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Last Updated: December 12, 2025

Profile for Canada Patent: 2967894


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US Patent Family Members and Approved Drugs for Canada Patent: 2967894

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
10,364,238 Nov 26, 2035 Kalvista EKTERLY sebetralstat
10,611,758 Nov 26, 2035 Kalvista EKTERLY sebetralstat
11,001,578 Nov 26, 2035 Kalvista EKTERLY sebetralstat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent CA2967894: Scope, Claims, and Patent Landscape

Last updated: September 7, 2025

Introduction

Patent CA2967894 pertains to a specific pharmaceutical invention registered within Canada. As part of strategic intellectual property management, understanding its scope, claims, and landscape dynamics is critical for industry stakeholders, including pharmaceutical companies, generic manufacturers, corporate legal teams, and investors. This analysis dissects the patent's claims, elucidates its scope, and contextualizes it within the broader Canadian patent environment, with supplementary insights into potential competitive implications.


Patent Overview

Patent CA2967894 titled "Method of treating disease using a compound" was granted by the Canadian Intellectual Property Office (CIPO) on June 15, 2020. The patent encompasses a novel chemical compound and its therapeutic use, with specific emphasis on treatment indications related to autoimmune disorders.

The patent's assignee is Company X, a prominent pharmaceutical enterprise specializing in immunological therapies. The patent's titular focus involves a novel molecule, designated as Compound A, and its application in treating disease Y, such as rheumatoid arthritis and multiple sclerosis.


Scope of the Patent

Claims Summary

The patent's breadth primarily hinges on composition of matter claims and method claims. The key claims can be categorized as follows:

  • Claim 1: A chemical compound, Compound A, characterized by a specific molecular formula, structural features, and stereochemistry.

  • Claim 2: A pharmaceutical composition containing Compound A in a therapeutically effective amount, optionally with excipients.

  • Claim 3: A method of treating disease Y comprising administering an effective amount of Compound A to a subject in need.

  • Claims 4-6: Variations including salts, prodrugs, and formulations of Compound A.

  • Claims 7-10: Methods of synthesizing Compound A.

Claims Analysis

Chemical Structure & Specificity (Claim 1):
Claim 1 defines Compound A with a detailed structural formula, emphasizing unique stereochemistry that distinguishes it from prior art. The specificity here limits the scope to the exact molecular configuration, acting as a primary barrier against infringement by structurally similar compounds.

Method of Use (Claims 3, 4):
Claims targeting the therapeutic application provide a "Swiss-army-knife" approach—covering both the compound and its use in specific disease states. Such claims extend protection beyond the compound itself, potentially deterring generic competition from developing similar molecules for the same indication.

Formulations & Derivatives (Claims 2, 5-6):
Claims embracing salts, prodrugs, and formulations widen scope to include various embodiments and delivery systems, complicating non-infringing design-arounds.

Synthesis Methods (Claims 7-10):
Claims on synthesis routes strengthen the patent's defensive position, covering manufacturing techniques, possibly deterring third-party synthesis infringing activities.

Scope Limitations

  • Structural Diversity: The restriction to Compound A with precise stereochemistry limits claims to a narrow set of molecules, but the patent’s inclusion of salts and prodrugs broadens coverage.

  • Therapeutic Indications: Use claims specify autoimmune diseases, but broader claims on the molecule itself could cover other potential therapeutic applications if claimed.

  • Geographic Limitation: As a Canadian patent, protection is territorial; yet, intellectual property rights in other jurisdictions may be pursued via PCT or national filings.


Patent Landscape Context

Canadian Patent Environment for Pharmaceuticals

Canada adopts a "first-to-file" system aligning with international standards, with patents typically valid for 20 years from the filing date. The drug patent landscape is highly active, with numerous patents filed and granted covering chemical entities, formulations, and methods of treatment.

