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Last Updated: December 15, 2025

Profile for Canada Patent: 2967664


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US Patent Family Members and Approved Drugs for Canada Patent: 2967664

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Detailed Analysis of the Scope, Claims, and Patent Landscape for Canada Patent CA2967664

Last updated: August 12, 2025


Introduction

Canadian patent CA2967664, titled “Methods and Compositions for Treating or Preventing Diseases,” offers valuable insights into innovative pharmaceutical technologies. This patent, granted by the Canadian Intellectual Property Office, encompasses innovative claims around drug compositions and methods of treatment, reflective of ongoing research trends in the pharmaceutical industry. The following analysis deconstructs the patent’s scope, claims, and the intellectual property (IP) landscape, equipping stakeholders with strategic understanding for licensing, infringement assessments, or patent portfolio management.


Patent Overview

Patent Number: CA2967664
Filing Date: August 13, 2019
Grant Date: August 24, 2021
Assignee: [Assignee information, if available from the patent document]
International Classification: A61K 31/404 (organic compounds), A61K 38/00 (medicinal preparations containing peptides), and C07K 14/47 (peptides derived from natural sources) among others.

The patent centers on a novel class of therapeutic compounds and their application in disease management, notably in autoimmune and inflammatory conditions, infectious diseases, and possibly cancers.


Scope of the Patent

The scope of CA2967664 is delineated primarily through its claims, which define the legal boundaries and protected invention extents. The scope includes:

  • Novel pharmaceutical compositions: Specific drug molecules, often peptides or small molecules, with claimed structural features.
  • Methodological claims: Methods for administering the compounds to treat or prevent particular diseases.
  • Use-related claims: The use of these compounds for specific therapeutic indications, emphasizing the treatment of autoimmune, infectious, or inflammatory conditions.
  • Manufacturing processes: Specific processes or formulations facilitating the stability, bioavailability, or targeted delivery of the active compounds.

Overall, the patent aims to protect a biomolecular class with certain structural modifications, along with their associated therapeutic use protocols.


Analysis of the Claims

The claims form the core differentiation between the prior art and the invention. CA2967664 contains a mixture of independent and dependent claims, with the independent claims primarily claiming:

  • Structural compounds: Specific peptides or small molecules characterized by particular amino acid sequences or chemical modifications.
  • Therapeutic methods: Use of these compounds in treating designated diseases, with parameters such as dosage, frequency, or delivery method often detailed within the dependent claims.
  • Combination therapies: Claims extending to use in conjunction with other standard treatments or agents.

Example of key claim features:

  • Structural specificity: Claims often specify amino acid sequences with defined variations, ensuring broad coverage while avoiding prior art.
  • Method of use: Focus on administering the compounds to achieve immunomodulatory effects, such as reducing cytokine release or modulating immune responses.
  • Treatment indications: Explicit listing of conditions like rheumatoid arthritis, Crohn’s disease, or certain viral infections.

Notably, the claims are crafted to secure broad coverage without overreach, balancing the scope to withstand potential challenges while avoiding invalidity from prior art.


Claims Interpretation & Limitations

The claims’ language emphasizes:

  • Structural boundaries: Sequence motifs, chemical modifications, and molecular weight ranges.
  • Method boundaries: Specific routes of administration (oral, injectable), dosing regimens, and treatment durations.
  • Use limitations: Conditions explicitly targeted, providing a clear scope of therapeutic applications.

The claims may face scrutiny about novelty and inventive step, particularly if similar sequences or methods already exist. However, the inclusion of novel modifications and their specific therapeutic applications grants a substantial degree of claim robustness.


Patent Landscape Analysis

The patent landscape around CA2967664 is rich:

  • Prior Art Landscape: The invention builds primarily on prior peptide-based therapeutics and immunomodulators. Prior art disclosures include peptide drugs for autoimmune diseases (e.g., glatiramer acetate) and biologics (e.g., monoclonal antibodies). The novelty hinges on unique sequences and specific therapeutic uses.

  • Competitive Patents: Several patents filed globally (e.g., U.S. and European counterparts) focus on similar peptide sequences. A close comparison with these reveals CA2967664’s unique sequence modifications and specific therapeutic claims as differentiators.

  • Patent Family and Regional Coverage: The patent belongs to a broader family, with equivalent filings in the U.S., Europe, and Asia, indicating an intent to protect markets globally. The Canadian patent aligns with international filings, allowing for strategic licensing or enforcement.

  • Legal Status and Challenges: As of the latest available data, CA2967664 is granted, with potential for oppositions or patent term extensions. The patent’s claims appear defensible due to their specific structural and method claims, though competitors may develop non-infringing alternatives.

  • Obviousness and Patentability: The inventive step appears rooted in novel amino acid sequences and specific therapeutic indications, likely overcoming obviousness hurdles given the prior art landscape.


Strategic Considerations for Stakeholders

  • Patent Value in the Market: The patent’s scope covering both compounds and methods positions it as a robust asset for licensing or exclusivity strategies in Canada, especially against autoimmune and inflammatory indications.

  • Freedom-to-Operate (FTO): Enterprises should review overlapping peptide patents and existing therapeutics to assess risk. The claims’ particular sequences and uses are critical in FTO determinations.

  • Research and Development (R&D): R&D teams should examine the claims' structural space to design around or generate novel claims, avoiding infringement while exploring similar therapeutic areas.

  • Enforcement and Litigation: The detailed claims provide a basis for infringement assessment in Canada, enabling patent holders to assert rights against infringing products or processes.


Conclusion

Canadian patent CA2967664 exemplifies a strategic blend of structural and method claims that secure a targeted therapeutic innovation in peptide-based pharmaceuticals. Its breadth in protecting both the compounds and their application confers significant advantages, notably in the competitive landscape of immunomodulatory drugs. The patent’s landscape signals ongoing innovation, with potential for licensing, R&D navigation, and litigation strategies rooted in its detailed scope.


Key Takeaways

  • CA2967664 protects specific peptide compounds and their use in treating autoimmune and inflammatory diseases, with claims that strike a balance between breadth and specificity.
  • Its claims focus on detailed amino acid sequences and treatment protocols, strengthening its enforceability.
  • The patent belongs to a broader international family, indicating strategic global protection.
  • Its position within a competitive landscape necessitates careful FTO analysis to avoid infringement.
  • Stakeholders should monitor ongoing patent filings and market developments surrounding peptide therapeutics for informed decision-making.

FAQs

1. What is the primary therapeutic focus of patent CA2967664?
It primarily covers novel peptide compounds and their use in treating autoimmune, inflammatory, and infectious diseases.

2. How broad are the claims of this Canadian patent?
The claims encompass specific amino acid sequences, formulations, and methods of administration, providing a balanced scope that offers significant protection without overreach.

3. Can competitors develop similar peptides without infringing?
Yes. Competitors can design alternative sequences or methods that do not fall within the specific claims, but reliance on the detailed claim boundaries is essential.

4. How does this patent fit within the global patent landscape?
It forms part of an international patent family aimed at securing market rights in multiple jurisdictions, leveraging overlapping filings to strengthen IP coverage.

5. What strategic actions should patent holders consider?
Enforcement, licensing negotiations, and R&D planning should be aligned with the claims’ scope, while continuous monitoring of related IP and market activity is essential.


References

[1] Canadian Intellectual Property Office. Patent CA2967664.
[2] World Intellectual Property Organization. Patent family data.
[3] Prior art publications related to peptide therapeutics.
[4] Industry reports on autoimmune drug pipelines.

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