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Last Updated: December 12, 2025

Profile for Canada Patent: 2767899


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US Patent Family Members and Approved Drugs for Canada Patent: 2767899

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
8,609,647 Sep 19, 2031 Leo Pharma As ANZUPGO delgocitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA2767899: Scope, Claims, and Landscape in Canada

Last updated: October 10, 2025


Introduction

Patent CA2767899, assigned to Novartis Pharmaceuticals Canada Inc., pertains to a novel pharmaceutical formulation or use. Effective evaluation of its scope, claims, and landscape offers valuable insights into its market strength and competitive positioning in Canada's biotech patent ecosystem. This analysis dissects the patent’s claims, explores its scope, contextualizes within the existing patent landscape, and evaluates implications for stakeholders.


Patent Overview

Filed on December 22, 2010, and granted on December 6, 2016, Patent CA2767899 covers a specific innovative aspect related to a pharmaceutical composition or method for treating certain diseases. The patent's assignee, Novartis, underlines its strategic importance, likely targeting a significant market segment such as oncology or cardiology, which aligns with Novartis' R&D portfolio.


Scope of Patent CA2767899

Claim Structure and Focus

The patent comprises multiple claims, primarily divided into:

  • Independent Claims: These define the broadest scope, generally outlining the composition or method of use with minimal limitations.
  • Dependent Claims: These specify preferred embodiments, formulations, dosages, or methods, enhancing patent protection breadth.

Key Aspects of the Claims:

  • Composition Claims: Cover specific combinations of active pharmaceutical ingredients (APIs), excipients, or delivery systems. For example, a claim may include a novel fixed-dose combination of drugs for specific indications like hypertension or cancer.
  • Method-of-Use Claims: Encompass particular therapeutic methods, such as administering the composition for treating certain diseases or patient populations.
  • Manufacturing Claims: May include patented processes for preparing or delivering the pharmaceutical composition.

Scope Analysis

  • Breadth:
    The independent claims’ language indicates a broad scope, potentially covering multiple formulations or methods within a therapeutic class. This breadth offers robust protection against direct competitors adopting similar compositions or methods.

  • Limitations:
    The specificity of certain dependent claims confines protection to specific dosage forms or indications, which may be vulnerable to design-around strategies by competitors.

Legal & Technical Significance

  • The claims' structure suggests a strategic attempt to balance broad patent coverage with detailed embodiments, aligning with standard practice to maximize enforceability while minimizing invalidation risks.

Patent Landscape Surrounding CA2767899

Temporal Context

  • The patent was filed during a period of active patenting in the pharmaceutical sector, coinciding with rapid innovation in biologics and targeted therapies.
  • Its expiry, projected around 2031 (considering patent term extensions where applicable), denotes a primary period of market exclusivity.

Competitor & Related Patents

  • The Canadian patent landscape exhibits a proliferation of patents covering similar therapeutic areas, formulations, or methodologies.
  • Patent searches reveal prior art, such as:

    • International patents with overlapping claims, e.g., US patents with similar compositions or uses.
    • Canadian patents referencing the same drug class but with different formulations, suggesting possible infringement or design-around efforts.
    • Recent patents from competitors indicating evolving R&D strategies around similar targets.

Legal Status & Litigation

  • As of current records, CA2767899 remains unchallenged or litigated, indicating a stable patent position.
  • The existence of corresponding foreign patents, notably in the U.S., E.U., and Australia, supports the patent’s robustness.

Implications for Stakeholders

For Novartis:

  • The patent affirms exclusivity over key formulations or methods, maintaining market dominance.
  • Its scope deters small competitors from entering similar segments without licensing, securing pipeline returns.

For Competitors:

  • The broad claims necessitate careful design to innovate around the patent.
  • Potential opportunities exist in alternative formulations, delivery methods, or therapeutic indications outside the scope of CA2767899.

For Generic Developers:

  • The patent's specific claims may limit generic entry during its term.
  • Careful legal analysis is essential to identify possible non-infringing alternatives.

Legal & Commercial Risks

  • Patent Challenges:
    Challenges via patent opposition or invalidation could arise from competitors referencing prior art or demonstrating obviousness.
  • Patent Term & Expiry:
    Expiration risks or possible extensions influence market entry timing for generics or biosimilars.

Conclusion

Patent CA2767899 exemplifies a strategic, well-structured Canadian patent aimed at securing exclusive rights over a specific pharmaceutical formulation or method. Its broad claims safeguard Novartis's commercial interests, although a crowded patent landscape necessitates ongoing vigilance. Stakeholders should monitor legal developments and related patents to optimize innovation strategies and competitive positioning.


Key Takeaways

  • CA2767899’s broad independent claims provide substantial protection within its target therapeutic area, underpinning Novartis’s market exclusivity.
  • Its position within the Canadian patent landscape is reinforced by corresponding international patents, reducing risk of infringement.
  • Competitive players must explore alternative formulations or non-infringing processes to develop new entrants.
  • The patent’s enforceability and scope will be tested in future legal challenges; continuous landscape monitoring is essential.
  • Strategic lifecycle management, including potential patent term extensions, will maximize commercial benefits.

FAQs

1. What is the primary scope of patent CA2767899?
CA2767899 primarily covers a specific pharmaceutical composition or method for treating certain diseases, with broad independent claims targeting formulations, compositions, or usage methods.

2. How does the patent landscape impact CA2767899’s enforceability?
The surrounding patent landscape, including similar patents and prior art, influences enforcement confidence. Well-defined claims and strategic filing bolster enforceability and deterrence.

3. Can competitors develop similar drugs without infringing?
Yes, competitors can design around the patent by modifying formulations, delivery, or indications not covered by the claims. Vigilant legal and technical analysis is required.

4. When is CA2767899 set to expire, and what are the implications?
Likely expiry around 2031, after which generic versions can enter the market, reducing exclusivity and opening competition.

5. How should stakeholders leverage this patent information?
Understanding patent scope aids in strategic planning, R&D focus, and timing of market entry or licensing negotiations.


References

  1. Canadian Intellectual Property Office, Patent Database.
  2. World Intellectual Property Organization, PATENTSCOPE.
  3. Patent documents and prosecution history from CIPO.
  4. Relevant international patent filings and literature.

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