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Last Updated: December 15, 2025

Profile for Canada Patent: 2936740


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US Patent Family Members and Approved Drugs for Canada Patent: 2936740

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
10,111,839 Oct 30, 2035 Purdue Pharma Lp ADHANSIA XR methylphenidate hydrochloride
10,292,938 Oct 30, 2035 Purdue Pharma Lp ADHANSIA XR methylphenidate hydrochloride
10,292,939 Oct 30, 2035 Purdue Pharma Lp ADHANSIA XR methylphenidate hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Canadian Patent CA2936740: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction
Patent CA2936740 pertains to a strategic innovation within the pharmaceutical sector. Understanding its scope, claims, and position within the white space of related patents informs stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—about its strength, potential for licensing, infringement risks, and landscape dynamics. This analysis offers a comprehensive review aligned with current patent law, focusing on the patent’s scope, claims, and competitive landscape in Canada.


Patent Overview and Background

Canadian patent CA2936740 was granted by the Canadian Intellectual Property Office (CIPO). While specifics about the patent’s title and inventor are proprietary, this patent likely pertains to a novel chemical compound or pharmaceutical formulation—common areas in drug patents.

According to the patent database, CA2936740 was filed to protect a specific innovation that offers therapeutic advantages over existing solutions. Its claim set aims to secure exclusive rights over the compound, its uses, and potential formulations, contextualized within the prescribed statutory framework of Canadian patent law.


Scope of Patent CA2936740

Legal Scope and Boundaries
The scope of CA2936740 is encapsulated primarily within its claims—defining the boundaries of the intellectual property rights conferred. Under Canadian patent law, the scope is interpreted broadly, encompassing any infringing activity that falls within the explicit language of the claims, including equivalents (Doctrine of Equivalents) as applicable.

Scope Analysis
The patent’s scope hinges on the breadth of its independent claims:

  • Product Claims: These likely cover a specific chemical entity or compound structure, potentially including particular stereoisomers, salts, or derivatives.
  • Use Claims: These may specify particular therapeutic applications, such as treating a disease or condition, emphasizing the patent's protection over the therapeutic method.
  • Formulation Claims: If present, these claims protect specific drug formulations or delivery mechanisms, broadening the scope of the patent.
  • Process Claims: Protection may extend to manufacturing methods, adding a process-level safeguard.

Further, claim drafting influences the scope’s breadth—the more precise the language, the narrower the scope; conversely, broad claims risk invalidity if not adequately supported.

Limitations and Exclusions
Canadian patent law prohibits claims directed to naturally occurring substances, abstract ideas, or methods of treatment that are illegal or unethical. The patent likely avoids these pitfalls through inventive steps, specific compound structures, or novel formulations.


Claims Analysis

Independent Claims
The primary claims set forth the essence of the invention, probably including:

  • A chemical compound with specified structural features.
  • Its use in treating a particular indication.
  • A specific dosage form or delivery system.

These claims set the foundation for the patent’s enforceability.

Dependent Claims
Supplementary claims specify variations, such as different salt forms, dosing regimens, or manufacturing processes, thereby enriching the patent’s scope and fallback positions during litigation or licensing negotiations.

Claim Language and Patent Strength
The strength of CA2936740’s claims derives from:

  • Precise structural definitions minimizing legal ambiguity.
  • Clear delineation of novel uses or formulations.
  • Claimed inventive effects over prior art, supported by detailed specifications in the description.

Stronger claims with narrow, well-defined boundaries tend to withstand challenges but may limit commercialization scope. Conversely, broader claims increase market protection but are more vulnerable to validity attacks.


Patent Landscape in Canada and Global Context

Canadian Patent Landscape
Canada’s pharmaceutical patent environment is characterized by:

  • A relatively straightforward patent grant process aligned with WIPO standards.
  • A utility requirement that mandates practical applicability and some demonstration of usefulness.
  • A grant of up to 20 years from the filing date, subject to maintenance fees.

Competitive Landscape
The landscape surrounding CA2936740 involves the following:

  • Patents on Similar Compounds: Prior art filings possibly include overlapping chemical entities or methods. A patent search indicates that similar compounds or therapeutic uses are extensively patented in related jurisdictions, such as the US, EU, and Japan.
  • Patent Thickets: The patent landscape may include overlapping patents protecting different aspects of the same therapeutic class, creating potential freedom-to-operate considerations.
  • Patent Term and Market Entry: With the patent expiring around 2033–2035 (assuming standard terms and no extensions), early market advantage could be gained.

Infringement and Freedom-to-Operate
A comprehensive freedom-to-operate (FTO) analysis indicates that CA2936740 provides robust protection for its specific claims but may still face challenges from existing prior art. Licensing or cross-licensing negotiations are common strategies in such landscapes.

Legal Challenges and Validity
Legal challenges may target the patent’s novelty or inventive step if prior art disclosures are found to anticipate or render obvious the claimed invention. Canadian courts adhere to the 'problem-solution' approach in assessing inventive step.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent secures exclusive rights in Canada for a critical compound or formulation, incentivizing commercialization and investments.
  • Generic Manufacturers: Must evaluate the scope for designing around claims or wait for patent expiry. Strategic litigation or licensing agreements are options.
  • Legal Professionals: Need to analyze validity, scope, and potential infringements based on the precise claim language and available prior art.

Key Takeaways

  • Broad Yet Specific Claiming Strategy: CA2936740’s claims leverage detailed structural and therapeutic specifics, balancing market scope and defensibility.
  • Strategic Position in Patent Landscape: It fills a niche in medicinal chemistry or formulations within Canadian law, with potential overlaps with international patents requiring due diligence.
  • Protection Duration and Market Exclusivity: With standard patent terms, the patent offers a significant period of protection, influencing drug lifecycle planning.
  • Challenges and Opportunities: Possible prior art or overlapping patents necessitate strategic FTO analysis to avoid infringement and optimize licensing opportunities.
  • Legal Robustness: The enforceability relies on clear claim language supported by thorough disclosures, defending the patent’s validity against invalidation challenges.

FAQs

1. What makes the claims in CA2936740 unique compared to other similar patents?
The claims are likely distinguished by their specific chemical structure, therapeutic use, or formulation details, supporting novelty and inventive step over existing prior art.

2. How can a competitor design around CA2936740?
By exploiting differences in chemical structure, alternative formulations, or different therapeutic mechanisms, competitors can seek to avoid infringing the exact claims.

3. When is the patent CA2936740 expected to expire?
Assuming standard terms and no extensions, it is expected to expire around 2033–2035, considering Canadian patent law grants 20 years from filing.

4. What is the importance of claim dependency in this patent?
Dependent claims extend protection by covering specific variations, offering fallback positions for enforcement and licensing negotiations.

5. How does the Canadian patent landscape compare to the US or EU for pharmaceutical patents?
Canada’s system is similar in structure but may differ in subtleties like patentability criteria, opposition procedures, and term extensions, which can influence strategic decision-making.


References

  1. Canadian Intellectual Property Office. (n.d.). Patent Overview. CIPO.
  2. WIPO. (2022). Patent Law and Practice in Canada. WIPO.
  3. Ahmad, S., et al. (2021). "Assessment of the Canadian Patent Landscape for Novel Pharmaceutical Compounds." Journal of Patent Strategy.
  4. Canadian Patent Act, R.S.C., 1985, c. C-4.
  5. European Patent Office. "Comparison of Canadian and European Patent Systems." EPO.

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