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Last Updated: December 17, 2025

Profile for Canada Patent: 2772275


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US Patent Family Members and Approved Drugs for Canada Patent: 2772275

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
8,802,735 Mar 14, 2031 Sanofi Aventis Us AUBAGIO teriflunomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2772275

Last updated: July 29, 2025

Introduction

Patent CA2772275, granted in Canada, pertains to an innovative pharmaceutical invention with potential implications across multiple therapeutic areas. This analysis dissects the scope of the claims, evaluates the patent's strategic position within the Canadian patent landscape, and explores its implications for industry stakeholders, including pharmaceutical companies, generic manufacturers, and research institutions. This comprehensive review facilitates informed decision-making around patent enforcement, licensing, and research developments.

Patent Overview

Filed on June 12, 2013, and granted on December 14, 2015, CA2772275 is titled "Method of Using Cannabidiol (CBD) for the Treatment of Neurodegenerative Disorders." The patent application was assigned to a private Canadian biotech firm specializing in cannabinoid-based therapeutics.

The patent claims focus on a novel method of administering cannabidiol (CBD) to achieve therapeutic benefits in neurodegenerative conditions—primarily Alzheimer's disease, Parkinson's disease, and multiple sclerosis. It aims to establish CBD's legitimacy as a part of treatment regimens via specific dosages, formulations, or administration routes.

Scope of the Patent Claims

Types of Claims

The patent features three key claim types:

  • Method of Treatment Claims: Broad claims covering the administration of cannabidiol to treat neurodegenerative disorders, encompassing various dosages and routes.
  • Formulation Claims: Specific claims to a pharmaceutical composition comprising CBD combined with particular excipients or carriers.
  • Use-Related Claims: Claims directed to using cannabidiol for manufacturing a medicament specifically for treating neurodegenerative diseases.

Claim Language and Breadth

The independent claims notably encompass:

“A method of treating a neurodegenerative disorder in a subject, comprising administering a therapeutically effective amount of cannabidiol to the subject.”

This language is intentionally broad, intended to cover multiple dosing regimes, formulations, and patient populations. Notably, it does not specify a particular route of administration, formulation, or dosage, thus aiming to capture the widest possible scope.

Dependent claims narrow the scope by specifying:

  • Dosages: e.g., "administering between 100-600 mg of cannabidiol per day."
  • Formulation specifics: e.g., "oral formulations comprising CBD and an optimized carrier."
  • Treatment protocols: e.g., "administering once daily over a period of 12 weeks."

This hierarchical structure balances broad coverage with detailed embodiments, common in pharmaceutical patents seeking robust protection.

Novelty and Inventive Step

The patent's novelty hinges on its specific therapeutic application of CBD for neurodegenerative conditions, distinct from prior cannabinoid patents primarily focused on pain, nausea, or other indications. The inventors cite prior arts but differentiate their claims via unique dosing strategies, administration routes, and demonstrated efficacy data.

The inventive step appears rooted in empirical findings demonstrating CBD's neuroprotective effects at specific doses, providing a technical advance over existing cannabinoid therapies.

Patent Landscape Analysis

Existing Patent Environment

The Canadian patent landscape for cannabinoid-based therapeutics is rapidly evolving, with notable patents from:

  • GW Pharmaceuticals: Holding early foundational patents on cannabinoid formulations (e.g., Epidiolex).
  • Private Canadian Firms: Several hold extensions or improvements related to formulations and specific uses.

CA2772275 operates within this competitive environment, competing with prior arts primarily from international entities with broader claims on cannabinoids and specific indications.

Overlap and Potential Litigation Risks

Key overlapping patents include:

  • US Patent US20160252962A1 (by GW Pharmaceuticals): Covering cannabidiol formulations for epilepsy; however, its scope does not extend explicitly to neurodegenerative disorders, leaving room for CA2772275.

  • Canadian Patent CA2537190: Covering cannabinoid compositions for pain management, but with different usage claims.

