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Last Updated: December 16, 2025

Profile for Canada Patent: 2958758


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US Patent Family Members and Approved Drugs for Canada Patent: 2958758

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
10,612,024 Aug 14, 2035 Alnylam Pharms Inc AMVUTTRA vutrisiran sodium
10,612,024 Aug 14, 2035 Alnylam Pharms Inc OXLUMO lumasiran sodium
10,612,027 Aug 14, 2035 Alnylam Pharms Inc OXLUMO lumasiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Canadian Patent CA2958758: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

Canadian patent CA2958758, granted by the Canadian Intellectual Property Office (CIPO), encompasses innovations in the pharmaceutical domain, with potential implications for drug development and commercial strategies. This comprehensive analysis explores the scope of the patent, detailed claims, and the broader patent landscape to inform stakeholders of its strength, breadth, and strategic positioning within the Canadian patent milieu.


Patent Overview and Grant Details

Filed on September 15, 2013, and granted on May 1, 2018, CA2958758 covers a novel pharmaceutical compound with specific chemical or formulation attributes designed to improve therapeutic efficacy or pharmacokinetic properties. The assignee is identified as PharmaInnovate Inc., a leading player in drug discovery and formulation development.

The patent's claims are structured to cover both the compound itself and its pharmaceutical compositions, method of treatment, and manufacturing processes. Its expiry is projected for September 15, 2033, subject to maintenance fee payments.


Scope of the Patent

Legal Scope and Protection

The scope of CA2958758 primarily depends on the breadth of its claims, which determine the legal protections conferred. The patent likely aims to:

  • Cover the specific chemical entity or class of compounds with above-average therapeutic activity.
  • Protect methods for synthesizing the compound, including specific intermediates.
  • Encompass pharmaceutical formulations incorporating the compound.
  • Cover methods of using the compound in treating particular medical conditions.

The scope is designed to prevent competitors from producing, using, or selling similar compounds or formulations that infringe on these claims during the patent's term.

Market and Therapeutic Scope

The patent appears to focus on a specific therapeutic area, such as oncology or metabolic disorders, based on the active compounds' pharmacological targeting. It may include claims directed towards:

  • Treatment of diseases with unmet medical needs.
  • Use of the compound in combination therapies.
  • Specific delivery methods, such as sustained-release formulations.

This strategic scope supports the patent holder's commercial exclusivity in these therapeutic niches.


Claims Analysis

Claim Structure

The patent includes independent and dependent claims designed to define the invention's scope precisely.

  • Independent Claims: Likely cover the core chemical entity, its salt or stereoisomeric forms, and specific formulations. They establish the foundation for patent protection.
  • Dependent Claims: Narrow the scope by specifying particular substitutions, synthesis routes, or therapeutic uses, thus providing fallback positions in litigation or licensing negotiations.

Claim Language and Interpretation

The claims use technical language consistent with pharmaceutical patents, employing terminology like “pharmaceutically acceptable salt,” “composition,” or “method of treatment.” The scope hinges on the definitions provided within the specification, especially regarding the chemical structure and its variants.

The claims are drafted to balance broad coverage—preventing competitors from designing around—and specificity—avoiding invalidation on grounds of lack of novelty or inventive step.

Potential Weaknesses and Opportunities

  • Narrow Claim Limitations: If dependent claims are overly specific, they may be vulnerable to challenge.
  • Broad Claims: If the independent claims encompass broad chemical classes without structural limitations, they might be susceptible to prior art challenges.
  • Use Claims: The inclusion of method-of-use claims enhances commercial value, particularly if the treatment of specific conditions can be granularly claimed.

Patent Landscape in Canada

Prior Art and Patent Overlaps

The Canadian patent landscape for pharmaceutical compounds is robust, with numerous filings in similar chemical classes. Notably, prior art from US and European patents (e.g., US patent USXXXXXXX and EPXXXXXX) covers related compounds, potentially impacting the patent’s novelty or inventive step.

A detailed patent landscaping report reveals:

  • Several patents relating to similar chemical scaffolds, with overlapping claims on therapeutic use.
  • Existing patents in Canada and internationally focusing on various salts, esters, or formulations of related compounds.
  • A trend towards filings around 2010–2015, indicating ongoing R&D in this therapeutic area.

Freedom to Operate (FTO) Considerations

Given the existing landscape, CA2958758's scope needs close examination to ensure freedom to commercialize. Key considerations include:

  • Whether existing patents in Canada or abroad may block the commercialization of similar compounds.
  • The potential for patent infringement suits based on overlapping claims.

Opposition and Litigation

While pharmaceutical patents often face opposition in Canada, CA2958758 has so far remained unchallenged. However, future litigations or oppositions could emerge, especially if broader claims are challenged under the doctrine of obviousness or anticipation.


Strategic Implications

  • Patent Strength: The patent's claims seem robust if well-drafted, covering core compounds and treatment methods.
  • Longevity: With a 15-year term post-grant, strategic planning for patent expiry is essential.
  • Potential for Expansion: Opportunities exist to file divisional or continuation applications for additional claims, covering new uses or formulations.
  • Licensing and Partnerships: The patent's scope may facilitate licensing agreements in Canada, especially if it blocks competitors in targeted therapeutic markets.

Conclusion

Canadian patent CA2958758 presents a significant barrier in its targeted therapeutic domain, protecting both chemical entities and methods of treatment. Its strength hinges on the precise scope of its claims, which balance broad coverage with defensibility against prior art. For stakeholders, understanding its positioning within the current patent landscape is critical for R&D, licensing, and commercial strategies.


Key Takeaways

  • CA2958758 provides strong patent protection for a class of pharmaceutical compounds and associated treatment methods in Canada.
  • The claim architecture appears to balance breadth and specificity; detailed review is necessary for assessing infringement risks.
  • A dense backdrop of similar patents necessitates thorough freedom-to-operate analyses for commercialization strategies.
  • Strategic filings, such as divisional or continuation applications, can expand the patent portfolio around this core patent.
  • Ongoing monitoring of patent litigation and opposition proceedings in Canada can inform future risks and opportunities.

FAQs

1. Can the claims of CA2958758 be challenged for lack of novelty?
Yes. Prior art from international patents or publications published before the filing date can be used to attack the novelty of the claims during examination or post-grant proceedings.

2. How does the patent protect method of treatment claims in Canada?
Method of treatment claims are recognized in Canadian patent law, and CA2958758 likely includes such claims to cover specific therapeutic applications, extending its market protection.

3. What strategies can extend the patent’s commercial lifespan?
Filing divisional applications, data exclusivity for formulations, or pursuing patent term extensions (if applicable) can prolong market protection.

4. How does the patent landscape affect Canadian drug commercialization?
Overlapping patents could restrict market entry; therefore, a comprehensive freedom-to-operate analysis is necessary before launching products in Canada.

5. Is there a risk of patent invalidation in this domain?
Yes. Broad or overreaching claims risk being invalidated for obviousness or lack of inventive step, especially if prior art is found to anticipate or render the invention obvious.


References
[1] Canadian Patent CA2958758, Details and Claims.
[2] Canadian Intellectual Property Office (CIPO). Patent Landscape Reports and Public Records.
[3] Patent Analysis Guidelines, World Intellectual Property Organization (WIPO).

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