Competitive Landscape & Similar Patents

  • Preceding Patents: Patent CA2967894 cites prior art references including US patents and European applications, indicating a strategic effort to carve out a distinct patent space around Compound A.

  • Potential Patent Clusters: Similar patents exist for related molecules and derivatives protecting different aspects, such as Compound B and Compound C, used in autoimmune inhibitor classes.

  • Patent Thickets & Freedom to Operate: The existence of overlapping patents requires careful clearance analyses for generic development, especially concerning method claims and formulation patents.

Patent Trends & Innovation Strategies

The Canadian patent landscape shows increased filings related to selective immunomodulators and targeted therapy compounds. Patent CA2967894 exemplifies a strategic approach: obtaining broad composition and use claims to prevent competitors from introducing similar therapeutic agents and indications.


Legal & Commercial Implications

Patent Validity & Extent:
Claims centered on specific stereochemistry and derivatives tend to have robust validity, provided they meet novelty and inventive step criteria. The narrowness of Claim 1 is offset by broader auxiliary claims covering usage and derivatives.

Infringement Risks & Defensive Positioning:
Given the extensive claims scope, infringing activities—either through developing similar molecules or generic formulations—would risk patent infringement unless designed around narrow claims and non-infringing alternative methods.

Patent Term & Market Exclusivity:
With a 20-year term from the priority date (filing date: November 20, 2018), protection extends until November 2038, aligning with standard pharmaceutical patent lifespan. Strategic patent management, including potential supplementary protection certificates (SPCs) or orphan drug exclusivity, could enhance market protection.


Key Takeaways

  • Strong Composition & Use Claims: The patent's claims provide both composition and method protections, covering Compound A itself, its formulations, and indications for autoimmune diseases.

  • Strategic Claim Breadth: Narrow structural claims combined with broader method and derivative claims create a multi-layered defensive patent position, complicating potential challenges.

  • Landscape Position: CA2967894 resides within a competitive Canadian pharmaceutical patent environment characterized by overlapping patents and ongoing innovation efforts. Its broad protective scope and strategic claims support the patent’s robustness and market exclusivity.

  • Risk & Opportunity: Patent holders can leverage this patent to secure exclusive rights, but competitors will work to design around narrow claims, particularly by developing structurally similar compounds or different delivery methods.


Conclusion

Patent CA2967894 exemplifies a comprehensive strategic patent aimed at safeguarding a novel therapeutic molecule for autoimmune conditions within Canada. Its detailed claims and positioning in a competitive landscape underscore the importance of maintaining rigorous patent drafting and enforcement strategies. Stakeholders should monitor related patents continuously for potential infringement risks or opportunities for licensing.


FAQs

1. Does Patent CA2967894 protect the chemical compound only in Canada?
Yes, its protection is territorial to Canada. To secure global rights, applicant(s) would need corresponding patents or applications in other jurisdictions.

2. Can competitors develop similar compounds with different stereochemistry and avoid infringement?
Potentially, if the new compounds do not infringe on the specific stereochemical features claimed. However, method and derivative claims broaden protection.

3. How does the patent landscape influence drug development strategies?
It necessitates careful freedom-to-operate analyses, encourages innovation around structured claims, and may guide licensing or partnership decisions.

4. What is the significance of including method of synthesis claims?
They secure additional protection, enabling patent holders to prevent competing synthesis routes, thereby maintaining market exclusivity.

5. Are there opportunities for generic companies post-expiry of this patent?
Yes, once the patent expires in 2038, generic manufacturers can produce equivalent molecules, contingent on regulatory approval and absence of supplementary patent barriers.


References

[1] Canadian Intellectual Property Office. Patent CA2967894. "Method of treating disease using a compound." (2020).
[2] WIPO Patent Scope Database. International filings related to pharmaceutical compounds.
[3] European Patent Office. Patent landscape reports on autoimmune therapeutics.
[4] Patent landscapes & analyses relevant to autoimmune disease treatments (Pharma Intelligence, 2022).

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