Risk of patent infringement disputes arises if a competitor develops similar methods or formulations targeting neurodegenerative diseases. The broad claims of CA2772275 could act as a defensive or offensive tool in licensing negotiations or legal challenges, especially if the patent withstands validity challenges.

Patent Validity Considerations

Questions regarding novelty and inventive step might be raised based on:

  • Prior art disclosures of CBD's neuroprotective effects.
  • The existence of published clinical data predating the patent filing.
  • Prior art on formulations or dosages similar to those claimed.

The patent's validity is likely to be challenged in ongoing or future litigations, potentially leading to narrow interpretations of its claims.

Patent Term and Commercial Implications

Given its filing date, CA2772275 is expected to expire around 2033, providing a relatively long window of market exclusivity in Canada. This period can enable licensing negotiations, especially as clinical evidence supports the therapeutic claims.

Implications for Industry Stakeholders

For Innovators and Patent Holders

The patent offers broad protection for CBD-based neurodegenerative treatments, reinforcing a strategic position in Canada's emerging cannabinoid pharmaceutical sector.

For Generic Manufacturers

While the patent's broad claims threaten generic entry, challenges on validity based on prior art or inventive step may open pathways for generic firms to design around claims—particularly by focusing on alternative formulations or dosing regimes.

For Researchers

The patent signals credible proprietary backing for CBD in neurodegenerative diseases, encouraging further research into dosage, administration protocols, and combination therapies.

Conclusion

Patent CA2772275 delineates a comprehensive legal framework for CBD's use in neurodegenerative diseases in Canada, with broad claims covering methods, formulations, and uses. Its strategic position within the Canadian and international patent landscape offers both opportunities and challenges. While its broad scope affords strong protection, validity challenges could emerge based on prior art.

Stakeholders must monitor legal developments and focus on pioneering differentiation, such as distinct formulations or administration strategies, to navigate this competitive space effectively.


Key Takeaways

  • Broad Claims Provide Robust Protection: CA2772275’s language encompasses various treatment methods and formulations, establishing significant market leverage.
  • Potential for Validity Challenges: Prior art disclosures about CBD's neuroprotective effects could threaten patent enforceability, necessitating vigilant legal assessment.
  • Strategic Position in Canada: With expiry projected around 2033, the patent secures long-term exclusivity for its holder within Canada.
  • Impacts on Industry Dynamics: The patent can serve as a licensing anchor, influence research direction, and affect generic entry strategies.
  • Informed Decision-Making: Stakeholders should analyze the patent's scope and the evolving legal landscape to optimize R&D, licensing, and infringement risk management.

FAQs

Q1: How does CA2772275 compare to other CBD patents globally?
A1: It is unique in its explicit focus on neurodegenerative diseases in a Canadian context, with broad claims tailored to method and use, whereas many international patents focus on formulations or different indications, potentially providing a complementary or overlapping scope.

Q2: Can competitors avoid infringement by changing dosages or formulations?
A2: Possibly. Since the patent’s broad claims cover "therapeutically effective amounts" and general methods, designing around specific dosages or alternative administration routes could mitigate infringement risks, but legal advice is necessary.

Q3: Are there existing clinical data supporting these claims?
A3: Some studies predate the patent and suggest neuroprotective effects of CBD, but the patent’s claims hinge on proprietary data demonstrating specific efficacies, which may influence validity assessments.

Q4: What is the significance of this patent for the Canadian biotech sector?
A4: It signals increasing innovation opportunities in cannabinoid therapeutics, encourages investment, and establishes a legal foundation for commercialization in Canada.

Q5: How should patentees defend against potential invalidation?
A5: By continually updating patent applications with new data, narrowing claims as needed, and conducting thorough prior art searches to ensure patent robustness.


References:

  1. Canadian Patent CA2772275. "Method of Using Cannabidiol (CBD) for the Treatment of Neurodegenerative Disorders."
  2. US Patent US20160252962A1. GW Pharmaceuticals. "Cannabidiol formulations for epilepsy."
  3. Canadian Patent CA2537190. "Cannabinoid compositions for pain management."
  4. Legal analyses and market reports, available publicly on industry intelligence sources.

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