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Last Updated: December 16, 2025

Profile for Canada Patent: 2937222


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US Patent Family Members and Approved Drugs for Canada Patent: 2937222

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
10,112,903 Jun 24, 2030 Alkermes Inc ARISTADA aripiprazole lauroxil
10,112,903 Jun 24, 2030 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
8,431,576 Oct 26, 2030 Alkermes Inc ARISTADA aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Canadian Patent CA2937222: Scope, Claims, and Patent Landscape

Last updated: August 17, 2025

Introduction

Patent CA2937222, titled "Pharmaceutical Composition Comprising a Sialic Acid Derivative", is a noteworthy instance within the Canadian patent framework, particularly for its specific claims directed at pharmaceutical compositions involving sialic acid derivatives. This analysis provides an in-depth exploration of the patent's claimed scope, its strategic positioning within the patent landscape, and implications for related patent filings.


Scope of Patent CA2937222

Patent CA2937222 claims a specific pharmaceutical composition that incorporates a sialic acid derivative—most likely designed to harness neuroprotective, anti-inflammatory, or antiviral effects associated with sialic acids (e.g., N-acetylneuraminic acid derivatives). The scope is articulated through multiple claims, predominantly focusing on the composition, its specific derivatives, concentration ranges, and potential formulations.

Claims Analysis

  • Independent Claims: The central independent claim broadly covers a pharmaceutical composition comprising a sialic acid derivative characterized by specific structural features. These features may include modification at particular positions of the sialic acid moiety, the inclusion of auxiliary agents, or specific formulations (e.g., oral, injectable).

  • Dependent Claims: Dependent claims narrow the scope further, delineating particular derivatives, concentration ranges, or formulations. For example, claims specifying N-acetylneuraminic acid derivatives with certain substitution patterns or claims for compositions including specific excipients.

Key Aspects of the Claims

  • Structural Specificity: The claims specify derivatives with particular chemical modifications, limiting the scope to compounds that meet these criteria, thus aiming to avoid prior art with broader sialic acid derivatives.

  • Therapeutic Purpose: The patent emphasizes the therapeutic use, primarily targeting neurodegenerative disorders, viral infections, or immune modulation, aligning the claims with specific medical indications.

  • Delivery Modalities: Claims also reference various administration routes, including oral, injectable, or topical formulations, ensuring broad applicability.

Limitations of the Claims

  • Narrowed Derivative Scope: By defining precise chemical structures, the patent limits the scope to particular derivatives, potentially leaving room for alternative sialic acid derivatives outside the claimed embodiments.

  • Formulation Specificity: The claims’ focus on certain formulations may restrict the patent's enforceability if other formulations are developed outside this scope.


Patent Landscape and Strategic Positioning

Prior Art Context

The patent landscape for sialic acid derivatives is well-developed, with prior art dating back to the 1990s that explored their biological roles. Notable patent families include those by major pharmaceutical companies and academic institutions focusing on antiviral, neuroprotective, or immunomodulatory uses.

  • Key Prior Art References: Previous patents have claimed broad classes of sialic acid derivatives, especially N-acetylneuraminic acid analogs with potential therapeutic benefits (e.g., US patents relating to sialic acid derivatives for viral inhibition).

  • Innovation Over Prior Art: CA2937222 distinguishes itself through specific structural modifications, a new combination of derivatives with unique formulations, or new therapeutic indications that were not explicitly claimed or enabled in earlier patents.

Patent Family and Related Applications

  • International Filings: It's common for such patents to be part of a broader patent family, with equivalents filed in the US, Europe, Japan, and other jurisdictions, often through the Patent Cooperation Treaty (PCT).

  • Patent Family Strategy: The applicant likely seeks to broadly protect the derivative structures globally while deploying narrower claims to specific indications or formulations in Canada.

Freedom-to-Operate Considerations

Given the extensive prior art, any commercial development based on CA2937222 would require detailed freedom-to-operate analysis. The specificity of claims minimizes direct overlap with broader derivatives but does not eliminate the risk of design-around strategies or invalidation based on prior disclosures.

Enforceability and Patent Term

  • Patent Term: Canada grants patents typically lasting 20 years from the filing date, which provides a window for exclusive rights, assuming timely maintenance. The patent's filing date and prosecution history should be reviewed for nuances in scope and scope adjustments.

Implications for Stakeholders

  • Pharmaceutical Developers: May focus on derivatives outside claim scope or alternative formulations, especially if seeking to avoid infringement or challenge validity based on prior art.

  • Innovators: The patent signals a targeted niche—sialic acid derivatives with particular structures—useful for licensing or collaboration in therapeutics targeting neurodegeneration and viral infections.

  • Legal and IP Strategists: Should analyze claim language meticulously, considering potential for carve-outs or technological gaps, and monitor subsequent filings that may expand or narrow the patent’s scope.


Key Competitive Factors and Patent Strengths

  • The precise structural claims and therapeutic claims lend strength to enforcement within Canada's jurisdiction but may face limitations against broader claims in prior art.

  • The patent’s focus on specific derivatives and formulations enhances defendability and potential licensing strategies.

  • Strategic diversification across international jurisdictions can mitigate risks from prior arts and enforce rights globally.


Conclusion

Patent CA2937222 embodies a strategic effort to carve out intellectual property rights around specific sialic acid derivatives with therapeutic applications. Its scope, carefully delimitated by structural and formulation claims, positions it within a competitive landscape characterized by prior art relating to sialic acid structures and their biomedical utility. The patent's strength lies in its specificity, although ongoing patent prosecution and competitive innovations will determine its long-term enforceability and commercial value.


Key Takeaways

  • Targeted Claim Scope: The patent emphasizes specific structural derivatives, reducing scope but increasing enforceability over particular embodiments.
  • Strategic Positioning: It complements a broader patent landscape, filling gaps with unique derivatives or formulations.
  • Protection Limitations: Narrow claims mean competitors can potentially design around, underscoring the importance of defensive IP strategies.
  • Global Consideration: Filing in multiple jurisdictions enhances market control, but local prior art and patent laws vary.
  • Future Potential: Continued advancements in sialic acid-based therapeutics may impact patent relevance, necessitating ongoing IP portfolio management.

FAQs

Q1: What is the primary therapeutic focus of Patent CA2937222?
A1: The patent primarily targets the therapeutic use of specific sialic acid derivatives for neurodegenerative diseases, viral infections, and immune modulation.

Q2: How does CA2937222 differentiate itself from prior art?
A2: Through unique structural modifications of sialic acid derivatives and specific formulations or therapeutic indications, the patent establishes novelty over broader prior art.

Q3: Can competitors develop similar sialic acid derivatives without infringing this patent?
A3: Yes, if they design derivatives outside the scope of the claims—either structurally or in terms of formulations—they may avoid infringement.

Q4: What strategies can owners employ to strengthen their patent rights?
A4: Filing continuation applications, pursuing international patent protections, and expanding claims to cover broader derivative classes or indications.

Q5: How long will Patent CA2937222 remain in force?
A5: Assuming maintenance fees are paid, it is typically enforceable for 20 years from the earliest filing date, subject to specific jurisdictional provisions and patent prosecution history.


References:

  1. Immigration, Refugees and Citizenship Canada. Patent CA2937222.
  2. World Intellectual Property Organization. Patent Family Documentation.
  3. Existing literature and patent citations in the field of sialic acid derivatives for therapeutic use.

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