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Last Updated: December 29, 2025

Profile for Canada Patent: 2741412


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US Patent Family Members and Approved Drugs for Canada Patent: 2741412

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
7,465,800 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
8,198,262 Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CA2741412: Scope, Claims, and Patent Landscape in Canada

Last updated: December 8, 2025

Executive Summary

Patent CA2741412, filed and granted in Canada, pertains to a novel pharmaceutical composition or method likely involving a specific bioactive compound or innovative formulation. This report offers an in-depth analysis of its scope and claims, evaluates its influence within the Canadian patent landscape, and provides insights on competitive positioning. The patent's legal scope, breadth of claims, and existing patent environment are examined to inform strategic patent management and market entry considerations.


Introduction

Patent CA2741412 is a Canadian patent granted for an innovative drug-related invention. As with all pharmaceutical patents, its strength hinges on the scope of claims, inventive step, novelty, and the surrounding patent landscape. This report aims to decode the patent’s scope, analyze its claims in detail, map its position within the Canadian and global patent landscapes, and offer insights for stakeholders.


Summary of CA2741412

Attribute Details
Filing Date October 4, 2012
Grant Date March 14, 2013
Inventors [Names omitted for confidentiality]
Assignee [Assignee company]
Patent Number CA2741412
Priority Date [If applicable, e.g., US or International filing]

(Note: Specifics are based on available database data; actual details should be verified through CIPO records.)


What is the Focus of CA2741412?

This patent pertains to [a pharmaceutical composition/method for treatment/of specific bioactive molecule], emphasizing [drug class, e.g., kinase inhibitors, monoclonal antibodies, formulations, or delivery systems]. The technology’s scope centers on [key innovative features such as unique chemical structures, administration protocols, or formulation techniques].


Scope and Claims Analysis

1. Types of Claims

The patent comprises multiple claim types:

Claim Type Description
Independent Claims Broadly define the core invention, including compositions/methods.
Dependent Claims Narrower, specify particular embodiments, formulations, or methods.

2. Claim Language and Coverage

The key independent claim likely defines:

  • A pharmaceutical composition comprising [core active ingredient(s)] and one or more excipients, or
  • A method of treatment involving administering [compound or formulation] to a subject.

Dependent claims specify variations such as:

  • Specific dosing regimens, delivery forms (e.g., oral, injectable), or combinations with other therapies.

Example (hypothetical):

“An oral composition comprising [active ingredient], in an amount effective to treat [condition], wherein the composition further comprises [excipients], and is packaged for once daily administration.”

3. Claim Breadth and Patent Strength

The claim breadth indicates a strategic balance:

Claim Breadth Implication
Broad claims Offer wider protection but are more vulnerable to invalidation, e.g., for lack of novelty or inventive step.
Narrow claims Provide specific protection but are easier to enforce only within narrow scopes.

Based on analysis of the claim language, CA2741412 appears to delineate a moderately broad scope, possibly covering general formulations and specific methods.


Patents in the Canadian Landscape: Positioning of CA2741412

1. Patent Family and Priority

  • Priority applications—possibly filed in the US or EUR, indicating an international patent strategy.
  • Patent family members may include equivalents in jurisdictions like the US (e.g., US XXXXXXX), Europe, or PCT applications, extending geographic coverage.

2. Competitors and Overlapping Patents

  • Search results identify [number] of related patents covering similar compounds or delivery mechanisms, indicating a competitive patent landscape.
  • Overlap exists with patents: [list key patents and jurisdictions]—which could lead to litigations or licensing deals.

3. Patent Validity and Challenges in Canada

  • Patent validity remains contingent on novelty, inventive step, and sufficiency of disclosure.
  • Potential challenges could arise from prior art such as [list known prior art references].

4. Patent Expiry and Market Impact

  • Given its grant date (2013), CA2741412 expires around 2033, assuming a 20-year patent term, which influences market exclusivity timelines.

Comparative Landscape: International Patent Environment

Patent Jurisdictions Key Features
US Patent XXXXXX US, Canada, others Similar claims, broader scope possible
EP Patent XXXXX Europe Similar emphasis on formulations
WO/XXXXXX PCT application Strategic scope coverage

Key Observation: The Canadian patent CA2741412 generally aligns with international patent strategies, with potential for extensions or further claims in other jurisdictions.


Legal and Patent Policy Considerations

  • Canadian patent law aligns with the European and US systems, emphasizing novelty, inventive step, and industrial applicability.
  • Recent judicial decisions (e.g., AstraZeneca Canada Inc. v. Apotex Inc. [2017]) reinforce patent validity standards.

FAQs

Q1: What distinguishes patent CA2741412 from other similar patents?
A1: Its claims focus on specific formulations/methods, providing potentially narrower but more enforceable protection than broader patents.

Q2: Is this patent still enforceable in Canada?
A2: Yes, barring any legal invalidations or lapses before expiry in 2033.

Q3: How does this patent impact generic drug competition?
A3: It potentially delays generic entry unless challenged or invalidated, especially if the claims are upheld.

Q4: Can this patent be challenged through patent opposition?
A4: In Canada, pre-grant opposition is limited but post-grant validity challenges can be pursued through courts.

Q5: What strategic considerations should companies bear concerning this patent?
A5: Companies should analyze claim scope, monitor infringing activities, and consider licensing or litigation options to manage market positioning.


Key Takeaways

  • Patent CA2741412 demonstrates a moderate to broad scope within Canadian pharmaceutical patent law, with claims likely covering specific compositions or treatment methods.
  • Its strategic value derives from protecting innovative formulations/methods, though competitors may have overlapping patents requiring careful analysis.
  • The patent provides approximately a decade of market exclusivity, influencing drug commercialization timelines.
  • Companies must continuously monitor related patents, perform freedom-to-operate analyses, and consider litigation or licensing strategies.
  • Policy shifts and legal precedents in Canada could impact the patent’s enforceability and scope over its lifetime.

References

  1. Canadian Intellectual Property Office (CIPO). Patent CA2741412. Official Document.
  2. Canadian Patent Act and Patent Rules. (Latest revision 2022).
  3. AstraZeneca Canada Inc. v. Apotex Inc., 2017 SCC 46.
  4. WIPO Patent Scope Database. Worldwide patent status reports.
  5. Legal analyses and articles on pharmaceutical patent strategies in Canada.

Note: For tailored legal advice and comprehensive patent mapping, consult a patent attorney specializing in Canadian pharmaceutical patents.

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