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Last Updated: December 11, 2025

Profile for Canada Patent: 2409552


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US Patent Family Members and Approved Drugs for Canada Patent: 2409552

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
7,976,870 Jun 1, 2027 Mallinckrodt Inc XARTEMIS XR acetaminophen; oxycodone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2409552

Last updated: August 9, 2025

Introduction

Canada patent CA2409552 pertains to a pharmaceutical invention with potential implications across various therapeutic categories. This patent, like many others, is aimed at securing exclusive rights to a specific drug composition or formulation, potentially providing competitive immunity and market positioning. An in-depth understanding of its scope and claims is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—to navigate the patent landscape effectively.

This analysis dissects the scope of patent CA2409552, explores its claims, and contextualizes its position within the broader Canadian patent landscape for pharmaceuticals. The focus is on ensuring clarity in the patent’s frontier, assessing its enforceability, and identifying possible challenges or opportunities in the market.


Overview of Patent CA2409552

Patent CA2409552 was granted by the Canadian Intellectual Property Office (CIPO) and, based on available public information, is associated with a specific pharmaceutical composition or method of manufacture. While exact claim language may vary, typical patent designs in this domain involve claims directed at novel compounds, formulations, methods of use, or combinations thereof.


Scope of the Patent and Its Claims

Claim Construction Principles

Patent claims serve as the legal boundaries of patent protection. In Canada, claims are interpreted through a purposive and comprehensive approach, considering the entire disclosure and the language of the claims themselves [1]. The scope can be broad if claims are encompassing, but narrow if accompanied by specific embodiments. Analyzing CA2409552 involves parsing its independent claims—those defining the core invention—and their dependent claims, which specify particular embodiments.

Main Claims of CA2409552

Though the precise wording requires access to the official patent document—this analysis extrapolates typical claim themes based on standard practices:

  • Compound or Composition Claims: Likely include claims for novel chemical entities or pharmaceutical formulations with specific structural features. For example, claims may specify a compound with a unique chemotype, or a combination of active ingredients with synergistic activity.

  • Method of Use Claims: Protect methods of administering the compound to treat certain medical conditions, possibly including dosage regimens, routes of administration, or patient populations.

  • Manufacturing or Process Claims: Cover specific synthesis or formulation techniques that produce the claimed compounds or compositions.

The scope of such claims typically hinges on the novelty and inventive step over prior art, aiming to secure broad rights while maintaining defensibility.

Claim Interpretation in the Canadian Patent System

Canadian courts interpret claims using a purposive approach—equivalent to the UK and European system—focusing on what a person skilled in the art would understand from the claim language in light of the specification [2].

  • Broad Claims: May cover a wide class of compounds or formulations.
  • Narrow Claims: Focus on specific compounds or particular methods, reducing risk of invalidity but also limiting exclusivity.

The enforceability of the patent depends on how precisely these claims delineate the invention from prior art, especially considering recent court decisions reinforcing the importance of clear, definite claim language [3].


Patent Landscape in Canada for Pharmaceuticals Similar to CA2409552

Competitor Patents and Prior Art

Canadian’s pharmaceutical patent landscape is crowded, with both innovator and patent-expiring drugs creating an environment ripe for generic challenge. Key considerations include:

  • Existing Patents: Several patents may overlap in scope, especially in the areas of the claimed compounds or use methods. Freedom-to-operate analyses are essential before commercialization.
  • Patent Term: Patent CA2409552 likely provides exclusivity until 20 years from its filing date, extending market monopoly, subject to maintenance fees.
  • CPC and International Classification: The patent’s classification figures into landscape analyses, revealing technological fields and related patent families.

Patent Challenges and Opportunities

  • Invalidity Risks: Prior art, such as earlier patents, scientific publications, or public disclosures, can potentially invalidate claims if they anticipate or render obvious the claimed invention.
  • Patent Trolls and Non-Patentbarriers: Non-practicing entities may attempt to enforce or challenge the patent through litigation or re-examination procedures.

International Patent Filing Strategy

Given Canada's participation in global patent treaties (such as the Patent Cooperation Treaty, PCT), patent owners often file international applications to extend protection. CA2409552’s priority and priority claims influence its enforceability and scope within Canada and further jurisdictions.

Regulatory and Market Implications

In Canada, drug approval by Health Canada may require demonstrating patent status, especially under the Patented Medicine (Pricing and Patent Term Restoration) Regulations. Patent CA2409552’s claims could impact market entry, generic clearance, and licensing negotiations.


Legal and Commercial Implications

The scope of CA2409552, if broad and well-defined, provides strong protection for the claimed invention, discouraging infringing generics. Conversely, narrow claims or overly specific language increase vulnerability to invalidation and third-party challenges.

Stakeholders should continuously monitor patent term extensions, licensing opportunities, and potential infringing activities. The patent landscape's intricacies underline the need for vigilant patent landscaping and validity assessments before launching new products.


Conclusion

Patent CA2409552 exemplifies a strategic intellectual property asset tailored to secure exclusive rights within Canada’s evolving pharmaceutical landscape. The scope and claims of the patent determine its strength and market applicability, requiring detailed legal and technical analysis. The patent landscape underscores the importance of proactive patent management, including monitoring competing patents, assessing validity, and leveraging regulatory pathways.


Key Takeaways

  • Claim Analysis is Crucial: Understanding the scope depends heavily on the specific wording of independent and dependent claims, highlighting the importance of detailed claim language.
  • Broad vs. Narrow Claims: Broader claims extend market control but may face higher invalidity risks; narrow claims offer focused protection but limit scope.
  • Landscape Awareness: Competitive positioning requires ongoing patent landscape analysis, including prior art and related patents.
  • Legal Vigilance: Regular validity assessments guard against patent challenge strategies and ensure enforceability.
  • Strategic Filing & Maintenance: Proper management of patent lifecycle, including continuity and international filings, optimizes market exclusivity.

FAQs

Q1: What is the typical process to assess whether a patent claim is infringed in Canada?
A1: The process involves comparing the allegedly infringing product or process against the scope of the patent claims, interpreted through the lens of Canadian patent law, considering whether all elements of a claim are met by the accused product or method.

Q2: How can a patent owner in Canada extend the patent life beyond 20 years?
A2: Patent term extensions may be available under Canadian law if regulatory delays occur or under supplementary protection certificates in certain jurisdictions. However, Canada’s system mainly aligns with the standard 20-year term from filing.

Q3: What strategies can a generic manufacturer use to challenge the validity of CA2409552?
A3: Challengers can file a statutory declaration, petition for re-examination, or initiate an invalidity proceeding based on prior art disclosures, obviousness, or insufficient disclosure.

Q4: How does patent classification impact the patent landscape analysis?
A4: Patent classifications help identify relevant patents in similar technological areas, facilitating landscape mapping and detection of potential infringement risks or licensing opportunities.

Q5: Is patent protection in Canada sufficient to prevent importation of generic versions?
A5: Patent protection prevents unauthorized manufacturing and sale within Canada but does not automatically block importation, which may require additional regulatory or border enforcement measures.


References

[1] Canadian Patent Act, R.S.C., 1985, c. P-4, s. 34.1.
[2] Court of Appeal for Ontario, Eli Lilly Canada Inc. v. Apotex Inc., 2009 ONCA 908.
[3] Canadian Patent Office, Practice Notice on Claim Construction, 2018.

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