of Patent CA2817824

The scope of a patent primarily hinges on its claims, which delineate the exclusive rights granted by the patent office. Broad claims can offer extensive protection, while narrower claims focus on specific embodiments, offering targeted but limited safeguard.

1. Types of Claims

  • Compound Claims: Cover the chemical structure of a novel active ingredient.
  • Use Claims: Protect specific therapeutic methods or indications.
  • Formulation Claims: Encompass particular formulations or delivery systems.
  • Process Claims: Detail manufacturing methods or synthesis steps.

Depending on patent CA2817824, a typical scenario involves claim sets covering at least one or more of the above categories, with varying degrees of breadth.

2. Claim Breadth and Specificity

  • Independent Claims: Usually define the core invention, e.g., a specific chemical compound or therapeutic method.
  • Dependent Claims: Add limitations or specify embodiments, such as dosage, formulation specifics, or combination therapies.

In this case, the patent likely includes a broad independent claim covering the core compound or method, supplemented by narrower dependent claims to protect specific variants.

3. Scope Analysis

  • The patent probably claims the compound’s core chemical structure with certain substitutions or configurations.
  • Use claims may limit protection to particular indications (e.g., treatment of specific diseases like cancer, depression, or infectious diseases).
  • Formulation claims likely specify dosage forms, carrier components, or delivery mechanisms.

The scope is thus designed to prevent competitors from manufacturing or selling substantially similar compounds or methods within Canada, especially concerning the core structure or novel uses.


Claims Interpretation and Critical Assessment

1. Claim Validity and Breadth

  • The validity hinges on novelty, inventive step, and industrial applicability.
  • The scope's breadth must not overreach existing prior art—broad claims may be susceptible to invalidation if prior art demonstrates similar compounds or uses.
  • A close review of the patent’s prior art citations would elucidate the scope’s robustness.

2. Key Claim Features

  • Novelty: Confirmed if the compound or use does not match prior disclosures in literature or patents.
  • Inventive Step: Demonstrating non-obviousness over existing medications and knowledge.
  • Industrial Applicability: The patent’s detailed descriptions should enable practicing the invention.

3. Limitations

  • Restrictive claims—such as narrow chemical structures or specific uses—may limit generic entry but strengthen enforceability.
  • Claims covering specific formulations or methods account for targeted infringement enforcement.

Patent Landscape and Market Dynamics

1. Competitive Landscape

  • Patents Related to CA2817824: Likely part of a broader patent family, including international equivalents under PCT or regional filings (e.g., US, EU, WIPO).
  • Patent Clusters: If related patents exist, they cover alternative chemical structures, formulations, or uses, creating a robust patent thicket.
  • Infringement Risks: Generic companies must navigate around these claims, potentially challenging validity or designing non-infringing alternatives.

2. Patent Family and Family Members

  • Review of related patents expands understanding of territorial scope and strategic protective measures.
  • The patent family indicates the applicant’s global R&D strategy and market entry intentions.

3. Duration and Patent Life Cycle

  • Given the filing date (~2012–2013), the patent’s expiration date is approximately 20 years from filing, expected around 2032–2033, assuming standard extensions.
  • The timing influences generic competition.

Legal Status and Enforcement

  • The patent’s legal status should be confirmed through official Canadian Patent Office records to verify whether it remains active, subject to maintenance fees, or has faced oppositions.
  • Active claims provide a competitive barrier, but their enforceability depends on legal compliance and potential patent challenges.

Implications for Stakeholders

1. For Innovators and Patent Holders:
Holding a broad patent scope restricts competitors, allowing market exclusivity for the designated therapeutic or chemical space. Maintaining patent fortifications and monitoring potential invalidation threats are essential.

2. For Generics and Competitors:
Analyzing the scope reveals areas susceptible to “evergreening” strategies or designing non-infringing alternatives. Validations of novelty and inventive step are critical when challenging the patent’s validity.

3. For Regulatory and Legal Strategists:
Successfully navigating patent landscapes requires robust patent landscaping, prior art searches, and strategic litigation planning.


Conclusion and Key Takeaways

  • Patent CA2817824 appears to have a strategic scope covering specific chemical compounds or therapeutic uses with potential broad claims targeted at a niche market within Canada.
  • The claims’ breadth is fundamental in determining enforceability and market exclusivity; however, they must withstand scrutiny against prior art to forestall invalidation.
  • The patent landscape context includes related patents, likely forming a comprehensive protection system, influencing both R&D directions and generic market entry.

Actionable insights:

  • Continuous monitoring of patent status and related filings is essential for stakeholders.
  • Clear understanding of claim scope influences licensing opportunities, litigation risk mitigation, and development strategies.
  • Broad claims necessitate thorough invalidity and infringement analyses to optimize legal and commercial positioning.

FAQs

1. How does Patent CA2817824 protect the applicant’s commercial interests in Canada?
It grants exclusive rights to produce, use, or sell the claimed compound or use within Canada for the patent’s duration, preventing competitors from entering the market with similar products or methods.

2. Can competitors develop similar drugs without infringing the patent claims?
Yes. If they design molecules or use methods outside the scope of the patent claims, they can avoid infringement but must thoroughly analyze patent claims to confirm non-infringement.

3. What strategies can competitors use to challenge the validity of CA2817824?
They can conduct prior art searches to identify earlier disclosures that invalidate novelty or inventive step claims, or file legal challenges such as patent oppositions or nullity proceedings.

4. How do patent families influence the scope of protection for this drug?
Patent families extend patent rights across multiple jurisdictions, creating a broad protective network and complicating generic dissemination except through litigation or licensing negotiations.

5. When does Patent CA2817824 expire, and what are the implications?
The expiry date is approximately 20 years from the filing date, around 2032–2033, after which generic manufacturers can produce equivalents, assuming no supplementary protections.


References

  1. Canadian Intellectual Property Office (CIPO). Patent Database.
  2. WIPO. Patent Landscape Reports.
  3. Relevant patent documents and claims from CA patent database entries.
  4. Regulatory filings and patent prosecution records.

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