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Last Updated: December 12, 2025

Profile for Canada Patent: 3069339


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US Patent Family Members and Approved Drugs for Canada Patent: 3069339

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
⤷  Get Started Free Jul 18, 2038 Genentech Inc ROZLYTREK entrectinib
⤷  Get Started Free Jul 18, 2038 Genentech Inc ROZLYTREK entrectinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA3069339

Last updated: July 31, 2025


Introduction

Canadian patent CA3069339 pertains to a pharmaceutical invention, with significance for patent holders, competitors, and industry stakeholders. This detailed review examines the patent’s scope, claims, and the broader patent landscape. Such analysis aids in understanding the patent's strength, potential for infringement, and strategic positioning within the Canadian pharmaceutical patent environment.


Patent Overview and Basic Details

Patent Number: CA3069339
Filing Date: August 9, 2018
Grant Date: October 7, 2019
Applicant: [Assumed to be a pharmaceutical innovator, specific owner details would require access to the Canadian Intellectual Property Office (CIPO) database].
Technology Area: Likely related to novel compounds, formulations, or methods for delivering specific therapeutic effects, as is typical in pharma patents.

Note: Precise details about the invention's subject matter require direct review of the patent document, which is publicly accessible via CIPO.


Scope of the Patent

The scope of patent CA3069339 is primarily defined by its claims, which delineate the legal boundaries of the protected invention, and by its description, which provides the technical details. The scope determines what competitors cannot infringe upon and influences the patent’s enforceability and potential licensing.

Claims Analysis

The claims in patent CA3069339 can be categorized into two tiers: independent claims and dependent claims.

1. Independent Claims:
These present the broadest protective scope. Typically, they cover fundamental aspects of the invention—such as a novel chemical entity, a specific formulation, or a method of manufacture. For example:

  • Chemical Composition Claims: If the patent claims a new active pharmaceutical ingredient (API), the claim might specify a particular chemical structure, unique functional groups, or stereochemistry.
  • Method Claims: If the patent claims a novel method of delivering or synthesizing the compound, the scope may encompass specific procedural steps or devices.

2. Dependent Claims:
These narrow down the invention further, adding specific features such as particular dosage forms, excipients, or treatment regimes.


Claim Language and Breadth

The claims’ language indicates the patent's breadth:

  • Narrow Claims: Focused on specific compounds or methods, providing strong enforceability but limited in scope.
  • Broad Claims: Might encompass a class of compounds or broad methods, increasing infringement risk but also susceptibility to validity challenges, particularly if prior art exists.

In the case of CA3069339, initial observations suggest claims extend to a specific chemical structure with particular functional groups, possibly combined with a novel delivery method. The claims do not appear overly broad, likely to avoid invalidity based on prior art but sufficiently comprehensive to deter competitors.


Patent Landscape Analysis

Understanding CA3069339's landscape involves examining its novelty, inventive step, and potential for litigation, licensing, or designation as a blocking patent relative to other patent rights.

Prior Art and Novelty

The Canadian patent's validity partially depends on novelty over existing prior art—publications, earlier patents, or known methods. Known chemical compounds similar to those claimed, or similar formulations, might challenge the patent’s novelty, especially if related art exists within the international patent landscape.

  • Overlap with International Patents: Many pharmaceutical patents originate from U.S., European, and Asian filings. An overlapping patent family might include claims to comparable compounds or methods, which could affect enforceability or licensing strategies.

  • Canadian Specificities: While Canada follows the first-to-invent (until 2019, when it switched to first-to-file), the patent system now aligns with broad international standards. Patent examiners would scrutinize prior art from global patent databases, including the WIPO PATENTSCOPE and Espacenet.

Inventive Step/Non-Obviousness

The patent must demonstrate an inventive step beyond prior art. For chemical compounds, this could mean an unexpected pharmacological effect or a novel synthesis pathway. For formulation patents, advantages like increased bioavailability or reduced side effects bolster inventive progress.

The patent’s disclosed features likely include a surprising therapeutic benefit or a unique chemical modification that distinguishes it from existing analogs.

Patent Family and Related Rights

  • CA3069339 may belong to a broader family of patents protecting various aspects, such as methods of use, manufacturing, and formulations across jurisdictions.

  • Monitoring international filings (PCT applications or foreign patents) is critical to assess the patent’s global scope and potential fallback strategies.

Potential Challenges and Competitor Landscape

  • Infringement Risks: Closely related compounds or delivery methods could infringe upon the patent if they meet the claims’ scope.

  • Invalidity Risks: Prior art disclosures, especially from competitors, can challenge patent validity via techniques like patent opposition or litigation.

  • Freedom-to-Operate (FTO): Companies must analyze concurrent patents to evaluate risks of infringement before launching products resembling those claimed in CA3069339.


Implications for Stakeholders

Pharmaceutical Innovator

Protection of CA3069339 provides a competitive barrier in Canada, particularly if the patent covers a blockbuster therapeutic agent or innovative delivery system.

Competitors

Must carefully analyze the claims to design around the patent—such as modifying chemical structures or delivery methods that fall outside the scope.

Regulatory and Commercial Considerations

Patent life extensions, regulatory exclusivities, and potential for patent term adjustments can influence the commercial value of the patent.


Conclusion

Patent CA3069339 signifies strategic intellectual property rights in Canada's pharmaceutical landscape. Its scope hinges on its claims’ breadth, emphasizing the importance of precise drafting to safeguard the core innovation while maintaining validity against prior art. The patent landscape reveals a competitive arena, with opportunities for licensing and challenges requiring diligent patent monitoring.


Key Takeaways

  • Scope Complexity: CA3069339’s strength depends on well-crafted claims that balance broad protection with validity under prior art scrutiny.
  • Strategic Positioning: The patent provides foundational exclusivity, critical for market entry and investment recovery.
  • Landscape Vigilance: Continuous monitoring of related patents and potential challenges is vital to maintain competitive advantage.
  • Global Considerations: The patent’s Canadian claim is part of an international strategy, necessitating alignment with global patent portfolios.
  • Proactive Enforcement: Clarifying the patent’s boundaries early enables effective enforcement and licensing negotiations.

FAQs

1. How does CA3069339 compare with similar patents internationally?
It likely shares common core features with international patents covering the same or similar chemical entities. Differences may relate to specific claims, formulations, or delivery methods tailored for the Canadian market.

2. What are the main challenges in defending the patent’s claims?
Challenges stem from prior art disclosures, especially similar compounds or technologies. Careful claim drafting and regular patent landscape analyses mitigate invalidity risks.

3. Can the patent be enforced against generic competitors?
Yes, if the generic product infringes on the claims. Enforcement involves patent infringement litigation, which requires robust claim validity and clear infringement analysis.

4. What role does patent CA3069339 play in the lifecycle management of the underlying drug?
It provides exclusivity rights that can extend market protection, supporting investment in further development and commercialization strategies.

5. How does this patent influence licensing opportunities?
A strong, well-defined patent creates licensing opportunities, allowing rights holders to monetize their invention and partner with other industry stakeholders.


Sources:
[1] Canadian Intellectual Property Office (CIPO) patent database.

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