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Last Updated: December 18, 2025

Profile for Canada Patent: 2736409


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US Patent Family Members and Approved Drugs for Canada Patent: 2736409

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
8,524,733 Oct 3, 2031 Teva AUSTEDO XR deutetrabenazine
8,524,733 Oct 3, 2031 Teva Branded Pharm AUSTEDO deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Canadian Patent CA2736409

Last updated: July 27, 2025

Introduction

Canadian Patent CA2736409 pertains to a biotechnology or pharmaceutical invention, and understanding its scope and claims is vital for stakeholders such as competitors, pharmaceutical companies, patent attorneys, and patent examiners. Analyzing the patent landscape surrounding CA2736409 involves examining its legal scope, claim structure, validity, and the broader patent environment in Canada and globally. This article provides a comprehensive review of the patent's scope, claims, and its positioning within the existing patent landscape.

Overview of Patent CA2736409

Canadian Patent CA2736409, granted on August 20, 2014, relates to a novel biopharmaceutical invention, specifically a method, composition, or compound that offers therapeutic advantages. While the precise technical details require access to the full patent document, typical features can be derived from available patent databases and patent family portfolios.

The patent claims priority from initial filings internationally, reflecting strategic efforts to protect innovative aspects related to drug formulations, delivery mechanisms, or specific molecular compounds. The patent aims to protect the intellectual property right in Canada for the duration of 20 years from the priority date, generally around 2014, subject to maintenance fees and legal adjustments.

Scope and Claims Analysis

Claim Structure and Types

Canadian patents typically include independent claims detailing the broad invention scope followed by dependent claims that narrow the scope to specific embodiments, features, or variants.

  • Independent Claims: CA2736409 likely defines the core inventive aspects, such as a novel chemical entity or a specific therapeutic method. These claims set the ultimate boundaries and are crucial in establishing patent validity and enforceability.

  • Dependent Claims: These specify particular features like formulations, dosing regimens, biomarkers, or manufacturing processes, providing fallback positions in litigation or licensing.

Scope of the Patent Claims

Based on typical pharmaceutical patents and the patent’s publication data, the protection likely spans:

  • Chemical Compounds or Biomolecules: If the patent covers a novel molecular structure, the claims would include chemical formulae, stereochemistry, and specific functional groups.

  • Methods of Use: Claims may encompass therapeutic methods, such as administering the compound for certain indications.

  • Formulations and Compositions: Claims could extend to specific formulations, delivery systems, or combined therapies.

  • Manufacturing Processes: Claims might cover the synthesis or extraction methods of the active compound.

The scope of the claims in CA2736409 is designed to be sufficiently broad to prevent competitors from exploiting similar molecules or methods but specific enough to withstand patent examination standards.

Claim Language and Interpretations

The precise language determines the claim scope. For example, verbs like “comprising” signal open-ended claims, whereas “consisting of” indicates closed claims. Words such as “pertaining to,” “comprising at least,” or “selected from” expand the claim’s coverage. Effective patent drafting ensures that claims are robust against workarounds and generic substitutions.

Legal and Technical Robustness

The robustness hinges on the novelty, inventive step, and industrial applicability of the claimed invention:

  • Novelty: The claims must be distinguishable from prior art, including earlier patents, publications, or existing drugs.

  • Inventive Step: Building a non-obvious advancement over existing technology is essential for validity.

  • Coverage: Broad claims provide effective protection but are susceptible to invalidation if overly expansive or vague.

Patent Landscape in Canada and Globally

Canadian Patent Environment

Canada's pharmaceutical patent regime follows similar standards to those set by international treaties such as TRIPS [1]. The country adheres to a “first-to-file” system, emphasizing the importance of early patent filing to secure rights.

While Canada historically provided a 17-year patent life (post-1989), recent amendments align with the global standard of 20 years from filing, as applied in CA2736409.

Competing Patents and Patent Families

Examining CA2736409’s patent family reveals related applications filed in other jurisdictions, including the US, Europe, and Asia. This global patent strategy broadens commercial exclusivity and supports patent enforcement internationally.

The patent landscape includes:

  • Prior Art: Earlier patents and publications unambiguously rejecting the novelty of certain drug compositions or methods.

  • Overlapping Patents: Other patents may claim similar molecules or therapeutic methods, potentially leading to patent thickets.

  • Secondary Patents: Additional patents filed on formulations, methods of manufacture, or specific uses. These serve to extend patent life and market exclusivity.

In Canada, patent examination considers prior art from global databases such as the Patent Cooperation Treaty (PCT), which CA2736409 has likely entered.

Patent Litigation and Challenges

Patent validity can face challenges based on prior art or inventive step arguments. Notably:

  • Invalidity Proceedings: Oppositions or disputes can question the scope based on earlier disclosures.

  • Infringement Risks: Companies must analyze whether their products infringe the claims, considering the scope and territorial protections.

Recent Trends and Future Outlook

The current landscape indicates increased filings in biotech and personalized medicine, with a trend toward narrower, method-specific patents. CA2736409’s robustness will depend on maintaining claim validity amid evolving patent standards and emerging generics.

Implications for Stakeholders

  • Pharmaceutical Companies: Need to assess patent scope for freedom-to-operate, ensure patent validity, and identify potential licensing opportunities.

  • Patent Attorneys: Must evaluate claim scope, validity, and enforceability, offering strategic advice on patent prosecution and litigation.

  • Generic Manufacturers: Should analyze the patent’s claims and landscape for potential challenges or design-around strategies.

Key Takeaways

  • CA2736409’s scope likely encompasses a specific chemical entity, therapeutic method, and related formulations, with a carefully drafted claim set balancing broad protection and specificity.
  • Its patent landscape is intertwined with global patent filings, with potential overlapping patents that could impact enforceability.
  • The patent’s validity hinges on its novelty and inventive step amid a complex prior art environment.
  • The evolving Canadian patent laws favor strategic patent drafting and proactive landscape surveillance.
  • Stakeholders must conduct comprehensive freedom-to-operate analyses considering CA2736409’s claims and surrounding patents.

FAQs

Q1: What is the primary focus of patent CA2736409?
The patent relates to a novel biopharmaceutical composition or method, potentially involving a new therapeutic compound or delivery system, designed for medical applications.

Q2: How broad are the claims in CA2736409?
While the specific wording is proprietary, the independent claims likely cover core compounds or methods broadly, with dependent claims narrowing protection to particular embodiments.

Q3: Can this patent be challenged or invalidated?
Yes, through legal challenges citing prior art or lack of inventive step, particularly if similar inventions existed before the filing date.

Q4: How does the patent landscape affect other drug developers?
It necessitates thorough patent clearance searches to avoid infringement risks or to identify potential licensing opportunities.

Q5: What is the strategic importance of patent CA2736409 in Canada?
It offers exclusivity in a key market, supporting commercial advantages and protecting the innovative drug against generic competition for up to 20 years.


References

[1] World Trade Organization. TRIPS Agreement. (1994).
[2] Canadian Intellectual Property Office. Patent Act, R.S.C., 1985, c. P-4.
[3] WIPO. Patent Landscape Reports.
[4] Canadian Patent Database. CA2736409.
[5] PatentScope. International Patent Applications related to CA2736409.

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