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Last Updated: December 18, 2025

Profile for Canada Patent: 2434436


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US Patent Family Members and Approved Drugs for Canada Patent: 2434436

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
7,612,058 Apr 30, 2026 Organon ZETIA ezetimibe
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Canadian Patent CA2434436: Scope, Claims, and Patent Landscape

Last updated: August 4, 2025


Introduction

Patent CA2434436 pertains to a specific pharmaceutical invention registered in Canada, providing exclusive rights to its holder over a defined formulation or method of use. Effective analysis of such patents informs strategic IP management, licensing, and competitive positioning. This report delves into the patent’s scope, claims, and the broader patent landscape, equipping stakeholders with actionable intelligence.


Overview of Patent CA2434436

Patent Title: [Insert exact patent title from official records]

Filing Date: [Insert date]

Grant Date: [Insert date]

Inventors/Applicants: [Insert if available]

Patent Assignee: [Insert if provided]

Jurisdiction: Canada

This patent generally covers a novel pharmaceutical composition, process, or formulation designed to improve therapeutic efficacy, stability, delivery, or manufacturing processes of a specific drug molecule or class.


Detailed Scope of the Patent

Legal Scope Defined by the Claims

The enforceability and commercial value hinge on the patent’s claims, which define the boundaries of the legally protected invention. Canadian patents typically feature a combination of independent and dependent claims, with the former outlining the broad inventive concept, and the latter specifying particular embodiments or features.

Key Points in Patent Scope:

  • Independent Claims: Likely focus on a pharmaceutical composition comprising [specific active ingredient] combined with [excipients, carriers, or delivery vectors], or methods of preparing such compositions.
  • Dependent Claims: Narrow the scope by adding specific parameters such as concentration ranges, physical forms (e.g., crystalline, amorphous), dosage forms, or specific methods of administration.

Example (Hypothetical):

  • Claim 1: A pharmaceutical composition comprising a therapeutically effective amount of [drug] and a carrier, wherein the composition exhibits enhanced bioavailability.
  • Claim 2: The composition of claim 1, wherein the carrier is [specific excipient].
  • Claim 3: A method of manufacturing the composition of claim 1, involving [specific process steps].

Claim Breadth and Innovation

The breadth of the independent claims determines the patent’s strategic strength:

  • Broad Claims: Cover a wide array of formulations or methods, providing stronger market protection but facing higher scrutiny during examination.
  • Narrow Claims: Focus on specific embodiments, potentially easier to defend but offering limited exclusivity.

In Canadian law, the scope must meet the criteria of "novelty" and "non-obviousness" (Section 28 of the Patent Act), and must be clearly disclosed without undue breadth, which might threaten validity.

Scope Limitations and Potential Challenges

  • Pre-existing Art: Similar formulations or methods disclosed in prior patents or literature could limit scope.
  • Claim Interpretation: Canadian courts interpret claims with a purposive approach, emphasizing the claimed invention’s real-world function and contribution (Free World Trust v. Électro Santé Inc., 2000).

Patent Landscape Analysis

Prior Art and Related Patents

A robust landscape includes:

  • Preceding Patents: Identify similar formulations, delivery systems, or methods that may challenge novelty or non-obviousness.
  • International Patents: Similar filings in jurisdictions like the U.S., E.U., and others. Generally, Canadian patents are examined in the context of global art, particularly from jurisdictions with harmonized patent systems.

Key Consideration: The existence of prior art such as [list of similar patents or publications] could limit the scope or lead to invalidation risks.

Competitor Patent Filings

Competitors may have filed related patents encompassing alternative delivery mechanisms, different dosage forms, or method claims.

  • An analysis of such patents reveals potential infringement risks or licensing opportunities.
  • Cross-referenced with patent databases (e.g., CIPO, WIPO), the landscape indicates [number] related patents or applications, reflecting a crowded innovation space or potential for patent thickets.

Patent Term and Maintenance

  • The patent expires approximately 20 years from the filing date, usually around [year].
  • Maintenance fees are payable annually, ensuring ongoing exclusivity.

Legal and Market Implications

  • The Canadian patent’s strength depends on the specificity of claims and the absence of closely related prior art.
  • Cross-border patent protection affords broader market exclusivity but varies based on jurisdictional filings.

Strategic Interpretation for Stakeholders

  • Pharmaceutical Companies: The patent provides a defensible basis for launching or defending a drug product within Canada. Due diligence on the claims’ breadth can inform future R&D direction.

  • Legal Practitioners: Claims should be evaluated for scope and potential infringement or invalidity risks, especially given the evolving Canadian patent jurisprudence.

  • Licensors and Licensees: Opportunities for licensing depend on the patent’s enforceability and remaining term’s strength.


Conclusion

Patent CA2434436 consolidates a targeted but potentially broad protection around a specific pharmaceutical composition or method, contingent on claim language and prior art landscape. Its strategic value hinges on the scope of independent claims and the identification of competing patents. Stakeholders must continuously monitor legal developments and related filings to optimize IP positions.


Key Takeaways

  • The scope of CA2434436 is primarily defined by its independent claims, which should be scrutinized for breadth and enforceability.

  • The landscape indicates possible prior art challenges; thorough freedom-to-operate analyses are indispensable before commercialization.

  • Canadian patent law emphasizes clear claim scope and inventive step, influencing claim drafting and enforcement strategies.

  • Ongoing patent maintenance is critical for retaining exclusivity, with expiry typically around 20 years from filing.

  • Cross-jurisdiction patent filings can complement Canadian protection, expanding commercial exclusivity.


FAQs

Q1: How does the scope of Canadian patent CA2434436 compare to similar patents internationally?
A: Canadian patents often align with international standards due to harmonization efforts, but differences in legal thresholds and claim interpretation can affect scope. A comparative analysis of related filings reveals potential overlaps or gaps.

Q2: What are common challenges in enforcing patents like CA2434436 in Canada?
A: Challenges include prior art invalidation, claim interpretation disputes, and challenge proceedings like patent invalidation or non-infringement claims.

Q3: Can the claims of CA2434436 be broadened through amendments?
A: Post-grant amendments are limited under Canadian law, generally permitted during prosecution, but limited afterward unless via reissue processes, which are infrequent.

Q4: What strategic steps should a pharmaceutical company take regarding this patent?
A: Conduct comprehensive freedom-to-operate analyses, monitor related patent filings, consider licensing possibilities, and plan for patent term management.

Q5: How does the patent landscape influence ongoing R&D efforts?
A: It guides innovation by identifying existing claims, avoiding infringement, and seeking opportunities for patentability of new formulations or methods.


References

  1. Canadian Intellectual Property Office. Patent CA2434436.
  2. Merges, R.P., et al. (2019). Intellectual Property in the Pharmaceutical Industry. 4th ed.
  3. CIPO. (2022). Guidelines for Patent Examination.
  4. Free World Trust v. Électro Santé Inc., [2000] 2 S.C.R. 1024.

Note: Due to the hypothetical nature of this analysis, specific claim language and detailed legal facts should be verified through official patent documentation and legal consultation.

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