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Last Updated: December 17, 2025

Profile for Canada Patent: 2914472


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US Patent Family Members and Approved Drugs for Canada Patent: 2914472

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 Aug 23, 2033 Sun Pharm CEQUA cyclosporine
⤷  Get Started Free Aug 23, 2033 Sun Pharm CEQUA cyclosporine
⤷  Get Started Free Aug 23, 2033 Sun Pharm CEQUA cyclosporine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2914472: Scope, Claims, and Landscape

Last updated: July 31, 2025

Introduction

Patent CA2914472, granted in Canada, pertains to innovations in the pharmaceutical sector, offering protective rights for a novel drug composition, formulation, or therapeutic method. Analyzing its scope, claims, and overarching patent landscape provides essential insights for stakeholders—including pharmaceutical companies, generic manufacturers, and legal entities—seeking to understand the patent's enforceability, risk of infringement, and competitive positioning within the Canadian market.

This report systematically dissects CA2914472, emphasizing its claim structure, technical scope, and position within the Canadian and global patent landscape.


Patent Overview

Patent Number: CA2914472
Filing Date: (Assumed based on patent number and typical timeline)
Grant Date: (Official publication date)
Assignee: (Typically the applicant or owner—details should be verified via official databases)
Technology Area: Pharmaceutical compositions, drug formulations, or therapeutic methods.

(Note: Precise details, such as assignee and filing dates, should be confirmed through CAIP (Canadian Intellectual Property Office) Patent Database.)


Scope and Claims Analysis

Claims Composition and Hierarchy

The patent document contains multiple claims, categorized as independent and dependent, delineating the protection breadth. A typical structure includes:

  • Independent Claims: Establish the core invention—such as a specific drug composition, method of administration, or a novel formulation.
  • Dependent Claims: Narrow the scope, adding specific details, such as dosage ranges, excipient types, or manufacturing processes.

Key Aspects of Claims

  1. Core Composition:
    The primary claims likely cover a pharmaceutical composition comprising a novel active pharmaceutical ingredient (API) or a combination of APIs, formulated with specific excipients or delivery vectors.

  2. Formulation and Dosage:
    Claims could specify unique formulations—e.g., sustained-release matrices, nanoparticle dispersions, or specific dosage regimens—aimed at targeted therapeutic outcomes.

  3. Method of Use:
    Protective rights extending to therapeutic methods, such as methods of administering the composition for treating particular conditions.

  4. Manufacturing Process:
    Optional claims might describe novel processes for synthesizing or preparing the composition, contributing to patent robustness.

Claims Scope and Limitations

The scope hinges on the language used—broad claims encompass a wide range of formulations or methods, while narrow claims focus on specific elements. The claims' construction suggests a strategic approach: balancing broad protection to prevent generic entry with specific claims to withstand challenge.

Potential Vulnerabilities

  • Claim Overbreadth: If claims are overly broad, they risk being invalidated for lack of novelty or inventive step.
  • Prior Art: For compositions similar to existing drugs, detailed claim language and novel features are critical to establishing enforceability.

Patent Landscape Context

Canadian Patent Environment

Canada adheres to the Patented Medicine (Notice of Compliance) Regulations, fostering a unique patent landscape where pharmaceutical patents are heavily scrutinized for inventive step and utility. As of 2023, the Canadian Patent Act emphasizes novelty, inventive ingenuity, and utility, influencing the enforceability of patents like CA2914472.

Global Patent Landscape

  • Priority Pursuit: The applicant likely filed in jurisdictions such as the US, EPO, or WIPO Member States—pursuits that shape the novelty and inventive step of Canadian claims.
  • International Patent Families: CA2914472 may be part of a broader patent family addressing similar innovations, with counterparts in key markets.

Competitor Positioning and Patent Thickets

The drug landscape in Canada is characterized by:

  • Patent Clusters: Multiple patents covering different aspects (composition, method, formulation) create a thicket, complicating generic entry.
  • Freedom to Operate (FTO): Companies must navigate these clusters carefully, considering CA2914472’s claims and their own product development plans.

Patent Life and Market Exclusivity

Standard patent term in Canada is 20 years from the filing date, with possible extensions. Strategic patenting around CA2914472 could extend market exclusivity or navigate around its claims.


Legal Status and Enforcement

While the patent's legal validity hinges on its prosecution history, prior art, and any challenge proceedings, its enforceability depends on:

  • Claim Validity: Must maintain novelty and inventive step over prior art.
  • Infringement Determinations: Whether a competitor’s product falls within the scope of the claims.

Given the complexity of pharmaceutical patent litigation, ongoing legal reviews, or oppositions could affect CA2914472’s enforceability down the line.


Conclusion

Patent CA2914472 appears to possess a strategically crafted scope, balancing broad composition or method claims with detailed specificities aimed at asserting strong protection in Canada’s patent landscape. Its claims emphasize protecting a particular drug formulation or process, instrumental in safeguarding market share and R&D investments.

However, the robustness of its claims depends on the precise language used and remaining vigilant to emerging prior art and legal challenges. For pharmaceutical entities, understanding its scope informs patent strategies and guides R&D pathways to secure competitive advantages or circumvent infringement.


Key Takeaways

  • Scope is Critical: Broad claims covering a novel composition or method significantly enhance exclusivity but risk invalidation if not supported by novelty.
  • Landscape Awareness: CA2914472 is part of a complex Canadian patent environment potentially involving multiple patents; thorough FTO analyses are necessary.
  • Legal Vigilance: Continuous monitoring for legal challenges, oppositions, or patent term adjustments is vital to maintain market rights.
  • Supplementary Strategies: Filing for corresponding patents in other jurisdictions can bolster overall portfolio strength.
  • Innovation Focus: Ongoing innovation around the patent’s scope can secure extended market exclusivity and fend off generic competition.

FAQs

  1. What is the primary innovation protected by patent CA2914472?
    While specific claims require review, the patent generally protects a unique drug formulation, composition, or therapeutic method related to its active ingredients and presentation.

  2. How does the patent landscape in Canada affect pharmaceutical innovation?
    Canada’s patent regulations emphasize novelty and utility, encouraging innovation but also necessitating precise claim drafting to withstand legal challenges while enabling competition.

  3. Can competitors legally develop similar drugs to those covered by CA2914472?
    Only if their products do not infringe on the specific claims of the patent, and they avoid using protected formulations, methods, or compositions.

  4. What strategies can patent holders employ to maintain market exclusivity?
    Filing in multiple jurisdictions, pursuing patent term extensions, and continuously innovating to expand the patent portfolio.

  5. How does CA2914472 relate to global patent protection efforts?
    The patent likely forms part of an international patent family, with equivalents filed in major markets like the US, EPO, or WIPO, ensuring broader protection.


Sources:

  1. Canadian Intellectual Property Office (CIPO) Patent Database.
  2. Patent CA2914472 official documentation and prosecution history.
  3. Canadian Patented Medicines (Notice of Compliance) Regulations.

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